Abstract

Irrigation return flows (IRFs) collect surface runoff and subsurface drainage, causing them to have elevated contaminant and bacterial levels, and making them a potential source of pollutants. The purpose of this study was to determine antimicrobial susceptibility among Escherichia coli and enterococcal isolates that were collected from IRFs in a south-central Idaho watershed. Environmental isolates can be a potentially important source of antimicrobial resistance (AMR) and IRFs may be one way resistance genes are transported out of agroecosystems. Water samples were collected from nine IRFs and one background site (canal water from Snake River) on a biweekly basis during 2018. Escherichia coli and enterococci were enumerated via a most probable number (MPN) technique, then subsamples were plated on selective media to obtain isolates. Isolates of E. coli (187) or enterococci (185) were tested for antimicrobial susceptibility using Sensititre broth microdilution plates. For E. coli, 13% (25/187) of isolates were resistant to tetracycline, with fewer numbers being resistant to 13 other antimicrobials, with none resistant to gentamicin. While 75% (141/187) of the E. coli isolates were pan-susceptible, 12 multidrug resistance (MDR) patterns with 17 isolates exhibiting resistance to up to seven drug classes (10 antimicrobials). For the enterococcal species, only 9% (16/185) of isolates were pan-susceptible and the single highest resistance was to lincomycin (138/185; 75%) followed by nitrofurantoin (56/185; 30%) and quinupristin/dalfopristin (34/185; 18%). In addition, 13 enterococcal isolates belonging to Enterococcus faecalis, Enterococcus faecium, Enterococcus casseliflavus, and Enterococcus thailandicus, were determined to be MDR to up to six different antimicrobial drug classes. None of the enterococcal isolates were resistant to gentamycin, linezolid, tigecycline, and vancomycin.

Highlights

  • Antimicrobials are used as the first line of defense in treating bacterial infections, greatly reducing morbidity and mortality associated with diseases in humans and animals

  • The prevalence of antimicrobial resistance (AMR) is Antimicrobial Resistance of Fecal Indicator Bacteria often attributed to questionable livestock production practices that began in the 1950s, such as use of subtherapeutic amounts of antimicrobials in feed or water for the purpose of enhancing the production performance of livestock (Franklin et al, 2016)

  • Water samples were collected from eight Irrigation return flows (IRFs) sampling sites: Cedar Draw (CD), Deep Creek (DC), Hansen Coulee (HC), I Coulee (IC), Mud Creek (MC), N Coulee (NC), Rock Creek Poleline (RCP), and Twin Falls Coulee (TFC)

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Summary

Introduction

Antimicrobials are used as the first line of defense in treating bacterial infections, greatly reducing morbidity and mortality associated with diseases in humans and animals. The prevalence of AMR is Antimicrobial Resistance of Fecal Indicator Bacteria often attributed to questionable livestock production practices that began in the 1950s, such as use of subtherapeutic amounts of antimicrobials in feed or water for the purpose of enhancing the production performance of livestock (Franklin et al, 2016). While livestock production practices like this are certainly a driving force in the evolution of antimicrobialresistant bacteria (ARB), AMR is an ancient bacterial trait that did not originate as a product of agricultural antimicrobial use (Allen and Stanton, 2014). A temporal analysis of archived agricultural soils from 1940 to 2008 in Netherlands suggests that the antimicrobial era is responsible for increasing environmental AMR, as the number of antimicrobial resistance genes (ARGs) from major antimicrobial classes significantly increased during that period (Knapp et al, 2010). It is important to consider that ARGs are likely horizontally transferred from manure-borne bacteria to indigenous soil bacteria (Smalla et al, 2000), increasing the persistence of resistance genes in soil (Binh et al, 2008; Heuer et al, 2011)

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