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Characterization of Chinese Haemophilus parasuis Isolates by Traditional Serotyping and Molecular Serotyping Methods

机译:传统血清分型和分子血清分型方法表征副猪嗜血杆菌

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摘要

Haemophilus parasuis is classified mainly through serotyping, but traditional serotyping always yields non-typable (NT) strains and unreliable results via cross-reactions. Here, we surveyed the serotype prevalence of Chinese H. parasuis isolates using traditional serotyping (gel immuno-diffusion test, GID) and molecular serotyping (multiplex PCR, mPCR). We also investigated why discrepant results between these methods were obtained, and investigated mPCR failure through whole-genome sequencing. Of the 100 isolate tested, 73 (73%) and 93 (93%) were serotyped by the GID test and mPCR, respectively, with a concordance rate of 66% (66/100). Additionally, mPCR reduced the number of NT isolates from 27 (27%) for the GID testing, to seven (7%). Eleven isolates were sequenced, including nine serotype-discrepant isolates from mPCR and GID typing (excluding strains that were NT by GID only) and two NT isolates from both methods, and their in silico serotypes were obtained from genome sequencing based on their capsule loci. The mPCR results were supported by the in silico serotyping of the seven serotype-discrepant isolates. The discrepant results and NT isolates determined by mPCR were attributed to deletions and unknown sequences in the serotype-specific region of each capsule locus. Compared with previous investigations, this study found a similar predominant serotype profile, but a different prevalence frequency for H. parasuis, and the five most prevalent serotypes or strain groups were serotypes 5, 4, NT, 7 and 13 for mPCR, and serotypes 5, NT, 4, 7 and 13/10/14 for GID. Additionally, serotype 7 was recognized as a principal serotype in this work.
机译:副猪嗜血杆菌主要通过血清分型来分类,但是传统的血清分型总是产生不可分型的菌株,并且通过交叉反应产生不可靠的结果。在这里,我们使用传统的血清分型(凝胶免疫扩散试验,GID)和分子血清分型(多重PCR,mPCR)调查了中国副猪嗜血杆菌的血清型患病率。我们还调查了为什么获得这些方法之间的结果不一致,并通过全基因组测序调查了mPCR失败。在进行测试的100个分离株中,分别通过GID测试和mPCR进行了血清分型(分别为73(73%)和93(93%)),一致性率为66%(66/100)。此外,mPCR将NT分离株的数量从GID测试的27个(27%)减少到了7个(7%)。对11种分离物进行了测序,包括9种来自mPCR和GID分型的血清型差异分离株(不包括仅通过GID进行NT分离的菌株)和两种方法的两种NT分离株,并根据其胶囊基因座从基因组测序中获得了其计算机病毒血清型。 mPCR结果得到了七个血清型差异分离株的计算机血清分型的支持。通过mPCR确定的差异结果和NT分离物归因于每个荚膜基因座血清型特异性区域的缺失和未知序列。与以前的研究相比,本研究发现相似的主要血清型谱,但副猪嗜血杆菌的流行频率不同,五个最普遍的血清型或菌株组分别为mPCR的血清型5、4,NT,7和13,以及血清型5 ,NT,4、7和13/10/14的GID。另外,血清型7被认为是这项工作的主要血清型。

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