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Antimicrobial Resistance in Humans, Animals, Water and Household Environs in Rural Andean Peru: Exploring Dissemination Pathways through the One Health Lens

Author

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  • Stella M. Hartinger

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru
    Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, 4002 Basel, Switzerland
    Swiss Tropical and Public Health Institute, University of Basel, 4001 Basel, Switzerland)

  • Maria Luisa Medina-Pizzali

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru)

  • Gabriela Salmon-Mulanovich

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru
    Institute for Nature, Earth and Energy, Pontificia Universidad Católica del Perú, Lima 15088, Peru)

  • Anika J. Larson

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru
    School of Medicine, University of Washington, Seattle, WA 98195, USA)

  • María Pinedo-Bardales

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru)

  • Hector Verastegui

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru
    Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, 4002 Basel, Switzerland
    Swiss Tropical and Public Health Institute, University of Basel, 4001 Basel, Switzerland)

  • Maribel Riberos

    (School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima 15102, Peru)

  • Daniel Mäusezahl

    (Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, 4002 Basel, Switzerland
    Swiss Tropical and Public Health Institute, University of Basel, 4001 Basel, Switzerland)

Abstract

Antimicrobial resistance (AMR) is a global public health threat, especially for low and middle-income countries (LMIC) where the threat has not been fully identified. Our study aims to describe E. coli AMR in rural communities to expand our knowledge on AMR bacterial contamination. Specifically, we aim to identify and describe potential dissemination routes of AMR-carrying bacteria in humans (children’s stools), community water sources (reservoirs and household sources), household environments (yard soil) and domestic animals of subsistence farmers in rural Andean areas. Our cross-sectional study was conducted in rural households in the region of Cajamarca, Peru. A total of 266 samples were collected. Thirty-four point six percent of reservoir water and 45% of household water source samples were positive for thermotolerant coliforms. Of the reservoir water samples, 92.8% were positive for E. coli , and 30.8% displayed resistance to at least one antibiotic, with the highest resistance to tetracycline. E. coli was found in 57.1% of the household water sources, 18.6% of these isolates were multidrug-resistant, and displayed the highest resistance to tetracycline (31.3%). Among samples from the children’s drinking water source, 32.5% were positive for thermotolerant coliforms, and 57.1% of them were E. coli . One third of E. coli isolates were multidrug-resistant and displayed the highest AMR to tetracycline (41.6%) and ampicillin (25%). Thermotolerant coliforms were found in all the soil samples, 43.3% of the isolates were positive for E. coli , 34.3% of the E. coli isolates displayed AMR to at least one antibiotic, and displayed the highest AMR to tetracycline (25.7%). We determined thermotolerant coliforms in 97.5% of the child feces samples; 45.3% of them were E. coli , 15.9% displayed multidrug resistance, and displayed the highest resistance to ampicillin (34.1%). We identified thermotolerant coliforms in 67.5% of the animal feces samples. Of those, 38.7% were E. coli , and 37.7% were resistant to at least one antibiotic. For all the samples, the prevalence of resistance to at least one antibiotic in the E. coli and Klebsiella spp. isolates was almost 43% and the prevalence of MDR in the same isolates was nearly 9%, yet the latter nearly doubled (15.9%) in children’s stools. Our results provide preliminary evidence for critical pathways and the interconnectedness of animal, human and environmental transmission but molecular analysis is needed to track dissemination routes properly.

Suggested Citation

  • Stella M. Hartinger & Maria Luisa Medina-Pizzali & Gabriela Salmon-Mulanovich & Anika J. Larson & María Pinedo-Bardales & Hector Verastegui & Maribel Riberos & Daniel Mäusezahl, 2021. "Antimicrobial Resistance in Humans, Animals, Water and Household Environs in Rural Andean Peru: Exploring Dissemination Pathways through the One Health Lens," IJERPH, MDPI, vol. 18(9), pages 1-16, April.
  • Handle: RePEc:gam:jijerp:v:18:y:2021:i:9:p:4604-:d:544005
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    Citations

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    Cited by:

    1. Maria Luisa Medina-Pizzali & Stella M. Hartinger & Gabriela Salmon-Mulanovich & Anika Larson & Maribel Riveros & Daniel Mäusezahl, 2021. "Antimicrobial Resistance in Rural Settings in Latin America: A Scoping Review with a One Health Lens," IJERPH, MDPI, vol. 18(18), pages 1-18, September.
    2. Pedro Padilla González & Carlos Bautista-Capetillo & Antonio Ruiz-Canales & Julián González-Trinidad & Hugo Enrique Júnez-Ferreira & Ada Rebeca Contreras Rodríguez & Cruz Octavio Robles Rovelo, 2022. "Characterization of Scale Deposits in a Drinking Water Network in a Semi-Arid Region," IJERPH, MDPI, vol. 19(6), pages 1-15, March.

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