Molecular characterization and recombination analysis of Gyrovirus homsa2 in chickens.

IF 2.5 2区 农林科学 Q1 VETERINARY SCIENCES
Zhibin Zhang, Weichi Li, Xin Xu, Dandan Li, Jun Ji, Lunguang Yao, Yingzuo Bi, Qingmei Xie
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引用次数: 0

Abstract

ABSTRACTGyrovirus homsa2 (GyVh2), originally identified in Tunisian children with diarrhea, was previously known as Gyrovirus 6. In this study, chickens from 36 poultry farms across four major poultry-producing provinces in China (Henan, Hubei, Anhui, and Jiangsu) were screened for GyVh2 using polymerase chain reaction (PCR) from 2022 to 2024. As a result, 12 farms positive for GyVh2 were detected and subsequently conducted whole-genome sequencing for GyVh2. The genomes of the 12 GyVh2 from positive farms were all 2,282 nucleotides (nt) in length. Sequence similarity analysis showed high similarity (94.87%-99.65%) among the obtained and reference GyVh2 strains with no significant determining of years or geographic distribution, but low similarity (48.99%-57.60%) with other Gyrovirus species (Gyrovirus chickenanemia, Gyrovirus galga1, Gyrovirus galga2 and Gyrovirus homsa1). Phylogenetic analysis of the whole genome sequences of all 12 positive farms GyVh2 revealed that they formed a unique branch, clearly separated from other Gyrovirus species. Recombination analysis suggested that HN220604 (accession NO.: 9595.1) and HN221228 (accession NO.: 9596.1) may have originated from recombination with the human-derived GyVh2 strain (accession NO.: NC_022789.1). A hypervariable region (located at sites 140-152) and highly mutated sites at positions 149, 254 and 380 were identified in the capsid protein through amino acid mutation analysis. The observed association between GyVh2 cross-species transmission and complex mutations and recombination offers a basis for future studies on its molecular epidemiology and evolution.

鸡homsa2型回旋病毒的分子特征及重组分析。
Gyrovirus homsa2 (GyVh2)最初在突尼斯腹泻儿童中被发现,以前被称为Gyrovirus 6。本研究采用聚合酶链反应(PCR)技术,从2022年至2024年对中国4个主要家禽生产省份(河南、湖北、安徽和江苏)的36家家禽养殖场的鸡进行了GyVh2筛选。结果,检测到12个GyVh2阳性的猪场,并随后对GyVh2进行了全基因组测序。阳性农场的12株GyVh2的基因组长度均为2,282个核苷酸(nt)。序列相似性分析显示,获得的GyVh2毒株与参考毒株具有较高的相似性(94.87% ~ 99.65%),与其他旋病毒种属(鸡贫血旋病毒、galga1旋病毒、galga2旋病毒和homsa1旋病毒)的相似性较低(48.99% ~ 57.60%)。对所有12个阳性农场GyVh2的全基因组序列进行系统发育分析,发现它们形成了一个独特的分支,与其他回旋病毒物种明显分离。重组分析表明,HN220604 (accession NO.;编号:9595.1)和HN221228 (accession NO. 5)。基因号:9596.1)可能起源于与人源性GyVh2菌株的重组。: NC_022789.1)。通过氨基酸突变分析,在衣壳蛋白中发现了一个高变区(位于位点140-152)和高度突变位点149、254和380。观察到GyVh2跨物种传播与复杂突变和重组的关系,为进一步研究其分子流行病学和进化奠定了基础。
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来源期刊
Avian Pathology
Avian Pathology 农林科学-兽医学
CiteScore
4.50
自引率
10.70%
发文量
68
审稿时长
1 months
期刊介绍: Avian Pathology is the official journal of the World Veterinary Poultry Association and, since its first publication in 1972, has been a leading international journal for poultry disease scientists. It publishes material relevant to the entire field of infectious and non-infectious diseases of poultry and other birds. Accepted manuscripts will contribute novel data of interest to an international readership and will add significantly to knowledge and understanding of diseases, old or new. Subject areas include pathology, diagnosis, detection and characterisation of pathogens, infections of possible zoonotic importance, epidemiology, innate and immune responses, vaccines, gene sequences, genetics in relation to disease and physiological and biochemical changes in response to disease. First and subsequent reports of well-recognized diseases within a country are not acceptable unless they also include substantial new information about the disease or pathogen. Manuscripts on wild or pet birds should describe disease or pathogens in a significant number of birds, recognizing/suggesting serious potential impact on that species or that the disease or pathogen is of demonstrable relevance to poultry. Manuscripts on food-borne microorganisms acquired during or after processing, and those that catalogue the occurrence or properties of microorganisms, are unlikely to be considered for publication in the absence of data linking them to avian disease.
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