Canine Leptospirosis in a Northwestern Region of Colombia: Serological, Molecular and Epidemiological Factors
1
Facultad de Medicina Veterinaria y Zootecnia, Universidad CES, Medellín 050021, Colombia
2
Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ 86011, USA
3
Escuela de Graduados, Universidad CES, Medellín 050021, Colombia
*
Author to whom correspondence should be addressed.
Pathogens 2022, 11(9), 1040; https://doi.org/10.3390/pathogens11091040
Submission received: 26 July 2022
/
Revised: 5 September 2022
/
Accepted: 8 September 2022
/
Published: 13 September 2022
(This article belongs to the Special Issue 10th Anniversary of Pathogens—Feature Papers)
Abstract
:Canine leptospirosis is a zoonosis of epidemiological importance. Dogs are recognized as primary reservoirs of Leptospira interrogans serogroup Canicola and a source of infection to the environment through urine. This study aimed to determine the presence of antibodies against Leptospira in canines from 49 municipalities in the Department of Antioquia, Colombia. We performed a cross-sectional study of dogs included in a neutering control program. We collected 1335 sera samples, assayed by a microagglutination test (MAT), and performed PCR detection in 21 urine samples. We also surveyed 903 dog owners. We found a seroreactivity of 11.2% (150/1335) in Antioquia with titers ≥1:50. Municipalities with the highest number of cases were Belmira (46.1%), Turbo (34.5%), and Concepción (31.0%). L. santarosai was identified by phylogenetic analysis in one urine sample from the municipality of Granada. The most important factor associated with a positive result was the lack of vaccination against leptospirosis (PR 3.3, p ≤ 0.014). Environmental factors such as water presence and bare soil around the household were also associated with Leptospira seroreactivity in the Department of Antioquia. We reviewed a national epidemiological surveillance database for human cases in those municipalities. We found a correlation between the high number of cases in canines and humans, especially in the Uraba. Serological and molecular results showed the circulation of Leptospira. Future public health efforts in the municipalities with the highest numbers of seroreactivity should be directed towards vaccination to prevent animal disease and decrease the probability of transmission of Leptospira. Dogs actively participate in the Leptospira cycle in Antioquia and encourage the implementation of vaccination protocols and coverage.
1. Introduction
Leptospirosis is a re-emerging zoonotic disease of global distribution caused by pathogenic spirochetes of the genus Leptospira, which contains more than 300 pathogenic serovars. Pathogenic species can remain in the water and alkaline soils but are mostly confined to the kidneys of a wide range of hosts. Humans, some domestic animals, and wildlife are highly susceptible to Leptospira, presenting mild and moderate clinical manifestations that may have a fatal outcome. Other animals have adapted to some serovars or serogroups of Leptospira and develop clinical manifestations that tend to be asymptomatic and chronic. They are considered maintenance hosts and disseminators of the bacterium and can shed on occasion throughout their lifetime. Urine in these infected animals is the primary source of infection for susceptible animals [1,2].
Canine leptospirosis is widespread worldwide, and dogs are incidental hosts for some Leptospira serovars and maintenance hosts for L. interrogans serovar Canicola. The relationship between leptospirosis in humans and their dogs could provide evidence of intra- and interspecific transmission or exposure to the same risk factors [3,4].
Dogs with leptospirosis can manifest clinical jaundice, uremia, or acute hemorrhagic diathesis [5]. The Canicola serogroup causes most clinical cases in canines, first reported in 1933 with the first isolate of the strain Hond Ultrech IV [2]. Dogs infected with this serogroup present a mild to moderate symptomatology, and they recover without relevant sequelae. Other Leptospira serogroups, mainly Icterohaemorrhagiae, cause severe and fatal canine leptospirosis cases. Canine leptospirosis has been considered a re-emergent disease in some countries due to changes in the serogroups responsible, clinical signs, and disease outcomes [5,6]. The serogroups Canicola and Icterohaemorrhagiae are the most commonly found in dogs and are used widely in vaccines. Vaccination has decreased the worldwide incidence of canine leptospirosis by these serovars in the last two decades. Vaccination prevents canine disease and subsequent zoonosis transmission to humans. However, changes in the incidence of serogroups affecting dogs have resulted in low effectiveness for canine vaccination when new serovars have been included in commercially available vaccines [7,8]. Additionally, vaccines would be more effective with knowledge of the serogroups of Leptospira circulating in the geographical area where the canine population originated [9].
In Colombia, the pathogenic group Leptospira interrogans sensu lato is the most frequent serogroup in canine leptospirosis recorded since 1966. These serogroups include Canicola, Ballum, Pyrogenes, and Icterohaemorrhagiae, and in the last few years, Pomona, Grippotyphosa, Australis, Sejroe, and Panama [10,11,12,13,14,15]. From the perspective of veterinary medicine and public health, it is necessary to identify the serogroups circulating in local areas and recognize the role of dogs in the epidemiology of the disease. This study aimed to determine the presence of the two main serogroups of Leptospira in dogs (Canicola and Icterohaemorrhagiae) in asymptomatic canines from 49 municipalities in the Department of Antioquia, Colombia. Using serology and molecular testing, we will explore other serogroups circulating in this region, describe epidemiological risk factors through owners self-reporting characteristics, and correlate with human leptospirosis cases reported in the National Surveillance System in Antioquia.
2. Results
Canines were 78.3% female, and although canines of 23 different breeds were included, the highest proportion was mixed breeds, at 73.3%. Dogs from urban areas comprised 57.3%.
Seroreactivity was 11.2% (150/1335), with positive MAT to at least one of the evaluated serogroups. Figure 1 shows the frequency of positive reactive cases by sub-region in the Department of Antioquia.
The highest percentage was obtained in the Uraba region (22.4%) with 35 seropositive dogs, and the lowest in the west region with 17 dogs (7.3%). Of the 49 municipalities, 24 presented seropositivity above the level obtained for the entire Department (11.2%), as shown in Table 1.
The municipality with the highest seroreactivity was Belmira (46.15%), followed by Turbo (34.4%) and Concepción (31.0%). Ten municipalities did not have any canines with a positive microagglutination test, as shown in Table 1. We found a statistically significant association between the presence of antibodies against Leptospira and municipalities (p ≤ 0.000) as well as the study regions (p ≤ 0.000).
The proportion of the sampled animals included in the study was calculated with the reported canine population by municipality (Figure 2). We found no statistical correlation between the presence of reactive canines in the municipalities and the incidence of human cases (p ≤ 0.1563). However, a significant relationship existed between municipalities of the Urabá region, with more than 19 cases per 100,000 inhabitants and almost 40% of canine reactive cases.
2.1. Serogroups Circulating
We analyzed all samples (1335) against the Canicola and Icterohaemorrhagiae serogroups. Serogroup Canicola had the highest number of cases, 50.6% (76/150), and the highest antibody titers, 1:3200. Furthermore, 28.6% (43/150) of seropositive dogs were reactive to the Icterohaemorrhagiae serogroup, with titers between 1:100 and 1:200 (Figure 3).
A set of 212 randomly selected sera from all regions was processed with a panel of nine serogroups, including a local strain JET, as described in Table 2. Extended MAT results include L. interrogans serovar Pomona (8/150), L. interrogans serovar Hardjo (5/150), L. kirschneri serovar Grippothyposa (3/150), L. borgpetersenii serovar Tarassovi (2/150), L. borgpetersenii serovar Ballum (6/150), L. borgpetersenii serovar Bratislava (3/150), and L. santarosai serovar Alice strain JET (4/150). Coaglutination defined as positive to both serogroups was found in 30 dogs.
Including all the tested serogroups, the percentage of seroreactivity was increased by 0.74% for ten additional positive canines (150/1335). We found two samples with co-agglutination between L. Interrogans serogroup Canicola (strain Utrecht) and L. santarosai serogroup Grippothyposa (strain JET).
2.2. Molecular Characterization
Of 21 urine samples collected, only one was positive by PCR for Leptospira 16S gene. This male mix breed dog lived in an urban household in the municipality of Granada, subregion Eastern region; it was 30 months old, seronegative, and had no history of the disease or vaccination. The dog spent most of the time outside the home and with other canines. The molecular analysis allowed us to define a 99% similarity to Leptospira santarosai.
2.3. Owners, Housing, and Dog Information
Only in two dogs did the owners report a history compatible with leptospirosis. Both cases were negative in the microagglutination test. The median age for reactive dogs was 24 months and 18 months for the non-reactive dogs, which was found to be a statistically significant difference (p ≤ 0.029).
When looking at signs of disease as presented by owners, none of the animals presented orchitis, three reported hematuria (0.39%; 3/770), five reported jaundice (0.67%, 5/742), and 15 had abortions (2.48%; 15/603). Reports of abortion presented three times more in seroreactive dogs than in those who had a negative MAT test (CI 95% 1.27–5.66, p ≤ 0.034).
Vaccination against leptospirosis was reported by 67 owners, equivalent to 8.47%, as shown in Table 3. Non-vaccinated MAT reactive dogs comprised 14.09% (102/724), and MAT reactive and vaccinated comprised 4.48% (3/67). Association between positivity and vaccination status was statistically significant (p ≤ 0.014).
We evaluated the interaction of dogs with their owners through time spent inside households; 14.71% (64/435) of dogs that remained inside the house most of the day were MAT positive, and 14.94% (49/328) slept inside the owner’s room.
When evaluating the presence of animals in the same household, 86% of the dogs shared with other potential Leptospira animal reservoirs: 92% cohabited with other canines and 51.3% with felines. Of the seroreactive dogs, 29.2% lived in homes with self-reported presence of rodents. Figure 4 describes the percentages of coexistence with all animal species as reported by owners. We also included the number of reactive canines by the microagglutination test. It should be noted that the largest number was recorded for the serogroup Icterohaemorrhagiae for intra-species coexistence and the Canicola serogroup for both intra- and inter-species coexistence.
We found that 65.4% of the canine owners were females. The most frequent occupations reported were “housewife” and “retired”, at 45.3%, and 12.8% were workers in the agricultural or primary economic sectors. Only one of the owners reported clinical symptoms compatible with leptospirosis. She lived in the urban area of the municipality of Turbo. Her pet was a 3-year-old female with no clinical history of the disease and positive microagglutination for the Canicola and Tarassovi serogroups, with titers of 1:100 and 1:200, respectively.
Housing characteristics of MAT reactive dogs include 14.06% with concrete or tile roofing, 15.15% with concrete walls, and 14.25% with ceramic and concrete flooring. However, dirt or wood flooring (traditional materials) were more common in reactive dogs than in those with negative MAT (p < 0.06). The peridomiciliary environment for the reactive dogs was mainly water sources (30.61%), forests (23.53%), and crops (16.42%). Water sources were 2.2 times more frequent in seroreactive dogs (CI 95% 1.29–3.62; p < 0.006). Other peridomiciliary characteristics in MAT reactive dogs were the presence of roads in 23.60% of dwellings and bare soil in 34.78% (Table 4). Seroreactive dogs were three times more frequent in households with an outdoor kitchen than in houses where food preparation was done in an indoor kitchen as an independent house space (p < 0052). Although most houses had municipal services for garbage collection, aqueducts, and sewerage, there were more cases of seroreactive dogs in homes with open field garbage and human waste disposal.
3. Discussion
The presence of canine leptospirosis in Colombia is known and commonly associated with the Canicola serogroup. In the Department of Antioquia, this study reports the presence of antibodies in 11.2% of asymptomatic canines by MAT. In addition, we found evidence of other circulating serogroups in the pathogenic group Leptospira interrogans serogroups Icterohaemorrhagiae, Pomona, Sejroe, Grippothyposa, Tarassovi, Ballum, and Australis. The presence of Leptospira antibodies in dogs highlights the circulation of this microorganism in susceptible hosts. Dogs could be indicators of Leptospira intra- or inter-specific infection.
Our results provided molecular evidence for the presence of Leptospira santarosai in the urine of an asymptomatic dog. There is only one known report on this Leptospira species in dogs in Colombia [16]. This finding suggests that canine leptospirosis in Antioquia has a unique and changing dynamic from a classic to a re-emergent presentation, as evident in other Latin American regions such as Brazil [17].
We found variable seropositivity of canine leptospirosis by MAT in 49 municipalities of the Department of Antioquia when compared to previous reports in other cities and regions in Colombia. It was lower than the highest reported in an indigenous territory in Colombia of 79.9% [18] but higher than the last report for the principal city of the same Department of this study of 8.4% [19]. A limitation in our results is that analysis must be done by region or municipality. This is an important factor because there may be considerable differences in the vaccination status and epidemiological characteristics. In addition, we must consider differences in climate, environmental and geographical conditions, and the diversity of domestic, livestock, and wild animal species.
A concrete example is the Uraba region, which had seropositivity of 22.4%. This highlights the highest frequencies per municipality, such as Turbo (proportion of sampled canines by municipality of 0.76%) with 34.4%, with 14 positive results of 31 sampled canines. Additionally, Mutata, Chigorodo, Carepa, San Pedro de Uraba, and Arboletes had frequencies between 20 and 30% in the same area. In 2007, a study on the human population reported a seroprevalence of 12.5% and positivity with serogroups associated with rodents and canines [20]. Previous studies in this area had generated consideration of the ownership of pets and wild animals [21,22] as a risk factor for disease in humans due to the isolation of L. santarosai in humans and canines [16]. However, there were no previous reports of seroprevalence of Leptospira in canines in this region. An outbreak was reported by the Colombian military forces in this area, describing a zoonotic link between six affected people who had contact with a canine presenting clinical signs and who were later diagnosed with the disease.
The serological and molecular results obtained in the present study provided evidence of the circulation of this organism in this susceptible population, and vaccination would have a high probability of preventing and decreasing the transmission of Leptospira in Antioquia. An important finding from the geographical analysis pertains to the municipality of Belmira, in the northern region of the Department. It had the highest canine seroprevalence of all the municipalities included in the study (46.15% of a proportion sampled for this municipality of 1.39%). This municipality is known for having many bovine farms, with the recognized seroprevalence in this species. However, according to official reports from the National Surveillance System in 2015, this municipality did not report human leptospirosis cases between 2007 and 2015. It is essential to actively search for cases in different animal populations and humans.
We found an absence of human cases in the Northeast municipalities included in the study, with a prevalence of 8.7% against zero cases of human leptospirosis in 2015. In this study, six of the ten municipalities that did not report canines with positive microagglutination tests did not report human leptospirosis cases in 2015 in the National Surveillance System. This absence could be due to a lack of circulation of Leptospira in these municipalities or case underreporting, since they meet all the environmental, demographic, and epidemiological risk factors for leptospirosis transmission. The proportion of canines sampled in some municipalities (Table 2) could represent an information bias that does not allow us to draw clear-cut conclusions on the actual status of the municipalities in potential epidemiological underreporting.
The Canicola serogroup was the most common serogroup found, as we expected, in dogs [2]. Furthermore, the presence of the Icterohaemorrhagiae serogroup confirms what is evident in other regions of Colombia: the epidemiological nexus of cases with typical synanthropic sources of infection such as rodents [10,11,12,13,14,15]. Titers might indicate that these dogs were susceptible hosts and may be asymptomatic while affected by the bacterium. Dogs can have greater exposure to this rodent-related serogroup than humans because they have free access to urine-contaminated environments, hunt rodents, and often their drinking water can be contaminated with the urine of these synanthropic species. A study in Brazil found evidence of the relationship between serovars and MAT titers, concluding that the Canicola serogroup could have higher titers than the Icterohaemorrhagiae serogroup [23,24].
The present study illustrates the great variety of serovars found in studies of the prevalence of Leptospira in a highly biodiverse country such as Colombia. Finding a pathogenic Leptospira santarosai by molecular techniques in an asymptomatic canine should be further studied. MAT results need to be correlated with direct techniques, because there are extrinsic and intrinsic factors that can produce variability in titers [25].
Vaccination against leptospirosis was reported by 67 owners, equivalent to 8.47% (67/791). Our MAT test found that 97.10% of positive dogs were not vaccinated (102/105), while only 4.48% of the vaccinated animals had antibodies in the microagglutination test (3/67). We found a low rate of seroreactivity in vaccinated dogs compared with those that were unvaccinated. This association was statistically significant (p < 0.029). In this study, titers in vaccinated dogs did not exceed 1:200, a value not associated with recent vaccination [26].
The frequency of Leptospira by PCR in urine samples was considerably low. Although low, this finding suggests the latent risk that humans become infected by direct or indirect contact with the urine of infected animals. Most canines (86%) coexisted with at least one other animal in the same house—mainly dogs, cats, and rodents. The proximity between canines and rodents is a risk factor for disease transmission in urban environments. A study in Brazil reported the behavior of “hunting mice” as an important risk factor in canine leptospirosis [27]. Therefore, it is important to continue an integrated control of rats and mice and the follow-up of reservoirs that have historically been considered the primary source of Leptospira infection in humans and other animals.
Dogs’ natural and instinctive behaviors could be risk factors, including urine marking, drinking water outdoors from an untreated source, and hunting small mammals (rodents, bats, or marsupials). We explored the presence of natural and untreated water sources in the peridomicile as a risk factor for canine leptospirosis (RP 2.46; p < 0.038) as well as the risk factors of being exposed to high urine contamination and risk interactions such as playing, swimming, and drinking. As an indirect measurement of the interaction between dogs and their owners, we identified the percentage of canines sharing the same space at night with their owners. It was high in this study (45.3%), promoting contact situations with urine, such as marking territory, using pee pads, sniffing, licking genitals, or locating a humid area within the dwelling. Those practices facilitate the microorganism spreading quickly [28]. Moreover, the probability of infection could be higher, not only for humans but also for other animals in the same household.
Canines should be considered sentinel species of leptospirosis in the human population. Active surveillance could help in the early detection of sources of Leptospira, such as infected animals and contaminated water. In addition, direct interventions such as canine vaccination, antimicrobial treatment in susceptible species, and implementation of control measures for reservoirs such as rodents are likely to minimize the risk factors that increase disease presentation in susceptible species.
4. Materials and Methods
4.1. Ethical Considerations
The study was approved by the Institutional Committee for the Care and Use of animals (CICUA) of Universidad CES, Acta 16 of 20 October 2015. All owners signed informed consent before collecting the sample and conducting surveys.
4.2. Study Area
We included surveys of 49 municipalities distributed in seven regions of the Department of Antioquia. The study was developed during a neutering program, “Animóvil”, sponsored by the Antioquia Government.
4.3. Type of Study
A cross-sectional study was carried out in which we obtained 1335 blood and 21 urine samples. We also administered 903 surveys to dog owners who voluntarily participated in the animal neutering program or were responsible for two of the municipal shelters included in the study performed in 2015. Some owners were responsible for more than one animal.
4.4. Procedures
A group of veterinarians evaluated all dogs to identify clinical signs or abnormalities. Only healthy canines were included in the study. We included all dogs whose owners allowed collection of samples, and urine samples were taken from animals that had urine in the bladder or spontaneously urinated at the clinical examination. Blood samples were taken from the cephalic vein (ADC BD Yellow Cap Tube, BD Vacutainer®, Fisher Scientific, Pittsburg, PA, USA), a urine sample was collected, and 1–2 mL of each was placed in a sterile vial. Both samples were kept for a maximum of four hours at room temperature until the completion of the entire sampling for each day. They were later stored at 4 °C until processing at the laboratory. A survey was also performed to obtain dog information and leptospirosis vaccination status and explore household risk factors.
4.5. Microagglutination Test (MAT)
All MATs were performed when the final collection of serum samples was completed. Samples were stored at −20 °C until processed and thawed in a cold bath for at least 15 min before performing the test. We tested all samples against the conventional canine serogroups, Canicola and Icterohaemorrhagiae. Each test included a positive control serum (internal control of the test for each serogroups) and negative control (only phosphate buffer saline pH 7.4, PBS). We performed serial dilutions with PBS (1:25) to determine antibody titers, beginning with 1:25. A 1:50 dilution was used as a cutoff for seroreactivity [28]. Tests were read after one-hour incubation using a dark field microscope with a 4× objective without a coverslip; agglutination of 50% of the field was used as a positivity indicator in a sample of 20 μL of the antigen-serum mixture.
Additionally, we tested a random selection of 212 sera samples (15% of total samples) against a panel of eight reference serogroups (Pomona, Sejroe, Grippothyposa, Tarassovi, Ballum, and Australis). We also included a local Leptospira strain belonging to the Grippothyphosa serogroup of Leptospira santarosai. A full description of the panel used for evaluation is presented in Table 2.
4.6. Molecular Characterization
We performed DNA extraction of urine samples using a commercial kit (Wizard Genomic DNA purification Kit®. Promega Corp., Madison, WI. USA). Samples were stored at 4 °C in Tris-EDTA buffer until processing. PCR was used to amplify the 16S ribosomal gene, and products were separated by electrophoresis in agarose gels as previously reported [15]. Products were subsequently sequenced (Macrogen Inc®. Seoul, Korea 2016) to determine the Leptospira sp.
4.7. Information Analysis
Surveys were analyzed using the IBM® SPSS® Statistics 21.0 (IBM Corporation®. Armond, NY, USA. Universidad CES license) and Epidat® 3.1 and 4.2 (Organización Panamericana de la Salud (OPS-OMS), Universidad CES. Coruña, España 2016). We performed a descriptive analysis by municipality according to the case definition: seroreactivity for the serogroups Canicola and Icterohaemorrhagiae with titers over 1:50. A Chi-square test or Fisher test association analysis analyzed the significance between the MAT positivity and epidemiological variables. Quantitative variables were tested using the Shapiro-France test and Mann-Whitney U test to determine correlation with the presence of disease.
The Antioquia Government provided animal populations. In each municipality, epidemiological surveillance information of human cases of leptospirosis included in the study was downloaded from the official website to correlate with the proportion of positive animals per place. The Spearman correlation test analyzed the significance between both variables. All tests used a 95% significance level, and statistical significance was assessed with a p < 0.05 value. We used free Piktochart (Piktochart Sdn. Bhd. Penang, Malaysia. www.piktochart.com, accessed on 11 September 2022) to create graphs and maps designed in ArcGIS® 10.4 (Esri Redlands, CA, USA. Universidad CES license).
Author Contributions
Conceptualization, methodology, and investigation: J.P.-G. and P.A.-F.; writing—original draft preparation, review and editing: J.P.-G., P.A.-F. and F.P.M. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by Facultad de Medicina Veterinaria y Zootecnia (Universidad CES). F.P.M. was a recipient of a US Scholar Fulbright Fellowship.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Ethics Committee for animal experimentation of Universidad CES in the Act 16, 20 October 2015.
Informed Consent Statement
Not applicable.
Data Availability Statement
Nucleotide sequence from the single Lepstopira 16S positive PCR may be made available upon request.
Acknowledgments
We thank our sponsor, the Antioquia Government (Colombia), and graduate and undergraduate students and professors who participated in sampling and fieldwork.
Conflicts of Interest
The authors declare no conflict of interest in the content of this manuscript.
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Figure 1.
Distribution percentage of canine leptospirosis obtained by subregion in the Department of Antioquia. The right side shows the number of reactive canines by microagglutination and the total number of dogs included in the study by region (Antioquia, 2015).
Figure 1.
Distribution percentage of canine leptospirosis obtained by subregion in the Department of Antioquia. The right side shows the number of reactive canines by microagglutination and the total number of dogs included in the study by region (Antioquia, 2015).
Figure 2.
The geographical distribution of the percentages of seropositivity to canine leptospirosis and human leptospirosis reported in the Department of Antioquia in 2015 by the National Surveillance System. The blue color shows human case distribution (rates per 100,000 inhabitants). Points denote canine cases obtained in the present study.
Figure 2.
The geographical distribution of the percentages of seropositivity to canine leptospirosis and human leptospirosis reported in the Department of Antioquia in 2015 by the National Surveillance System. The blue color shows human case distribution (rates per 100,000 inhabitants). Points denote canine cases obtained in the present study.
Figure 3.
Distribution of seroreactive cases based on antibody titers in the microagglutination test (MAT). Reactivity against serogroup (Canicola) was used as an adaptability marker of reservoirs and the susceptibility serogroup (Icterohaemorrhagiae) as an incidental host in Antioquia 2015. The dotted line describes hypothetical antibody titers for each serogroup in asymptomatic canines. The presence of high antibody titers suggests canine leptospirosis.
Figure 3.
Distribution of seroreactive cases based on antibody titers in the microagglutination test (MAT). Reactivity against serogroup (Canicola) was used as an adaptability marker of reservoirs and the susceptibility serogroup (Icterohaemorrhagiae) as an incidental host in Antioquia 2015. The dotted line describes hypothetical antibody titers for each serogroup in asymptomatic canines. The presence of high antibody titers suggests canine leptospirosis.
Figure 4.
The proportion of seroreactive dogs cohabiting in the same household with other animals and showing positivity in the microagglutination test. The value in each row indicates the number of dog positives for the serogroup. Co-agglutination was included when there was reactivity to more than two serogroups at the same titer and was evaluated separately.
Figure 4.
The proportion of seroreactive dogs cohabiting in the same household with other animals and showing positivity in the microagglutination test. The value in each row indicates the number of dog positives for the serogroup. Co-agglutination was included when there was reactivity to more than two serogroups at the same titer and was evaluated separately.
Table 1.
Description of the microagglutination test results found in each of the municipalities. Samples are described by municipality with respect to the data of the canine census and the proportion sampled by the municipality in Antioquia, 2015.
Table 1.
Description of the microagglutination test results found in each of the municipalities. Samples are described by municipality with respect to the data of the canine census and the proportion sampled by the municipality in Antioquia, 2015.
| Municipality | Reactive MAT | Not Reactive MAT | Sample by Municipality | Canine Population by Municipality | Proportion Sampled by Municipality | ||
|---|---|---|---|---|---|---|---|
| n | % | n | % | n | n | % | |
| Uraba region | |||||||
| Apartadó | 2 | 11.76% | 15 | 88.24% | 17 | 3369 | 0.50% |
| Arboletes | 3 | 20.00% | 12 | 80.00% | 15 | 2930 | 0.51% |
| Carepa | 3 | 27.27% | 8 | 72.73% | 11 | 1642 | 0.67% |
| Chigorodó | 4 | 25.00% | 12 | 75.00% | 16 | 4026 | 0.40% |
| Mutatá | 8 | 29.63% | 19 | 70.37% | 27 | 1280 | 2.11% |
| Necoclí | 2 | 6.67% | 28 | 93.33% | 30 | 3680 | 0.82% |
| San Pedro de Urabá | 2 | 25.00% | 6 | 75.00% | 8 | 2400 | 0.33% |
| Turbo | 11 | 34.38% | 21 | 65.63% | 32 | 4220 | 0.76% |
| Magdalena medio region | |||||||
| Puerto Berrio | 3 | 16.67% | 15 | 83.33% | 18 | 2375 | 0.76% |
| Puerto Triunfo | 5 | 15.63% | 27 | 84.38% | 32 | 1120 | 2.86% |
| Valle de Aburra region | |||||||
| Envigado | 14 | 17.50% | 66 | 82.50% | 80 | 7350 | 1.09% |
| Itagüí | 0 | 0.00% | 15 | 100.0% | 15 | 8690 | 0.17% |
| North region | |||||||
| Angostura | 3 | 11.54% | 23 | 88.46% | 26 | 1127 | 2.31% |
| Belmira | 6 | 46.15% | 7 | 53.85% | 13 | 933 | 1.39% |
| Campamento | 0 | 0.00% | 29 | 100.0% | 29 | 1130 | 2.57% |
| Carolina | 3 | 9.09% | 30 | 90.91% | 33 | 2020 | 1.63% |
| Entrerrios | 0 | 0.00% | 21 | 100.0% | 21 | 1024 | 2.05% |
| Guadalupe | 4 | 20.00% | 16 | 80.00% | 20 | 594 | 3.37% |
| Ituango | 1 | 6.25% | 15 | 93.75% | 16 | 1450 | 1.10% |
| San Andrés | 1 | 5.56% | 17 | 94.44% | 18 | 788 | 2.28% |
| Toledo | 2 | 12.50% | 14 | 87.50% | 16 | 375 | 4.27% |
| Eastern region | |||||||
| Alejandría | 1 | 2.86% | 34 | 97.14% | 35 | 594 | 5.89% |
| Argelia | 2 | 8.33% | 22 | 91.67% | 24 | 1010 | 2.38% |
| Cocorná | 4 | 12.50% | 28 | 87.50% | 32 | 936 | 3.42% |
| Concepción | 9 | 31.03% | 20 | 68.97% | 29 | 1100 | 2.64% |
| El Carmen | 2 | 5.41% | 35 | 94.59% | 37 | 2800 | 1.32% |
| El Peñol | 1 | 2.00% | 49 | 98.00% | 50 | 2669 | 1.87% |
| Granada | 2 | 8.33% | 22 | 91.67% | 24 | 600 | 4.00% |
| Guarne | 2 | 13.33% | 13 | 86.67% | 15 | 2815 | 0.53% |
| Guatapé | 1 | 3.57% | 27 | 96.43% | 28 | 843 | 3.32% |
| La Ceja | 0 | 0.00% | 19 | 100.0% | 19 | 2100 | 0.90% |
| Marinilla | 1 | 4.17% | 23 | 95.83% | 24 | 2825 | 0.85% |
| Nariño | 0 | 0.00% | 23 | 100.0% | 23 | 1250 | 1.84% |
| Santuario | 0 | 0.00% | 18 | 100.0% | 18 | 1800 | 1.00% |
| San Carlos | 2 | 5.56% | 34 | 94.44% | 36 | 1240 | 2.90% |
| San Francisco | 3 | 14.29% | 18 | 85.71% | 21 | 463 | 4.54% |
| San Rafael | 14 | 22.95% | 47 | 77.05% | 61 | 1410 | 4.33% |
| San Vicente | 6 | 16.22% | 31 | 83.78% | 37 | 1929 | 1.92% |
| Sonsón | 0 | 0.00% | 26 | 100.0% | 26 | 4357 | 0.60% |
| Northeast region | |||||||
| Anorí | 1 | 3.03% | 32 | 96.97% | 33 | 801 | 4.12% |
| San Roque | 5 | 13.89% | 31 | 86.11% | 36 | 1920 | 1.88% |
| West region | |||||||
| Armenia | 7 | 17.50% | 33 | 82.50% | 40 | 604 | 6.62% |
| Cañas Gordas | 3 | 14.29% | 18 | 85.71% | 21 | 1398 | 1.50% |
| Ebéjico | 1 | 4.35% | 22 | 95.65% | 23 | 2450 | 0.94% |
| Frontino | 3 | 7.32% | 38 | 92.68% | 41 | 1593 | 2.57% |
| Olaya | 0 | 0.00% | 22 | 100.0% | 22 | 570 | 3.86% |
| Santafé de Antioquia | 0 | 0.00% | 27 | 100.0% | 27 | 2050 | 1.32% |
| Sopetran | 0 | 0.00% | 48 | 100.0% | 48 | 1470 | 3.27% |
| Uramita | 3 | 25.00% | 9 | 75.00% | 12 | 890 | 1.35% |
| Total, municipalities | 150 | 11.24% | 1185 | 88.76% | 1335 | 97,010 | 1.38% |
| under study | |||||||
Table 2.
Description of the panel of Leptospira sp. serogroups used in the microagglutination test (MAT) and the number of positive dogs with titers ≥ 1:50 in the Department of Antioquia. Canicola and Icterohaemorrhagiae serogroups were tested in 1335 dogs and other serogroups in a subset of 212 dogs.
Table 2.
Description of the panel of Leptospira sp. serogroups used in the microagglutination test (MAT) and the number of positive dogs with titers ≥ 1:50 in the Department of Antioquia. Canicola and Icterohaemorrhagiae serogroups were tested in 1335 dogs and other serogroups in a subset of 212 dogs.
| No. | Species | Serogroup | Serovar | Strain | Number of Positives |
|---|---|---|---|---|---|
| 1 | L. interrogans | Icterohaemorrhagiae | Icterohaemorrhagiae | RGA | 43 |
| 2 | L. interrogans | Canicola | Canicola | Hond Utrecht IV | 76 |
| 3 | L. interrogans | Pomona | Pomona | Pomona | 8 |
| 4 | L. interrogans | Sejroe | Hardjo | Hardjoprajitno | 5 |
| 5 | L. interrogans | Grippothyposa | Grippothyposa | Moskva | 3 |
| 6 | L. borgpetersenii | Tarassovi | Tarassovi | Perepelitsin | 2 |
| 7 | L. borgpetersenii | Ballum | Castellonis | Castellon 3 | 6 |
| 8 | L. borgpetersenii | Australis | Bratislava | Jez Bratislava | 3 |
| 9 | L. santarosai | Grippothyposa | Alice | JET | 4 |
Table 3.
Prevalence ratio (PR) of the dog characteristics by the MAT results with the serogroups Canicola and Icterohaemorrhagiae, Antioquia, 2015.
Table 3.
Prevalence ratio (PR) of the dog characteristics by the MAT results with the serogroups Canicola and Icterohaemorrhagiae, Antioquia, 2015.
| Reactive MAT | Not Reactive MAT | Total † | PR (CI 95%) | p-Value | ||||
|---|---|---|---|---|---|---|---|---|
| n | % | n | % | n | % | |||
| Sex | ||||||||
| Male | 25 | 13.44% | 161 | 86.56% | 186 | 100% | 1.075 (0.79–1.63) | 0.4080 |
| Female | 84 | 12.50% | 588 | 87.50% | 672 | 100% | ||
| Breed | ||||||||
| Purebred | 25 | 11.52% | 192 | 88.48% | 217 | 100% | 0.85 (0.558–1.293) | 0.2610 |
| Cross | 81 | 13.57% | 516 | 86.43% | 597 | 100% | ||
| Housing area | ||||||||
| Rural | 44 | 13.54% | 281 | 86.46% | 325 | 100% | 1.014 (0.959–1.072) | 0.3540 |
| Urban | 54 | 12.36% | 383 | 87.64% | 437 | 100% | ||
| History of leptospirosis | ||||||||
| Yes | 0 | 0.00% | 2 | 100.00% | 2 | 100% | 0.7490 | |
| No | 102 | 13.51% | 653 | 86.49% | 755 | 100% | ||
| Vaccination against leptospirosis | ||||||||
| Yes | 3 | 4.48% | 64 | 95.52% | 67 | 100% | 0.318 (0.104–0.975) | 0.014 * |
| No | 102 | 14.09% | 622 | 85.91% | 724 | 100% | ||
| History of clinical signs | ||||||||
| Jaundice | ||||||||
| Yes | 1 | 20.00% | 4 | 80.00% | 5 | 100% | 1.504 (0.258–8.766) | 0.5120 |
| No | 98 | 13.30% | 639 | 86.70% | 737 | 100% | ||
| Hematuria | ||||||||
| Yes | 0 | 0.00% | 3 | 100.00% | 3 | 100% | 0.6530 | |
| No | 102 | 13.30% | 655 | 85.40% | 767 | 100% | ||
| Abortion | ||||||||
| Yes | 5 | 33.33% | 10 | 66.67% | 15 | 100% | 2.685 (1.272–5.668) | 0.034 * |
| No | 73 | 12.41% | 515 | 87.59% | 588 | 100% | ||
| Canine habits | ||||||||
| Most frequented place | ||||||||
| Interior | 64 | 14.71% | 371 | 85.29% | 435 | 100% | 1.37 (0.908–2.067) | 0.0800 |
| Exterior | 29 | 10.74% | 241 | 89.26% | 270 | 100% | ||
| Resting place | ||||||||
| Exterior | 43 | 11.50% | 331 | 88.50% | 374 | 100% | 0.77 (0.525–1.127) | 0.1080 |
| Interior | 49 | 14.94% | 279 | 85.06% | 328 | 100% | ||
† There are missing values in surveys. Absolute number of total patients can change between each variable. * Value p < 0.05.
Table 4.
Prevalence ratio (PR) of the peri- and domiciliary characteristics of dog owners’ households and seropositive dogs by microagglutination test with the serogroups Canicola and Icterohaemorrhagiae in Antioquia, 2015.
Table 4.
Prevalence ratio (PR) of the peri- and domiciliary characteristics of dog owners’ households and seropositive dogs by microagglutination test with the serogroups Canicola and Icterohaemorrhagiae in Antioquia, 2015.
| Reactive MAT | Not Reactive MAT | Total † | PR (CI 95%) | p-Value | ||||
|---|---|---|---|---|---|---|---|---|
| n | % | n | % | n | % | |||
| Roof materials | ||||||||
| Modern materials | 44 | 14.06% | 269 | 85.94% | 313 | 100% | 0.714 (0.408–1.48) | 0.164 |
| Traditional materials | 13 | 19.70% | 53 | 80.30% | 66 | 100% | ||
| Wall materials | ||||||||
| Modern materials | 45 | 15.15% | 252 | 84.85% | 297 | 100% | 1.010 (0.562–1.817) | 0.566 |
| Traditional materials | 12 | 15.00% | 68 | 85.00% | 80 | 100% | ||
| Floor materials | ||||||||
| Modern materials | 50 | 14.25% | 301 | 85.75% | 351 | 100% | 0.509 (0.258–1.003) | 0.066 |
| Traditional materials | 7 | 28.00% | 18 | 72.00% | 25 | 100% | ||
| History of flooding | ||||||||
| Yes | 5 | 27.78% | 13 | 72.22% | 18 | 100% | 1.670 (0.772–3.641) | 0.176 |
| No | 78 | 16.63% | 391 | 83.37% | 469 | 100% | ||
| Peridomiciliary housing | ||||||||
| Yes | 40 | 15.04% | 226 | 84.96% | 266 | 100% | 0.602 (0.347–1.043) | 0.064 |
| No | 13 | 25.00% | 39 | 75.00% | 52 | 100% | ||
| Peridomiciliary forest | ||||||||
| Yes | 12 | 23.53% | 39 | 76.47% | 51 | 100% | 1.532 (0.867–2.708) | 0.112 |
| No | 41 | 15.36% | 226 | 84.64% | 267 | 100% | ||
| Peridomiciliary crops | ||||||||
| Yes | 11 | 16.42% | 56 | 83.58% | 67 | 100% | 0.981 (0.535–1.800) | 0.558 |
| No | 42 | 16.73% | 209 | 83.27% | 251 | 100% | ||
| Peridomiciliary water | ||||||||
| Yes | 15 | 30.61% | 34 | 69.39% | 49 | 100% | 2.167 (1.296–3.624) | 0.006 * |
| No | 38 | 14.13% | 231 | 85.87% | 269 | 100% | ||
| Peridomiciliary Bare soil | ||||||||
| Yes | 16 | 34.78% | 30 | 65.22% | 46 | 100% | 2.557 (1.558–4.200) | 0.001 * |
| No | 37 | 13.60% | 235 | 86.40% | 272 | 100% | ||
| Peridomiciliary roads | ||||||||
| Yes | 21 | 23.60% | 68 | 76.40% | 89 | 100% | 1.689 (1.031–2.764) | 0.031 * |
| No | 32 | 13.97% | 197 | 86.03% | 229 | 100% | ||
| Source of drinking water | ||||||||
| Treated water | 71 | 15.71% | 381 | 84.29% | 452 | 100% | 1.055 (0.673–1.652) | 0.467 |
| Untreated water | 21 | 14.89% | 120 | 85.11% | 141 | 100% | ||
| Place of food preparation | ||||||||
| Outside of the house | 86 | 15.28% | 477 | 84.72% | 563 | 100% | 0.306 (0.134–0.696) | 0.052 |
| Inside the house | 3 | 50.00% | 3 | 50.00% | 6 | 100% | ||
| Municipal garbage collection service | ||||||||
| Yes | 72 | 15.55% | 391 | 84.45% | 463 | 100% | 0.855 (0.569–1.285) | 0.266 |
| No | 26 | 18.18% | 117 | 81.82% | 143 | 100% | ||
| Municipal sewer service | ||||||||
| Yes | 61 | 15.06% | 344 | 84.94% | 405 | 100% | 0.846 (0.577–1.240) | 0.231 |
| No | 34 | 17.80% | 157 | 82.20% | 191 | 100% | ||
† There are missing values in surveys. Absolute number of total patients can change between each variable. * Value p < 0.05.
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Perez-Garcia, J.; Monroy, F.P.; Agudelo-Florez, P. Canine Leptospirosis in a Northwestern Region of Colombia: Serological, Molecular and Epidemiological Factors. Pathogens 2022, 11, 1040. https://doi.org/10.3390/pathogens11091040
AMA Style
Perez-Garcia J, Monroy FP, Agudelo-Florez P. Canine Leptospirosis in a Northwestern Region of Colombia: Serological, Molecular and Epidemiological Factors. Pathogens. 2022; 11(9):1040. https://doi.org/10.3390/pathogens11091040
Chicago/Turabian StylePerez-Garcia, Janeth, Fernando P. Monroy, and Piedad Agudelo-Florez. 2022. "Canine Leptospirosis in a Northwestern Region of Colombia: Serological, Molecular and Epidemiological Factors" Pathogens 11, no. 9: 1040. https://doi.org/10.3390/pathogens11091040
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