Journals / Acta Veterinaria Eurasia / 2022 / Cilt: 48 - Sayı: 1

Tetracycline Resistance Genes in Escherichia coli Strains Isolated From Biofilm of Drinking Water System in Poultry Farms

Pages
64–68
Publication Date
2022-10-12
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The microbiological results showed that 20 samples (20%) yielded E. coli.

📌 3 Key Takeaways

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Objective & Hypothesis:The frequency of resistance genes in clinical and environmental isolates increases the need for molecular knowledge about the antibiotics used in the prevention and treatment of infectious diseases.
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Key Findings & Data:Hence, in present study, 100 water biofilm samples were collected from poultry water systems from 20 randomly chosen broiler farms in Isfahan province, Iran.
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Conclusion & Impact:The microbiological results showed that 20 samples (20%) yielded E. coli.
🔬Design:Research Article
📍Scope:20 samples
⚙️Variables:Domain Parameters

Abstract

The frequency of resistance genes in clinical and environmental isolates increases the need for molecular knowledge about the antibiotics used in the prevention and treatment of infectious diseases. Hence, in present study, 100 water biofilm samples were collected from poultry water systems from 20 randomly chosen broiler farms in Isfahan province, Iran. Escherichia coli strains were identified by conventional microbiological and biochemical characterization. All E. coli strains were evaluated for sensitivity to commercially important antibiotics by the disc diffusion method. Furthermore, the tetracycline (TC) resistance genes tetA, tetB, tetC, tetD, tetE, tetG, tetK, tetL, tetM, tetO, tetS were investigated using three multiplex polymerase chain reactions (PCR). The microbiological results showed that 20 samples (20%) yielded E. coli. Fourteen isolates (70%) were resistant to TC. The results of PCR revealed that 12 TC-resistant E. coli strains (85.71%) harbored the examined tet genes (four, seven and one TC-resistant E. coli isolates harbored tetA, tetB, and tetA plus tetB genes, respectively). All the E. coli strains that harbored tet genes were resistant to TC. Although these strains did not derive from clinical samples, the prevalence of tet genes among E. coli strains in water biofilm suggests the possible transmission of resistance genes from water to the environment, animals, and humans, and can play role in spreading tet genes. Therefore, the sanitation of water in poultry farms can decrease the bacterial infections and antibiotic resistance in poultry and humans.

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Cite This Article

AHANGARAN, M. G., ZINSAZ, P., POURMAHDI, O., AHMADI-DASTGERDI, A., OSTADPOUR, M., SOLTANI, M. (2022). Tetracycline Resistance Genes in Escherichia coli Strains Isolated From Biofilm of Drinking Water System in Poultry Farms. Acta Veterinaria Eurasia, Cilt: 48 - Sayı: 1, 64–68. https://ajindex.com/articles/428029

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References (2)

  1. Angulo, F. J., Nunnery, J. A., & Bair, H. D. (2004). Antimicrobial resistance in zoonotic enteric pathogens. Revue Scientifique et Technique, 23, 485–496. [CrossRef] Bryan, A., Shapir, N., & Sadowsky, M. J. (2004). Frequency and distribution of tetracycline resistance genes in genetically divers, nonselected and nonclinical Escherichia coli strains isolated from diverse human and animal sources. Applied and Environmental Microbiology, 70, 2503–2507. [CrossRef] Chopra, I., & Roberts, M. (2001). Tetracycline antibiotics: Mode of action, applications, molecular biology, and epidemiology of bacterial resistance. Microbiology and Molecular Biology Reviews, 65, 232–260. [CrossRef] Clinical and Laboratory Standards Institute (CLSI) (2018). Performance standards for antimicrobial susceptibility testing (28th ed, pp. 1–258).
  2. Wayne, PA. Coleman, B. L., Salvadori, M. I., McGeer, A. J., Sibley, K. A., Neumann, N. F., & Bondy, S. J. (2012).The role of drinking water in the transmission of antimicrobial resistant E. coli. Epidemiology and Infection, 140, 633–642. [CrossRef] Dai, Y., Liu, M., Li, J., Yang, S., Sun, Y., Sun, Q., Liu, Z. (2020). A review on pollution situation and treatment methods of tetracycline in groundwater. Separation Science and Technology, 55, 1005–1021. [CrossRef] Deckert, A., Gow, S., Rosengren, L., Léger, D., Avery, B., Daignault, D., Irwin, R. (2010). Canadian integrated program for antimicrobial resistance surveillance (CIPARS) farm program: Results from finisher pigs surveillance. Zoonoses and Public Health, 57, 71–84. [CrossRef] Feng, P., Weagant, S., & Grant, M. (2002). Enumeration of Escherichia coli and the coliform bacteria (Bacteriological analytical manual). Washington DC: US FDA Center for Food safety and Applied Nutrition Publishing. Gholami-Ahangaran, M., Karimi-Dehkord, M., Miranzadeh-Mahabadi, E., & Ahmadi-Dastgerdi, A. (2021). The frequency of tetracycline resistance genes in Escherichia coli strains isolated from healthy and diarrheic pet birds. Iranian Journal of Veterinary Research. [CrossRef] Gholami-Ahangaran, M., & Zia-Jahromi, N. (2014). Identification of shiga toxin and intimin genes in Escherichia coli detected from canary (Serinus canaria domestica). Toxicology and Industrial Health, 30, 724–727. [CrossRef] Kang, S. G., Lee, D. Y., Shin, S. J., Ahn, J. M., & Yoo, H. S. (2005). Change in patterns of antimicrobial susceptibility and class 1 intergron carriage among Escherichia coli isolates. Journal of Veterinary Science,