Law Dennis K S, Lefebvre Brigitte, Gilca Rodica, Deng Saul, Zhou Jianwei, De Wals Philippe, Tsang Raymond S W
Vaccine Preventable Bacterial Diseases, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, R3E 3R2, Winnipeg, MB, Canada.
Laboratoire de santé publique du Québec, Institut national de santé publique du Québec, 20045 chemin Sante-Marie, Ste-Anne-de-Bellevue, H9X 3R5, Québec, Canada.
BMC Microbiol. 2015 Jul 25;15:143. doi: 10.1186/s12866-015-0469-6.
The epidemiology of invasive meningococcal disease (IMD) in Québec, Canada, has been dominated in the past decade by a clone of serogroup B (MenB) Neisseria meningitidis defined by multi-locus sequence typing (MLST) as sequence type (ST)-269. With the licensure of a new MenB vaccine Bexsero (4CMenB) in Canada, this study characterized invasive N. meningitidis recovered in Québec from 2009 to 2013, with an objective to examine the diversity of the 4CMenB vaccine antigens. Isolates were serogrouped by antisera and genogrouped by PCR, and further typed by whole cell ELISA for serotype and serosubtype antigens. Clonal analysis was done by MLST. Isolates were genotyped by analysis of their 4CMenB vaccine antigen genes of PorA, factor H binding protein (fHbp), Neisserial Heparin Binding Antigen (NHBA), and Neisseria Adhesin A (NadA).
Of the 263 IMD isolates analysed, 229, 16, 10, 7, and 1 belonged to MenB, MenY, MenW, MenC, and MenX, respectively. Of the 229 MenB, 159 (69.4 %) were typed as ST-269 clonal complex (CC); and they possessed a restricted number of three fHbp and five nhba gene alleles. Nine N. meningitidis isolates (eight MenB and one MenY) were found to possess at least one gene that encoded for an antigen that matched exactly with protein variants in the 4CMenB vaccine. Two MenB expressed PorA antigen P1.4 and possessed the nhba gene for peptide 2; four other MenB were predicted to have NHBA peptide 2; another two MenB were predicted to encode fHbp peptide 1.1; and a single MenY was found to have nadA gene for NadA peptide 8. In addition, another 172 isolates were found to possess genes for variant 1 fHbp peptides other than peptide 1.1 or NadA variant 1-2/3 peptides other than peptide 8; and therefore, may potentially be covered by 4CMenB.
The most prevalent clone of N. meningitidis in Quebec was ST-269 CC; and 96 % of the isolates in this CC were predicted to be covered by 4CMenB vaccine. Extensive genetic diversity was found in the other IMD isolates in Québec which might suggest a lower coverage by the vaccine when compared to the ST-269 MenB.
在过去十年中,加拿大魁北克侵袭性脑膜炎球菌病(IMD)的流行病学情况主要由B群(MenB)脑膜炎奈瑟菌的一个克隆主导,该克隆通过多位点序列分型(MLST)被定义为序列型(ST)-269。随着新型MenB疫苗Bexsero(4CMenB)在加拿大获得许可,本研究对2009年至2013年在魁北克分离出的侵袭性脑膜炎奈瑟菌进行了特征分析,目的是检测4CMenB疫苗抗原的多样性。通过抗血清对分离株进行血清群分型,通过PCR进行基因群分型,并通过全细胞ELISA对血清型和血清亚型抗原进行进一步分型。通过MLST进行克隆分析。通过分析分离株的4CMenB疫苗抗原基因PorA(孔蛋白A)、因子H结合蛋白(fHbp)、奈瑟菌肝素结合抗原(NHBA)和奈瑟菌粘附素A(NadA)对分离株进行基因分型。
在分析的263株IMD分离株中,229株、16株、10株、7株和1株分别属于MenB、MenY、MenW、MenC和MenX血清群。在229株MenB分离株中,159株(69.4%)被分型为ST-269克隆复合体(CC);它们具有数量有限的三种fHbp和五种nhba基因等位基因。发现9株脑膜炎奈瑟菌分离株(8株MenB和1株MenY)至少拥有一个编码与4CMenB疫苗中蛋白质变体完全匹配的抗原的基因。两株MenB表达PorA抗原P1.4并拥有肽2的nhba基因;另外4株MenB预计具有NHBA肽2;另外两株MenB预计编码fHbp肽1.1;并且发现一株MenY具有NadA肽8的nadA基因。此外,还发现另外172株分离株拥有除肽1.1以外的fHbp肽变体1基因或除肽8以外的NadA变体1-2/3肽基因;因此,可能潜在地被4CMenB疫苗覆盖。
魁北克最常见的脑膜炎奈瑟菌克隆是ST-269 CC;预计该CC中的96%的分离株可被4CMenB疫苗覆盖。在魁北克的其他IMD分离株中发现了广泛的遗传多样性,这可能表明与ST-269 MenB相比,该疫苗的覆盖率较低。