The First Case of Antimicrobial-Resistant Stanley ST29 Diagnosed Secondary to Acute Cholecystitis.

Objective: To analyze the phenotypic and genomic characteristics of a non-typhoidal bile isolate from a patient with chronic diarrhoea secondary to acute cholecystitis.

Methods: The patient presented with chronic diarrhoea lasting for two weeks, which was secondary to acute cholecystitis. The non-typhoidal bile isolate was identified using biochemical tests, mass spectrometry, serum agglutination tests, and antimicrobial susceptibility testing. Subsequently, whole-genome sequencing (WGS) was performed to predict and annotate the serotype, multilocus sequence typing (MLST), antimicrobial resistance genes (AMR), mobile genetic elements (MGEs), and virulence genes of the isolate.

Results: The isolate was identified as spp. by biochemical tests and mass spectrometry. The serotype of the isolate identified by serum agglutination tests was consistent with WGS prediction and was identified as Stanley (1,4,5,12: d:1,2, ST29). It was resistant to six antimicrobial agents, including ampicillin, ciprofloxacin, cefotaxime, azithromycin, trimethoprim/sulfamethoxazole, and chloramphenicol. Five major classes of antimicrobial agents, comprising a total of 14 resistance genes were screened, including β-lactam resistance genes: , , and ; quinolone resistance gene: and '; macrolide resistance genes: , and , and folate pathway inhibitor resistance genes: , and ; chloramphenicol resistance genes: and . T57S mutation in the gene was detected in the quinolone resistance-determining region (QRDR). Three plasmid replicons () and three insertion MGEs were predicted. Forty-two virulence genes were predicted, of which 25 were secretion and transporter genes, and ten were fimbrial adherence genes. Only one invasive protein-regulated gene() was found in Pathogenicity Islands 1(SPI-1), and no Typhoid toxin genes were predicted.

Conclusion: The case of Stanley ST29 isolated from a patient with diarrhoea lasting 55 days secondary to cholecystitis aligns with the characteristics of high drug resistance and relatively low virulence. This highlights the need for increased vigilance in clinical practice regarding invasive cases and the significant disease burden associated with the intestinal migration of antimicrobial-resistant isolates.