Longitudinal Molecular Epidemiology and Genomic Surveillance of Carbapenem-Resistant Klebsiella pneumoniae in the Gut of Healthy Individuals in China

Zelin Yan , Yan Li , Yi Sun , Qiaoling Sun , Congcong Liu , Yanyan Zhang , Yuchen Wu , Hongwei Zhou , Shangshang Qin , Gongxiang Chen , Ruichao Li , Rong Zhang

MedComm ›› 2026, Vol. 7 ›› Issue (8) : e70814

PDF (5048KB)
MedComm ›› 2026, Vol. 7 ›› Issue (8) :e70814 DOI: 10.1002/mco2.70814
ORIGINAL ARTICLE
Longitudinal Molecular Epidemiology and Genomic Surveillance of Carbapenem-Resistant Klebsiella pneumoniae in the Gut of Healthy Individuals in China
Author information +
History +
PDF (5048KB)

Abstract

Carbapenem-resistant Klebsiella pneumoniae (CRKP) was identified by the World Health Organization in 2024 as a key priority bacterium for the development of novel control strategies. While most surveillance studies have focused on clinical isolates, the prevalence and genomic characteristics of CRKP in healthy populations remain poorly understood. Here, we present a nationwide longitudinal descriptive genomic analysis of CRKP isolates from healthy individuals in China in 2016 and from 2019 to 2024. Within this hospital-based health-check cohort, CRKP prevalence was higher in southern regions. Descriptive temporal changes in carbapenemase gene composition were observed, with blaNDM variants, especially blaNDM-5, more frequently detected in later years and often associated with IncHI2-IncHI2A plasmids. ST11, primarily represented by capsular types KL47 and KL64, remained the predominant lineage throughout the study period. Gene presence/absence association analysis identified several ST11-enriched loci related to iron acquisition, capsular polysaccharide synthesis, and secretion-associated functions, highlighting candidate lineage-associated features. Comparative genomic analysis with 113 clinical CRKP isolates revealed high genetic similarity (SNP < 100) between some healthy-carrier and clinical strains, suggesting possible clonal relatedness. These findings indicate that healthy individuals in this hospital-based cohort can harbor clinically relevant CRKP, supporting surveillance beyond symptomatic infections while emphasizing the descriptive scope of the present study.

Keywords

Carbapenem-resistant Klebsiella pneumoniae / Healthy individuals / Carbapenemase genes / ST11 / IncHI2-IncHI2A

Cite this article

Download citation ▾
Zelin Yan, Yan Li, Yi Sun, Qiaoling Sun, Congcong Liu, Yanyan Zhang, Yuchen Wu, Hongwei Zhou, Shangshang Qin, Gongxiang Chen, Ruichao Li, Rong Zhang. Longitudinal Molecular Epidemiology and Genomic Surveillance of Carbapenem-Resistant Klebsiella pneumoniae in the Gut of Healthy Individuals in China. MedComm, 2026, 7 (8) : e70814 DOI:10.1002/mco2.70814

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

J. A. Bengoechea and J. Sa Pessoa, “Klebsiella pneumoniae Infection Biology: Living to Counteract Host Defences,” FEMS Microbiology Review 43 (2019): 123–144.

[2]

S. Hala, M. Malaikah, J. Huang, et al., “The Emergence of Highly Resistant and Hypervirulent Klebsiella pneumoniae CC14 Clone in a Tertiary Hospital Over 8 Years,” Genome Med 16 (2024): 58.

[3]

M. Wang, M. Earley, L. Chen, et al., “Clinical Outcomes and Bacterial Characteristics of Carbapenem-Resistant Klebsiella pneumoniae Complex Among Patients From Different Global Regions (CRACKLE-2): A Prospective, Multicentre, Cohort Study,” The Lancet Infectious Diseases 22 (2022): 401–412.

[4]

D. Pu, J. Zhao, K. Chang, X. Zhuo, and B. Cao, “Superbugs‘’ With Hypervirulence and Carbapenem Resistance in Klebsiella pneumoniae: The Rise of Such Emerging Nosocomial Pathogens in China,” Science Bulletin 68 (2023): 2658–2670.

[5]

D. Gu, H. Lv, Q. Sun, L. Shu, and R. Zhang, “Emergence of Tet(A) and blaKPC-2 Co-Carrying Plasmid From a ST11 Hypervirulent Klebsiella pneumoniae Isolate in Patient's Gut,” International Journal of Antimicrobial Agents 52 (2018): 307–308, https://doi.org/10.1016/j.ijantimicag.2018.06.003.

[6]

F. Hu, Y. Pan, H. Li, et al., “Carbapenem-Resistant Klebsiella pneumoniae Capsular Types, Antibiotic Resistance and Virulence Factors in China: A Longitudinal, Multi-Centre Study,” Nature Microbiology 9 (2024): 814–829.

[7]

S. Pei, F. Liljeros, and J. Shaman, “Identifying Asymptomatic Spreaders of Antimicrobial-Resistant Pathogens in Hospital Settings,” Proceedings of National Academy of Sciences 118 (2021): e2111190118.

[8]

K. Marimuthu, I. Venkatachalam, V. Koh, et al., “Whole Genome Sequencing Reveals Hidden Transmission of Carbapenemase-Producing Enterobacterales,” Nature Communications 13 (2022): 3052.

[9]

R. G. Elbaiomy, A. H. El-Sappah, R. Guo, et al., “Antibiotic Resistance: A Genetic and Physiological Perspective,” MedComm 6 (2025): e70447.

[10]

R. Zhang, N. Dong, Y. Huang, et al., “Evolution of Tigecycline- and Colistin-Resistant CRKP (Carbapenem-Resistant Klebsiella pneumoniae) in Vivo and Its Persistence in the GI Tract,” Emerging Microbes & Infections 7 (2018): 127, https://doi.org/10.1038/s41426-018-0129-7.

[11]

B. Fu, J. Xu, D. Yin, et al., “Transmission of blaNDM in Enterobacteriaceae Among Animals, Food and Human,” Emerging Microbes & Infections 13 (2024): 2337678.

[12]

R. Bai, X. Wang, Z. Zou, et al., “Limited Transmission of Carbapenem-Resistant Klebsiella pneumoniae Between Animals and Humans: A Study in Qingdao,” Emerg Microbes Infect 13 (2024): 2387446.

[13]

W. Wu, Y. Feng, G. Tang, F. Qiao, A. McNally, and Z. Zong, “NDM Metallo-β-Lactamases and Their Bacterial Producers in Health Care Settings,” Clinical Microbiology Reviews 32 (2019): e00115–118.

[14]

C.-C. Tsai, J.-C. Lin, P.-C. Chen, et al., “A 20-Year Study of Capsular Polysaccharide Seroepidemiology, Susceptibility Profiles, and Virulence Determinants of Klebsiella pneumoniae From Bacteremia Patients in Taiwan,” Microbiology Spectrum 11 (2023): e0035923.

[15]

T. A. Russo and C. M. Marr, “Hypervirulent Klebsiella pneumoniae,” Clinical Microbiology Reviews 32 (2019): e00001–19.

[16]

D. Zhao, M. Tang, Z. Ma, et al., “Synergy of Bacteriophage Depolymerase With Host Immunity Rescues Sepsis Mice Infected With Hypervirulent Klebsiella pneumoniae of Capsule Type K2,” Virulence 15 (2024): 2415945.

[17]

K. Zhou, T. Xiao, S. David, et al., “Novel Subclone of Carbapenem-Resistant Klebsiella pneumoniae Sequence Type 11 With Enhanced Virulence and Transmissibility,” Emerging Infectious Diseases 26 (2020): 289–297.

[18]

D. Gu, N. Dong, Z. Zheng, et al., “A Fatal Outbreak of ST11 Carbapenem-resistant Hypervirulent Klebsiella pneumoniae in a Chinese Hospital: A Molecular Epidemiological Study,” The Lancet Infectious Diseases 18 (2018): 37–46.

[19]

J. He, Q. Shi, Z. Chen, et al., “Opposite Evolution of Pathogenicity Driven by in Vivo Wzc and wcaJ Mutations in ST11-KL64 Carbapenem-Resistant Klebsiella pneumoniae,” Drug Resistance Updates 66 (2023): 100891.

[20]

P. Lan, Y. Lu, Y. Fu, Y. Yu, and J. Zhou, “Siderophores and Beyond: A Comprehensive Review of Iron Acquisition in Klebsiella pneumoniae,” Virulence 16 (2025): 2550621.

[21]

M. E. S. Guerra, G. Destro, B. Vieira, et al., “Klebsiella pneumoniae Biofilms and Their Role in Disease Pathogenesis,” Frontiers in Cellular and Infection Microbiology 12 (2022): 877995.

[22]

B. Davido, B. Merrick, E. Kuijper, et al., “How Can the Gut Microbiome be Targeted to Fight Multidrug-Resistant Organisms?,” The Lancet Microbe 6 (2025): 101063.

[23]

Y. Li, Y. Zhang, X. Sun, et al., “National Genomic Epidemiology Investigation Revealed the Spread of Carbapenem-Resistant Escherichia coli in Healthy Populations and the Impact on Public Health,” Genome Medicine 16 (2024): 57.

[24]

J. Zhang, J. Xu, S. Shen, et al., “Comparison of Three Colloidal Gold Immunoassays and GeneXpert Carba-R for the Detection of Klebsiella pneumoniae blaKPC-2 Variants,” Journal of Clinical Microbiology 62 (2024): e0015424.

[25]

R. M. Humphries, J. Ambler, S. L. Mitchell, et al., “CLSI Methods Development and Standardization Working Group Best Practices for Evaluation of Antimicrobial Susceptibility Tests,” Journal of Clinical Microbiology 56 (2018): e01934-17.

[26]

A. G. Elliott, D. Ganesamoorthy, L. Coin, M. A. Cooper, and M. D. Cao, “Complete Genome Sequence of Klebsiella Quasipneumoniae subsp. Similipneumoniae Strain ATCC 700603,” Genome Announcements 4 (2016): e00438-16.

[27]

T. D. Minogue, H. A. Daligault, K. W. Davenport, et al., “Complete Genome Assembly of Escherichia coli ATCC 25922, a Serotype O6 Reference Strain,” Genome Announcements 2 (2014): e00969-14.

[28]

T. Seemann, “Prokka: Rapid Prokaryotic Genome Annotation,” Bioinformatics 30 (2014): 2068–2069.

[29]

A. C. Schürch, S. Arredondo-Alonso, R. J. L. Willems, and R. V. Goering, “Whole Genome Sequencing Options for Bacterial Strain Typing and Epidemiologic Analysis Based on Single Nucleotide Polymorphism Versus Gene-by-Gene-Based Approaches,” Clinical Microbiology and Infection 24 (2018): 350–354.

[30]

M. M. C. Lam, R. R. Wick, S. C. Watts, L. T. Cerdeira, K. L. Wyres, and K. E. Holt, “A Genomic Surveillance Framework and Genotyping Tool for Klebsiella pneumoniae and Its Related Species Complex,” Nature Communications 12 (2021): 4188.

[31]

A. Carattoli, E. Zankari, A. García-Fernández, et al., “In Silico Detection and Typing of Plasmids Using PlasmidFinder and Plasmid Multilocus Sequence Typing,” Antimicrobial Agents and Chemotherapy 58 (2014): 3895–3903.

[32]

B. Liu, D. Zheng, S. Zhou, L. Chen, and J. Yang, “VFDB 2022: A General Classification Scheme for Bacterial Virulence Factors,” Nucleic Acids Research 50 (2022): D912–917.

[33]

C. Bertelli, M. R. Laird, K. P. Williams, et al., “IslandViewer 4: Expanded Prediction of Genomic Islands for Larger-Scale Datasets,” Nucleic Acids Research 45 (2017): W30–35.

[34]

K. L. Wyres, S. M. Cahill, K. E. Holt, R. M. Hall, and J. J. Kenyon, “Identification of Acinetobacter baumannii Loci for Capsular Polysaccharide (KL) and Lipooligosaccharide Outer Core (OCL) Synthesis in Genome Assemblies Using Curated Reference Databases Compatible With Kaptive,” Microbial Genomics 6 (2020): e000339.

[35]

M. N. Price, P. S. Dehal, and A. P. Arkin, “FastTree: Computing Large Minimum Evolution Trees With Profiles Instead of a Distance Matrix,” Molecular Biology and Evolution 26 (2009): 1641–1650.

[36]

A. J. Page, C. A. Cummins, M. Hunt, et al., “Roary: Rapid Large-Scale Prokaryote Pan Genome Analysis,” Bioinformatics 31 (2015): 3691–3693.

[37]

I. Letunic and P. Bork, “Interactive Tree of Life (iTOL) v5: An Online Tool for Phylogenetic Tree Display and Annotation,” Nucleic Acids Res 49 (2021): W293–296.

[38]

O. Brynildsrud, J. Bohlin, L. Scheffer, and V. Eldholm, “Rapid Scoring of Genes in Microbial Pan-Genome-Wide Association Studies With Scoary,” Genome Biology 17 (2016): 238.

[39]

X. Liu, E. W.-C. Chan, and S. Chen, “Transmission and Stable Inheritance of Carbapenemase Gene (blaKPC-2 or blaNDM-1)-Encoding and Mcr-1-encoding Plasmids in Clinical Enterobacteriaceae Strains,” Journal of Global Antimicrobial Resistance 26 (2021): 255–261.

[40]

L. Yang, Y. Shen, J. Jiang, et al., “Distinct Increase in Antimicrobial Resistance Genes Among Escherichia coli During 50 Years of Antimicrobial Use in Livestock Production in China,” Nature Food 3 (2022): 197–205.

Rights & permissions

2026 The Author(s). MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

PDF (5048KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉