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2009 - 2013年加拿大侵袭性脑膜炎奈瑟菌C群(MenC)病例分离株在MenC结合疫苗时代的基因和抗原特征分析

Genetic and antigenic characterization of Canadian invasive Neisseria meningitidis serogroup C (MenC) case isolates in the post-MenC conjugate vaccine era, 2009-2013.

作者信息

Tsang Raymond S W, Hoang Linda, Tyrrell Gregory, Horsman Greg, Wylie John, Jamieson Frances B, Lefebvre Brigitte, Taha Muhamed-Kheir

机构信息

Vaccine Preventable Bacterial Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

BC Public Health Microbiology and Reference Laboratory, Vancouver, British Columbia, Canada.

出版信息

J Med Microbiol. 2015 Feb;64(Pt 2):174-9. doi: 10.1099/jmm.0.000006-0.

DOI:10.1099/jmm.0.000006-0
PMID:25627205
Abstract

We previously reported a shift in the electrophoretic type (ET) of invasive MenC in Canada from predominantly ET-15 to ET-37 in the post-MenC conjugate vaccine period. This study sought to confirm this trend by examining all culture-confirmed invasive MenC case isolates in Canada in the period from 1 January 2009 to 31 December 2013. Of the 50 MenC isolates, 18 belonged to ET-15, 28 belonged to ET-37 (but not ET-15), and four belonged to other clonal types. Analysis of the serotype and serosubtype antigens, porA and fetA gene sequences provided data to show that invasive MenC belonging to ET-15 and ET-37 were two very different subpopulations within the ST-11 clonal complex. Sequence analysis of the fHbp genes suggested that 12 different types of factor H-binding protein were found among the ET-15 isolates while 86 % of ET-37 isolates were found to have fHbp genes predicted to encode peptide 22. The nadA gene in 12 MenC isolates was disrupted due to IS1301 insertion and 11 of these 12 isolates belonged to ET-15. Ten per cent of the invasive MenC were found to have a frame-shift mutation in their fHbp genes that predicted no fHbp produced. Significant diversity and frame-shift mutations of fHbp genes were found in invasive MenC strains in Canada.

摘要

我们之前报道过,在加拿大,接种结合疫苗后的时期内,侵袭性C群脑膜炎奈瑟菌(MenC)的电泳类型(ET)从主要为ET-15转变为ET-37。本研究旨在通过检查2009年1月1日至2013年12月31日期间加拿大所有经培养确诊的侵袭性MenC病例分离株来证实这一趋势。在50株MenC分离株中,18株属于ET-15,28株属于ET-37(但不属于ET-15),4株属于其他克隆类型。对血清型和血清亚型抗原、porA和fetA基因序列的分析提供的数据表明,属于ET-15和ET-37的侵袭性MenC是ST-11克隆复合物中的两个非常不同的亚群。fHbp基因的序列分析表明,在ET-15分离株中发现了12种不同类型的因子H结合蛋白,而86%的ET-37分离株被发现具有预测编码肽22的fHbp基因。12株MenC分离株中的nadA基因由于IS1301插入而中断,这12株分离株中有11株属于ET-15。发现10%的侵袭性MenC在其fHbp基因中有移码突变,预测不会产生fHbp。在加拿大的侵袭性MenC菌株中发现了fHbp基因的显著多样性和移码突变。

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