Shoucri Sherif, Blair Nicholas J, Seeram Dwayne, Gomez-Simmonds Angela, Shi Qiuhu, Lowy Franklin D, Uhlemann Anne-Catrin
Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Department of Public Health, New York Medical College, Valhalla, New York, USA.
Open Forum Infect Dis. 2025 May 21;12(6):ofaf304. doi: 10.1093/ofid/ofaf304. eCollection 2025 Jun.
(SA) bacteremia is a morbid complication of injection drug use (IDU), yet little is known about the biological and clinical factors that drive morbidity due to these infections in persons who inject drugs (PWID).
We reviewed all cases of community-associated bacteremia (SAB) over a 2-year period at a large tertiary care medical center in New York City. We identified 29 PWID with community-associated SAB, who were matched randomly in a 4:1 (control:case) ratio to 112 comparisons with SAB but no IDU. Whole-genome sequencing and phylogenetic analysis were performed on SAB isolates to identify genetic and molecular similarities.
The PWID group was younger, more unstably housed, and more frequently diagnosed with endocarditis. Genotyping results showed comparable proportions of SA sequence types (STs) between PWID and comparisons, and ST8 accounted for a plurality of infections. Phylogenetic analysis showed 2 related pairs of SA isolates, only 1 of which occurred among PWID. The highest proportion of endocarditis episodes occurred in patients with SA isolates belonging to ST5, ST7, and ST97, but we were unable to identify significant associations between complications and specific SA virulence factors.
Among PWID, we did not identify specific clusters of SA, which was clonally diverse. Possible explanations include nonoverlapping IDU networks and the fact that New York is a syringe-exchange state, which may reduce the risk of shared exposures to PWID demonstrate higher rates of infective endocarditis than controls and should be targeted for early multidisciplinary intervention.
金黄色葡萄球菌(SA)菌血症是注射吸毒(IDU)的一种严重并发症,但对于促使注射毒品者(PWID)发生这些感染相关发病的生物学和临床因素知之甚少。
我们回顾了纽约市一家大型三级医疗中心两年期间所有社区相关性菌血症(SAB)病例。我们确定了29例患有社区相关性SAB的PWID,他们以4:1(对照:病例)的比例与112例有SAB但无IDU的对照进行随机匹配。对SAB分离株进行全基因组测序和系统发育分析,以确定遗传和分子相似性。
PWID组更年轻,居住状况更不稳定,且更频繁地被诊断为心内膜炎。基因分型结果显示,PWID和对照组之间SA序列类型(STs)的比例相当,ST8占感染的多数。系统发育分析显示有2对相关的SA分离株,其中只有1对出现在PWID中。心内膜炎发作比例最高的是SA分离株属于ST5、ST7和ST97的患者,但我们未能确定并发症与特定SA毒力因子之间的显著关联。
在PWID中,我们未发现SA的特定聚集群,其克隆具有多样性。可能的解释包括IDU网络不重叠,以及纽约是一个注射器交换州,这可能降低了共同暴露的风险。PWID的心内膜炎发生率高于对照组,应针对其进行早期多学科干预。