Research Article: Baicalin potentiates cefquinome against animal-origin ESBL- Escherichia coli by attenuating resistance-associated phenotypes and intestinal injury
Abstract:
Animal-origin extended-spectrum ? -lactamase-producing Escherichia coli (ESBL- E. coli ) undermines cefquinome (CEF) efficacy in veterinary medicine, necessitating strategies that enhance antibacterial activity while protecting intestinal integrity. Here, we evaluated baicalin (BAI), a flavonoid from Scutellaria baicalensis , as a CEF adjuvant against animal-origin ESBL- E. coli . In a mouse intestinal infection model, BAI combined with CEF significantly improved survival, mitigated intestinal pathology, and downregulated Tlr4 , Myd88 , and NF-?B signaling. The combination preserved mucosal architecture and partially restored intestinal microbiota composition. In vitro , BAI potentiated CEF activity by suppressing blaCTX-M gene expression, reducing ESBL-mediated CEF hydrolysis, and limiting the emergence of reduced CEF susceptibility during serial passage. Docking suggested a potential interaction of BAI with the catalytic site of CTX-M-9; together with reduced cefquinome hydrolysis in whole-cell suspensions, this suggests interference with ESBL-mediated hydrolysis. These results demonstrate that BAI functions as a CEF sensitizer, integrating pathogen-directed and host-protective effects, and offer a translationally relevant strategy for veterinary antibiotic adjuvant therapy.
Introduction:
Animal-origin extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli (ESBL- E. coli ) has become an increasing challenge in veterinary medicine because of its pathogenicity, resistance burden, and dissemination potential ( 1 , 2 ). As important reservoirs of mobile beta-lactam resistance determinants, particularly blaCTX-M -type genes, ESBL- E. coli substantially compromises the clinical efficacy of cephalosporins such as cefquinome (CEF) and complicates anti-infective treatment in animals ( 3 ). CEF…
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