Center for Diagnostics and Vaccine Development, Centers for Disease Control, Taichung, Taiwan.
Department of Microbiology and Immunology, School of Medicine, China Medical University, Taichung, Taiwan.
Microbiol Spectr. 2022 Aug 31;10(4):e0088222. doi: 10.1128/spectrum.00882-22. Epub 2022 Jul 11.
We present the demographic features of invasive meningococcal disease (IMD) in Taiwan between 1993 and 2020 and the genetic characteristics of Neisseria meningitidis isolates recovered from 2003 to 2020. IMD was rare in Taiwan between 1993 and 2020, with an annual incidence ranging from 0.009 to 0.204 per 100,000 people. The case fatality rate (CFR) declined from 18.1% for patients in 1993 to 2002 to 9.8% in 2003 to 2020. Infants less than 12 months were most susceptible to the disease. N. meningitidis serogroup B (NmB) was most predominant, responsible for 81.2% (134/165) of the IMD cases in 2003 to 2020. The majority of the isolates recovered from 2003 to 2020 belonged to 4 worldwide-spread hyperinvasive clonal complexes (cc), cc4821 (30.3%), cc32 (19.4%), cc41/44 (12.7%), cc23 (7.3%), and also a newly assigned clonal complex, cc3439 (10.3%). Core genome multilocus sequence typing (cgMLST) profile comparisons revealed that the cc4821 isolates with a T-to-I substitution at position 91 in were closely related to those originating from China. Of the 165 isolates, 20.0% and 53.3% were predicted to be covered by the Bexsero and Trumenba vaccines, respectively, whereas, 77.0% and 46.7% remained indeterminate. In conclusion, N. meningitidis isolates recovered in Taiwan between 2003 and 2020 were mostly highly diverse. Most IMD cases appeared sporadically and were caused by localized strains, although some patients were infected by recently introduced strains. cgMLST is a powerful tool for the rapid comparison of genetic relatedness among a large number of isolates. cgMLST profiling, based on 1,241 core genes, and strain tracking can be performed on the website of cgMLST@Taiwan (http://rdvd.cdc.gov.tw/cgMLST/). N. meningitidis can cause life-threatening invasive meningococcal disease (IMD), including meningitis and sepsis, resulting in a high CFR and long-term sequelae in survivors. Here, we report the demographic features of IMD in Taiwan over a 28-year period (1993 to 2020) and the genetic characteristics of N. meningitidis isolates recovered from patients with IMD over an 18-year period (2003 to 2020). We conducted a whole-genome sequence analysis to characterize the genetic features of the isolates and developed a cgMLST scheme for epidemiological investigation and strain tracking. The findings can be beneficial in understanding the epidemiology of IMD in Taiwan, the genetic characteristics of the bacterial strains, and the distribution of vaccine antigens for vaccine development and implementation.
我们呈现了 1993 年至 2020 年期间台湾侵袭性脑膜炎奈瑟菌病(IMD)的人口统计学特征,以及 2003 年至 2020 年期间从分离株中恢复的脑膜炎奈瑟氏球菌的遗传特征。1993 年至 2020 年期间,台湾 IMD 罕见,年发病率为每 10 万人 0.009 至 0.204。病例死亡率(CFR)从 1993 年至 2002 年的 18.1%下降到 2003 年至 2020 年的 9.8%。12 个月以下的婴儿最易患这种疾病。脑膜炎奈瑟氏球菌血清群 B(NmB)是最主要的,占 2003 年至 2020 年 IMD 病例的 81.2%(134/165)。从 2003 年至 2020 年恢复的大多数分离株属于 4 个全球传播的超侵袭性克隆复合体(cc),cc4821(30.3%)、cc32(19.4%)、cc41/44(12.7%)、cc23(7.3%)和一个新分配的克隆复合体,cc3439(10.3%)。核心基因组多位点序列分型(cgMLST)谱比较显示,位置 91 处 T 到 I 取代的 cc4821 分离株与来自中国的分离株密切相关。在 165 株分离株中,20.0%和 53.3%分别预测被 Bexsero 和 Trumenba 疫苗覆盖,而 77.0%和 46.7%仍不确定。总之,2003 年至 2020 年期间在台湾恢复的脑膜炎奈瑟氏球菌分离株大多高度多样化。大多数 IMD 病例呈散发性出现,由局部菌株引起,尽管一些患者感染了最近引入的菌株。cgMLST 是对大量分离株进行遗传相关性快速比较的有力工具。cgMLST 分析基于 1241 个核心基因,可以在 cgMLST@Taiwan(http://rdvd.cdc.gov.tw/cgMLST/)网站上进行菌株跟踪。脑膜炎奈瑟氏球菌可引起危及生命的侵袭性脑膜炎奈瑟菌病(IMD),包括脑膜炎和败血症,导致高 CFR 和幸存者长期后遗症。在这里,我们报告了 28 年来(1993 年至 2020 年)台湾 IMD 的人口统计学特征,以及 18 年来(2003 年至 2020 年)从 IMD 患者中恢复的脑膜炎奈瑟氏球菌分离株的遗传特征。我们进行了全基因组序列分析,以描述分离株的遗传特征,并为流行病学调查和菌株跟踪制定了 cgMLST 方案。这些发现有助于了解台湾 IMD 的流行病学、细菌株的遗传特征以及疫苗抗原的分布,以进行疫苗开发和实施。