Guo Xi, Wang Min, Wang Lu, Wang Yao, Chen Tingting, Wu Pan, Chen Min, Liu Bin, Feng Lu
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education-Tianjin Economic-Technological Development Area, Tianjin, China.
Tianjin Key Laboratory of Microbial Functional Genomics, Tianjin Economic-Technological Development Area, Tianjin, China.
Front Microbiol. 2018 Mar 19;9:501. doi: 10.3389/fmicb.2018.00501. eCollection 2018.
Serotyping based on surface polysaccharide antigens is important for the clinical detection and epidemiological surveillance of pathogens. Polysaccharide gene clusters (PSgcs) are typically responsible for the diversity of bacterial surface polysaccharides. Through whole-genome sequencing and analysis, eight putative PSgc types were identified in 23 strains from several geographic areas, allowing us to present the first molecular serotyping system for . A conventional antigenic scheme was also established and correlated well with the molecular serotyping system that was based on PSgc genetic variation, indicating that PSgc-based molecular typing and immunological serology provide equally valid results. Further, a multiplex Luminex-based array was developed, and a double-blind test was conducted with 97 clinical specimens from Shanghai, China, to validate our array. The results of these analyses indicated that strains containing PSgc4 and PSgc7 comprised the predominant groups. We then examined 86 publicly available strain genomes and identified an additional seven novel PSgc types, with PSgc10 being the most abundant type. In total, our study identified 15 PSgc types in , providing the basis for a molecular serotyping scheme. From these results, differing epidemic patterns were identified between strains that were predominant in different regions. Our study highlights the feasibility and reliability of a serotyping system based on PSgc diversity, and for the first time, presents a molecular serotyping system, as well as an antigenic scheme for , providing the basis for molecular diagnostics and epidemiological surveillance of this important emerging pathogen.
基于表面多糖抗原的血清分型对于病原体的临床检测和流行病学监测至关重要。多糖基因簇(PSgcs)通常决定了细菌表面多糖的多样性。通过全基因组测序和分析,在来自几个地理区域的23株菌株中鉴定出8种假定的PSgc类型,这使我们能够首次提出针对[病原体名称未给出]的分子血清分型系统。还建立了一种传统的抗原分型方案,该方案与基于PSgc基因变异的分子血清分型系统相关性良好,表明基于PSgc的分子分型和免疫血清学提供了同样有效的结果。此外,开发了一种基于Luminex的多重检测芯片,并对来自中国上海的97份临床标本进行了双盲测试,以验证我们的芯片。这些分析结果表明,含有PSgc4和PSgc7的菌株构成了主要群体。然后,我们检查了86个公开可用的[病原体名称未给出]菌株基因组,又鉴定出另外7种新型PSgc类型,其中PSgc10是最丰富的类型。总的来说,我们的研究在[病原体名称未给出]中鉴定出15种PSgc类型,为分子血清分型方案提供了基础。从这些结果中,我们确定了不同地区主要菌株之间存在不同的流行模式。我们的研究突出了基于PSgc多样性的血清分型系统的可行性和可靠性,并首次提出了一种分子血清分型系统以及针对[病原体名称未给出]的抗原分型方案,为这种重要的新兴病原体的分子诊断和流行病学监测提供了基础。