Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, H-1143, Budapest, Hungária krt. 21., Hungary.
Istituto Zooprofilattico Sperimentale delle Venezie, Viale dell'Università 10, 35020, Legnaro, PD, Italy.
Vet Microbiol. 2018 Nov;226:41-49. doi: 10.1016/j.vetmic.2018.10.012. Epub 2018 Oct 15.
Control of one of the most important avian mycoplasmas, Mycoplasma synoviae, and tracing the spread of the infection can be challenging as the pathogen is transmissible by both horizontal and vertical routes, and it can be disseminated through long distances via the hatching eggs, day-old chicks or pullets during intensive international trade. Genetic information provided by molecular typing methods support control programmes and epizootiologic studies. The aims of the present study were to develop a multi-locus variable number of tandem-repeats analysis (MLVA) method for the typing of M. synoviae isolates and to evaluate the currently used molecular typing methods which are applicable directly on clinical samples. Tandem repeat (TR) regions were selected from the whole genome sequence of the M. synoviae type strain (WVU1853) to characterise the genetic diversity of 86 M. synoviae strains originating from 15 countries. The strains were also submitted to multi-locus sequence typing (MLST) assays, vlhA gene sequence analysis and to assays designed to differentiate live vaccine strains from field strains. The developed MLVA involves the examination of seven TR regions and provides similar genetic resolution as the tested MLST assays by identifying 35 genotypes among the tested strains. Differentiation of the live vaccine strains from field strains was also successful with the developed assay. The provided MLVA method proved to be a highly discriminative, rapid and cost-effective alternative typing technique for the genetic characterisation of M. synoviae and it is also suitable for the complementation of live vaccine strain differentiating assays in ambiguous cases.
控制其中一种最重要的禽类支原体,滑液支原体,以及追踪感染的传播可能具有挑战性,因为病原体可通过水平和垂直途径传播,并且可以通过长途孵化蛋、一日龄小鸡或育成鸡在密集的国际贸易中传播。分子分型方法提供的遗传信息支持控制计划和流行病学研究。本研究的目的是开发一种用于滑液支原体分离株分型的多位点可变串联重复分析(MLVA)方法,并评估目前可直接应用于临床样本的分子分型方法。从滑液支原体标准株(WVU1853)的全基因组序列中选择串联重复(TR)区域,以表征源自 15 个国家的 86 株滑液支原体的遗传多样性。这些菌株还进行了多位点序列分型(MLST)分析、vlhA 基因序列分析以及区分活疫苗株和田间株的分析。开发的 MLVA 涉及七个 TR 区域的检查,通过在测试菌株中识别 35 种基因型,提供与测试 MLST 分析相似的遗传分辨率。该检测还成功区分了活疫苗株和田间株。所提供的 MLVA 方法被证明是一种高度区分、快速且具有成本效益的替代技术,用于滑液支原体的遗传特征分析,并且在不确定情况下也适合补充活疫苗株区分检测。