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哥伦比亚犬丝虫病中的微丝蚴感染:形态学和分子诊断中的一项挑战

Microfilaremic infection in canine filariosis in Colombia: a challenge in morphological and molecular diagnostics.

作者信息

Esteban-Mendoza María Victoria, Arcila-Quiceno Victor Hernán, Ríos Chacón Catalina, Jaimes Dueñez Jeiczon Elim, Tique Oviedo Marisol, Díaz Bustos Alejandro, Castellanos María Fernanda, Morchón Rodrigo

机构信息

Grupo GRICA, Facultad de Medicina Veterinaria y Zootecnia, Maestría en Salud y Producción Animal, Universidad Cooperativa de Colombia, Bucaramanga, Santander, Colombia.

Biovet Diagnóstico Veterinario Bga, Laboratorio Clínico Veterinario, Floridablanca, Santander, Colombia.

出版信息

Front Vet Sci. 2024 Mar 27;11:1368307. doi: 10.3389/fvets.2024.1368307. eCollection 2024.

DOI:10.3389/fvets.2024.1368307
PMID:38601908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11005679/
Abstract

Canine filariosis is caused by filiform nematodes and affects several species of animals as well as humans. The disease produces a wide range of symptoms that can often be confused with other diseases, which increases the complexity of its diagnosis. The search for methodologies to facilitate its diagnosis is a challenge, and specific and differential identification of the parasite species causing the disease holds key to a successful diagnosis. In Colombia, there is a problem of underdiagnosis of filariosis in microfilaremic dogs infected by and , and of microfilaremias not related to heartworm disease. The highest prevalences have been reported for infections, although new cases of infections are beginning to appear. The aim of this study was to differentiate the microfilariae infections caused by and by a morphological and molecular characterization of microfilariae so as to facilitate an accurate diagnosis of canine filariosis in the metropolitan area of Bucaramanga (Colombia). For this purpose, 400 blood samples with anticoagulants were collected from the dogs and analyzed with the help of a commercial immunochromatography kit for the detection of circulating antigen. The Woo, Knott, and polymerase chain reaction (PCR) techniques were employed for determining the parasite count, morphological observation, and molecular identification of microfilariae present in the dogs respectively. The prevalence of microfilaremic dogs in Bucaramanga metropolitan area was 18.75% (75/400). The prevalence of dogs that tested positive for in the antigen and in PCR tests was 1.25% (5/400) and 1% (4/400), respectively. Furthermore, the PCR test revealed that 17.75% of the microfilaremic dogs tested positive for (71/400) (first report in the metropolitan area of Bucaramanga), with one animal co-infected by both species, and 0% for (0/400). However, by morphological characterization, 4% of the microfilariae (3/75) corresponded to , 20% (15/75) to , and 76% (57/75) to . The use of molecular diagnostic methods such as PCR aids in the specific identification of the parasite, thus making it a more accurate method than the morphological characterization of microfilariae. The identification of the parasites by PCR helps improve the veterinary diagnosis of canine filariosis in Colombia, which would lead to the establishment of an appropriate treatment protocol for each species of filaria and also to the generation of reliable data to be used at the clinical and epidemiological levels.

摘要

犬丝虫病由丝状线虫引起,可感染多种动物及人类。该病症状多样,常与其他疾病混淆,增加了诊断的复杂性。寻找便于诊断的方法是一项挑战,准确鉴别引起该病的寄生虫种类是成功诊断的关键。在哥伦比亚,感染 和 的微丝蚴血症犬的丝虫病诊断不足,以及与心丝虫病无关的微丝蚴血症问题较为突出。尽管 感染的新病例开始出现,但据报道 感染的患病率最高。本研究旨在通过对微丝蚴进行形态学和分子特征分析,区分由 和 引起的微丝蚴感染,以便在布卡拉曼加市(哥伦比亚)大都市区准确诊断犬丝虫病。为此,从犬只采集了400份抗凝血液样本,并借助用于检测 循环抗原的商业免疫层析试剂盒进行分析。分别采用吴(Woo)氏法、诺特(Knott)氏法和聚合酶链反应(PCR)技术测定犬体内微丝蚴的数量、进行形态学观察及分子鉴定。布卡拉曼加大都市区微丝蚴血症犬的患病率为18.75%(75/400)。抗原检测和PCR检测呈阳性的犬的患病率分别为1.25%(5/400)和1%(4/400)。此外,PCR检测显示,17.75%的微丝蚴血症犬 检测呈阳性(71/400)(布卡拉曼加大都市区的首次报告),有1只动物同时感染了这两种寄生虫, 检测呈阳性的比例为0%(0/400)。然而,通过形态学特征分析,4%的微丝蚴(3/75)对应 ,20%(15/75)对应 ,76%(57/75)对应 。使用PCR等分子诊断方法有助于特异性鉴定寄生虫,因此它比微丝蚴的形态学特征分析更准确。通过PCR鉴定寄生虫有助于改善哥伦比亚犬丝虫病的兽医诊断,这将有助于为每种丝虫建立适当的治疗方案,并生成可靠的数据用于临床和流行病学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/b366e5ad1220/fvets-11-1368307-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/7ac7bfb3082f/fvets-11-1368307-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/fba1df5c8f6e/fvets-11-1368307-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/bbd28c8bbbe3/fvets-11-1368307-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/b366e5ad1220/fvets-11-1368307-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/7ac7bfb3082f/fvets-11-1368307-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/fba1df5c8f6e/fvets-11-1368307-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/bbd28c8bbbe3/fvets-11-1368307-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fb/11005679/b366e5ad1220/fvets-11-1368307-g004.jpg

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