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侵袭性人源猪链球菌感染的临床特征、90天功能结局、抗菌药物敏感性及探索性基因组分析:中国多中心回顾性研究

Clinical Characteristics, 90-Day Functional Outcomes, Antimicrobial Susceptibility, and Exploratory Genomic Analysis of Invasive Human Streptococcus suis Infection: A Multicenter Retrospective Study in China.

临床研究耳科IF 3.7Q1

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中文摘要

背景: 猪链球菌是一种人畜共患病原体;侵袭性感染幸存者可能存在持续性听觉或前庭后遗症。为弥补中国多中心证据的不足,我们描述了90天结局、抗菌药物敏感性及探索性基因组发现。
方法: 我们回顾性研究了2017年至2025年间在中国四个省份八家医院收治的34例侵袭性猪链球菌感染患者。不良结局定义为90天内死亡或第90天时存在持续性后遗症。最低抑菌浓度采用CLSI草绿色链球菌群替代折点重新判读;对6株可回收分离株进行了全基因组测序。
结果: 急性耳蜗前庭受累发生于11/27(40.7%)的脑膜炎患者和0/7的非脑膜炎型菌血症/脓毒症患者。不良结局发生于17/34(50.0%)患者,包括2例死亡;12/32(37.5%)幸存者存在听力相关后遗症。急性耳蜗前庭受累在不良结局患者中更为常见(64.7%对0%;P < 0.001)。所有可评估分离株对青霉素(21/21)、头孢噻肟(19/19)和头孢曲松(5/5)敏感。在接受红霉素、克林霉素和四环素检测的分离株中,分别有17/20、16/20和20/20观察到耐药。序列型为ST1(n = 3)、ST7(n = 2)和ST25(n = 1);epf和sly各在5株分离株中检出,mrp在4株中检出。
结论: 显著的听力相关疾病负担支持开展结构化的听力学随访。临床关联和基因组发现仍属探索性,不能确立独立预后价值或基因型-表型因果关系。

英文摘要

BACKGROUND: Streptococcus suis is a zoonotic pathogen; survivors of invasive infection may have persistent auditory or vestibular sequelae. To address limited multicenter evidence from China, we characterized 90-day outcomes, antimicrobial susceptibility, and exploratory genomic findings.
METHODS: We retrospectively studied 34 patients with invasive S. suis infection at eight hospitals in four Chinese provinces (2017-2025). Unfavorable outcome was defined as death within 90 days or persistent sequelae at day 90. Minimum inhibitory concentrations were reinterpreted using CLSI viridans-group streptococcal surrogate breakpoints; six recoverable isolates underwent whole-genome sequencing.
RESULTS: Acute cochleovestibular involvement occurred in 11/27 (40.7%) patients with meningitis and 0/7 with nonmeningitic bacteremia/sepsis. Unfavorable outcomes occurred in 17/34 (50.0%) patients, including two deaths; 12/32 (37.5%) survivors had hearing-related sequelae. Acute cochleovestibular involvement was more frequent among patients with unfavorable outcomes (64.7% versus 0%; P < 0.001). All evaluable isolates were susceptible to penicillin (21/21), cefotaxime (19/19), and ceftriaxone (5/5). Resistance was observed in 17/20, 16/20, and 20/20 isolates tested for erythromycin, clindamycin, and tetracycline, respectively. Sequence types were ST1 (n = 3), ST7 (n = 2), and ST25 (n = 1); epf and sly were each detected in five isolates, and mrp in four.
CONCLUSIONS: Substantial hearing-related morbidity supports structured audiological follow-up. Clinical associations and genomic findings remain exploratory and do not establish independent prognostic value or genotype-phenotype causality.