Detecting, mapping, and suppressing the spread of a decade-long Pseudomonas aeruginosa nosocomial outbreak with genomics

Author:

Stribling William1ORCID,Hall Lindsey R.1,Powell Aubrey12,Harless Casey1ORCID,Martin Melissa J.1ORCID,Corey Brendan W.1ORCID,Snesrud Erik1,Ong Ana1,Maybank Rosslyn1,Stam Jason1ORCID,Bartlett Katie1ORCID,Jones Brendan T.1ORCID,Preston Lan N.1,Lane Katherine F.1,Thompson Bernadette3,Young Lynn M.3,Kwak Yoon I.1,Barsoumian Alice E.4,Markelz Ana-Elizabeth4,Kiley John L.4,Cybulski Robert J.15,Bennett Jason W.1,Mc Gann Patrick T.1ORCID,Lebreton Francois1ORCID

Affiliation:

1. Multidrug-Resistant Organism Repository and Surveillance Network (MRSN), Walter Reed Army Institute of Research

2. Department of Pathology, Brooke Army Medical Center, Joint Base San Antonio-Fort Sam Houston

3. Infection Prevention & Control, Brooke Army Medical Center, Joint Base San Antonio-Fort Sam Houston

4. Infectious Disease Service, Department of Medicine, Brooke Army Medical Center, Joint Base San Antonio Fort Sam Houston

5. Bacterial Disease Branch, Walter Reed Army Institute of Research

Abstract

Whole-genome sequencing is revolutionizing bacterial outbreak investigation but its application to the clinic remains limited. In 2020, prospective and retrospective surveillance detected a Pseudomonas aeruginosa outbreak with 254 isolates collected from 82 patients in 27 wards of a hospital. Its origin was dated to the late 90s, just after the facility opened, and patient-to-patient and environment-to-patient cases of transmission were inferred. Over time, two epidemic subclones evolved in separate hosts and hospital areas, including newly opened wards, and hospital-wide sampling confirmed reservoirs persisted in the plumbing. Pathoadaptive mutations in genes associated with virulence, cell wall biogenesis, and antibiotic resistance were identified. While the latter correlated with the acquisition of phenotypic resistances to 1st (cephalosporin), 2nd (carbapenems) and 3rd (colistin) lines of treatment, maximum parsimony suggested that a truncation in a lipopolysaccharide component coincided with the emergence of a subclone prevalent in chronic infections. Since initial identification, extensive infection control efforts guided by routine, near real-time surveillance have proved successful at slowing transmission.Every year, millions of hospital-associated infections are threatening patient lives. This, in a world in which rates of resistances to existing antibiotics are increasing. And this, at a time dubbed the post-antibiotic era when new drugs are scarce. But now is also the golden age of genomics. Here, applying this transformative technology to the clinic revealed an outbreak of Pseudomonas aeruginosa , resistant to last line antibiotics, that had escaped detection for decades. The mapping of transmission chains, through hospital floors, pointed to environmental reservoirs in intensive care units but also provided critical insights into the evolution and adaptation of this pathogen. Genomic data, shared in near real-time with the hospital, resulted in targeted interventions and the prevention of new cases.

Publisher

eLife Sciences Publications, Ltd

Reference50 articles.

1. Pseudomonas aeruginosa: a formidable and ever-present adversary;Journal of Hospital Infection,2009

2. Prevalence of bacterial pathogens in biofilms of drinking water distribution systems

3. Intrinsic and Environmental Mutagenesis Drive Diversification and Persistence of Pseudomonas aeruginosa in Chronic Lung Infections;J. Infect. Dis,2012

4. Prioritization of pathogens to guide discovery, research and development of new antibiotics for drug resistant bacterial infections, including tuberculosis;World Health Organization;Essential medicines and health products,2017

5. Epidemiology and characteristics of metallo-ß-lactamase-producing Pseudomonas aeruginosa;Infect. Chemother,2015

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3