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<p>Extended-spectrum β-lactamases (ESBLs) constitute one of the principal mechanisms underlying multidrug resistance (MDR) in avian pathogenic <i>Escherichia coli</i> (APEC). The coexistence of ESBL-encoding genes, particularly <i>blaCTX-M</i>, together with the plasmid-mediated colistin resistance gene <i>mcr-1</i> in APEC raises serious concern, as it undermines the effectiveness of third-generation cephalosporins and colistin. To clarify the current epidemiological status and potential transmission risks associated with the co-occurrence of ESBL and <i>mcr-1</i> genes in southern Xinjiang, 133 liver samples from chickens that had died after exhibiting clinical signs consistent with colibacillosis were collected, from which 100 of these isolates (75.2%, 100/133) were confirmed as APEC. The double-disk diffusion test revealed that 65 strains (65.0%, 65/100) were ESBL-producing. Among these ESBL-producing APEC isolates, resistance rates to ampicillin, cefazolin, ceftiofur, and cefoxitin were 100% (65/65), 100% (65/65), 92.3% (60/65), and 4.6% (3/65, intermediate/susceptible), respectively. PCR detection revealed that 95.4% (62/65) carried <i>blaCTX-M</i> and 93.8% (61/65) carried <i>blaTEM</i> and five isolates (7.7%, 5/65) were resistant to colistin and carried the <i>mcr-1</i> gene. Integron analysis revealed that int1 was detected in 98.5% (64/65) of the ESBL-APEC isolates. Notably, all five <i>mcr-1</i>-positive strains co-harbored int1. These five isolates exhibited MDR phenotypes and were assigned to phylogenetic groups A (<i>n</i> = 1), B1 (<i>n</i> = 3), and D (<i>n</i> = 1). Whole-genome sequencing (WGS) revealed that the five <i>mcr-1</i>-positive APEC strains belonged to four sequence types (STs): ST6792 (<i>n</i> = 1), ST1196 (<i>n</i> = 2), ST155 (<i>n</i> = 1), and ST162 (<i>n</i> = 1), and harbored three <i>blaCTX-M</i> subtypes (<i>blaCTX-M-55</i> [<i>n</i> = 3], <i>blaCTX-M-64</i> [<i>n</i> = 1], and <i>blaCTX-M-65</i>[<i>n</i> = 1]). Furthermore, these strains carried IncI2 or IncFIB plasmid replicons alongside the int1 integrase gene, highlighting the co-occurrence of critical resistance determinants with mobile genetic elements known to facilitate horizontal dissemination. The coexistence of <i>blaCTX-M</i> and <i>mcr-1</i> in high-risk clones such as ST155 and ST162, which are associated with human infections worldwide, indicates that the region faces a threat from multidrug-resistant strains and a potential risk of cross-species transmission. Given the limited geographic scope and sample size, our findings should be considered a preliminary warning. Future studies with expanded sampling and experimental validation of horizontal transfer are needed to fully assess the transmission risks.</p>

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Co-existence of blaCTX-M and mcr-1 in avian pathogenic Escherichia coli in Southern Xinjiang: current status and antimicrobial resistance characteristics

  • 期刊论文

  • 发表日期：

    2026年5月6日

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  • Bin Yang,
  • Guofeng Xing,
  • Wenxuan Ma,
  • Meng Qi,
  • Bo Jing,
  • Jing Li,
  • Jing Wu

摘要

Extended-spectrum β-lactamases (ESBLs) constitute one of the principal mechanisms underlying multidrug resistance (MDR) in avian pathogenic Escherichia coli (APEC). The coexistence of ESBL-encoding genes, particularly blaCTX-M, together with the plasmid-mediated colistin resistance gene mcr-1 in APEC raises serious concern, as it undermines the effectiveness of third-generation cephalosporins and colistin. To clarify the current epidemiological status and potential transmission risks associated with the co-occurrence of ESBL and mcr-1 genes in southern Xinjiang, 133 liver samples from chickens that had died after exhibiting clinical signs consistent with colibacillosis were collected, from which 100 of these isolates (75.2%, 100/133) were confirmed as APEC. The double-disk diffusion test revealed that 65 strains (65.0%, 65/100) were ESBL-producing. Among these ESBL-producing APEC isolates, resistance rates to ampicillin, cefazolin, ceftiofur, and cefoxitin were 100% (65/65), 100% (65/65), 92.3% (60/65), and 4.6% (3/65, intermediate/susceptible), respectively. PCR detection revealed that 95.4% (62/65) carried blaCTX-M and 93.8% (61/65) carried blaTEM and five isolates (7.7%, 5/65) were resistant to colistin and carried the mcr-1 gene. Integron analysis revealed that int1 was detected in 98.5% (64/65) of the ESBL-APEC isolates. Notably, all five mcr-1-positive strains co-harbored int1. These five isolates exhibited MDR phenotypes and were assigned to phylogenetic groups A (n = 1), B1 (n = 3), and D (n = 1). Whole-genome sequencing (WGS) revealed that the five mcr-1-positive APEC strains belonged to four sequence types (STs): ST6792 (n = 1), ST1196 (n = 2), ST155 (n = 1), and ST162 (n = 1), and harbored three blaCTX-M subtypes (blaCTX-M-55 [n = 3], blaCTX-M-64 [n = 1], and blaCTX-M-65[n = 1]). Furthermore, these strains carried IncI2 or IncFIB plasmid replicons alongside the int1 integrase gene, highlighting the co-occurrence of critical resistance determinants with mobile genetic elements known to facilitate horizontal dissemination. The coexistence of blaCTX-M and mcr-1 in high-risk clones such as ST155 and ST162, which are associated with human infections worldwide, indicates that the region faces a threat from multidrug-resistant strains and a potential risk of cross-species transmission. Given the limited geographic scope and sample size, our findings should be considered a preliminary warning. Future studies with expanded sampling and experimental validation of horizontal transfer are needed to fully assess the transmission risks.