# Increased Antimicrobial and Multidrug Resistance Downstream of Wastewater Treatment Plants in an Urban Watershed

**Authors:** Maitreyee Mukherjee, Edward Laird, Terry J. Gentry, John P. Brooks, Raghupathy Karthikeyan

PMC · DOI: 10.3389/fmicb.2021.657353 · Frontiers in Microbiology · 2021-05-24

## TL;DR

This study shows that wastewater treatment plant discharges increase antimicrobial and multidrug resistance in nearby water, highlighting a public health risk.

## Contribution

The study provides empirical evidence linking WWTP discharges to increased AMR and MDR in urban watersheds.

## Key findings

- E. coli isolates downstream of WWTPs showed higher resistance to multiple antibiotics compared to upstream sites.
- Abundance of antibiotic resistance genes (ARG) was significantly higher downstream of WWTP discharges.
- Class I integron (intI1) gene concentrations were about 20 times higher downstream compared to upstream.

## Abstract

Development and spread of antimicrobial resistance (AMR) and multidrug resistance (MDR) through propagation of antibiotic resistance genes (ARG) in various environments is a global emerging public health concern. The role of wastewater treatment plants (WWTPs) as hot spots for the dissemination of AMR and MDR has been widely pointed out by the scientific community. In this study, we collected surface water samples from sites upstream and downstream of two WWTP discharge points in an urban watershed in the Bryan-College Station (BCS), Texas area, over a period of nine months. E. coli isolates were tested for resistance to ampicillin, tetracycline, sulfamethoxazole, ciprofloxacin, cephalothin, cefoperazone, gentamycin, and imipenem using the Kirby-Bauer disc diffusion method. Antimicrobial resistant heterotrophic bacteria were cultured on R2A media amended with ampicillin, ciprofloxacin, tetracycline, and sulfamethoxazole for analyzing heterotrophic bacteria capable of growth on antibiotic-containing media. In addition, quantitative real-time polymerase chain reaction (qPCR) method was used to measure eight ARG – tetA, tetW, aacA, ampC, mecA, ermA, blaTEM, and intI1 in the surface water collected at each time point. Significant associations (p < 0.05) were observed between the locations of sampling sites relative to WWTP discharge points and the rate of E. coli isolate resistance to tetracycline, ampicillin, cefoperazone, ciprofloxacin, and sulfamethoxazole together with an increased rate of isolate MDR. The abundance of antibiotic-resistant heterotrophs was significantly greater (p < 0.05) downstream of WWTPs compared to upstream locations for all tested antibiotics. Consistent with the results from the culture-based methods, the concentrations of all ARG were substantially higher in the downstream sites compared to the upstream sites, particularly in the site immediately downstream of the WWTP effluent discharges (except mecA). In addition, the Class I integron (intI1) genes were detected in high amounts at all sites and all sampling points, and were about ∼20 times higher in the downstream sites (2.5 × 107 copies/100 mL surface water) compared to the upstream sites (1.2 × 106 copies/100 mL surface water). Results suggest that the treated WWTP effluent discharges into surface waters can potentially contribute to the occurrence and prevalence of AMR in urban watersheds. In addition to detecting increased ARG in the downstream sites by qPCR, findings from this study also report an increase in viable AMR (HPC) and MDR (E. coli) in these sites. This data will benefit establishment of improved environmental regulations and practices to help manage AMR/MDR and ARG discharges into the environment, and to develop mitigation strategies and effective treatment of wastewater.

## Linked entities

- **Genes:** tet(A) (tetracycline efflux MFS transporter Tet(A)) [NCBI Gene 33941499], tet(W) (tetracycline resistance ribosomal protection protein Tet(W)) [NCBI Gene 29696589], aacA (aminoglycoside 6'-N-acetyltransferase) [NCBI Gene 304361609], ampC (beta-lactamase) [NCBI Gene 878149], mecA (adaptor protein controlling oligomerization of the AAA+ protein ClpC) [NCBI Gene 936406], TMEM94 (transmembrane protein 94) [NCBI Gene 9772], intI1 (class 1 integron integrase IntI1) [NCBI Gene 29367876]
- **Chemicals:** ampicillin (PubChem CID 6249), tetracycline (PubChem CID 54675776), sulfamethoxazole (PubChem CID 5329), ciprofloxacin (PubChem CID 2764), cephalothin (PubChem CID 6024), cefoperazone (PubChem CID 44187), gentamycin (PubChem CID 3467), imipenem (PubChem CID 104838)

## Full-text entities

- **Genes:** integrase [NCBI Gene 16489578], blaTEM [NCBI Gene 13905334], ampC [NCBI Gene 7872529], aacA [NCBI Gene 9846058], intI1 [NCBI Gene 7872749]
- **Diseases:** ARG (MESH:D004761), MDR (MESH:D018088), Infectious Diseases (MESH:D003141), AMR (MESH:D060467), fungal (MESH:D009181), HPC (MESH:C537243)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606], Sus scrofa (pig, species) [taxon 9823], Pseudomonas aeruginosa (species) [taxon 287], activated sludge metagenome (species) [taxon 942017], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Aeromonas (genus) [taxon 642]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC8181147/full.md

## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC8181147/full.md

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Source: https://tomesphere.com/paper/PMC8181147