Parasitology Diseases in Large Animals

A special issue of Veterinary Sciences (ISSN 2306-7381). This special issue belongs to the section "Veterinary Microbiology, Parasitology and Immunology".

Deadline for manuscript submissions: 16 September 2024 | Viewed by 5081

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Nature Research Centre, Akademijos Str. 2, LT-08412 Vilnius, Lithuania
Interests: parasitology; population genetics; taxonomy; phylogeny; conservation genetics; bioinformatics; molecular biology
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Special Issue Information

Dear Colleagues,

Parasites in animals are not uncommon. Parasitic diseases impair the health, reproduction, growth, and productivity of large animals, and more severe cases can lead to death. Parasitic infections can cause digestive tract, lung, skin, or other dysfunction in large animals, then trigger heavy economic losses. While it is not always possible to avoid parasites in the first place, being able to reduce the risk of infection, identify the type of parasite, and treat the infection helps ensure the continued health and safety of the large animal.

We invite you to submit your original research article, review, and communication to our Special Issue. The Special Issue topic includes, but is not limited to:

  1. Livestock parasites;
  2. One health;
  3. Gastrointestinal parasites;
  4. The economic impact of parasites;
  5. Effects of parasites on animals;
  6. Roundworms;
  7. Pinworms;
  8. Ticks;
  9. Threadworms.

Dr. Dalius Butkauskas
Guest Editor

Manuscript Submission Information

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Keywords

  • large animals
  • parasitic diseases
  • parasitic infections
  • one health

Published Papers (3 papers)

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Research

12 pages, 1319 KiB  
Article
Analysis of Trypanosoma equiperdum Recombinant Proteins for the Serological Diagnosis of Dourine
by Mirella Luciani, Gisella Armillotta, Tiziana Di Febo, Ivanka Krasteva, Simonetta Ulisse, Chiara Di Pancrazio, Caterina Laguardia, Fabrizia Perletta, Anna Serroni, Marta Maggetti, Lilia Testa, Flavio Sacchini, Mariangela Iorio, Diamante Rodomonti, Manuela Tittarelli and Maria Teresa Mercante
Vet. Sci. 2024, 11(3), 127; https://doi.org/10.3390/vetsci11030127 - 13 Mar 2024
Viewed by 1151
Abstract
The significance of Trypanosoma equiperdum as the causative agent of dourine cannot be understated, especially given its high mortality rate among equids. International movement of equids should be subject to thorough health checks and screenings to ensure that animals are not infected with [...] Read more.
The significance of Trypanosoma equiperdum as the causative agent of dourine cannot be understated, especially given its high mortality rate among equids. International movement of equids should be subject to thorough health checks and screenings to ensure that animals are not infected with Trypanosoma equiperdum. This involves the implementation of quarantine protocols, testing procedures, and the issuance of health certificates to certify the health status of the animals. Three proteins, the peptidyl-prolyl cis-trans isomerase (A0A1G4I8N3), the GrpE protein homolog (A0A1G4I464) and the transport protein particle (TRAPP) component, putative (A0A1G4I740) (UniProt accession numbers SCU68469.1, SCU66661.1 and SCU67727.1), were identified as unique to T. equiperdum by bioinformatics analysis. The proteins were expressed as recombinant proteins and tested using an indirect ELISA and immunoblotting test with a panel of horse positive and negative sera for dourine. The diagnostic sensitivity, specificity and accuracy of the i-ELISAs were 86.7%, 53.8% and 59.0% for A0A1G4I8N3; 53.3%, 58.7% and 57.9% for A0A1G4I464; and 73.3%, 65.0% and 66.3% for A0A1G4I740, respectively, while the diagnostic sensitivity, specificity and accuracy of immunoblotting were 86.7%, 92.5% and 91.6% for A0A1G4I8N3; 46.7%, 81.3% and 75.8% for A0A1G4I464; and 80.0%, 63.8% and 66.3% for A0A1G4I740. Among the three proteins evaluated in the present work, A0A1G4I8N3 provided the best results when tested by immunoblotting; diagnostic application of this protein should be further investigated using a greater number of positive and negative sera. Full article
(This article belongs to the Special Issue Parasitology Diseases in Large Animals)
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12 pages, 6183 KiB  
Article
Molecular Detection of Candidatus Anaplasma camelii in Naturally Infected Dromedary Camels (Camelus dromedarius) in Abu Dhabi Emirate, United Arab Emirates, 2019–2023
by Hassan Zackaria Ali Ishag, Shameem Habeeba, El Tigani Ahmed El Tigani-Asil, Mohd Farouk Yuosf, Zulaikha Mohamed Abdel Hameed Al Hammadi, Abraham Nii Okai Commey, Hashel Talal Aboud Amer Bin Hraiz, Asma Abdi Mohamed Shah and Abdelmalik Ibrahim Khalafalla
Vet. Sci. 2024, 11(3), 123; https://doi.org/10.3390/vetsci11030123 - 7 Mar 2024
Viewed by 2177
Abstract
The recent emergence of anaplasmosis in camels has raised global interest in the pathogenicity and zoonotic potential of the pathogen causing it and the role of camels as reservoir hosts. In the United Arab Emirates (UAE), molecular studies and genetic characterization of camel-associated [...] Read more.
The recent emergence of anaplasmosis in camels has raised global interest in the pathogenicity and zoonotic potential of the pathogen causing it and the role of camels as reservoir hosts. In the United Arab Emirates (UAE), molecular studies and genetic characterization of camel-associated Anaplasma species are limited. This study aimed to characterize molecularly Anaplasmataceae strains circulating in dromedary camels in the UAE. Two hundred eighty-seven whole-blood samples collected from dromedary camels across regions of the Abu Dhabi Emirate were received between 2019 and 2023 at the Abu Dhabi Agriculture and Food Safety Authority (ADAFSA) veterinary laboratories for routine diagnosis of anaplasmosis. The animals were sampled based on field clinical observation by veterinarians and their tentative suspicion of blood parasite infection on the basis of similar clinical symptoms as those caused by blood parasites in ruminants. The samples were screened for Anaplasmataceae by PCR assay targeting the groEL gene. Anaplasmataceae strains were further characterized by sequencing and phylogenetic analysis of the groEL gene. Thirty-five samples (35/287 = 12.2%) tested positive for Anaplasmataceae spp. by PCR assay. Nine positive samples (9/35 = 25.7%) were sequenced using groEL gene primers. GenBank BLAST analysis revealed that all strains were 100% identical to the Candidatus A. camelii reference sequence available in the GenBank nucleotide database. Phylogenetic analysis further indicated that the sequences were close to each other and were located in one cluster with Candidatus A. camelii sequences detected in Saudi Arabia, Morocco, and the UAE. Pairwise alignment showed that the UAE sequences detected in this study were completely identical and shared 100% identity with Candidatus A. camelii from Morocco and Saudi Arabia and 99.5% identity with Candidatus A. camelii from the UAE. This study demonstrates the presence of Candidatus A. camelii in UAE dromedary camels. Further critical investigation of the clinical and economical significance of this pathogen in camels needs to be carried out. Full article
(This article belongs to the Special Issue Parasitology Diseases in Large Animals)
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12 pages, 2046 KiB  
Article
Sarcocystis Species Richness in Sheep and Goats from Lithuania
by Alina Marandykina-Prakienė, Dalius Butkauskas, Naglis Gudiškis, Evelina Juozaitytė-Ngugu, Dovilė Laisvūnė Bagdonaitė, Muza Kirjušina, Rafael Calero-Bernal and Petras Prakas
Vet. Sci. 2023, 10(8), 520; https://doi.org/10.3390/vetsci10080520 - 11 Aug 2023
Cited by 4 | Viewed by 1107
Abstract
Contradictory data is available on the intermediate host specificity of Sarcocystis spp. in farm animals. Therefore, the current work aimed at molecularly testing samples of sheep and goats reared in Lithuania to identify Sarcocystis species described in other intermediate hosts but suspected to [...] Read more.
Contradictory data is available on the intermediate host specificity of Sarcocystis spp. in farm animals. Therefore, the current work aimed at molecularly testing samples of sheep and goats reared in Lithuania to identify Sarcocystis species described in other intermediate hosts but suspected to be non-canonical parasites to these small ruminants. For this purpose, muscle samples from 47 domestic sheep and nine goats were examined. Sarcocystis species were identified using direct and nested PCR targeting cox1 and sequencing of positive amplified products. Along with the detection of the canonical Sarcocystis spp. in their respective intermediate hosts, the DNA of S. capracanis and S. morae was detected in sheep, although these species were previously thought to be specific to goats and deer, respectively. In addition, DNA from S. arieticanis and S. tenella was found in goats, even though these two species were believed to be sheep-specific. Notably, under light microscopy, only sarcocysts of S. capracanis specific to goats were observed. Thus, future research on the life cycle and host-specificity of Sarcocystis spp. examined is warranted. Full article
(This article belongs to the Special Issue Parasitology Diseases in Large Animals)
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