Xu Bin, Chen Xi, Lu Fengying, Sun Yu, Sun Huawei, Zhang Jingfeng, Shen Liya, Pan Qunxing, Liu Chuanmin, Zhang Xiaofei
Key Laboratory of Veterinary Biological Engineering and Technology of Ministry of Agriculture, Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
National Center for Engineering Research of Veterinary Bio-products, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Front Vet Sci. 2021 Feb 19;8:640067. doi: 10.3389/fvets.2021.640067. eCollection 2021.
is an important pathogen of poultry, causing significant economic losses in this industry. Analysis of the unique genes and shared genes among different strains and among related species is helpful for studying the molecular pathogenesis of and provides valuable molecular diagnostic targets to facilitate the identification of species. We selected a total of 46 strains, including six strains, from 25 major animal (including avian) species/subspecies that had complete genome sequences and annotation information published in GenBank, and used them for comparative genomic analysis. After analysis, 16 common genes were found in the 46 strains. Thirteen single-copy core genes and the 16s rRNA genes were used for genetic evolutionary analysis. was found to have a distant evolutionary relationship not only with other arthritis-causing mycoplasmas, but also with another major avian pathogen, , that shares the major virulence factor with . Subsequently, six unique coding genes were identified as shared among these strains that are absent in other species with published genome sequences. Two of the genes were found to be located in the genetically stable regions of the genomes of and were determined to be present in all isolated strains ( = 20) and -positive clinical samples ( = 48) preserved in our laboratory. These two genes were used as molecular diagnostic targets for which SYBR green quantitative PCR detection methods were designed. The two quantitative PCR methods exhibited good reproducibility and high specificity when tested on positive plasmid controls and genomic DNA extracted from different strains, other major avian pathogenic bacteria/mycoplasmas, and low pathogenic Mycoplasma species. The detection limit for the two genes was 10 copies or less per reaction. The clinical sensitivity and specificity of the quantitative PCR methods were both 100% based on testing chicken hock joint samples with positive or negative infection. This research provides a foundation for the study of species-specific differences and molecular diagnosis of .
是家禽的一种重要病原体,给该行业造成重大经济损失。分析不同菌株之间以及相关物种之间的独特基因和共享基因,有助于研究其分子发病机制,并提供有价值的分子诊断靶点,以促进该物种的鉴定。我们从25种主要动物(包括禽类)物种/亚种中总共挑选了46株菌株,其中包括6株该菌株,这些物种/亚种在GenBank上已发表了完整的基因组序列和注释信息,并将它们用于比较基因组分析。经过分析,在这46株菌株中发现了16个共同基因。使用13个单拷贝核心基因和16s rRNA基因进行遗传进化分析。结果发现,该菌株不仅与其他引起关节炎的支原体具有较远的进化关系,而且与另一种主要的禽病原体也具有较远的进化关系,该禽病原体与该菌株共享主要毒力因子。随后,鉴定出6个独特的编码基因在这些菌株中是共享的,而在已发表基因组序列的其他物种中不存在。发现其中两个基因位于该菌株基因组的遗传稳定区域,并且确定存在于我们实验室保存的所有该菌株分离株(n = 20)和该菌株阳性临床样本(n = 48)中。这两个基因被用作分子诊断靶点,并设计了SYBR Green定量PCR检测方法。当在阳性质粒对照以及从不同该菌株、其他主要禽病原细菌/支原体和低致病性支原体物种中提取的基因组DNA上进行测试时,这两种定量PCR方法表现出良好的重现性和高特异性。这两个基因的检测限为每个反应10个拷贝或更少。基于对鸡跗关节样本进行该菌株感染阳性或阴性检测,定量PCR方法的临床敏感性和特异性均为100%。本研究为该菌株的物种特异性差异研究和分子诊断提供了基础。