Transmission of <i>bla</i> <sub>NDM</sub> in Enterobacteriaceae among animals, food and human

Bo Fu, Jian Xu, Dandan Yin, Chengtao Sun, Dejun Liu, Weishuai Zhai, Rina Bai, Yue Cao, Qin Zhang, Shizhen Ma,

Emerging Microbes & Infections · 2024 · 26 citations · 36 references

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Abstract

Despite carbapenems not being used in animal, Carbapenem-Resistant-Enterobacterales (CRE), particularly New-Delhi-metallo-β-lactamase-producing-CRE (NDM-CRE), are prevalent in livestock. Concurrently, the incidence of human infections caused by NDM-CRE is rising, particularly in children. Although positive association between livestock production and human NDM-CRE infections at national level was identified, the evidence of direct transmission of NDM originating from livestock to humans remains largely unknown. Here we conducted a cross-sectional study in Chengdu, Sichuan Province to examine the prevalence of NDM-CRE in chickens and pigs along the breeding-slaughtering-retail chains, in pork in cafeterias of schools, and in colonisations and infections from a children's hospital, and examined the correlation of NDM-CRE among animals, foods and humans. Overall, the blaNDM increases gradually along the chicken and pig breeding (4.70%/2.0%) - slaughtering (7.60%/22.40%) - retail (65.56%/34.26%) chains. The slaughterhouse has become a hotspot for cross-contamination and amplifier of blaNDM. Notably, 63.11% pork from school cafeteria were positive for blaNDM. The prevalence of blaNDM in intestinal and infection samples from children's hospital was 21.68% and 19.80%, respectively. WGS analysis revealed the sporadic, not large-scale, clonal spread of NDM-CRE along the chicken and pig breeding-slaughtering-retail chain, with further spreading via IncX3-blaNDM plasmid within each stage of whole chains. Whist clonal transmission of NDM-CRE is predominant in children's hospital. The IncX3-blaNDM plasmid was highly prevalent among animals and humans and accounted for 57.7% in Escherichia coli and 91.3% in Klebsiella pneumoniae. Attention should be directed towards the IncX3 plasmid to control the transmission of blaNDM between animals and humans.

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