Detection of Parasites Using Traditional and Advanced Molecular Techniques

A special issue of Animals (ISSN 2076-2615). This special issue belongs to the section "Veterinary Clinical Studies".

Deadline for manuscript submissions: closed (1 August 2023) | Viewed by 4808

Special Issue Editors


E-Mail Website
Guest Editor
1. College of Life Science and Engineering, Foshan University, Foshan 528231, China
2. Faculty of Science, Kafrelsheikh University, Kafr El-Shaikh, Egypt
Interests: parasitology; immunology; veterinary medicine and next - generation sequencing (MiSeq and HiSeq)
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Associate Professor, King Abdulaziz City for Science and Technology, Riyadh 12354, Saudi Arabia
Interests: animal infectious and parasitic diseases; zoonoses; molecular parasitology

E-Mail Website
Guest Editor
Faculty of Science, Menofia University, Shibeen El-Kom, Egypt
Interests: molecular microbiology; DNA barcoding; population genetics; biodiversity and gene evolution

Special Issue Information

Dear Colleagues,

The global death toll from parasitic diseases has been reduced, partly due to the widespread use of molecular tests in the diagnosis, therapy, and epidemiological research of these illnesses. Techniques, such as optical microscopy, are employed in the laboratory for the morphological identification of parasites, which is the standard practice in parasitology. Nonetheless, the inconsistency in detecting these parasite forms may reduce the sensitivity of such approaches. To overcome these obstacles, molecular techniques are used to identify parasites that cause parasitic illnesses. Molecular approaches have been demonstrated in several studies to be very effective and sensitive in detecting parasite infections. The utility of molecular techniques in epidemiological studies is particularly striking because studies of this nature involve the genetic diversity of populations, their susceptibility to infection and the possibility of mutation, the geographical spread of parasite illnesses, and their association with hosts and clinical manifestations. 

Parasites can be identified using a variety of laboratory diagnostic assays, including the microsatellite marker method, PCR, AFLP, real-time PCR, RAPD, RFLP, LAMP, Luminex xMAP-based technology(nucleic-acid-based multiplex assays), and CRISPR-based detection. Many molecular epidemiology approaches are available for parasite detection and strain typing. These approaches include nested ITS-PCR, which is based on ITS gene-size variation, and MGE-PCR, which is based on mobile genetic element location variation (MGE).

Nanotechnology and nanomaterial advancements provide novel, adaptable, and intriguing diagnostic platforms. Nucleic-acid-detection techniques for in vitro molecular diagnostics using nanobiosensors and surface-enhanced Raman scattering (SERS) have been developed. The chip-based method employs SERS-active Nanowave chips for single-step multiplex detection. Sandwich hybridization using magnetic beads, target sequences, and SERS nanorattle nanoparticles is used in the nanoparticle-based method.

Recent breakthroughs in molecular methods have aided in the identification of taxonomic groupings at all levels (species, subspecies, populations, strains, and isolates). Next-generation sequencing (NGS) of amplicons allows for massive parallelization of sequencing operations and more efficient identification of low-abundance genotypes in mixed infections. Metabarcoding is a technique for identifying numerous species inside a sample at high throughput. It is a popular approach for identifying bacterial populations because it targets the ubiquitous bacterial 16S ribosomal RNA (rRNA) gene. Recent research has revealed that eukaryotic species may be similarly described by targeting the 18S rRNA gene.

This Special Issue aims to provide original research and reviews on the utility of molecular techniques in parasite detection, identification of taxonomic groupings at all levels (species, subspecies, populations, strains, and isolates), and epidemiological studies.

Prof. Dr. Saeed El-Ashram
Dr. Abdulaziz Alouffi
Prof. Dr. Sobhy Elsayed Hassab El-Nabi
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Animals is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2400 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • polymerase chain reaction
  • random amplified polymorphic DNA
  • amplified fragment-length
  • polymorphism
  • restriction fragment-length polymorphism
  • microsatellite marker method
  • luminex xMAP-based technology
  • nanobiosensors
  • surface-enhanced Raman scattering
  • CRISPR-based detection
  • next-generation sequencing
  • epidemiology
  • drug resistance
  • diagnosis
  • population structure
  • identification of taxonomic groupings

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

18 pages, 3307 KiB  
Article
First Report of Rickettsia conorii in Hyalomma kumari Ticks
by Shafi Ullah, Abdulaziz Alouffi, Mashal M. Almutairi, Nabila Islam, Gauhar Rehman, Zia Ul Islam, Haroon Ahmed, Itabajara da Silva Vaz Júnior, Marcelo B. Labruna, Tetsuya Tanaka and Abid Ali
Animals 2023, 13(9), 1488; https://doi.org/10.3390/ani13091488 - 27 Apr 2023
Cited by 7 | Viewed by 1744
Abstract
As a vector of wide range of pathogenic agents, ticks pose health threats to wild and domestic animals, and humans. Information is unavailable about the prevalence and spatial survey of Hyalomma kumari ticks and associated Rickettsia spp. in Pakistan. Concerning this knowledge gap, [...] Read more.
As a vector of wide range of pathogenic agents, ticks pose health threats to wild and domestic animals, and humans. Information is unavailable about the prevalence and spatial survey of Hyalomma kumari ticks and associated Rickettsia spp. in Pakistan. Concerning this knowledge gap, the present study aimed to molecularly detect Rickettsia species associated with H. kumari infesting small ruminants in Khyber Pakhtunkhwa (KP), Pakistan. A total of 409 H. kumari ticks were collected from 163/295 infested hosts with an infestation rate of 55.25%. A total of 204 females, 158 males, and 47 nymphs were collected. Goats were heavily infested by 224 ticks having an infestation rate of 58.33% (98/168), whereas sheep were infested by 185 ticks having a lesser infestation rate of 51.18% (65/127). Genomic DNA extracted from ticks was used for the amplification of tick (cox I, 16S rRNA, ITS-2) species and Rickettsia (gltA, ompA, and ompB) partial genes. Eighty-three ticks were subjected to PCR, and 8/83 (9.6%) were found positive for rickettsial agents. The cox I and 16S rRNA sequences of H. kumari showed 98.90–99.74% identity with H. kumari sequences reported from Pakistan, and phylogenetically clustered to the corresponding species reported from Pakistan and India. The obtained rickettsial gltA, ompA, and ompB sequences showed 100% identity with Rickettsia sp. of the Rickettsia conorii reported from Pakistan. In the phylogenetic trees, rickettsial sequences clustered with uncharacterized Rickettsia sp. from Pakistan and R. conorii from Israel, Russia, South Africa, and India. The present molecular based detection of H. kumari-associated R. conorii will facilitate effective surveillance in the region. Full article
Show Figures

Figure 1

10 pages, 1325 KiB  
Article
A Monogenean Gill Parasite within the Genus Haliotrema (Ancyrocephalidae) Infecting Argyrops filamentosus Fish: Morphology and Molecular Studies
by Rewaida Abdel-Gaber, Masheil Alghamdi, Saleh Al Quraishy, Esam M. Al-Shaebi, Manal F. Elkhadragy, Saeed El-Ashram and Mohamed A. Dkhil
Animals 2023, 13(6), 1010; https://doi.org/10.3390/ani13061010 - 10 Mar 2023
Viewed by 1959
Abstract
Due to the presence of different parasite taxa and other disease-causing agents, all fish species are extremely prone to dangers. As a result, the current study focused on some of the monogenean parasites that infect one of the economically important fish species, the [...] Read more.
Due to the presence of different parasite taxa and other disease-causing agents, all fish species are extremely prone to dangers. As a result, the current study focused on some of the monogenean parasites that infect one of the economically important fish species, the soldier bream Argyrops filamentosus, from the Red Sea coast of Jeddah, Saudi Arabia. Following that, thirty A. filamentosus fish specimens were examined for monogenean parasites. The parasitic species were isolated and morphologically and molecularly studied. The presence of one monogenean species of Haliotrema susanae (F: Ancyrocephalidae) infecting gills was observed in 50% of the investigated fish species. The ancyrocephalid species Haliotrema susanae is characterized by having all generic features within the genus Haliotrema. It could be distinguished from other species within this genus by the male copulatory organ including a copulatory tube with no accessory piece and a haptor made up of two pairs of anchors, two bars, and seven pairs of marginal hooks. As ectoparasitic taxa of the investigated sparid fish, the current study of Haliotrema species constitutes the first report of this genus. A molecular phylogenetic analysis based on the partial 28S rRNA gene region was analyzed to investigate the phylogenetic affinity of this parasite with the genus Haliotrema belonging to Ancyrocephalidae. This study considers the addition of a new genetic sequence for this parasite species. Full article
Show Figures

Figure 1

Back to TopTop