接种疫苗和未接种疫苗的种鸡所产肉鸡禽类腺病毒的分子流行病学。

Tansu Bıçakcıoğlu, Hamit Kaan Müştak, Seyyide Sarıçam İnce, Şimal Yörük, Gültekin Ünal
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摘要

鸡禽流感病毒(FAdVs)广泛分布于家禽群体中,导致各种疾病、免疫抑制和经济损失。循环FAdV分离株的分子特征和系统发育分析在流行病学研究中起着至关重要的作用,有助于控制、监测和预防相关疾病的爆发。本研究旨在确定 FAdV 的血清型并揭示肉鸡群中的分子流行病学。根据疫苗接种情况、鸡龄和传播途径等流行病学重要参数采集样本。从报告疑似 FAdV 临床症状和死亡的鸡群中随机抽取了 20 个接种疫苗的鸡群(VF,源自接种疫苗的种鸡品系的鸡群)和 20 个未接种疫苗的鸡群(NVF,源自未接种疫苗的种鸡品系的鸡群)。在 12 和 18 周龄时,使用商业灭活疫苗对鸡群的胸肌进行肌肉注射。在两个不同的生产周期和三个不同的年龄组(1 日龄、14 日龄和 28 日龄鸡)中,从每个鸡群采集肝脏和泄殖腔拭子样本。利用针对 hexon loop-1 基因的 PCR 技术对肝脏和泄殖腔交换样本进行了 FAdV 分析。分子检测结果显示,所有鸡群中有 30.0%(24/80)的鸡呈 FAdV 阳性,其中 50.0%(20/40)的鸡呈 NVF 阳性,10.0%(4/40)的鸡呈 VF 阳性。对 hexon loop-1 基因的序列分析表明,所有样本均为 FAdV-8b 血清型(OR670689-OR670712),相似度为 100.0%。随机抽取的一个 FAdV-8b 样本进行了全基因组序列分析。这是土耳其首次将 FAdV 全基因组序列(44 139 bp)存入 GenBank 数据库(PP236873)。鉴于VF中的FAdV阳性率明显低于NVF,研究结果表明,接种疫苗是预防FAdV相关感染的有效工具。
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Molecular Epidemiology of Fowl Aviadenoviruses in Broiler Chickens from Vaccinated and Nonvaccinated Breeders.

Fowl aviadenoviruses (FAdVs) are widely distributed among poultry populations, leading to various diseases, immunosuppression, and economic losses. Molecular characterization and phylogenetic analysis of circulating FAdV isolates play a critical role in epidemiologic studies, contributing to the control, monitoring, and prevention of related outbreaks. This study aimed to determine the serotypes of FAdV and reveal the molecular epidemiology in broiler chicken flocks. Samples were taken based on epidemiologically important parameters, such as vaccination status, age, and transmission route. A total of 20 vaccinated flocks (VF, flocks originated from vaccinated breeder lines) and 20 nonvaccinated flocks (NVF, flocks originated from nonvaccinated breeder lines) were randomly selected from flocks reporting suspected FAdV clinical symptoms and deaths. Vaccination was administered by intramuscular injection into the pectoral muscle with a commercial inactivated vaccine at 12 and 18 wk. Liver and cloacal swab samples were collected from each flock over two different production cycles and for three different age groups (1-day-old, 14-day-old, and 28-day-old chickens). The liver and cloacal swap samples were analyzed for FAdV using PCR targeting the hexon loop-1 gene. Molecular detection revealed that 30.0% (24/80) of all flocks were FAdV positive, with 50.0% (20/40) positivity in NVF and 10.0% (4/40) in VF. Sequence analysis of the hexon loop-1 gene revealed that all samples were FAdV-8b serotype (OR670689-OR670712), with 100.0% similarity. One randomly selected FAdV-8b sample was analyzed by whole-genome sequence analysis. This is the first study in Turkey to deposit an FAdV whole-genome sequence (44,139 bp) into the GenBank database (PP236873). Given the significantly lower FAdV positivity rates in VF compared to NVF, the findings indicate that vaccination is an effective tool for protecting against FAdV-related infections.

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