Journals / Mehmet Akif Ersoy Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi / 2023 / Cilt: 11 Sayı: 2

Molecular prevalence of canine leishmaniasis in Burdur, Türkiye

Pages
244–252
Publication Date
2023-08-31
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The importance of vector fly control has been remembered once again in order to protect from the disease both animals that can be host of parasites, especially dogs, and human society, since it is a zoonotic disease.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Canine leishmaniasis (CanL) is among the most important vector-borne parasitic diseases in dogs worldwide, except for Oceania, and can be fatal if left untreated.
📊
Key Findings & Data:Blood samples collected from 120 dogs were first examined for Leishmania spp. by genus-spesific PCR and then positives were examined for L. infantum/donovani complex by species-spesific PCR.
💡
Conclusion & Impact:The importance of vector fly control has been remembered once again in order to protect from the disease both animals that can be host of parasites, especially dogs, and human society, since it is a zoonotic disease.
🔬Design:Research Article
📍Scope:120 samples
⚙️Variables:Burdur · canine leishmaniasis · Leishmania infantum

Abstract

Canine leishmaniasis (CanL) is among the most important vector-borne parasitic diseases in dogs worldwide, except for Oceania, and can be fatal if left untreated. The present study aimed to investigate the molecular prevalence of L. infantum, the causative agent of CanL, in Burdur province of Türkiye. Blood samples collected from 120 dogs were first examined for Leishmania spp. by genus-spesific PCR and then positives were examined for L. infantum/donovani complex by species-spesific PCR. As a result, Leishmania DNA was detected in five out of the 120 samples in the first-stage PCR, resulting in a molecular positivity rate of 4.16% at the genus level. Among these five samples, four were positive for L. infantum in the second-stage PCR, leading to a prevalence of 3.33% for L. infantum. No statistically significant differences were found in terms of gender and age concerning L. infantum positivity. Additionally, blood smears were examined under a microscope, but no Leishmania amastigotes were observed in any of the samples. With this obtained data, the presence of Leishmania spp. and L. infantum in dogs in Burdur is reported for the first time using a molecular method. The importance of vector fly control has been remembered once again in order to protect from the disease both animals that can be host of parasites, especially dogs, and human society, since it is a zoonotic disease.

🔖

Cite This Article

ÖZEN, Ö., KÖSE, O. (2023). Molecular prevalence of canine leishmaniasis in Burdur, Türkiye. Mehmet Akif Ersoy Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi, Cilt: 11 Sayı: 2, 244–252. https://ajindex.com/articles/959638

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Akhoundi, M., Kuhls, K., Cannet, A., Votýpka, J., Marty, P., Delaunay, P., Sereno, D., 2016. A historical overview of the classification, evolution, and dispersion of Leishmania parasites and sandflies. PLoS Neglected Tropical Diseases 10, 1-40.
  2. Akman, L., Aksu, H.S., Wang, R.Q., Özensoy, S., Özbel, Y., Alkan, Z., Özcel, M.A., Çulha, G., Özcan, K., Uzun, S., Memişoglu, H.R., Chang, K.P., 2000. Multi-site DNA polymorphism analyses of Leishmania isolates define their genotypes predicting clinical epidemiology of leishmaniasis in a specific region. Journal of Eukaryotic Microbiology 47, 545-554.
  3. Alemayehu, B., Alemayehu, M., 2017. Leishmaniasis: A Review on Parasite, Vector and Reservoir Host. Health Science Journal 11, 519. Andrade, H.M., Reis, A.B., Santos, S.L., Volpini, A.C., Marques, M.J., Romanha, A.J., 2006. Use of PCR-RFLP to identify Leishmania species in naturally-infected dogs. Veterinary Parasitology 140, 231-238.
  4. Aslan Çelik, B., Şahin, T., Çelik, Ö., 2019. Retrospective Evaluation of Canine Leishmaniasis in Turkey. Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi 33, 123-130.
  5. Aydenizöz, M., Yağcı, B.B., Taylan Özkan, A., Duru, S.Y., Gazyağcı, A.N., 2010. Investigation of the prevalence of visceral leishmaniasis by the microculture method and IFAT in dogs in Kırıkkale. Türkiye Parazitoloji Dergisi 34, 1-5.
  6. Ayele, A., Seyoum, Z., 2016. A Review on Canine Leishmaniasis; Etiology, Clinical Sign, Pathogenesis, Treatment and Control Methods. Global Veterinaria 17, 343-352.
  7. Bakırcı, S., Bilgiç, H.B., Köse, O., Aksulu, A., Hacılarlıoğlu, S., Erdoğan, H., Karagenç, T., 2016. Molecular and seroprevalence of canine visceral leishmaniasis in West Anatolia, Turkey. Turkish Journal of Veterinary and Animal Sciences 40, 637-644.
  8. Bakırcı, S., Topçuoğlu, A.D., 2021. Molecular and Serological Analysis for Prevalence of Canine Visceral Leishmaniasis in the Muğla Region of Turkey. Türkiye Parazitoloji Dergisi 45, 11-16.
  9. Bamorovat, M., Sharifi, I., Dabiri, S., Mohammadi, M.A., Harandi, M.F., Mohebali, M., Aflatoonian, M.R., Keyhani, A., 2015. Leishmania tropica in Stray Dogs in Southeast Iran. Iranian Journal of Public Health 44, 1359-1366.
  10. Baneth, G., Koutinas, A.F., Solano-Gallego, L., Bourdeau, P., Ferrer, L., 2008. Canine leishmaniosis – new concepts and insights on an expanding zoonosis: part one. Trends in Parasitology 24, 324-330.
  11. Baneth, G., Zivotofsky, D., Nachum-Biala, Y., Yasur-Landau, D., Botero, A.M., 2014. Mucocutaneous Leishmania tropica infectio