无家可归成年人中侵袭性肺炎球菌疾病病例比例的增加为新的血清 4 型胶囊开关重组体创造了条件

Bernard Beall, Sopio Chochua, Ben Metcalf, Wuling Lin, Theresa Tran, Zhongya Li, Yuan Li, Meghan L Bentz, Mili Sheth, Gunars Osis, Lesley McGee
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摘要

背景 美国疾病控制和预防中心的主动细菌核心监测(ABCs)发现血清型 4 侵袭性肺炎球菌疾病(IPD)有所增加,尤其是在无家可归的成年人(AEH)中。方法 我们对 2016-2022 年期间的 IPD 病例进行了量化。通过对 IPD 分离物进行基于基因组的特征描述,我们确定了血清型转换变体。重组分析用于确定产生血清 4 型后代菌株的基因供体和受体菌株。我们对血清 4 型后代和血清 12F 型基因受体进行了系统发育分析,以确定遗传距离。结果 我们在 2022-2023 年期间发现了 30 个相互关联(0-21 个核苷酸差异)的 IPD 分离物,它们与血清 4 型胶囊开关变异株相对应。这种菌株是通过血清型 4/ST10172 和血清型 12F/ST220 亲本菌株之间的多片段重组事件产生的。30 例病例中有 25 例发生在俄勒冈州。在 29 例已知居住地的病例中,16 例发生在 AEH。变异株出现的同时,2022 年由血清型 4/ST10172 供体株引起的病例比 2019 年增加了 2.6 倍(从 57 例增加到 148 例),这也是变异株首次出现在俄勒冈州。2016-2022 年间,大多数血清型的 AEH IPD/所有 IPD 比率呈现连续增长(所有血清型合计,2022 年间为 247/2198,11.2%,而 2018-2019 年为 405/5317,7.6%,p<0.001)。在 2020-2022 年期间,血清型 4 和 12F 在 AEH 中造成的 IPD 多于其他任何血清型(合计报告病例 207 例,主要发生在西部 4 个州,占 AEH IPD 的 38%)。结论 4 型和 12F 型血清型在成人中的扩展和传播增加,可能导致最近产生了具有影响力的混合型 "血清型转换 "变体。
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Increased proportions of invasive pneumococcal disease cases amongs adults experiencing homelessness sets stage for new serotype 4 capsular-switch recombinant
Background The Centers for Disease Control and Prevention’s Active Bacterial Core surveillance (ABCs) identified increased serotype 4 invasive pneumococcal disease (IPD), particularly among adults experiencing homelessness (AEH). Methods We quantified IPD cases during 2016-2022. Employing genomic-based characterization of IPD isolates, we identified serotype-switch variants. Recombinational analyses were used to identify the genetic donor and recipient strains that generated a serotype 4 progeny strain. We performed phylogenetic analyses of the serotype 4 progeny and serotype 12F genetic recipient to determine genetic distances. Results We identified 30 inter-related (0-21 nucleotide differences) IPD isolates recovered during 2022–2023, corresponding to a serotype 4 capsular-switch variant. This strain arose through a multi-fragment recombination event between serotype 4/ST10172 and serotype 12F/ST220 parental strains. Twenty-five of the 30 cases occurred within Oregon. Of 29 cases with known residence status, 16 occurred in AEH. Variant emergence coincided with a 2.6-fold increase (57 to 148) of cases caused by the serotype 4/ST10172 donor lineage in 2022 compared to 2019 and its first appearance in Oregon. Most serotypes showed sequential increases of AEH IPD/all IPD ratios during 2016-2022 (for all serotypes combined, 247/2198, 11.2% during 2022 compared to 405/5317, 7.6% for 2018-2019, p<0.001). Serotypes 4 and 12F each caused more IPD than any other serotypes in AEH during 2020-2022 (207 combined reported cases primarily in 4 western states accounting for 38% of IPD in AEH). Conclusion Expansion and increased transmission of serotypes 4 and 12F among adults potentially led to recent genesis of an impactful hybrid “serotype-switch” variant.
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