College of Animal Science, Shanxi Agricultural University, Taiyuan, 030032, China.
College of Animal Science, Shanxi Agricultural University, Taiyuan, 030032, China.
Microb Pathog. 2024 Sep;194:106827. doi: 10.1016/j.micpath.2024.106827. Epub 2024 Jul 30.
Integration of nucleic acid sequences of Reticuloendotheliosis virus (REV) in Avipoxvirus(APV) has become commonplace. In this study, 4 strains of suspected Fowlpox virus (FPV) and 1 strain of suspected Pigeonpox virus (PPV) collected in Taiyuan, Shanxi Province were cultured in chicken embryos, and the 4b core protein gene was amplified by PCR, and the identity and genome similarity were determined by sequence analysis. The sequences between the end of ORF201 and the beginning of ORF203 of FPV and PPV were then amplified, sequenced, and subjected to sequence comparison to determine genome similarity. The results showed that the isolates were 4 strains of FPV and 1 strain of PPV. The 4 isolated strains of FPV belong to type A1 virus, with 100 % identity to each other and to the FWPV-09-Jilin strain isolated in Jilin, China, and the lowest identity to the type B2 virus TNPV5/NZL/2009, which is only 74 %. PPV belongs to type A2 virus, and its identity with local strain of fowlpox virus was 90.1 %, with the highest identity of 100 % with PPLH and ROPI/W370/ON/2012 and ow_2017_3 strains, which also belong to type A2 pigeonpox virus, and the lowest identity of 73.7 % with TNPV5/NZL/2009, a type B2 virus. The complete genome of REV sequences integrated into FPV and PPV were amplified, and 5 REV nucleic acid sequences were obtained after sequencing and concatenation, with lengths ranging from 7942 to 8005 bp. The identity analysis results indicate that it has high identity with isolates from Northeast China, Guangdong, and Guangxi regions in China. Based on its gp90 protein gene, the REV integrated into the poxvirus belong to type III, with the highest identity of 99.9% with strains such as APC-566 and CY1111, and the lowest identity with REV-Anhui1, at 95.4 %. The length of the pol gene varies among different strains of REV, and its encoded amino acid changes significantly after position 675, with deletions and alterations. This study indicates that all fowlpox viruses isolated in Taiyuan, Shanxi Province have integrated the entire REV gene sequence, with high identity between them. At the same time, it indicates that the pigeonpox virus isolate has also integrated the entire REV gene sequence, and has the highest identity with the integrated REV gene sequence in fowlpox virus.
禽痘病毒(APV)中整合的禽网状内皮组织增生病病毒(REV)核酸序列已很常见。本研究对山西省太原市采集的 4 株疑似禽痘病毒(FPV)和 1 株疑似鸽痘病毒(PPV)进行鸡胚培养,采用 PCR 扩增 4b 核心蛋白基因,通过序列分析确定其同源性和基因组相似性。然后扩增、测序、比较 FPV 和 PPV 末端 ORF201 与 ORF203 之间的序列,确定基因组相似性。结果显示,分离株为 4 株 FPV 和 1 株 PPV。4 株分离的 FPV 属于 A1 型病毒,彼此之间以及与中国吉林分离的 FWPV-09-Jilin 株完全相同,与 B2 型 TNPV5/NZL/2009 的最低同一性为 74%。PPV 属于 A2 型病毒,与当地禽痘病毒的同源性为 90.1%,与 PPLH 和 ROPI/W370/ON/2012 以及 ow_2017_3 株的同源性最高,均为 100%,也属于 A2 型鸽痘病毒,与 B2 型 TNPV5/NZL/2009 的最低同一性为 73.7%。扩增了整合到 FPV 和 PPV 中的 REV 完整基因组序列,测序拼接后获得了 5 条 REV 核酸序列,长度为 7942-8005bp。同源性分析结果表明,与中国东北地区、广东和广西地区的分离株具有高度同源性。根据其 gp90 蛋白基因,整合到痘病毒中的 REV 属于 III 型,与 APC-566 和 CY1111 等株的同源性最高,为 99.9%,与 REV-Anhui1 的同源性最低,为 95.4%。不同 REV 株的 pol 基因长度不同,其编码的氨基酸在 675 位后发生显著变化,存在缺失和改变。本研究表明,山西省太原市分离的所有禽痘病毒均整合了完整的 REV 基因序列,彼此之间具有高度同源性。同时表明,鸽痘病毒分离株也整合了完整的 REV 基因序列,与禽痘病毒整合的 REV 基因序列具有最高的同源性。