Marks Laura R, Calix Juan J, Wildenthal John A, Wallace Meghan A, Sawhney Sanjam S, Ransom Eric M, Durkin Michael J, Henderson Jeffrey P, Burnham Carey-Ann D, Dantas Gautam
Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO USA.
The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO USA.
Commun Med (Lond). 2021 Nov 30;1:52. doi: 10.1038/s43856-021-00053-9. eCollection 2021.
The ongoing injection drug use (IDU) crisis in the United States has been complicated by an emerging epidemic of IDU-associated bloodstream infections (IDU-BSI).
We performed a case-control study comparing IDU-BSI and non-IDU BSI cases identified in a large US Midwestern academic medical center between Jan 1, 2016 and Dec 21, 2019. We obtained the whole-genome sequences of 154 IDU-BSI and 91 non-IDU BSI cases, which were matched with clinical data. We performed phylogenetic and comparative genomic analyses to investigate clonal expansion of lineages and molecular features characteristic of IDU-BSI isolates.
Here we show that patients with IDU-BSI experience longer durations of bacteremia and have lower medical therapy completion rates. In phylogenetic analyses, 45/154 and 1/91 contemporaneous IDU-BSI and non-IDU BSI staphylococcal isolates, respectively, group into multiple, unique clonal clusters, revealing that pathogen community transmission distinctively spurs IDU-BSI. Lastly, multiple lineages deficient in canonical virulence genes are overrepresented among IDU-BSI, which may contribute to the distinguishable clinical presentation of IDU-BSI cases.
We identify clonal expansion of multiple lineages among IDU-BSI isolates, but not non-IDU BSI isolates, in a community with limited access to needle exchange facilities. In the setting of expanding numbers of staphylococcal IDU-BSI cases consideration should be given to treating IDU-associated invasive staphylococcal infections as a communicable disease.
美国持续存在的注射吸毒(IDU)危机因IDU相关血流感染(IDU-BSI)的新流行而变得复杂。
我们进行了一项病例对照研究,比较了2016年1月1日至2019年12月21日期间在美国中西部一家大型学术医疗中心确定的IDU-BSI病例和非IDU-BSI病例。我们获得了154例IDU-BSI病例和91例非IDU-BSI病例的全基因组序列,并将其与临床数据相匹配。我们进行了系统发育和比较基因组分析,以研究IDU-BSI分离株的谱系克隆扩增和分子特征。
我们在此表明,IDU-BSI患者的菌血症持续时间更长,药物治疗完成率更低。在系统发育分析中,分别有45/154和1/91例同期IDU-BSI和非IDU-BSI葡萄球菌分离株归入多个独特的克隆簇,表明病原体的社区传播显著促进了IDU-BSI的发生。最后,IDU-BSI中多个缺乏典型毒力基因的谱系占比过高,这可能导致IDU-BSI病例出现明显的临床表现。
在针头交换设施有限的社区中,我们在IDU-BSI分离株中而非非IDU-BSI分离株中发现了多个谱系的克隆扩增。在葡萄球菌IDU-BSI病例数量不断增加的情况下,应考虑将IDU相关的侵袭性葡萄球菌感染作为传染病进行治疗。