Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
PLoS One. 2019 May 28;14(5):e0217500. doi: 10.1371/journal.pone.0217500. eCollection 2019.
In 2015-2016, a cross-sectional carriage survey was performed in Tuscany Region, Italy, during an outbreak of invasive meningococcal disease due to Neisseria meningitidis serogroup C clonal complex 11 (MenC:cc11). This study aims to evaluate the genomic profile of meningococcal carriage isolates collected during the survey.
Whole-genome sequencing (WGS) was performed using Illumina MiSeq on 85 cultivated meningococcal carriage isolates received at the Dept. of Infectious Disease, National Institute of Health (Istituto Superiore di Sanità, ISS), as National Reference Laboratory (NRL) for Invasive Meningococcal Disease (IMD). De novo assembled genomes were scanned by the BIGSdb platform to assign: the genotypic profiles, the cgMLST, the vaccine antigen variants and allele types of antimicrobial resistance associated genes, together with denitrification pathway loci.
Capsule null and non-groupable meningococci accounted for 52.9% and 10.6%, respectively. Among the remaining carriage isolates, serogroup B was the predominant (71.0%). Serogroup C meningococci were culture negative and unavailable for WGS. Overall, 64 genotypic profiles were identified and, based on cgMLST, isolates clustered according to clonal complexes. Eight isolates (9.4%) harbored at least one gene encoding a 4CMenB vaccine antigen. Mutated penA alleles were found in more than 82%. Finally, complete aniA and norB coding sequences were detected among 71.8% of carriage isolates.
Meningococcal carriage isolates collected during the MenC:cc11 outbreak were characterized by an extensive genetic diversity. The lack of outbreak-related isolates among carriage might be attributable to the high transmissibility with low duration of colonization of MenC:cc11 meningococci.
2015-2016 年,意大利托斯卡纳地区发生了由 C 群脑膜炎奈瑟菌克隆复合体 11(MenC:cc11)引起的侵袭性脑膜炎球菌病疫情,在此期间进行了横断面带菌调查。本研究旨在评估调查期间采集的脑膜炎球菌带菌分离株的基因组特征。
国家卫生研究院传染病系(意大利卫生研究所,ISS)作为侵袭性脑膜炎球菌病(IMD)的国家参考实验室(NRL),使用 Illumina MiSeq 对 85 株培养的脑膜炎球菌带菌分离株进行全基因组测序(WGS)。使用 BIGSdb 平台对从头组装的基因组进行扫描,以分配基因型谱、cgMLST、疫苗抗原变异体和与抗菌药物耐药性相关的基因等位类型,以及硝酸盐还原途径基因座。
无荚膜和非分组脑膜炎球菌分别占 52.9%和 10.6%。在其余的带菌分离株中,B 群血清型占主导地位(71.0%)。C 群脑膜炎球菌培养呈阴性,无法进行 WGS。总体上,共鉴定出 64 种基因型谱,根据 cgMLST,分离株根据克隆复合体聚类。8 株(9.4%)携带至少一个编码 4CMenB 疫苗抗原的基因。超过 82%的分离株存在 penA 突变等位基因。最后,71.8%的带菌分离株中检测到完整的 aniA 和 norB 编码序列。
在 MenC:cc11 爆发期间采集的脑膜炎球菌带菌分离株具有广泛的遗传多样性。带菌者中缺乏与爆发相关的分离株可能归因于 MenC:cc11 脑膜炎球菌的高传染性和低定植持续时间。