Changes in antimicrobial resistance of clinical isolates of Proteus, Morganella, and Providencia species from regional hospitals in Zhejiang Province, 2020 ~ 2024
- 1Department of Laboratory Medicine, Second Affiliated Hospital of Zhejiang University, School of Medicine
- 2Clinical Laboratory of Chun’an First People’s Hospital, Zhejiang Provincial People’s Hospital Chun’an Branch
- 3Department of Microbiology Laboratory, Hangzhou Third People’s Hospital, Hangzhou Third Hospital Affiliated to Zhejiang Chinese Medical University
Abstract
Background Proteus, Morganella, and Providencia species are important opportunistic pathogens associated with healthcare- and community-acquired infections, but their recent epidemiological and antimicrobial resistance trends in regional secondary hospitals remain insufficiently characterized. This study investigated the distribution and antimicrobial resistance patterns of these three genera collected from 34 regional medical institutions in Zhejiang Province, China, between 2020 and 2024. Methods Clinical isolates of these three genera were collected from 34 secondary-level hospitals across seven regions of Zhejiang. Bacterial identification and antimicrobial susceptibility testing were performed primarily using VITEK-2. Results were interpreted according to Clinical and Laboratory Standards Institute (CLSI) M100 breakpoints. Duplicate isolates from the same patient were excluded. Isolates resistant to meropenem or ertapenem were defined as carbapenem-resistant Enterobacterales (CRE). Results A total of 7,329 nonduplicate isolates were collected, including 6,181 Proteus (84.4%), 847 Morganella (11.6%), and 301 Providencia (4.1%). Annual isolate counts increased from 2020 to 2024. The leading specimen sources were urine (approximately 42%), respiratory tract specimens (approximately 28%), and wound and secretion specimens (approximately 12%); approximately 2% were from bloodstream infections. Across all years, carbapenem resistance was lowest in Proteus and Morganella but highest in Providencia. In 2020, resistance rates for multiple antibiotics were higher than in 2021, and they increased again by 2024. Phylogenetic analysis revealed that the human intestinal tract may serve as a reservoir for blaNDM-1-carrying Providencia spp. and carbapenemase genes are broadly disseminated across genetically diverse M. morganii strains. Conclusions The rising prevalence of these bacteria, particularly carbapenem-resistant Providencia, highlights an urgent need for enhanced antimicrobial stewardship and infection control in secondary hospitals. Ongoing resistance surveillance in community healthcare settings is essential to curb the spread of these resistant pathogens.
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BibTeX
@article{zhang2026changes,
title = {{Changes in antimicrobial resistance of clinical isolates of Proteus, Morganella, and Providencia species from regional hospitals in Zhejiang Province, 2020 ~ 2024}},
author = {Zhengliang Zhang and Lingmei Fang and Hongwei Zhou and Rong Zhang and Shi Chen},
journal = {BMC Microbiology},
year = {2026},
month = jul,
doi = {10.1186/s12866-026-05407-8},
url = {https://doi.org/10.1186/s12866-026-05407-8},
note = {CC BY},
}
RIS
TY - JOUR
TI - Changes in antimicrobial resistance of clinical isolates of Proteus, Morganella, and Providencia species from regional hospitals in Zhejiang Province, 2020 ~ 2024
AU - Zhengliang Zhang
AU - Lingmei Fang
AU - Hongwei Zhou
AU - Rong Zhang
AU - Shi Chen
PY - 2026
DA - 2026/07/01
JO - BMC Microbiology
DO - 10.1186/s12866-026-05407-8
UR - https://doi.org/10.1186/s12866-026-05407-8
AB - Background Proteus, Morganella, and Providencia species are important opportunistic pathogens associated with healthcare- and community-acquired infections, but their recent epidemiological and antimicrobial resistance trends in regional secondary hospitals remain insufficiently characterized. This study investigated the distribution and antimicrobial resistance patterns of these three genera collected from 34 regional medical institutions in Zhejiang Province, China, between 2020 and 2024. Methods Clinical isolates of these three genera were collected from 34 secondary-level hospitals across seven regions of Zhejiang. Bacterial identification and antimicrobial susceptibility testing were performed primarily using VITEK-2. Results were interpreted according to Clinical and Laboratory Standards Institute (CLSI) M100 breakpoints. Duplicate isolates from the same patient were excluded. Isolates resistant to meropenem or ertapenem were defined as carbapenem-resistant Enterobacterales (CRE). Results A total of 7,329 nonduplicate isolates were collected, including 6,181 Proteus (84.4%), 847 Morganella (11.6%), and 301 Providencia (4.1%). Annual isolate counts increased from 2020 to 2024. The leading specimen sources were urine (approximately 42%), respiratory tract specimens (approximately 28%), and wound and secretion specimens (approximately 12%); approximately 2% were from bloodstream infections. Across all years, carbapenem resistance was lowest in Proteus and Morganella but highest in Providencia. In 2020, resistance rates for multiple antibiotics were higher than in 2021, and they increased again by 2024. Phylogenetic analysis revealed that the human intestinal tract may serve as a reservoir for blaNDM-1-carrying Providencia spp. and carbapenemase genes are broadly disseminated across genetically diverse M. morganii strains. Conclusions The rising prevalence of these bacteria, particularly carbapenem-resistant Providencia, highlights an urgent need for enhanced antimicrobial stewardship and infection control in secondary hospitals. Ongoing resistance surveillance in community healthcare settings is essential to curb the spread of these resistant pathogens.
SN - 1471-2180
ER -