Increasing antimicrobial resistance and potential human bacterial pathogens in an invasive land snail driven by urbanization

Yiyue Zhang, Jian Qiang Su, Hu Liao, Martin F. Breed, Haifeng Yao, Huayuan Shangguan, Hong Zhe Li, Xin Sun, Yong Guan Zhu

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

Our understanding of the role urbanization has in augmenting invasive species that carry human bacterial pathogens and antimicrobial resistance (AMR) remains poorly understood. Here, we investigated the gut bacterial communities, antibiotic resistance genes (ARGs) and potential antibiotic-resistant pathogens in giant African snails (Achatina fulica) collected across an urbanization gradient in Xiamen, China (n = 108). There was a lack of correlation between the microbial profiles of giant African snails and the soils of their habitats, and the resistome and human-associated bacteria were significantly higher than those of native snails as well as soils. We observed high diversity (601 ARG subtypes) and abundance (1.5 copies per 16S rRNA gene) of giant African snail gut resistome. Moreover, giant African snails in more urban areas had greater diversity and abundance of high-risk ARGs and potential human bacterial pathogens (e.g., ESKAPE pathogens). We highlight that urbanization significantly impacted the gut microbiomes and resistomes of these invasive snails, indicating that they harbor greater biological contaminants such as ARGs and potential human bacterial pathogens than native snails and soils. This study advances our understanding of the effect of urbanization on human bacterial pathogens and AMR in a problematic invasive snail and should help combat risks associated with invasive species under the One Health framework.

Original languageEnglish
Pages (from-to)7273-7284
Number of pages12
JournalEnvironmental Science and Technology
Volume57
Issue number18
DOIs
Publication statusPublished - 9 May 2023

Keywords

  • antibiotic resistance genes
  • biological invasion
  • ESKAPE pathogens
  • human bacterial pathogens
  • metagenome-assembled genomes
  • resistome

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