Reference Laboratory for Veterinary Quality Control on Poultry Production (RLQP), Animal Health Research Institute, Agriculture Research Center (ARC), Giza, 12618, Egypt.
Department of Biology, College of Science, King Khalid University, Abha, 61421, Saudi Arabia.
Poult Sci. 2023 Aug;102(8):102769. doi: 10.1016/j.psj.2023.102769. Epub 2023 May 3.
A total of 45 samples of vaccinated and non-vaccinated layer chickens were collected from farms in the Egyptian governorates of Sharqia, Ismailia, Menofia, Gharbia, Kafr El Sheikh, Qalyubia, and Dakahlia in the year 2022. They exhibited nodular lesions on their combs, mouth corners, and eyelids, suggesting they were infected with pox disease, which was associated with a 3 to 5% mortality rate. The samples were grown on the chorioallantoic-membrane of embryonated chicken eggs to ensure their viability. In both vaccinated and non-vaccinated farms, 35 of 45 virus isolates were confirmed positive via polymerase chain reaction (PCR) of fpv167 (P4b), based on the amplicon length of the fpv167 gene locus. The 6 strains from various Egyptian governorates were chosen for sequencing and genetic characterization. Phylogenetic investigation of the fpv167 (P4b) gene of sequenced strains clustered within sub clade A1 showed 100% correlation between FWPVD, TKPV13401 and fowlpox-AN2, fowlpox-AN3, and fowlpox-AN6, but only a 98.6% correlation between fowlpox-AN1, fowlpox-AN4, and fowlpox-AN5. Comparing the fowlpox-AN1, fowlpox-AN4, and fowlpox-AN5 strains with commercial vaccine strains (HP1-444-(FP9), vaccine-VSVRI), they had 98.6% identity, while other strains had 100% identity. The results of this study's mutation research showed that fowlpox-AN1, fowlpox-AN4, and fowlpox-AN5 had acquired novel mutations; fowlpox-AN1 had R201G and T204A; fowlpox-AN4 and fowlpox-AN5 had L141F and H157P. Further research is required to determine the effectiveness of the current vaccine in order to develop a new vaccine.
2022 年,从埃及 Sharqia、Ismailia、Menofia、Gharbia、Kafr El Sheikh、Qalyubia 和 Dakahlia 等省的农场中采集了 45 份接种和未接种疫苗的蛋鸡样本。它们的鸡冠、口角和眼睑上出现结节性病变,表明它们感染了痘病,死亡率为 3%至 5%。这些样本在鸡胚的尿囊膜上生长,以确保其存活。在接种和未接种疫苗的农场中,通过聚合酶链反应(PCR)对 fpv167(P4b)对 45 个病毒分离物中的 35 个进行了确认,基于 fpv167 基因座的扩增子长度。从埃及各个省选择了 6 个毒株进行测序和遗传特征分析。对测序株的 fpv167(P4b)基因进行系统发育研究,聚类在亚分支 A1 内,表明 FWPVD、TKPV13401 与禽痘-AN2、禽痘-AN3 和禽痘-AN6 之间存在 100%的相关性,而禽痘-AN1、禽痘-AN4 和禽痘-AN5 之间仅存在 98.6%的相关性。将禽痘-AN1、禽痘-AN4 和禽痘-AN5 株与商业疫苗株(HP1-444-(FP9)、疫苗-VSVRI)进行比较,它们的同一性为 98.6%,而其他株的同一性为 100%。本研究的突变研究结果表明,禽痘-AN1、禽痘-AN4 和禽痘-AN5 获得了新的突变;禽痘-AN1 有 R201G 和 T204A;禽痘-AN4 和禽痘-AN5 有 L141F 和 H157P。需要进一步研究以确定当前疫苗的有效性,以便开发新的疫苗。