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首页> 外文期刊>Veterinary World >2. Epidemiology and diagnosis of feline panleukopenia virus in Egypt: Clinical and molecular diagnosis in cats
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2. Epidemiology and diagnosis of feline panleukopenia virus in Egypt: Clinical and molecular diagnosis in cats

机译:2.埃及猫泛白细胞减少症病毒的流行病学和诊断:猫的临床和分子诊断

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Aim: This work aimed to study epidemiology and diagnosis of feline panleukopenia virus (FPV) using clinical examination, direct ELISA, RNA viral isolation and identification, and knowing phylogenetic tree of our isolate. Materials and Methods: One hundred and sixty-five cats of different ages and sex were examined. Each cat was examined clinically to detect the clinical manifestations of the disease showing symptoms suggestive of feline panleukopenia (FP) as well as ELISA, and polymerase chain reaction (PCR) amplification analyses were conducted. Results: Our finding includes (a) clinical signs detected in 165 of 165 cats were in the form of lethargy, fever, anorexia, thirst, vomiting, diarrhea, dehydration, and leukopenia. (b) ELISA results revealed that 66 of all examined cats were positive for FPV. (c) The amplification products from all positive samples were confirmed as FPV (VP1) gene by nucleotide sequences analysis, in which 75 samples were positive using PCR amplification for the FPV. (d) Statistical evaluation of ELISA results in comparison to PCR findings. ELISA showed 88%, 100%, and 94.5% for sensitivity, specificity, and accuracy, respectively, while the prevalence of FP among the examined population was 45%. No effect on sex, breed, and age on ELISA results as recorded using Chi-square analysis. Conclusion: The results of the sequence analysis indicated that PCR products of the FPV cDNA exhibited very low variation in their nucleotide sequence of all isolates compared with the published FPV genome, which could be suggested that FPV appears to be genomically stasis compared with other Parvoviruses. The genome sequence of FPLV strain in this study has been deposited in GenBank under the accession number KY466003. Our isolate closely related 100% to isolates from Portugal, which might be the origin of infection to Egypt through importation of cats.
机译:目的:这项工作旨在通过临床检查,直接ELISA,RNA病毒分离和鉴定以及了解我们分离株的系统树来研究猫泛白细胞减少症病毒(FPV)的流行病学和诊断。材料和方法:检查了165只不同年龄和性别的猫。每只猫均经过临床检查,以检测该疾病的临床表现,表现出表明猫泛白细胞减少症(FP)的症状以及ELISA,并进行了聚合酶链反应(PCR)扩增分析。结果:我们的发现包括(a)在165只猫中的165只猫中有165例检测到临床症状,表现为嗜睡,发烧,厌食,口渴,呕吐,腹泻,脱水和白细胞减少。 (b)ELISA结果表明,所有接受检查的猫中有66只FPV阳性。 (c)通过核苷酸序列分析将所有阳性样品的扩增产物确认为FPV(VP1)基因,其中使用FPV的PCR扩增对75个样品阳性。 (d)ELISA结果与PCR结果相比的统计评估。 ELISA检测的敏感性,特异性和准确性分别为88%,100%和94.5%,而被调查人群中FP的患病率为45%。使用卡方分析记录的结果对ELISA结果的性别,品种和年龄均无影响。结论:序列分析结果表明,与已公布的FPV基因组相比,FPV cDNA的PCR产物在所有分离株的核苷酸序列中均表现出非常低的变异,这可能表明FPV与其他细小病毒相比似乎在基因组上处于停滞状态。本研究中FPLV菌株的基因组序列已保藏在GenBank中,登录号为KY466003。我们的分离株与来自葡萄牙的分离株有100%的密切关系,这可能是通过猫的传入埃及感染的起源。

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