The fly route of extended-spectrum-β-lactamase-producing Enterobacteriaceae dissemination in a cattle farm: from the ecosystem to the molecular scale

IntroductionThis study aimed to understand the origin and to explain the maintenance of extended-spectrum β-lactamase (ESBL) Enterobacteriaceae isolated from food-producing animals in a third-generation cephalosporin (3GC)-free farm.MethodsCulture and molecular approaches were used to test molecules...

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Main Authors: Alann Caderhoussin (Author), David Couvin (Author), Gaëlle Gruel (Author), Isaure Quétel (Author), Matthieu Pot (Author), Rémy Arquet (Author), Alexis Dereeper (Author), Jean-Christophe Bambou (Author), Antoine Talarmin (Author), Séverine Ferdinand (Author)
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Published: Frontiers Media S.A., 2024-04-01T00:00:00Z.
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100 1 0 |a Alann Caderhoussin  |e author 
700 1 0 |a David Couvin  |e author 
700 1 0 |a Gaëlle Gruel  |e author 
700 1 0 |a Isaure Quétel  |e author 
700 1 0 |a Matthieu Pot  |e author 
700 1 0 |a Rémy Arquet  |e author 
700 1 0 |a Alexis Dereeper  |e author 
700 1 0 |a Jean-Christophe Bambou  |e author 
700 1 0 |a Antoine Talarmin  |e author 
700 1 0 |a Séverine Ferdinand  |e author 
245 0 0 |a The fly route of extended-spectrum-β-lactamase-producing Enterobacteriaceae dissemination in a cattle farm: from the ecosystem to the molecular scale 
260 |b Frontiers Media S.A.,   |c 2024-04-01T00:00:00Z. 
500 |a 2813-2467 
500 |a 10.3389/frabi.2024.1367936 
520 |a IntroductionThis study aimed to understand the origin and to explain the maintenance of extended-spectrum β-lactamase (ESBL) Enterobacteriaceae isolated from food-producing animals in a third-generation cephalosporin (3GC)-free farm.MethodsCulture and molecular approaches were used to test molecules other than 3GC such as antibiotics (tetracycline and oxytetracycline), antiparasitics (ivermectin, flumethrin, fenbendazol, and amitraz), heavy metal [arsenic, HNO3, aluminum, HNO3, cadmium (CdSO4), zinc (ZnCl2), copper (CuSO4), iron (FeCl3), and aluminum (Al2SO4)], and antioxidant (butylated hydroxytoluene) as sources of selective pressure. Whole-genome sequencing using short read (Illumina™) and long read (Nanopore™) technologies was performed on 34 genomes. In silico gene screening and comparative analyses were used to characterize the genetic determinants of resistance, their mobility, and the genomic relatedness among isolates.ResultsOur analysis unveiled a low diversity among the animal ESBL-producing strains. Notably, E. coli ST3268 was recurrently isolated from both flies (n = 9) and cattle (n = 5). These E. coli ST3268/blaCTX-M-15/blaTEM-1B have accumulated multiple plasmids and genes, thereby representing a reservoir of resistance and virulence factors. Our findings suggest that flies could act as effective mechanical vectors for antimicrobial gene transfer and are capable of transporting resistant bacteria across different environments and to multiple hosts, facilitating the spread of pathogenic traits. A significantly higher mean minimum inhibitory concentration of oxytetracycline (841.4 ± 323.5 mg/L vs. 36.0 ± 52.6 mg/L, p = 0.0022) in ESBL E. coli than in non-ESBL E. coli and blaCTX-M-15 gene overexpression in oxytetracycline-treated vs. untreated ESBL E. coli (RQOxy = 3.593, p = 0.024) confirmed oxytetracycline as a source of selective pressure in ESBL E. coli.DiscussionThe occurrence of ESBL E. coli in a farm without 3GC use is probably due to an as yet undefined human origin of Enterobacteriaceae blaCTX-M-15 gene transmission to animals in close contact with cattle farm workers and the maintenance of the local ESBL E. coli reservoir by a high fly diversity and oxytetracycline selective pressure. These findings highlight the critical need for stringent vector control to mitigate antimicrobial resistance spread for preserving public health. Addressing this issue necessitates a multifaceted approach combining microbial genetics, vector ecology, and farm management practices. 
546 |a EN 
690 |a ESBL 
690 |a Enterobacteriaceae 
690 |a ST3268 
690 |a oxytetracycline 
690 |a selective pressure 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Antibiotics, Vol 3 (2024) 
787 0 |n https://www.frontiersin.org/articles/10.3389/frabi.2024.1367936/full 
787 0 |n https://doaj.org/toc/2813-2467 
856 4 1 |u https://doaj.org/article/00ad1b0e85364a5c9b7d071c2b4b509d  |z Connect to this object online.