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伊朗鸡源支原体分离株 mgc2/pvpA 基因的全序列基于基因型分析。

Complete Sequence-Based Genotyping of mgc2/pvpA Genes in Chicken-Derived Mycoplasma gallisepticum Isolates of Iran.

机构信息

Department of Avian Disease Research and Diagnostic, Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization (AREEO), Karaj 3197619751, Iran.

出版信息

Avian Dis. 2020 Dec 1;64(4):507-516. doi: 10.1637/aviandiseases-D20-00032.

Abstract

Mycoplasma gallisepticum (MG) is a major pathogen of the poultry industry throughout the world. MG causes chronic respiratory disease in chickens and infectious sinusitis in turkeys. Despite constant improvements in the biosecurity of the poultry industry in Iran, MG infection still occurs and causes significant economic issues. To evaluate genetic variability, 10 Iranian MG isolates along with 17 available sequences were characterized by gene-targeted sequencing (GTS) analysis of complete mgc2/pvpA genes. According to the findings, 21 different sequence types within the sample set of 27 strains were typed by this method. The discriminatory power of this typing assay was established to be 0.97. Although no insertions and deletions of nucleotides were observed in the mgc2 gene among the Iranian strains, different lengths of pvpA genes with 1086, 1095, and 1101 nucleotides were detected within direct repeats (DRs) 1 and 2. Generally, eight tetrapeptides Pro-Arg-Pro-Met/Gln/Asn were found in the DRs of PvpA. Analysis of the carboxyl ends of PvpA proteins exhibited various repeats of prolines. In the phylogenetic tree of partial and complete mgc2/pvpA genes, all Iranian MG isolates were clustered into two distinct groups. Because this typing assay could provide a higher discriminatory power than the previously reported GTS scheme of partial mgc2/ pvpA genes, these results can be considered a blueprint for future national control and diagnostic strategies. Furthermore, consistent surveillance with larger datasets will be needed to clarify the epidemiologic characteristics of MG outbreaks in different poultry hosts.

摘要

鸡毒支原体(MG)是全球家禽业的主要病原体。MG 可引起鸡慢性呼吸道疾病和火鸡传染性窦炎。尽管伊朗家禽业的生物安全措施不断得到改善,但 MG 感染仍然存在,并造成重大经济问题。为了评估遗传变异,我们对 10 株伊朗 MG 分离株和 17 个可用序列进行了基因靶向测序(GTS)分析,以确定完整的 mgc2/pvpA 基因。根据研究结果,该方法将 27 株菌的样本集中分为 21 种不同的序列类型。该分型检测的区分力为 0.97。虽然在伊朗株中未观察到 mgc2 基因的核苷酸插入和缺失,但在直接重复(DR)1 和 2 内检测到不同长度的 pvpA 基因,分别为 1086、1095 和 1101 个核苷酸。通常,在 PvpA 的 DR 中发现 8 个四肽 Pro-Arg-Pro-Met/Gln/Asn。PvpA 羧基末端的分析显示各种脯氨酸重复。在部分和完整 mgc2/pvpA 基因的系统发育树中,所有伊朗 MG 分离株均聚为两个不同的组。由于这种分型检测比以前报道的部分 mgc2/ pvpA 基因的 GTS 方案具有更高的区分力,因此这些结果可以被视为未来国家控制和诊断策略的蓝图。此外,需要进行更大数据集的持续监测,以阐明不同家禽宿主中 MG 暴发的流行病学特征。

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