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A combinational approach of multilocus sequence typing and other molecular typing methods in unravelling the epidemiology of Erysipelothrix rhusiopathiae strains from poultry and mammals

机译:多位点序列分型和其他分子分型方法的组合方法,用于阐明家禽和哺乳动物的红斑丹毒丝菌病流行病学

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Erysipelothrix rhusiopathiae infections re-emerged as a matter of great concern particularly in the poultry industry. In contrast to porcine isolates, molecular epidemiological traits of avian E. rhusiopathiae isolates are less well known. Thus, we aimed to (i) develop a multilocus sequence typing (MLST) scheme for E. rhusiopathiae, (ii) study the congruence of strain grouping based on pulsed-field gel electrophoresis (PFGE) and MLST, (iii) determine the diversity of the dominant immunogenic protein SpaA, and (iv) examine the distribution of genes putatively linked with virulence among field isolates from poultry (120), swine (24) and other hosts (21), including humans (3). Using seven housekeeping genes for MLST analysis we determined 72 sequence types (STs) among 165 isolates. This indicated an overall high diversity, though 34.5% of all isolates belonged to a single predominant ST-complex, STC9, which grouped strains from birds and mammals, including humans, together. PFGE revealed 58 different clusters and congruence with the sequence-based MLST-method was not common. Based on polymorphisms in the N-terminal hyper-variable region of SpaA the isolates were classified into five groups, which followed the phylogenetic background of the strains. More than 90% of the isolates harboured all 16 putative virulence genes tested and only intI, encoding an internalin-like protein, showed infrequent distribution. MLST data determined E. rhusiopathiae as weakly clonal species with limited host specificity. A common evolutionary origin of isolates as well as shared SpaA variants and virulence genotypes obtained from avian and mammalian hosts indicates common reservoirs, pathogenic pathways and immunogenic properties of the pathogen.
机译:引起人们广泛关注的是再次出现了红斑丹毒丝菌性红斑病感染,特别是在禽类行业。与猪分离株相反,禽类风疹大肠杆菌分离株的分子流行病学特征尚不为人所知。因此,我们的目的是(i)为风疹病原体开发多基因座序列分型(MLST)方案,(ii)基于脉冲场凝胶电泳(PFGE)和MLST研究菌株分组的一致性,(iii)确定多样性(iv)检查家禽(120),猪(24)和其他宿主(21)包括人类(3)的田间分离株中与毒力相关的基因分布。使用七个管家基因进行MLST分析,我们确定了165个分离株中的72个序列类型(ST)。这表明总体上具有很高的多样性,尽管所有分离株的34.5%都属于单一的主要ST复合体STC9,该复合体将鸟类和哺乳动物(包括人)的菌株归为一类。 PFGE揭示了58个不同的簇,与基于序列的MLST方法的一致性并不常见。基于SpaA的N末端高变区中的多态性,将分离株分为五组,其遵循菌株的系统发育背景。超过90%的分离株具有所有测试的16种推定毒力基因,只有编码internalin-like蛋白的intI分布很少。 MLST数据确定了大肠埃希氏菌为宿主特异性有限的弱克隆物种。从禽类和哺乳动物宿主获得的分离株以及共享的SpaA变体和毒力基因型的共同进化起源表明病原体具有共同的储库,致病途径和免疫原性。

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