Volume 47, Issue 6
Free Access

Tetracycline‐resistance genes in Gram‐negative isolates from estuarine waters

I.S. Henriques

CESAM & Department of Biology, University of Aveiro, 3810‐193 Aveiro, Portugal

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F. Fonseca

CESAM & Department of Biology, University of Aveiro, 3810‐193 Aveiro, Portugal

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A. Alves

CESAM & Department of Biology, University of Aveiro, 3810‐193 Aveiro, Portugal

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M.J. Saavedra

CECAV, Department of Veterinary Science, University of Trás‐os‐Montes e Alto Douro, Vila Real, Portugal

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A. Correia

CESAM & Department of Biology, University of Aveiro, 3810‐193 Aveiro, Portugal

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First published: 19 November 2008
Citations: 18
Isabel S. Henriques, CESAM & Department of Biology, University of Aveiro, 3810‐193 Aveiro, Portugal. E‐mail: ihenriques@ua.pt

Abstract

Aims: To investigate the diversity and dissemination of tetracycline resistance genes in isolates from estuarine waters.

Methods and Results: Forty‐two out of 164 multi‐resistant isolates previously obtained were resistant or less‐susceptible to tetracycline, as evaluated by the disc diffusion method. Minimal inhibitory concentration for resistant bacteria ranged from 16 to 256 mg l−1. Screening of tet genes by polymerase chain reaction showed that 88% of the isolates carried at least one of the genes tested, namely tet (A) (present in 13 isolates), tet (B) (present in 13 isolates), tet (C) (present in 3 isolates), tet (D) (present in 1 isolate), tet (E) (present in 6 isolates) and tet (M) (present in 1 isolate). One isolate carried tet (A) and tet (M). To our knowledge, this study presents the first description of a tet (D) gene in Morganella morganii . Hybridization revealed that tet genes were plasmid‐located in 31% of the isolates. Those isolates were included as donors in conjugation experiments and 38% transferred tetracycline resistance.

Conclusions: A considerable diversity of tet genes was detected in the estuary. Frequently, these genes were associated with plasmids and could be transferred to Escherichia coli .

Significance and Impact of the Study: The results presented provide further evidence of the role played by estuarine reservoirs in antibiotic resistance maintenance and dissemination.

Number of times cited according to CrossRef: 18

  • Antibiotic-Resistant Bacteria in Greywater and Greywater-Irrigated Soils, Frontiers in Microbiology, 10.3389/fmicb.2018.02666, 9, (2018).
  • Monitoring of drug resistance amplification and attenuation with the use of tetracycline-resistant bacteria during wastewater treatment, E3S Web of Conferences, 10.1051/e3sconf/20172200063, 22, (00063), (2017).
  • Morganella morganii, a non-negligent opportunistic pathogen, International Journal of Infectious Diseases, 10.1016/j.ijid.2016.07.006, 50, (10-17), (2016).
  • Characterization of microbial community and antibiotic resistance genes in activated sludge under tetracycline and sulfamethoxazole selection pressure, Science of The Total Environment, 10.1016/j.scitotenv.2016.07.014, 571, (479-486), (2016).
  • Low Prevalence of Carbapenem-Resistant Bacteria in River Water: Resistance Is Mostly Related to Intrinsic Mechanisms, Microbial Drug Resistance, 10.1089/mdr.2015.0072, 21, 5, (497-506), (2015).
  • Influence of Tetracycline on Tetracycline-Resistant Heterotrophs and tet Genes in Activated Sludge Process, Current Microbiology, 10.1007/s00284-014-0731-4, 70, 3, (415-422), (2014).
  • Bacterial diversity and antibiotic resistance in water habitats: searching the links with the human microbiome, FEMS Microbiology Reviews, 10.1111/1574-6976.12062, 38, 4, (761-778), (2014).
  • Analysis of Antibiotic Resistance in Bacteria Isolated from the Surface Microlayer and Underlying Water of an Estuarine Environment, Microbial Drug Resistance, 10.1089/mdr.2012.0084, 19, 1, (64-71), (2013).
  • Effect of analgesics on the antibiotic resistance of ammonia-oxidizing organisms, Journal of Environmental Engineering and Science, 10.1680/jees.2013.0038, 8, 3, (382-390), (2013).
  • Genetic diversity and antimicrobial resistance of Escherichia coli from Tagus estuary (Portugal), Science of The Total Environment, 10.1016/j.scitotenv.2013.04.067, 461-462, (65-71), (2013).
  • A systematic quantitative proteomic examination of multidrug resistance in Acinetobacter baumannii, Journal of Proteomics, 10.1016/j.jprot.2013.03.008, 84, (17-39), (2013).
  • Phenotypic–genotypic resistance in Salmonella spp. isolated from cattle carcasses from the north central zone of the State of Mexico, Tropical Animal Health and Production, 10.1007/s11250-012-0323-x, 45, 4, (995-1000), (2012).
  • Co-occurrence of resistance to different antibiotics among aquatic bacteria, BMC Microbiology, 10.1186/1471-2180-12-225, 12, 1, (225), (2012).
  • Prevalence of Clinically Relevant Antibiotic Resistance Genes in Surface Water Samples Collected from Germany and Australia, Environmental Science & Technology, 10.1021/es302020s, 46, 17, (9716-9726), (2012).
  • Positive and negative selection towards tetracycline resistance genes in manure treatment lagoons, Journal of Applied Microbiology, 10.1111/j.1365-2672.2012.05252.x, 112, 5, (907-919), (2012).
  • Persistence and Profiles of Tetracycline Resistance Genes in Swine Farms and Impact of Operational Practices on Their Occurrence in Farms’ Vicinities, Water, Air, & Soil Pollution, 10.1007/s11270-011-0838-1, 223, 1, (49-62), (2011).
  • The occurrence, spatial and temporal distribution, and environmental routes of tetracycline resistance and integrase genes in Crassostrea virginica beds, Marine Pollution Bulletin, 10.1016/j.marpolbul.2010.08.016, 60, 12, (2215-2224), (2010).
  • Effect of analgesics on the antibiotic resistance of ammonia-oxidizing organismsA paper submitted to the Journal of Environmental Engineering and Science., Canadian Journal of Civil Engineering, 10.1139/L09-076, 36, 9, (1558-1566), (2009).