Next Article in Journal
Waddlia chondrophila and Male Infertility
Previous Article in Journal
Doing More with Less: A Comparison of 16S Hypervariable Regions in Search of Defining the Shrimp Microbiota
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Listeriosis Outbreak in South Africa: A Comparative Analysis with Previously Reported Cases Worldwide

by
Christ-Donald Kaptchouang Tchatchouang
1,
Justine Fri
1,
Mauro De Santi
2,3,
Giorgio Brandi
2,3,
Giuditta Fiorella Schiavano
3,
Giulia Amagliani
2 and
Collins Njie Ateba
1,4,*
1
Department of Microbiology, North-West University, Mafikeng Campus, Private Bag X2046, Mmabatho 2735, South Africa
2
Department of Biomolecular Sciences, University of Urbino Carlo Bo, via S. Chiara 27, 61029 Urbino (PU), Italy
3
Department of Humanities, University of Urbino Carlo Bo, via Bramante 17, 61029 Urbino (PU), Italy
4
Food Security and Safety Niche Area, Faculty of Natural and Agricultural Sciences, North-West University, Mafikeng Campus, Mmabatho, Mafikeng 2735, South Africa
*
Author to whom correspondence should be addressed.
Microorganisms 2020, 8(1), 135; https://doi.org/10.3390/microorganisms8010135
Submission received: 22 November 2019 / Revised: 26 December 2019 / Accepted: 27 December 2019 / Published: 17 January 2020
(This article belongs to the Section Food Microbiology)

Abstract

:
Listeria species are Gram-positive, rod-shaped, facultative anaerobic bacteria, which do not produce endospores. The genus, Listeria, currently comprises 17 characterised species of which only two (L. monocytogenes and L. ivanovii) are known to be pathogenic to humans. Food products and related processing environments are commonly contaminated with pathogenic species. Outbreaks and sporadic cases of human infections resulted in considerable economic loss. South Africa witnessed the world’s largest listeriosis outbreak, characterised by a progressive increase in cases of the disease from January 2017 to July 2018. Of the 1060 laboratory-confirmed cases of listeriosis reported by the National Institute of Communicable Diseases (NICD), 216 deaths were recorded. Epidemiological investigations indicated that ready-to-eat processed meat products from a food production facility contaminated with L. monocytogenes was responsible for the outbreak. Multilocus sequence typing (MLST) revealed that a large proportion (91%) of the isolates from patients were sequence type 6 (ST6). Recent studies revealed a recurrent occurrence of small outbreaks of listeriosis with more severe side-effects in humans. This review provides a comparative analysis of a recently reported and most severe outbreak of listeriosis in South Africa, with those previously encountered in other countries worldwide. The review focuses on the transmission of the pathogen, clinical symptoms of the disease and its pathogenicity. The review also focuses on the major outbreaks of listeriosis reported in different parts of the world, sources of contamination, morbidity, and mortality rates as well as cost implications. Based on data generated during the outbreak of the disease in South Africa, listeriosis was added to the South African list of mandatory notifiable medical conditions. Surveillance systems were strengthened in the South African food chain in order to assist in preventing and facilitating early detection of both sporadic cases and outbreaks of infections caused by these pathogens in humans.

1. Introduction

Listeria was reported for the first time in 1924 by Murray and colleagues due to the sudden deaths of six young rabbits and was named Bacterium monocytogenes [1]. Subsequently, in 1927, Pirie named the bacterium Listerella hepatolytica in honour of Sir Joseph Lister, a pioneer in the field of antisepsis after successfully isolating it from the liver of several gerbils (Latera lobenquiae) in South Africa [2]. In 1929, three patients suffered from infectious-mononucleosis, due to Listeria and were the first confirmed human cases in Denmark [3]. In 1940, the name Listeria monocytogenes was finally adopted to harmonise the nomenclature of the bacterium.
Listeria species are Gram-positive, catalase positive, oxidase negative and facultative anaerobic bacteria. Morphological identification presents cells as chains or single rods, non-sporulating, possessing peritrichous flagella, with a tumbling motility [4]. Listeria measures approximately 0.5 µm in diameter and 1–2 µm in length. The genus is classified under the family Listeriacaeae, which comprises 17 species, including L. monocytogenes, L. ivanovii, L. seeligeri, L. innocua, L. welshimeri, L. grayi, and the more recently characterised L marthii, L. rocourtiae, L weihenstephanensis and L. fleischmannii, L. floridensis, L. aquatica, L. cornellensis, L. riparia, L. grandensis, L. booriae and L. newyorkensis [5,6]. Listeria are capable of tolerating up to 10% salt, pH of 6–9 and temperatures of 0–45 °C with an optimal temperature range of 30–37 °C [7,8]. Listeria species are widespread in nature; however, among them, L. monocytogenes and L. ivanovii are human pathogens, causative agents of listeriosis [9,10]. Listeriosis caused by L. monocytogenes is a severe disease with a mortality rate of 20–30% [11]. This foodborne disease affects numerous individuals worldwide with a high fatality rate [1].
The pathogen is a major threat to the food industry as it can survive and proliferate in extreme conditions such as high salinity, acidity, and refrigeration temperatures [12]. Due to its ubiquitous and widespread nature, it was found in diverse natural environments such as plants, soil, silage, animals, sewage, and water. Contaminated food such as vegetables, dairy products, red meat, poultry, and seafood are implicated as sources of infection [13,14]. Sporadic and epidemic incidents of listeriosis were reported due to the consumption of ready-to-eat (RTE) foods, dairy products, seafood, pre-cooked or frozen meat, pork, and fresh produce. In the modern, fast-paced lifestyle, the population is consuming more RTE and ready-to-cook food products that entail minimal processing [15,16]. There is, therefore, a high risk of food contamination, which can cause severe clinical health effects in humans.

2. Potential Sources of Contamination with Listeria Species

Listeria monocytogenes is the causative agent of multiple outbreaks of listeriosis worldwide [17] associated with a variety of foods, such as milk and other dairy products, vegetables, salads, meat products and ready-to-eat foods (i.e., smoked salmon). Outbreaks caused by contaminated fishery products were also reported [18]. Poor manufacturing practices might result in food contamination by this pathogenic bacterium in the food supply chain [19]. A previous report showed that factors such as poor sanitary practices, contaminated processing environments and temperature abuse during overstay storage in retail outlets led to Listeria-contaminated vacuum-packed (VP) smoked fish products [20]. Numerous organisations worldwide such as World Health Organisation (WHO), Food and Agricultural Organisation (FAO) and Codex Alimentarius, among others have been applying the policy of “Zero Tolerance” for L. monocytogenes in RTE processed foods to reduce the high risk of food contamination and, consequently, reducing the spread of infection to the public [21,22]. Listeria is widely dispersed in nature and was isolated from soil, plants, sewage, and water [23]. From these sources, the bacterium can propagate, disseminate and contaminate food products, a source of infection to animals and humans. Due to the severity of the disease, stringent procedures must be established to detect the critical control point where contamination is at its maximum level. It is worthy to note that approximately 20–30% of both sporadic and outbreak L. monocytogenes cases are fatal [24,25].

3. Transmission of the Disease

The reservoirs of infection are the soil and the intestinal tracts of asymptomatic animals, such as wild and feral mammals, birds, fish, and crustaceans [26]. Infected animals can shed L. monocytogenes in their faeces [27], milk [28] and uterine discharges [29]. It is also found in aborted foetuses and, occasionally, in the nasal discharges and urine of symptomatic animals [30]. Soil or faecal contamination results in its presence in plants and silage [13]. Most infections are acquired through ingestion; however, Listeria can also be spread by inhalation or direct contact [31]. Venereal transmission might also be possible [32]. In ruminants, listeriosis typically occurs after the consumption of contaminated silage or other feed [33]. For humans, contaminated sources of food include raw meat and fish, unpasteurised dairy products and uncooked vegetables. L. monocytogenes has also been found in foods contaminated after processing, particularly soft cheeses, deli cold cuts, sliced or grated cheese and ice cream. The infective dose for oral transmission is unknown but it is thought to depend on the bacterial strain and the host susceptibility [34,35]. Processed food may get contaminated during the production process from the raw product to the final consumer. Due to the significant increase in the level of contamination and the risk of exposure of food to L. monocytogenes, food security and safety is of global concern [36]. Emphasis is now placed on the negligence of food production/processing facilities and rethinking consumer habits towards the consumption of convenient foods [37]. A major issue facing the chain of production is the fact that the Listeria pathogen can survive under low-temperatures, resulting in increased cases and high mortality rates due to the infection. It is worth mentioning that listeriosis due to L. monocytogenes, is not only prominent in humans but also life-threatening with various lethal symptoms [34,38]. Healthy people seem to consume most Listeria-contaminated foods without any clinical signs; however, in susceptible persons, the infective dose is probably about 10–100 organisms [39,40]. Vertical transmission is the usual source of infection in newborn human infants and ruminants; infections are transmitted either transplacentally or from an infected birth canal. Humans can also be infected by direct contact with infected animals during calving, lambing or necropsies. Cases were reported after contact with sick birds or the carcasses of asymptomatic poultry [41,42]. L. monocytogenes is relatively resistant to freezing, drying and heat. It will grow at temperatures from 1 °C to 45 °C and can even proliferate at refrigeration temperatures on contaminated foods. It can tolerate a pH from 3.6 to 9.5 and a sodium chloride content of up to 10%. A pH of greater than 5 (e.g., in spoiled silage) favours the growth of this organism; however, it has also been found in silage with a pH less than 4 [43,44,45].

4. Clinical Signs and Symptoms of Listeriosis

Listeriosis is a fatal infection that mostly affects pregnant women, newborns, the elderly and immunocompromised or debilitated hosts. In symptomatic individuals, common symptoms include diarrhoea, abdominal pain, fever, vomiting, mild and flu-like illness. Pregnant women may also experience chills, headache, slight dizziness, or gastroenteritis [46,47,48]. Sepsis (bacteraemia) in pregnant women may eventually lead to abortion, stillbirth, premature birth, or septicemia in the newborn. L. monocytogenes infection might result in side-effects on the central nervous system, such as encephalitis, rhombencephalitis (brainstem encephalitis), or focal signs suggestive of brain abscess formation [49]. Although common symptoms of relatively mild gastroenteritis are observed in healthy adults, it is severe in immune-compromised patients. Complication of the disease may result in meningitis, meningoencephalitis, or septicemia, with immune-suppressed individuals highly at risk [50].

4.1. Asymptomatic Carriage of L. monocytogenes

Listeria colonises at least 1–5% of healthy adults. Moreover, every year, humans experience multiple exposures to persons with transient carriage of the pathogen [47]. Research has shown that 2 out of 3 people experience episodes of faecal carriage, which takes less than 4 days and is asymptomatic. Approximately 20–25% of faecal carriage is displayed by people who come in contact with invasive Listeria disease [51].

4.2. Gastroenteritis Due to L. monocytogenes

Listeria-infected humans may experience gastroenteritis. There are several side-effects associated with gastroenteritis, such as fever (60–100% of cases), non-bloody diarrhoea (33–88%), arthromyalgia (20–100%) and headache (15–88%). Fever and vomiting are common in children with gastroenteritis, while diarrhoea and arthralgia are common in adults. The incubation period ranges from 6 hours to 10 days and the symptoms span from 1–3 days, although they can last for up to one week. Hospitalisation caused by gastroenteritis due to listeriosis is usually prominent in children and the elderly. Blood cultures from gastroenteritis patients may yield Listeria [52].

4.3. Listeriosis in Pregnancy

Listeriosis infection in pregnant women presents a serious side-effect because of its invasive nature. A previous study revealed the mean incubation period of listeriosis in pregnancy as 27.5 days, with a range of 17–67 days. Major side-effects include mild flu-like symptoms, with fever, backache, and headache, and some might lead to neonatal sepsis. Listeria infection in pregnancy usually occurs at the early stages, and the side-effects are observed during the third trimester. The disease often results in poorer neonatal outcomes. Serious side-effects associated with infections in pregnant women are spontaneous abortion, stillbirth, or preterm birth [53].

4.4. Neonatal Infections Due to L. monocytogenes

Listeria infection in neonates occurs through an endogenous transplacental transmission, inhalation of infected amniotic fluid, or following colonisation from the maternal gastrointestinal or vaginal carriage. A study revealed the isolation of Listeria pathogens from the genital tract and blood cultures of majority of mothers. The premature offspring experienced the onset of the disease within 36 hours, which represented transplacental neonatal infection. Neonates exhibited sepsis (90%), respiratory distress or pneumonia (40%), meningitis (25%) and, sometimes, with inflammatory granulomata (granulomatosis infantiseptica). The appearance of rash occurs with maculopapular or papulovesicular lesions on the trunk or extremities. Between 5–30 days postnatal period, the late-onset of the disease progresses and patients present the expansion of non-specific symptoms, sepsis and meningitis [54,55].

4.5. Bacteraemia Due to L. monocytogenes

Listeria monocytogenes can disseminate into the blood, leading to bacteraemia, one of the clinical presentations in some Listeria-infected persons. Bacteraemia due to Listeria might lead to gastroenteritis and, in most cases, associated with pregnancy or neonatal infection. Bacteremia in adults might be a clinical effect of HIV infection, chronic renal disease, steroid use, underlying malignancy, chemotherapy or age >65 years [56,57].

4.6. Meningitis Due to L. monocytogenes

Acute meningitis and encephalitis are considered to be some of the most severe symptoms of listeriosis. Other symptoms include rhomboencephalitis, which is the involvement of the midbrain, pons and/or cerebellum linked to cranial nerve involvement or cerebellar signs (ataxia, tremor), or the development of hemiparesis. The incubation period of meningitis is estimated to be 0–21 days, with an average of 10 days. Studies revealed that cases of neuroinvasive listeriosis, neck stiffness was found in 75% of cases, focal neurological signs in 30%, seizures in 30% and coma in 7%. Focal neurological symptoms comprised single or multiple cranial nerve involvement (most commonly the 6th and 7th cranial nerves), hemiparesis, ataxia, and aphasia [58,59].

5. Pathogenicity Factors and Virulence Potential

The pathogenicity of L. monocytogenes is due to the expression of different genes, which are responsible for its ability to penetrate, proliferate and spread in cells [60]. These capabilities are attributed to their inlAB internalisation locus, Listeria pathogenicity island-1 (LIPI-1), and hpt intracellular growth locus, respectively (Figure 1) [49]. InlAB internalisation locus encodes two surface proteins: InlA and InlB that bind their corresponding receptors on host cell surface through their Leucine-Rich Repeat (LRR) domains, i.e., InlA binds human E-cadherin, a calcium-dependent intercellular adhesion glycoprotein, while InlB binds hepatocyte growth factor receptor Met [61] and, together, mediate bacterial internalisation and invasion into host cells. LIPI-1 encodes a pore-forming toxin listeriolysin O (LLO) and two phospholipases C (PlcA and PlcB), which cooperate to lyse the phagocytic vacuole membrane of host cells [62]. The hpt intracellular growth locus encodes hexose-6-phosphate transporter and actin assembly inducing protein (ActA), which play an important role in intracellular bacterial growth, cell-to-cell spread and actin polymerisation [49].
The virulence of L. monocytogenes is mainly regulated by six genes (prfA, plcA, hly, mpl, actA and plcB) residing in PrfA-dependent virulent gene clusters and other virulence-related genes located outside this gene cluster [49]. Furthermore, L. monocytogenes carries a gene cluster of five genes termed stress survival islet 1 (SSI-1), contributing to the survival of cells under suboptimal conditions, including low pH and high salt concentrations especially within food environments [63].
The prfA virulent gene clusters of L. monocytogenes and L. ivanovii also contains a positive master-regulator that controls the expression of different virulence factors. In addition, these pathogenic strains possess the hlyA gene that encodes a 60-kDa sulfhydryl-activated pore-forming listeriolysin O (LLO) that is very essential for facilitating escape of invading bacterial cells from the phagosomes of host cells into the host cytosol. The LLO is, therefore, known to be the main virulence feature responsible for discharging bacterial cells from the primary and secondary intracellular vacuoles [64]. The species-specificity properties of the hlyA gene and the LLO makes them effective molecular identification targets for L. monocytogenes, especially in food samples [65], on-farm microbiological control initiatives [66], and for serological diagnosis of ovine listeriosis [67] as well as contamination in pregnant women [68]. On the other hand, the plcA and plcB code for phosphatidylinositol-specific phospholipase C and phosphatidylcholine phospholipase respectively that assist, can operate in concert to ensure lysis of host cell membranes [69]. Soni, Ghosh [64] state that virulent genes comprising members of the internalins protein family (inlA, inlB), encode cell wall proteins that are important for attachment and invasion of non-phagocytic host cells. These virulent genes can be expressed or repressed by a few environmental conditions, thus affecting the virulence of L. monocytogenes [70].

6. Antibiotic Resistance in Listeria monocytogenes

The first L. monocytogenes strains resistant to antimicrobials were detected in 1988 [72]. Since then, an increasing number of strains resistant to one or more antibiotics, isolated from humans, animals, food [73], such as food processing environments [74] and dairy farms [75], were reported in recent years.
Although L. monocytogenes are considered vulnerable to a wide range of antibiotics, intrinsic antibiotic resistance to first generation Quinolones, Fosfomycin, Monobactams and broad-spectrum Cephalosporins were described [76]. Moreover, clinical use of antibiotics contributed to the selection of resistant strains, particularly for antibiotics commonly used to treat listeriosis. β-lactams (Penicillin and Ampicillin), with or without Gentamicin, are the main antibiotics considered for the treatment of listeriosis; Vancomycin and Trimethoprim / Sulfamethoxazole can be used as alternative therapy for Penicillin-allergic patients [77].
Veterinary use of antimicrobials in food-producing animals, commonly administered for disease therapy, prophylaxis and as growth promoters, could also contribute to the emergence of resistant strains [78]. Antibiotic resistance and particularly multi-resistance represent public health problems since they may cause failure of therapeutic treatment. Therefore, monitoring changes in antibiotic resistance of L. monocytogenes due to the continuing emergence of resistant strains, particularly by integration of phenotypic and genotypic techniques, is needed.

7. Outbreak of Listeriosis

7.1. Outbreak of Listeriosis in the United States of America

In 1998, an outbreak occurred in 10 states linked to the consumption of hot dogs and possibly refrigerated, processed deli meat. Forty patients contaminated by a single strain, L.monocytogenes, were identified in early August 1998 from the States of Ohio (13 cases); New York (12); Tennessee, Massachusetts and West Virginia (three each); Michigan (two); Connecticut, Oregon, Vermont, and Georgia (one each). Out of the forty infected patients, information could only be accessed from 38 individuals comprising six newborns and 32 adults (median age: 69 years; range: 18–88 years) with 55% of patients female. Out of this number, deaths were recorded in one foetus and three elderly [79]. The same year, on 22 December, Bil Mar Food recalled the production lots EST P261 or EST 6911 of hot dogs and meat products that could be contaminated. This recall comprised the Ball Park, Bil Mar, Bryan Bunsize and Bryan 3-lb Club Pack, Grillmaster, Hygrade, Mr Turkey, Sara Lee Deli Meat and Sara Lee Home Roast brands [80].
Listeria monocytogenes was also isolated from 29 patients in 10 states between 17 May and 26 November 2000. Out of this number, majority of cases 26 (90%) occurred from 15 July to 26 November 2000, while fewer cases 3 (10%) were isolated in the earlier months. The 29 patients were distributed as follows: New York (15 cases); Georgia (3); Connecticut, Ohio and Michigan (2 each); California, Pennsylvania, Tennessee, Utah and Wisconsin (1 each). 21 patients were elderly (29–92 years) with a median age of 65 years while 8 were perinatal. Three cases of miscarriages or stillbirths and four deaths were reported [81]. Since then, outbreaks or sporadic cases of the infection have been reported almost every year. Table 1 provides a summary of outbreaks of listeriosis in the USA from 1976–2019.

7.2. Outbreaks of Listeriosis in the European Union

Cases of Listeriosis in the European Union were reported in 12 countries (667 cases) in 1999, rising to 1583 cases in 23 countries in 2006; a total of 667 cases were reported in 12 countries in 1999, 586 in 2000 (13 countries), 872 in 2001(13 countries), 909 in 2002 (15 countries), 1070 in 2003 (16 countries), 1264 in 2004 (22 countries), 1427 in 2005 (19 countries) and 1583 in 2006 (23 countries). This report shows that human cases of listeriosis are on the increase each year. Table 2 shows the numbers cases reported for Listeriosis in human beings in the EU from 1999–2006,
Based on the definition by the European of cases of outbreak, as of 6 March 2018, a multi-country foodborne outbreak was verified in five countries, involving 32 confirmed cases and six deaths due to or with the infection (Table 3) [104].
(1)
Austria reported two confirmed cases from 2016. Both cases were males, aged over 85 years at symptom onset, one case was fatal.
(2)
Denmark reported four confirmed cases with sampling dates in January 2017, May 2017, and February 2018 (two cases). Three cases were female patients and one male. Their ages ranged between 37 and 74 years while one case was fatal [105].
(3)
Finland reported 14 confirmed cases with sampling dates from September 2016 to January 2018. Nine cases were females and five males. Their ages ranged between 22 and 92 years while two cases were fatal.
(4)
Sweden reported six confirmed cases with isolates. Out of this number, five were females while one was a male with an age range between 70 and 94 years. Two cases were fatal.
(5)
The United Kingdom reported six confirmed cases between 2015 and 2018 with an age range of 22–84 years. Four cases were males and two females.

7.3. Outbreaks of Listeriosis in Australia

Listeria monocytogenes has become an invasive pathogen in foods and processed food products. In 2003, Australia experienced an outbreak of the disease with the highest mortality (30%) [99]. In 2009, there was contamination of chicken wraps sold on domestic flights while in 2010, L. monocytogenes contaminated melons and caused a multijurisdictional outbreak, with approximately 70 cases reported (Figure 2). The highest number of cases of Listeriosis was reported in 2014 and the most prevalent group affected were patients of 80 years and above (Figure 2). In 2018, the isolated L. monocytogenes strain was serotype 4b strain ST240 and affected 59% of females.

7.4. Outbreaks of Listeriosis in Asia

In the past few decades, Asia has experienced severe outbreaks of Listeriosis. Several reports in Asian countries such as Japan [106,107], Thailand (Bangkok) [108] and Taïwan [109,110] were documented for clinical cases of Listeriosis. Table 4 shows that L. monocytogenes targets immune-compromised individuals such as pregnant women and infants. This is displayed in reports of outbreaks in China in 1964 and 2010 [111].

7.5. Outbreaks of Listeriosis in Nigeria

Nigeria is considered to be the "Giant of Africa" due to the large population and growing economy. Regardless of this, there have been limited reports documented and surveillance systems of outbreaks of Listeriosis in the country. However, researchers successfully isolated Listeria in humans, animals, the environment, and food samples in Nigeria (Table 5). Listeria was shown to affect pregnant women and infants while ruminants dominated reports of incidences in animals.

7.6. Outbreaks of Listeriosis in South Africa

Currently, South Africa is experiencing severe outbreaks of Listeriosis. To date, this is the highest outbreak of Listeria in history affecting a single nation. A total of 820 cases of Listeriosis were reported by the National Institute of Communicable Diseases (NICD) from January 2017 to 23 January 2018. The highest number of cases originated from Gauteng Province (59%), followed by the Western Cape (13%) and Kwa Zulu-Natal (7%). Samples were collected from blood (71%) and Cerebral Spinal Fluid (CSF) with 23% in the public and private healthcare sectors. Approximately 66% were diagnosed from public and 34% from private healthcare sectors. The age distribution of cases ranged from birth to 93 years, with majority (96%) of cases neonates (≤28 days). The gender distribution was 55% females and 45% males [142]. Figure 3 shows the evolution of confirmed cases of Listeriosis from 1 January 2017 to 17 July 2018 in South Africa [23].
Fortunately, human Listeriosis is rare. However, there is a high case of fatality if the disease ensues. With the very long incubation period, which can range up to 60 days, attributing the illness to a specific food product becomes difficult [17]. In addition to several factors mentioned earlier, responsible for outbreaks of Listeriosis in the supply chain, resistance of microorganisms to antibiotics and disinfectants also play a role [143].

7.7. Estimated cost of the outbreak of Listeriosis in South Africa

Food spoilage caused by microbial pathogens results in massive economic loss to both the company responsible and the country. In developing countries, such as South Africa, outbreaks of Listeriosis are poorly documented [23], including the major outbreak in 2017–2018, which caused a deadly epidemic. Approximately, 1060 cases were reported with 216 deaths [23]. Processed meat products (Polony), produced by Tiger Brands Limited (South Africa), was identified as the responsible source. The accountable factories were Tiger Brand (Polokwane, Limpopo and Germiston, Johannesburg) [144]. The economic loss was projected to be US $260 million (R 3, 79 Billion) in terms of lethality, while cost of hospitalisation associated with one-month recovery of affected patients by the disease was US $10.4 million (R1, 5 Billion). Furthermore, more than US $15 million (R2, 19 Billion) was attributed to loss due to productivity and export of food processing companies due to the outbreak [145].

8. Conclusions

It is confirmed in this review that South Africa recorded the highest outbreaks of Listeriosis with a high mortality rate. L. monocytogenes was successfully isolated from contaminated possessed meat (Polony). South Africa is considered the economic capital of Africa and developing exponentially. The country also has strong regulations on food safety management and laws aligned with international standards. Despite this, the recent outbreak of Listeriosis showed some limitations in food safety policies. Authorities in the Department of Health (South Africa) recently reviewed the list of notifiable diseases to include Listeriosis.

Author Contributions

C.-D.K.T. wrote the first version of the manuscript; J.F., M.D.S., G.B., G.F.S., G.A. and C.N.A. reviewed and finalised the manuscript. C.N.A. and G.A. finalised the reviewed manuscript, approved and prepare it for submission. All authors have read and agreed to the published version of the manuscript.

Funding

The authors appreciate the financial assistance received from the North-West University.

Acknowledgments

The authors acknowledge the financial assistance received from the Postgraduate Bursary Office of the North-West University.

Conflicts of Interest

There are no conflicts of interests to be declared by the authors.

References

  1. Murray, E.G.D.; Webb, R.A.; Swann, M.B.R. A disease of rabbits characterised by a large mononuclear leucocytosis, caused by a hitherto undescribed bacillus Bacterium monocytogenes (n. sp.). J. Pathol. Bacteriol. 1926, 29, 407–439. [Google Scholar] [CrossRef]
  2. Pirie, J. A new disease of veld rodents, Tiger River disease. Publ. South Afr. Inst. Med Res. 1927, 3, 163–186. [Google Scholar]
  3. Schmidt, V.; Nyfeldt, A. Ueber Mononucleosis infectiosa und Meningoencephalitis. Acta Oto-Laryngol. 1938, 26, 680–688. [Google Scholar] [CrossRef]
  4. Bell, C.; Kyriakides, A. Listeria: A Practical Approach to the Organism and Its Control in Food, 2nd ed.; Wiley-Blackwell: Oxford, UK, 2005. [Google Scholar]
  5. Weller, D.; Andrus, A.; Wiedmann, M.; den Bakker, H.C. Listeria booriae sp. nov. and Listeria newyorkensis sp. nov., from food processing environments in the USA. Int. J. Syst. Evol. Microbiol. 2015, 65, 286–292. [Google Scholar] [CrossRef]
  6. Bell, C.; Kyriakides, A. Listeria: A Practical Approach to the Organism and Its Control in Foods; Springer Science & Business Media: Berlin, Germany, 2012. [Google Scholar]
  7. Lado, B.; Yousef, A.E. Characteristics of Listeria monocytogenes important to food processors. In Listeria, Listeriosis and Food Safety, 3rd ed.; CRC Press: Boca Raton, FL, USA, 2007; pp. 157–214. [Google Scholar]
  8. George, S.M.; Lund, B.M.; Brocklehurst, T. The effect of pH and temperature on initiation of growth of Listeria monocytogenes. Lett. Appl. Microbiol. 1988, 6, 153–156. [Google Scholar] [CrossRef]
  9. Lakicevic, B.; Nastasijevic, I.; Raseta, M. Sources of Listeria monocytogenes contamination in retail establishments. Procedia Food Sc. 2015, 5, 160–163. [Google Scholar] [CrossRef] [Green Version]
  10. Orsi, R.H.; Den Bakker, H.C.; Wiedmann, M. Listeria monocytogenes lineages: Genomics, evolution, ecology, and phenotypic characteristics. Int. J. Med. Microbiol. 2011, 301, 79–96. [Google Scholar] [CrossRef]
  11. Zhu, Q.; Gooneratne, R.; Hussain, M. Listeria monocytogenes in fresh produce: Outbreaks, prevalence and contamination levels. Foods 2017, 6, 21. [Google Scholar] [CrossRef] [Green Version]
  12. Likotrafiti, E.; Smirniotis, P.; Nastou, A.; Rhoades, J. Effect of Relative Humidity and Storage Temperature on the Behavior of L isteria monocytogenes on Fresh Vegetables. J. Food Saf. 2013, 33, 545–551. [Google Scholar] [CrossRef]
  13. Fenlon, D.R. Listeria monocytogenes in the natural environment. In Listeria, Listeriosis and Food Safety; Ryser, E.T., Marth, E.H., Eds.; Marcel Dekker, Inc.: New York, NY, USA, 1999; pp. 21–38. [Google Scholar]
  14. Marshall, B.M.; Levy, S.B. Food animals and antimicrobials: Impacts on human health. Clin. Microbiol. Rev. 2011, 24, 718–733. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Davis, D.E.; Stewart, H. Changing consumer demands create opportunities for US food system. Food Rev./Natl. Food Rev. 2002, 25, 19–23. [Google Scholar]
  16. Suresh, D. Enhancing the Safety of Ready-To-Eat Meats by Ultraviolet Light Intervention against L. monocytogenes and Its Influence on Product Quality. Master’s Thesis, Graduate Faculty of Auburn University, Auburn, AL, USA, 2013. Available online: https://etd.auburn.edu/handle/10415/3561?show=full (accessed on 22 April 2013).
  17. Farber, J.; Peterkin, P. Listeria monocytogenes, a food-borne pathogen. Microbiol. Mol. Biol. Rev. 1991, 55, 476–511. [Google Scholar] [CrossRef] [Green Version]
  18. Tham, W.; Ericsson, H.; Loncarevic, S.; Unnerstad, H.; Danielsson-Tham, M.L. Lessons from an outbreak of listeriosis related to vacuum-packed gravad and cold-smoked fish. Int. J. Food Microbiol. 2000, 62, 173–175. [Google Scholar] [CrossRef]
  19. Wirtanen, G.; Saarela, M.; Mattila-Sandholm, T. Biofilms—Impact on Hygiene in Food Industries. In Biofilms II: Process Analysis and Applications, 2nd ed.; Wiley-Liss, Inc.: New York, NY, USA, 2000; pp. 327–372. [Google Scholar]
  20. Tocmo, R.; Krizman, K.; Khoo, W.J.; Phua, L.K.; Kim, M.; Yuk, H.G. Listeria monocytogenes in vacuum-packed smoked fish products: Occurrence, routes of contamination, and potential intervention measures. Compr. Rev. Food Sci. Food Saf. 2014, 13, 172–189. [Google Scholar] [CrossRef]
  21. Molins, R.; Motarjemi, Y.; Käferstein, F. Irradiation: A critical control point in ensuring the microbiological safety of raw foods. Food Control 2001, 12, 347–356. [Google Scholar] [CrossRef]
  22. Todd, E.C. Microbiological safety standards and public health goals to reduce foodborne disease. Meat Sci. 2004, 66, 33–43. [Google Scholar] [CrossRef]
  23. National Institute of Communicable Diseases. Situation Report of Listeriosis in South Africa; National Listeria Incident Management Team: Pretoria, South Africa, 2008. [Google Scholar]
  24. Gasanov, U.; Hughes, D.; Hansbro, P.M. Methods for the isolation and identification of Listeria spp. and Listeria monocytogenes: A review. FEMS Microbiol. Rev. 2005, 29, 851–875. [Google Scholar] [CrossRef] [Green Version]
  25. Alessandria, V.; Rantsiou, K.; Dolci, P.; Cocolin, L. Molecular methods to assess Listeria monocytogenes route of contamination in a dairy processing plant. Int. J. Food Microbiol. 2010, 141, S156–S162. [Google Scholar] [CrossRef]
  26. Fenlon, D. Wild birds and silage as reservoirs of Listeria in the agricultural environment. J. Appl. Microbiol. 1985, 59, 537–543. [Google Scholar]
  27. Esteban, J.I.; Oporto, B.; Aduriz, G.; Juste, R.A.; Hurtado, A. Faecal shedding and strain diversity of Listeria monocytogenes in healthy ruminants and swine in Northern Spain. BMC Vet. Res. 2009, 5, 2. [Google Scholar] [CrossRef] [Green Version]
  28. Borucki, M.K.; Reynolds, J.; Gay, C.C.; McELWAIN, K.L.; Kim, S.H.; Knowles, D.P.; Hu, J. Dairy farm reservoir of Listeria monocytogenes sporadic and epidemic strains. J. Food Prot. 2004, 67, 2496–2499. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Dennis, S.M. Ovine listeriosis: A newley diagnosed cause of infectious abortion and lamb losses in Western Australia. J. Dep. Agric. West. Aust. Ser. 1963, 4, 641–643. [Google Scholar]
  30. Barr, B.C.; Anderson, M.L. Infectious diseases causing bovine abortion and fetal loss. Vet. Clin. N. Am. Food A. 1993, 9, 343–368. [Google Scholar] [CrossRef]
  31. Ho, J.L.; Shands, K.N.; Friedland, G.; Eckind, P.; Fraser, D.W. An outbreak of type 4b Listeria monocytogenes infection involving patients from eight Boston hospitals. Arch. Intern. Med. 1986, 146, 520–524. [Google Scholar] [CrossRef]
  32. Wiedmann, M.; Mobini, S.; Cole, J.J.; Watson, C.K.; Jeffers, G.T.; Boor, K.J. Molecular investigation of a listeriosis outbreak in goats caused by an unusual strain of Listeria monocytogenes. J. Am. Vet. Med. Assoc. 1999, 215, 340, 369–371. [Google Scholar]
  33. Fenlon, D.; Wilson, J.; Donachie, W. The incidence and level of Listeria monocytogenes contamination of food sources at primary production and initial processing. J. Appl. Bacteriol. 1996, 81, 641–650. [Google Scholar]
  34. Schuchat, A.; Swaminathan, B.; Broome, C.V. Epidemiology of human listeriosis. Clin. Microbiol. Rev. 1991, 4, 169–183. [Google Scholar] [CrossRef]
  35. Hazards, E.P.o.B.; Ricci, A.; Allende, A.; Bolton, D.; Chemaly, M.; Davies, R.; Escámez, P.S.F.; Girones, R.; Herman, L.; Koutsoumanis, K. Listeria monocytogenes contamination of ready-to-eat foods and the risk for human health in the EU. EFSA J. 2018, 16, e05134. [Google Scholar]
  36. Advisory Committee on the Microbiological Safety of Food: Annual Report 2007. Available online: https://acmsf.food.gov.uk/sites/default/files/mnt/drupal_data/sources/files/multimedia/pdfs/committee/acmsfar2007.pdf (accessed on 21 September 2008).
  37. Rocourt, J.; Bille, J. Foodborne listeriosis. World health statistics quarterly. Rapp. Trimest. Stat. Sanit. Mond. 1997, 50, 67–73. [Google Scholar]
  38. Lamont, R.F.; Sobel, J.; Mazaki-Tovi, S.; Kusanovic, J.P.; Vaisbuch, E.; Kim, S.K.; Uldbjerg, N.; Romero, R. Listeriosis in human pregnancy: A systematic review. J. Perinat. Med. 2011, 39, 227–236. [Google Scholar] [CrossRef]
  39. Hof, H.; Hefner, P. Pathogenicity of Listeria monocytogenes in comparison to other Listeria species. Infection 1988, 16, S141–S144. [Google Scholar] [CrossRef] [PubMed]
  40. Buchanan, R.L.; Gorris, L.G.; Hayman, M.M.; Jackson, T.C.; Whiting, R.C. A review of Listeria monocytogenes: An update on outbreaks, virulence, dose-response, ecology, and risk assessments. Food Control 2017, 75, 1–13. [Google Scholar] [CrossRef]
  41. McLauchlin, J. Listeria monocytogenes, recent advances in the taxonomy and epidemiology of listeriosis in humans. J. Appl. Bacteriol. 1987, 63, 1–11. [Google Scholar] [CrossRef] [PubMed]
  42. Nightingale, K.K.; Schukken, Y.H.; Nightingale, C.R.; Fortes, E.D.; Ho, A.J.; Her, Z.; Grohn, Y.T.; McDonough, P.L.; Wiedmann, M. Ecology and transmission of Listeria monocytogenes infecting ruminants and in the farm environment. Appl. Environ. Microbiol. 2004, 70, 4458–4467. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Ryser, E.T.; Arimi, S.M.; Donnelly, C.W. Effects of pH on distribution of Listeria ribotypes in corn, hay, and grass silage. Appl. Environ. Microbiol. 1997, 63, 3695–3697. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Vasseur, C.; Rigaud, N.; Hebraud, M.; Labadie, J. Combined effects of NaCl, NaOH, and biocides (monolaurin or lauric acid) on inactivation of Listeria monocytogenes and Pseudomonas spp. J. Food Prot. 2001, 64, 1442–1445. [Google Scholar] [CrossRef]
  45. Venkitanarayanan, K.S.; Lin, C.M.; Bailey, H.; Doyle, M.P. Inactivation of Escherichia coli O157: H7, Salmonella Enteritidis, and Listeria monocytogenes on apples, oranges, and tomatoes by lactic acid with hydrogen peroxide. J. Food Prot. 2002, 65, 100–105. [Google Scholar] [CrossRef]
  46. Craig, S.; Permezel, M.; Doyle, L.; Mildenhall, L.; Garland, S. Perinatal infection with Listeria monocytogenes. Aust. N. Z. J. Obstet. Gynaecol. 1996, 36, 286–290. [Google Scholar] [CrossRef]
  47. Goulet, V.; King, L.A.; Vaillant, V.; de Valk, H. What is the incubation period for listeriosis? BMC Infect. Dis. 2013, 13, 11. [Google Scholar] [CrossRef] [Green Version]
  48. Vázquez-Boland, J.A.; Krypotou, E.; Scortti, M. Listeria placental infection. MBio 2017, 8, e00949-17. [Google Scholar] [CrossRef] [Green Version]
  49. Vázquez-Boland, J.A.; Kuhn, M.; Berche, P.; Chakraborty, T.; Domínguez-Bernal, G.; Goebel, W.; González-Zorn, B.; Wehland, J.; Kreft, J. Listeria pathogenesis and molecular virulence determinants. Clin. Microbiol. Rev. 2001, 14, 584–640. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Anderson, N.M.; Keller, S.E.; Mishra, N.; Pickens, S.; Gradl, D.; Hartter, T.; Rokey, G.; Dohl, C.; Plattner, B.; Chirtel, S.; et al. Salmonella inactivation during extrusion of an oat flour model food. J. Food Sci. 2017, 82, 738–743. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Humphries, R.M.; Linscott, A.J. Laboratory diagnosis of bacterial gastroenteritis. Clin. Microbiol. Rev. 2015, 28, 3–31. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Opperman, C.; Bamford, C. Co-infection with Streptococcus pneumoniae and Listeria monocytogenes in an immunocompromised patient. South. Afr. Med. J. 2018, 108, 386–388. [Google Scholar] [CrossRef] [Green Version]
  53. Okpala, C.O.R.; Ifeoma, M.E. Food Hygiene/Microbiological Safety in the Typical Household Kitchen: Some Basic ‘Must Knows’ for the General Public. J. Pure Appl. Microbiol. 2019, 13, 2. [Google Scholar] [CrossRef] [Green Version]
  54. Visintine, A.M.; Oleske, J.M.; Nahmias, A.J. Listeria monocytogenes infection in infants and children. Am. J. Dis. Child. 1977, 131, 393–397. [Google Scholar] [CrossRef]
  55. Dyatlov, V.A.; Lawrence, D.A. Neonatal lead exposure potentiates sickness behavior induced by Listeria monocytogenes infection of mice. Brain Behav. Immun. 2002, 16, 477–492. [Google Scholar] [CrossRef] [Green Version]
  56. Jurado, R.L.; Farley, M.M.; Pereira, E.; Harvey, R.C.; Schuchat, A.; Wenger, J.D.; Stephens, D.S. Increased risk of meningitis and bacteremia due to Listeria monocytogenes in patients with human immunodeficiency virus infection. Clin. Infect. Dis. 1993, 17, 224–227. [Google Scholar] [CrossRef]
  57. Maayan, M.; Wajsman, C.; Nitzan, Y. Meningitis and bacteraemia due to Listeria monocytogenes in compromised hosts. Postgrad. Med. J. 1981, 57, 77–79. [Google Scholar] [CrossRef]
  58. Lavetter, A.; Leedom, J.M.; Mathies, A.W., Jr.; Ivler, D.; Wehrle, P.F. Meningitis due to Listeria monocytogenes: A review of 25 cases. N. Engl. J. Med. 1971, 285, 598–603. [Google Scholar] [CrossRef]
  59. Brouwer, M.C.; Beek, D.V.D.; Heckenberg, S.G.; Spanjaard, L.; Gans, J.D. Community-acquired Listeria monocytogenes meningitis in adults. Clin. Infect. Dis. 2006, 43, 1233–1238. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Orsi, R.H.; Wiedmann, M. Characteristics and distribution of Listeria spp., including Listeria species newly described since 2009. Appl. Microbiol. Biotechnol. 2016, 100, 5273–5287. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Shen, Y.; Naujokas, M.; Park, M.; Ireton, K. InlB-dependent internalization of Listeria is mediated by the Met receptor tyrosine kinase. Cell 2000, 103, 501–510. [Google Scholar] [CrossRef] [Green Version]
  62. Dussurget, O.; Pizarro-Cerda, J.; Cossart, P. Molecular determinants of Listeria monocytogenes virulence. Annu. Rev. Microbiol. 2004, 58, 587–610. [Google Scholar] [CrossRef] [PubMed]
  63. Ryan, S.; Begley, M.; Hill, C.; Gahan, C.G.M. A five-gene stress survival islet (SSI-1) that contributes to the growth of Listeria monocytogenes in suboptimal conditions. J. Appl. Microbiol. 2010, 109, 984–995. [Google Scholar] [CrossRef] [PubMed]
  64. Soni, D.K.; Ghosh, A.; Chikara, S.K.; Singh, K.M.; Joshi, C.G.; Dubey, S.K. Comparative whole genome analysis of Listeria monocytogenes 4b strains reveals least genome diversification irrespective of their niche specificity. Gene Rep. 2017, 8, 61–68. [Google Scholar] [CrossRef]
  65. Amagliani, G.; Petruzzelli, A.; Carloni, E.; Tonucci, F.; Foglini, M.; Micci, E.; Ricci, M.; Di Lullo, S.; Rotundo, L.; Brandi, G. Presence of Escherichia coli O157, Salmonella spp., and Listeria monocytogenes in raw ovine milk destined for cheese production and evaluation of the equivalence between the analytical methods applied. Foodborne Pathog. Dis. 2016, 13, 626–632. [Google Scholar] [CrossRef]
  66. Amagliani, G.; Petruzzelli, A.; Omiccioli, E.; Tonucci, F.; Magnani, M.; Brandi, G. Microbiological surveillance of a bovine raw milk farm through multiplex real-time PCR. Foodborne Pathog. Dis. 2012, 9, 406–411. [Google Scholar] [CrossRef] [Green Version]
  67. Amagliani, G.; Giammarini, C.; Omiccioli, E.; Merati, E.G.; Pezzotti, G.; Filippini, G.; Brandi, G.; Magnani, M. A combination of diagnostic tools for rapid screening of ovine listeriosis. Res. Vet. Sci. 2006, 81, 185–189. [Google Scholar] [CrossRef]
  68. Massacesi, M.; Oliva, N.; Pucci, L.; Brandi, G.; De Santi, M. Listeriolysin O antibodies detection in pregnant women: Results from an Italian pilot study. Ann. Ig. Med. Prev. Comunita 2019, 31, 326–332. [Google Scholar]
  69. Böckmann, R.; Dickneite, C.; Middendorf, B.; Goebel, W.; Sokolovic, Z. Specific binding of the Listeria monocytogenes transcriptional regulator PrfA to target sequences requires additional factor (s) and is influenced by iron. Mol. Microbiol. 1996, 22, 643–653. [Google Scholar] [CrossRef] [PubMed]
  70. Shi, H.; Trinh, Q.; Xu, W.; Luo, Y.; Tian, W.; Huang, K. The transcriptional response of virulence genes in Listeria monocytogenes during inactivation by nisin. Food Control 2013, 31, 519–524. [Google Scholar] [CrossRef]
  71. Cossart, P.; Pizarro-Cerda, J.; Lecuit, M. Invasion of mammalian cells by Listeria monocytogenes: Functional mimicry to subvert cellular functions. Trends Cell Biol. 2003, 13, 23–31. [Google Scholar] [CrossRef]
  72. Poyart-Salmeron, C.; Carlier, C.; Trieu-Cuot, P.; Courtieu, A.L.; Courvalin, P. Transferable plasmid-mediated antibiotic resistance in Listeria monocytogenes. Lancet 1990, 335, 1422–1426. [Google Scholar] [CrossRef]
  73. Noll, M.; Kleta, S.; Al Dahouk, S. Antibiotic susceptibility of 259 Listeria monocytogenes strains isolated from food, food-processing plants and human samples in Germany. J. Infect. Public Heal. 2018, 11, 572–577. [Google Scholar] [CrossRef]
  74. Haubert, L.; Mendonça, M.; Lopes, G.V.; de Itapema Cardoso, M.R.; da Silva, W.P. Listeria monocytogenes isolates from food and food environment harbouring tetM and ermB resistance genes. Lett. Appl. Microbiol. 2016, 62, 23–29. [Google Scholar] [CrossRef] [Green Version]
  75. Srinivasan, V.; Nam, H.M.; Nguyen, L.T.; Tamilselvam, B.; Murinda, S.E.; Oliver, S.P. Prevalence of antimicrobial resistance genes in Listeria monocytogenes isolated from dairy farms. Foodborne Pathog. Dis. 2005, 2, 201–211. [Google Scholar] [CrossRef]
  76. Hof, H. Therapeutic options. FEMS Immunol. Med. Microbiol. 2003, 35, 203–205. [Google Scholar] [CrossRef] [Green Version]
  77. Pagliano, P.; Arslan, F.; Ascione, T. Epidemiology and treatment of the commonest form of listeriosis: Meningitis and bacteraemia. Infez. Med. 2017, 25, 210–216. [Google Scholar]
  78. Lungu, B.; O’Bryan, C.A.; Muthaiyan, A.; Milillo, S.R.; Johnson, M.G.; Crandall, P.G.; Ricke, S.C. Listeria monocytogenes: Antibiotic resistance in food production. Foodborne Pathog. Dis. 2011, 8, 569–578. [Google Scholar] [CrossRef]
  79. Centers for Disease Control Prevention. Multistate outbreak of listeriosis--United States, 1998, in MMWR. Morb. Mortal. Wkly. Rep. 1998, 47, 1085–1086. [Google Scholar]
  80. Gaysinsky, S.; Taylor, T.M.; Davidson, P.M.; Bruce, B.D.; Weiss, J. Antimicrobial efficacy of eugenol microemulsions in milk against Listeria monocytogenes and Escherichia coli O157: H7. J. Food Prot. 2007, 70, 2631–2637. [Google Scholar] [CrossRef] [PubMed]
  81. Centers of Disease Control and Prevention. Multistate outbreak of listeriosis--United States, 2000. MMWR. Morb. Mortal. Wkly. Rep. 2000, 49, 1129. [Google Scholar]
  82. Fleming, D.W.; Cochi, S.L.; MacDonald, K.L.; Brondum, J.; Hayes, P.S.; Plikaytis, B.D.; Holmes, M.B.; Audurier, A.; Broome, C.V.; Reingold, A.L. Pasteurized milk as a vehicle of infection in an outbreak of listeriosis. N. Engl. J. Med. 1985, 312, 404–407. [Google Scholar] [CrossRef]
  83. Linnan, M.J.; Mascola, L.; Lou, X.D.; Goulet, V.; May, S.; Salminen, C.; Hird, D.W.; Yonekura, M.L.; Hayes, P.; Weaver, R.; et al. Epidemic listeriosis associated with Mexican-style cheese. N. Engl. J. Med. 1988, 319, 823–828. [Google Scholar] [CrossRef]
  84. Riedo, F.X.; Pinner, R.W.; Tosca, M.L.; Cartter, M.L.; Graves, L.M.; Reeves, M.W.; Weaver, R.E.; Plikaytis, B.D.; Broome, C.V. A point-source foodborne listeriosis outbreak: Documented incubation period and possible mild illness. J. Infect. 1994, 170, 693–696. [Google Scholar] [CrossRef]
  85. Centers of Disease Control and Prevention. Update: Multistate outbreak of listeriosis--United States, 1998–1999. MMWR. Morb. Mortal. Wkly. Rep. 1999, 47, 1117. [Google Scholar]
  86. Centers of Disease Control and Prevention. Outbreak of listeriosis associated with homemade Mexican-style cheese—North Carolina, October 2000–January 2001. MMWR. Morb. Mortal. Wkly. Rep. 2001, 50, 560. [Google Scholar]
  87. Centers of Disease Control and Prevention. Public health dispatch: Outbreak of listeriosis—Northeastern United States, 2002. MMWR Morb. Mortal. Wkly. Rep. 2002, 51, 950–951. [Google Scholar]
  88. Centers of Disease Control and Prevention. Salmonella typhimurium infection associated with raw milk and cheese consumption—Pennsylvania, 2007. MMWR. Morb. Mortal. Wkly. Rep. 2007, 56, 1161. [Google Scholar]
  89. Centers of Disease Control and Prevention. Outbreak of Listeria monocytogenes infections associated with pasteurized milk from a local dairy—Massachusetts, 2007. MMWR. Morb. Mortal. Wkly. Rep. 2008, 57, 1097. [Google Scholar]
  90. Gaul, L.K.; Farag, N.H.; Shim, T.; Kingsley, M.A.; Silk, B.J.; Hyytia-Trees, E. Hospital-acquired listeriosis outbreak caused by contaminated diced celery—Texas, 2010. Clin. Infect. Dis. 2012, 56, 20–26. [Google Scholar] [CrossRef] [PubMed]
  91. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Imported Frescolina Marte Brand Ricotta Salata Cheese (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2012.
  92. Centers of Disease Control and Prevention. Wholesome Soy Products, Inc. Sprouts and Investigation of Human Listeriosis Cases (Final Update). 2015. Available online: https://www.cdc.gov/listeria/outbreaks/bean-sprouts-11-14/index.html (accessed on 27 January 2015).
  93. Chen, Y.; Burall, L.S.; Luo, Y.; Timme, R.; Melka, D.; Muruvanda, T.; Payne, J.; Wang, C.; Kastanis, G.; Maounounen-Laasri, A.; et al. Listeria monocytogenes in stone fruits linked to a multistate outbreak: Enumeration of cells and whole-genome sequencing. Appl. Environ. Microbiol. 2016, 82, 7030–7040. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  94. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Blue Bell Creameries Products (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2015. Available online: https://www.cdc.gov/listeria/outbreaks/ice-cream-03-15/index.html (accessed on 10 June 2015).
  95. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Commercially Produced, Prepackaged Caramel Apples Made From Bidart Bros. Apples (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2015. Available online: http://www.cdc.gov/listeria/outbreaks/caramel-apples-12-14 (accessed on 12 September 2019).
  96. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Frozen Vegetables (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2016. Available online: https://www.cdc.gov/listeria/outbreaks/frozen-vegetables-05-16/index.html (accessed on 15 July 2015).
  97. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Raw Milk Produced by Miller’s Organic Farm in Pennsylvania (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2016. Available online: https://www.cdc.gov/listeria/outbreaks/raw-milk-03-16/index.html (accessed on 14 December 2016).
  98. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Packaged Salads Produced at Springfield, Ohio Dole Processing Facility (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2016. Available online: https://www.cdc.gov/listeria/outbreaks/bagged-salads-01-16/index.html (accessed on 26 March 2016).
  99. Centers of Disease Control and Prevention. Multistate Outbreak of Listeriosis Linked to Soft Raw Milk Cheese Made by Vulto Creamery (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2017. Available online: https://www.cdc.gov/listeria/outbreaks/soft-cheese-03-17/index.html (accessed on 3 May 2017).
  100. Centers of Disease Control and Prevention. Outbreak of Listeria Infections Linked to Pork Products (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2018. Available online: https://www.google.com.hk/url?sa=t&rct=j&q=&esrc=s&source=web&cd=11&ved=2ahUKEwi34dO8y4nnAhV0yIsBHctcBuYQFjAKegQIBRAB&url=https%3A%2F%2Fecdc.europa.eu%2Fsites%2Fportal%2Ffiles%2Fdocuments%2F2018_ECDC-EFSA_ROA_UI-444_Listeria-final-22-mar-2018.pdf&usg=AOvVaw1RJfBgpq43ApWXcFL6ado1 (accessed on 22 March 2018).
  101. Centers of Disease Control and Prevention. Outbreak of Listeria Infections Linked to Deli Ham (Final Update); Centers for Disease Control and Prevention: Atlanta, GA, USA, 2018. Available online: https://www.cdc.gov/listeria/outbreaks/countryham-10-18/index.html (accessed on 18 December 2018).
  102. Centers of Disease Control and Prevention. Outbreak of Listeria Infections Linked to Deli-Sliced Meats and Cheeses; Centers for Disease Control and Prevention: Atlanta, GA, USA, 2019. Available online: https://www.cdc.gov/listeria/outbreaks/deliproducts-04-19/index.html (accessed on 26 September 2019).
  103. Denny, J.; McLauchlin, J. Human Listeria monocytogenes infections in Europe-an opportunity for improved European surveillance. Eurosurveillance 2008, 13, 9–10. [Google Scholar]
  104. EFSA. Prevention, and Control. The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2017. Efsa J. 2018, 16, e05500. [Google Scholar]
  105. Helwigh, B.; Müller, L. Annual Report on Zoonoses in Denmark 2017; Technical University of Denmark: Lyngby, Denmark, 2018. [Google Scholar]
  106. Makino, S.I.; Kawamoto, K.; Takeshi, K.; Okada, Y.; Yamasaki, M.; Yamamoto, S.; Igimi, S. An outbreak of food-borne listeriosis due to cheese in Japan, during 2001. Int. J. Food Microbiol. 2005, 104, 189–196. [Google Scholar] [CrossRef]
  107. Okutani, A.; Okada, Y.; Yamamoto, S.; Igimi, S. Overview of Listeria monocytogenes contamination in Japan. Int. J. Food Microbiol. 2004, 93, 131–140. [Google Scholar] [CrossRef]
  108. Indrawattana, N.; Nibaddhasobon, T.; Sookrung, N.; Chongsa-Nguan, M.; Tungtrongchitr, A.; Makino, S.; Tungyong, W.; Chaicumpa, W. Prevalence of Listeria monocytogenes in raw meats marketed in Bangkok and characterization of the isolates by phenotypic and molecular methods. J. Health Popul. Nutr. 2011, 29, 26. [Google Scholar] [CrossRef]
  109. Hsieh, W.S.; Tsai, L.Y.; Jeng, S.F.; Hsu, C.H.; Lin, H.C.; Hsueh, P.R.; Chen, C.Y.; Chou, H.C.; Tsao, P.N.; Yang, P.H. Neonatal listeriosis in Taiwan, 1990–2007. Int. J. Infect. Dis. 2009, 13, 193–195. [Google Scholar] [CrossRef] [Green Version]
  110. Huang, Y.T.; Liao, C.H.; Yang, C.J.; Teng, L.J.; Wang, J.T.; Hsueh, P.R. Listeriosis, Taiwan, 1996–2008. Emerg. Infect. Dis. 2011, 17, 1731. [Google Scholar] [CrossRef]
  111. Feng, Y.; Wu, S.; Varma, J.K.; Klena, J.D.; Angulo, F.J.; Ran, L. Systematic review of human listeriosis in China, 1964–2010. Trop. Med. Int. Health 2013, 18, 1248–1256. [Google Scholar] [CrossRef] [PubMed]
  112. Nwaiwu, O. An overview of Listeria species in Nigeria. Int. Food Res. J. 2015, 22, 2. [Google Scholar]
  113. Onyemelukwe, G.C.; Lawande, R.V.; Egler, L.J.; Mohammed, I. Listeria monocytogenes in northern Nigeria. J. Infect. 1983, 6, 141–145. [Google Scholar] [CrossRef]
  114. Emele, F. Etiologic spectrum and pattern of antimicrobial drug susceptibility in bacterial meningitis in Sokoto, Nigeria. Acta Paediatr. 2000, 89, 942–946. [Google Scholar] [CrossRef] [PubMed]
  115. Chukwu, C.O.O. Studies of Listeria monocytogenes (Bacterium) in some selected Local Government Areas of Plateau State, Nigeria. Ph.D. Thesis, University of Jos, Jos, Nigeria, August 2007. [Google Scholar]
  116. Onyemelukwe, G.; Lawande, R. Listeriosis in a neonate and the mother. Trop. Geogr. Med. 1982, 34, 87–89. [Google Scholar]
  117. Ako-Nai, K.; Adejuyigbe, E.A.; Ajayi, F.M.; Onipede, A.O. The bacteriology of neonatal septicaemia in Ile-Ife, Nigeria. J. Trop. Pediatr. 1999, 45, 146–151. [Google Scholar] [CrossRef] [Green Version]
  118. Bolarinwa, R.A.; Aboderin, O.A.; Odetoyin, B.W.; Adegunloye, A.B. Bacterial contamination of blood and blood components in a tertiary hospital setting in Nigeria. Int. J. Infect. Control 2011, 7, 1–6. [Google Scholar]
  119. Esumeh, F.; Odugbemi, T. Screening for Listeria monocytogenes and other related species from faecal specimens at the Lagos University Teaching Hospital, Lagos. Afr. J. Med. Med. Sci. 1992, 21, 47–50. [Google Scholar]
  120. Lawan, F.A.; Tijjani, A.N.; Raufu, A.I.; Ameh, J.A.; Ngoshe, I.Y.; Auwal, M.S. Isolation and characterisation of Listeria species from ruminants in Maiduguri northeastern Nigeria. Afr. J. Biotechnol. 2013, 12, 6997–7001. [Google Scholar]
  121. Chukwu, C.; Muhammad, M.; Nwankpa, N.; Chukwu, I.; Olabode, A. Listeric septicaemia and abotion in African buffalo (Syncerus caffer). J. Anim. Prod. Res. Adv. 2006, 2, 194–196. [Google Scholar] [CrossRef]
  122. Chukwu, C.O.; Ogo, N.I.; Antiabong, J.F.; Muhammad, M.J.; Ogbonna, C.L.; Chukwukere, S.C. Epidemiological evidence of listeriosis in guinea pigs fed with cabbage (Brassica oleracea) in Nigeria. J. Anim. Prod. Res. Adv. 2006, 2, 248–252. [Google Scholar] [CrossRef]
  123. Oni, O.O.; Adesiyun, A.A.; Adekeye, J.O.; Sai’du, S.N. Sero-prevalence of agglutinins to Listeria monocytogenes in Nigerian domestic animals. Rev. Élev. Méd. Vét. Pays Trop. 1989, 42, 383–388. [Google Scholar] [PubMed]
  124. Eruteya, O.; Odunfa, S.; Lahor, J. Listeria spp. in raw cow and goat meat in port harcourt, Nigeria. Br. Biotechnol. J. 2014, 4, 204–214. [Google Scholar] [CrossRef]
  125. Akpavie, S.; Ikheloa, J. An outbreak of listeriosis in cattle in Nigeria. Rev. Élev. Méd. Vét. Pays Trop. 1992, 45, 263–264. [Google Scholar] [PubMed]
  126. Yakubu, Y.; Salihu, M.D.; Faleke, O.O.; Abubakar, M.B.; Junaidu, A.U.; Magaji, A.A.; Gulumbe, M.L.; Aliyu, R.M. Prevalence and antibiotic susceptibility of Listeria monocytogenes in raw milk from cattle herds within Sokoto Metropolis, Nigeria. Sokoto J. Vet. Sci. 2012, 10, 13–17. [Google Scholar] [CrossRef] [Green Version]
  127. Adetunji, V.O.; Olaoye, O.O. Incidence and antibiotic susceptibility pattern of Listeria monocytogenes isolates from milk of West African Dwarf and Red Sokoto breeds of goat from Southwestern Nigeria. N. Y. Sci. J. 2012, 5, 68–73. [Google Scholar]
  128. Magaji, A.A.; Saulawa, M.A.; Salihu, M.D.; Junaidu, A.U.; Shittu, A.; Gulumbe, M.L.; Chafe, U.M.; Buhari, S.; Raji, A.A. Oral microflora of stray domestic cats (Felis catus) found in the premises of two human hospitals in Sokoto, Nigeria. Sokoto J. Vet. Sci. 2008, 7, 9–12. [Google Scholar]
  129. Adeleke, M.A.; Akatah, H.A.; Hassan, A.O.; Adebimpe, W.O. Microbial load and multiple drug resistance of pathogenic bacteria isolated from feaces and body surfaces of cockroaches in an urban area of southwestern Nigeria. J. Microbiol. Biotechnol. Food Sci. 2012, 1, 1448. [Google Scholar]
  130. Adetunji, V.O.; Isola, T.O. Antibiotic resistance of Escherichia coli, Listeria and Salmonella isolates from retail meat tables in Ibadan municipal abattoir, Nigeria. Afr. J. Biotechnol. 2011, 10, 5795–5799. [Google Scholar]
  131. Nwachukwu, N.C.; Orji, F.A.; Iheukwumere, I.; Ekeleme, U.G. Antibiotic resistant environmental isolates of Listeria monocytogenes from anthropogenic lakes in Lokpa-Ukwu, Abia State of Nigeria. Aust. J. Basic Appl. Sci. 2010, 4, 1571–1576. [Google Scholar]
  132. Mawak, J.D.; Dashen, M.M.; Idolor, A.J.; Chukwu, O.O.C. Occurrence of Listeria monocytogenes in irrigation water and vegetable at Jos, Plateau State, Nigeria. Int. J. Trop. Agric. Food Syst. 2009, 3, 279–282. [Google Scholar]
  133. Kawo, A.; Adam, M.; Abdullahi, B.; Sani, N. Prevalence and public health implications of the microbial load of abused naira notes. Bayero J. Pure Appl. Sci. 2009, 2, 52–57. [Google Scholar] [CrossRef] [Green Version]
  134. Tambuwal, F.M.; Shittu, A.; Abubakar, M.B.; Salihu, M.D.; Junaidu, A.U.; Magaji, A.A.; Lawal, M.; Danyaro, M. A survey of veterinary hospitals in Nigeria for the presence of some bacterial organisms of nosocomial and zoonotic potential. Vet. Ital. 2009, 45, 235–241. [Google Scholar] [PubMed]
  135. David, O.; Odeyemi, A. Antibiotic resistant pattern of environmental isolates of Listeria monocytogenes from Ado-Ekiti, Nigeria. Afr. J. Biotechnol. 2007, 6, 2135–2139. [Google Scholar] [CrossRef] [Green Version]
  136. Shinkafi, S.; Ukwaja, V. Bacteria Associated with Fresh Tilapia Fish (Oreochromis niloticus) Sold At Sokoto Central Market in Sokoto, Nigeria. Nig. J. Basic Appl. Sci. 2010, 18, 217–221. [Google Scholar] [CrossRef] [Green Version]
  137. Ikeh, M.; Obi, S.; Ezeasor, D.; Ezeonu, I.; Moneke, A. Incidence and pathogenicity profile of Listeria spp. isolated from food and environmental samples in Nsukka, Nigeria. Afr. J. Biotechnol. 2010, 9, 4776–4782. [Google Scholar]
  138. Yusuf, M.; TengkuHaziyamin, A. Isolation and identification of Listeria spp. from ready-to-eat (rte) kilishi in retail outlet in Bauchi, Nigeria. Int. J. Pharm. Sci. Invent. 2013, 2, 22–25. [Google Scholar]
  139. Nwachukwu, N.; Orji, F.; Amaike, J. Isolation and characterization of Listeria monocytogenes from kunu, a locally produced beaverage marketed in different markets in Abia State of Nigeria. Aust. J. Basic Appl. Sci. 2009, 3, 4432–4436. [Google Scholar]
  140. Ijabadeniyi, A. Microbiological safety of gari, lafun and ogiri in Akure metropolis, Nigeria. Afr. J. Biotechnol. 2007, 6, 22. [Google Scholar] [CrossRef] [Green Version]
  141. Adetunji, V.O.; Odetokun, I.A. Antibiogram profiles of Escherichia coli, Salmonella and Listeria species isolated along the processing line of sale of frozen poultry foods. Res. J. Microbiol. 2012, 7, 235–241. [Google Scholar]
  142. NICD. National Institute of Communicable Diseases. Situation Report on Listeriosis Outbreak; National Health Laboratory Service (NHLS): Pretoria, South Africa, 2018. Available online: https://www.nhls.ac.za/situation-report-on-listeriosis-outbreak-south-africa-2017/ (accessed on 4 December 2017).
  143. Schirone, M.; Visciano, P.; Tofalo, R.; Suzzi, G. Foodborne pathogens: Hygiene and safety. Front. Microbiol. 2019, 10, 1974. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  144. Van der Vyver, A. The Listeriosis Outbreak in South Africa: A Twitter Analysis of Public Reaction. Int. Conf. Manag. Inf. Syst. Sept. 2018, 21, 22. [Google Scholar]
  145. Olanya, O.M.; Hoshide, A.K.; Ljabadeniyi, O.A.; Ukuku, D.O.; Mukhopadhyay, S.; Niemira, B.A.; Ayeni, O. Cost estimation of listeriosis (Listeria monocytogenes) occurrence in South Africa in 2017 and its food safety implications. Food Control 2019, 102, 231–239. [Google Scholar] [CrossRef]
Figure 1. Infection process of a host cell by L. monocytogenes [71].
Figure 1. Infection process of a host cell by L. monocytogenes [71].
Microorganisms 08 00135 g001
Figure 2. Outbreak of Listeriosis in Australia in 2003, 2009, 2010, 2014 and 2018.
Figure 2. Outbreak of Listeriosis in Australia in 2003, 2009, 2010, 2014 and 2018.
Microorganisms 08 00135 g002
Figure 3. Epidemic curve of laboratory-confirmed cases of Listeriosis according to date of collection of clinical specimen (N = 1060) and type of sequence (ST) (n = 636), South Africa, 1 January 2017 to 17 July 2018 [23].
Figure 3. Epidemic curve of laboratory-confirmed cases of Listeriosis according to date of collection of clinical specimen (N = 1060) and type of sequence (ST) (n = 636), South Africa, 1 January 2017 to 17 July 2018 [23].
Microorganisms 08 00135 g003
Table 1. Outbreaks of Listeriosis in the USA, 1976–2019.
Table 1. Outbreaks of Listeriosis in the USA, 1976–2019.
Listeriosis Outbreaks in the USA 1976–2019
YearNumber of Cases (Number of Deaths and Number of Miscarriages)FoodReferences
197620Raw salad[31]
198349Milk[82]
1985142 (41)Soft cheese[83]
19899 (1)Shrimps[84]
1998–1999108 (14; 4)Hot dog[85]
200029 (4; 3)Turkey meat[81]
200112Mexican style cheese[86]
200246 (7; 35)Fresh and frozen ready-to-eat turkey and chicken[87]
2007311 (52)Milk[88]
20075 (3)Dairy milk[89]
201010 (5)Pre-cut celery[90]
2011147 (33)Cantaloupe[40]
201222 (4)Ricotta salata Cheese[91]
20145 (2)Mung bean sprouts[92]
20144Stone fruit[93]
2010–201510 (3)Ice cream[94]
2014–20155 (3)Caramel apples[95]
20169 (3)Frozen vegetables[96]
20162 (1)Raw milk[97]
201619 (1)Packaged salads[98]
20178 (2)Soft Raw Milk Cheese Made by Vulto Creamery[99]
20184Pork Products[100]
20184 (1)Deli Ham[101]
20198 (1)Deli-Sliced Meats and Cheeses[102]
Table 2. Cases of Listeriosis reported among humans in Europe, 1999–2006 [103].
Table 2. Cases of Listeriosis reported among humans in Europe, 1999–2006 [103].
Country Number of Confirmed Cases
19992000200120022003200420052006
Austria1314916819910
Belgium6448574476706267
Cyprus 1
Czech Republic 161578
Denmark4439382829414656
Estonia1 221
Finland4618282041353645
France275261187218220236221290
Germany3133216240256296510508
Greece1235 3 6
Hungary 161014
Ireland 776611117
Italy171331 255151
Latvia 36 168532
Lithuania 2124
Luxembourg 4
Malta 0
Netherlands 163252559664
Poland 315102228
Portugal 38
Slovakia 768512
Slovenia 61 7
Spain32355749521006878
Sweden2746673948443542
United Kingdom116115156158255232223208
EU Total6675868729091070126414271583
Bulgariax 2000 6
Iceland 14
Liechtenstein 48
Norway 181718211427
Table 3. Cases of Listeriosis verified in five countries in Europe between 2015 and 2018.
Table 3. Cases of Listeriosis verified in five countries in Europe between 2015 and 2018.
CountryConfirmed Cases (Number of Deaths)Total Number of CasesTotal Number of Deaths
2015201620172018
Austria02 (1)0021
Denmark0022 (1)41
Finland0310 (2)1142
Sweden03 (1)3 (1)062
United Kingdom122160
Total1 (0)10 (2)17 (3)4 (1)326
Table 4. Reporting periods of clinical cases of Listeriosis for each subgroup in China, 1964–2010.
Table 4. Reporting periods of clinical cases of Listeriosis for each subgroup in China, 1964–2010.
Reporting PeriodNo. of Cases
Immune-Competent PatientsImmune-Compromised PatientsPregnant WomenNeonatesTotal
1964–197010012
1971–198010001
1981–1990820010
1991–20001275933
2001–201027122537101
Total48213047147
Table 5. Different sources of Listeria in Nigeria, such as humans, fish, water, animals, soil, and the environment [112].
Table 5. Different sources of Listeria in Nigeria, such as humans, fish, water, animals, soil, and the environment [112].
Source OriginReferences
HumanPatients with meningitis, septicaemia[113,114,115]
Neonatal and mother[116]
Neonates[117]
Blood samples[118]
Faecal specimens[119]
AnimalsCow faeces[120]
African buffalo[121]
Guinea pig[122]
Pig, dog, cattle, goat, horse, camel, chicken[123,124]
Animals dropping[125]
Raw cattle milk[126]
Raw goat milk[127]
Domestic cats[128]
Cockroach[129]
EnvironmentButcher’stable[130]
Lake[131]
Irrigation water[132]
Nairacurrency notes[133]
Veterinary surgical material[134]
Soil[135]
FoodFish[136]
Vegetables[137]
Dried beef Kilishi[138]
Kunu drink[139]
Wara soft cheese[140]
Fermented food (Gari etc…)[140]
Frozen poultry[141]

Share and Cite

MDPI and ACS Style

Kaptchouang Tchatchouang, C.-D.; Fri, J.; De Santi, M.; Brandi, G.; Schiavano, G.F.; Amagliani, G.; Ateba, C.N. Listeriosis Outbreak in South Africa: A Comparative Analysis with Previously Reported Cases Worldwide. Microorganisms 2020, 8, 135. https://doi.org/10.3390/microorganisms8010135

AMA Style

Kaptchouang Tchatchouang C-D, Fri J, De Santi M, Brandi G, Schiavano GF, Amagliani G, Ateba CN. Listeriosis Outbreak in South Africa: A Comparative Analysis with Previously Reported Cases Worldwide. Microorganisms. 2020; 8(1):135. https://doi.org/10.3390/microorganisms8010135

Chicago/Turabian Style

Kaptchouang Tchatchouang, Christ-Donald, Justine Fri, Mauro De Santi, Giorgio Brandi, Giuditta Fiorella Schiavano, Giulia Amagliani, and Collins Njie Ateba. 2020. "Listeriosis Outbreak in South Africa: A Comparative Analysis with Previously Reported Cases Worldwide" Microorganisms 8, no. 1: 135. https://doi.org/10.3390/microorganisms8010135

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop