TY - JOUR
T1 - Colonization dynamics of extended-spectrum beta-lactamase-producing Enterobacterales in the gut of Malawian adults
AU - Lewis, Joseph M.
AU - Mphasa, Madalitso
AU - Banda, Rachel
AU - Beale, Mathew A.
AU - Heinz, Eva
AU - Mallewa, Jane
AU - Jewell, Christopher
AU - Faragher, Brian
AU - Thomson, Nicholas R.
AU - Feasey, Nicholas A.
PY - 2022/10
Y1 - 2022/10
N2 - Drug-resistant bacteria of the order Enterobacterales which produce extended-spectrum beta-lactamase enzymes (ESBL-Enterobacterales, ESBL-E) are global priority pathogens. Antimicrobial stewardship interventions proposed to curb their spread include shorter courses of antimicrobials to reduce selection pressure but individual-level acquisition and selection dynamics are poorly understood. We sampled stool of 425 adults (aged 16–76 years) in Blantyre, Malawi, over 6 months and used multistate modelling and whole-genome sequencing to understand colonization dynamics of ESBL-E. Models suggest a prolonged effect of antimicrobials such that truncating an antimicrobial course at 2 days has a limited effect in reducing colonization. Genomic analysis shows largely indistinguishable diversity of healthcare-associated and community-acquired isolates, hence some apparent acquisition of ESBL-E during hospitalization may instead represent selection from a patient’s microbiota by antimicrobial exposure. Our approach could help guide stewardship protocols; interventions that aim to review and truncate courses of unneeded antimicrobials may be of limited use in preventing ESBL-E colonization.
AB - Drug-resistant bacteria of the order Enterobacterales which produce extended-spectrum beta-lactamase enzymes (ESBL-Enterobacterales, ESBL-E) are global priority pathogens. Antimicrobial stewardship interventions proposed to curb their spread include shorter courses of antimicrobials to reduce selection pressure but individual-level acquisition and selection dynamics are poorly understood. We sampled stool of 425 adults (aged 16–76 years) in Blantyre, Malawi, over 6 months and used multistate modelling and whole-genome sequencing to understand colonization dynamics of ESBL-E. Models suggest a prolonged effect of antimicrobials such that truncating an antimicrobial course at 2 days has a limited effect in reducing colonization. Genomic analysis shows largely indistinguishable diversity of healthcare-associated and community-acquired isolates, hence some apparent acquisition of ESBL-E during hospitalization may instead represent selection from a patient’s microbiota by antimicrobial exposure. Our approach could help guide stewardship protocols; interventions that aim to review and truncate courses of unneeded antimicrobials may be of limited use in preventing ESBL-E colonization.
KW - Drug-resistant bacteria
KW - colonization dynamics
KW - antimicrobial exposure
KW - antimicrobials
UR - http://www.scopus.com/inward/record.url?scp=85137425436&partnerID=8YFLogxK
UR - https://doi.org/10.5281/zenodo.5554081
U2 - 10.1038/s41564-022-01216-7
DO - 10.1038/s41564-022-01216-7
M3 - Article
C2 - 36065064
AN - SCOPUS:85137425436
VL - 7
SP - 1593
EP - 1604
JO - Nature microbiology
JF - Nature microbiology
IS - 10
ER -