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本文引用的文献

1
A robust PCR for the differentiation of potential virulent strains of Haemophilus parasuis.一种用于区分副猪嗜血杆菌潜在强毒株的稳健PCR方法。
BMC Vet Res. 2017 May 8;13(1):124. doi: 10.1186/s12917-017-1041-4.
2
Development of a Multiplex PCR Assay for Rapid Molecular Serotyping of Haemophilus parasuis.副猪嗜血杆菌快速分子血清分型多重PCR检测方法的建立
J Clin Microbiol. 2015 Dec;53(12):3812-21. doi: 10.1128/JCM.01991-15. Epub 2015 Sep 30.
3
The use of genome wide association methods to investigate pathogenicity, population structure and serovar in Haemophilus parasuis.利用全基因组关联方法研究副猪嗜血杆菌的致病性、群体结构和血清型。
BMC Genomics. 2014 Dec 24;15:1179. doi: 10.1186/1471-2164-15-1179.
4
Virulence and draft genome sequence overview of multiple strains of the swine pathogen Haemophilus parasuis.猪副猪嗜血杆菌多株菌株的毒力及基因组草图序列概述
PLoS One. 2014 Aug 19;9(8):e103787. doi: 10.1371/journal.pone.0103787. eCollection 2014.
5
Time course Haemophilus parasuis infection reveals pathological differences between virulent and non-virulent strains in the respiratory tract.时间进程副猪嗜血杆菌感染揭示了呼吸道中强毒力和非强毒力菌株的病理差异。
Vet Microbiol. 2014 Jun 4;170(3-4):430-7. doi: 10.1016/j.vetmic.2014.01.011. Epub 2014 Feb 3.
6
Characterization and proteome analysis of inosine 5-monophosphate dehydrogenase in epidemic Streptococcus suis serotype 2.猪链球菌 2 型肌苷 5′-单磷酸脱氢酶的鉴定及蛋白质组学分析。
Curr Microbiol. 2014 May;68(5):663-9. doi: 10.1007/s00284-014-0527-6. Epub 2014 Jan 24.
7
Simultaneous detection of antibodies against Apx toxins ApxI, ApxII, ApxIII, and ApxIV in pigs with known and unknown Actinobacillus pleuropneumoniae exposure using a multiplexing liquid array platform.使用多重液相芯片平台同时检测已知和未知胸膜肺炎放线杆菌暴露猪体内抗Apx毒素ApxI、ApxII、ApxIII和ApxIV的抗体。
Clin Vaccine Immunol. 2014 Jan;21(1):85-95. doi: 10.1128/CVI.00451-13. Epub 2013 Nov 13.
8
MEGA6: Molecular Evolutionary Genetics Analysis version 6.0.MEGA6:分子进化遗传学分析版本 6.0。
Mol Biol Evol. 2013 Dec;30(12):2725-9. doi: 10.1093/molbev/mst197. Epub 2013 Oct 16.
9
Advances in the quest for virulence factors of Haemophilus parasuis.副猪嗜血杆菌毒力因子研究进展。
Vet J. 2013 Dec;198(3):571-6. doi: 10.1016/j.tvjl.2013.08.027. Epub 2013 Sep 4.
10
Genetic diversity of Haemophilus parasuis from sick and healthy pigs.副猪嗜血杆菌病猪和健康猪的遗传多样性。
Vet Microbiol. 2013 Dec 27;167(3-4):459-67. doi: 10.1016/j.vetmic.2013.07.028. Epub 2013 Aug 9.

副猪嗜血杆菌的“分型”多重PCR检测:一种预测毒力的工具

"Pathotyping" Multiplex PCR Assay for Haemophilus parasuis: a Tool for Prediction of Virulence.

作者信息

Howell Kate J, Weinert Lucy A, Peters Sarah E, Wang Jinhong, Hernandez-Garcia Juan, Chaudhuri Roy R, Luan Shi-Lu, Angen Øystein, Aragon Virginia, Williamson Susanna M, Langford Paul R, Rycroft Andrew N, Wren Brendan W, Maskell Duncan J, Tucker Alexander W

机构信息

Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom

Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.

出版信息

J Clin Microbiol. 2017 Sep;55(9):2617-2628. doi: 10.1128/JCM.02464-16. Epub 2017 Jun 14.

DOI:10.1128/JCM.02464-16
PMID:28615466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5648699/
Abstract

is a diverse bacterial species that is found in the upper respiratory tracts of pigs and can also cause Glässer's disease and pneumonia. A previous pangenome study of identified 48 genes that were associated with clinical disease. Here, we describe the development of a generalized linear model (termed a pathotyping model) to predict the potential virulence of isolates of based on a subset of 10 genes from the pangenome. A multiplex PCR (mPCR) was constructed based on these genes, the results of which were entered into the pathotyping model to yield a prediction of virulence. This new diagnostic mPCR was tested on 143 field isolates of that had previously been whole-genome sequenced and a further 84 isolates from the United Kingdom from cases of related disease in pigs collected between 2013 and 2014. The combination of the mPCR and the pathotyping model predicted the virulence of an isolate with 78% accuracy for the original isolate collection and 90% for the additional isolate collection, providing an overall accuracy of 83% (81% sensitivity and 93% specificity) compared with that of the "current standard" of detailed clinical metadata. This new pathotyping assay has the potential to aid surveillance and disease control in addition to serotyping data.

摘要

是一种多样的细菌物种,存在于猪的上呼吸道中,也可引起格拉泽氏病和肺炎。先前对该细菌的泛基因组研究鉴定出48个与临床疾病相关的基因。在此,我们描述了一种广义线性模型(称为致病型分型模型)的开发,该模型基于泛基因组中的10个基因子集来预测该细菌分离株的潜在毒力。基于这些基因构建了多重PCR(mPCR),其结果输入致病型分型模型以得出毒力预测。这种新的诊断性mPCR在143株先前已进行全基因组测序的该细菌田间分离株以及另外84株于2013年至2014年期间从英国猪的相关疾病病例中收集的分离株上进行了测试。mPCR与致病型分型模型的组合对原始分离株集合预测分离株毒力的准确率为78%,对额外分离株集合的准确率为90%,与详细临床元数据的“当前标准”相比,总体准确率为83%(敏感性81%,特异性93%)。除血清分型数据外,这种新的致病型分型检测方法有潜力辅助监测和疾病控制。