Literature DB >> 34085858

Azithromycin and Ciprofloxacin Can Promote Antibiotic Resistance in Biosolids and Biosolids-Amended Soils.

Harmanpreet Sidhu1, Hee-Sung Bae1, Andrew Ogram1, George O'Connor1, Fahong Yu2.   

Abstract

Spread of biosolids-borne antibiotic resistance is a growing public and environmental health concern. Herein, we conducted incubation experiments involving biosolids, which are byproducts of sewage treatment processes, and biosolids-amended soil. Quantitative reverse transcription-PCR (RT-qPCR) was employed to assess responses of select antibiotic resistance genes (ARGs) and mobile elements to environmentally relevant concentrations of two biosolids-borne antibiotics, azithromycin (AZ) and ciprofloxacin (CIP). Additionally, we examined sequence distribution of gyrA (encoding DNA gyrase; site of action of CIP) to assess potential shifts in genotype. Increasing antibiotic concentrations generally increased the transcriptional activities of qnrS (encoding CIP resistance) and ermB and mefE (encoding AZ resistance). The transcriptional activity of intl1, a marker of class 1 integrons, was unaffected by CIP or AZ concentrations, but biosolids amendment increased intl1 activity in the soil by 4 to 5 times, which persisted throughout incubation. While the dominant gyrA sequences found herein were unrelated to known CIP-resistant genotypes, the increasing CIP concentrations significantly decreased the diversity of genes encoding the DNA gyrase A subunit, suggesting changes in microbial community structures. This study suggests that biosolids harbor transcriptionally active ARGs and mobile elements that could survive and spread in biosolids-amended soils. However, more research is warranted to investigate these trends under field conditions. IMPORTANCE Although previous studies have indicated that biosolids may be important spreaders of antibiotics and antibiotic resistance genes (ARGs) in environments, the potential activities of ARGs or their responses to environmental parameters have been understudied. This study highlights that certain biosolids-borne antibiotics can induce transcriptional activities of ARGs and mobile genetic elements in biosolids and biosolids-amended soil, even when present at environmentally relevant concentrations. Furthermore, these antibiotics can alter the structure of microbial populations expressing ARGs. Our findings indicate the bioavailability of the antibiotics in biosolids and provide evidence that biosolids can promote the activities and dissemination of ARGs and mobile genes in biosolids and soils that receive contaminated biosolids, thus, underscoring the importance of investigating anthropogenically induced antibiotic resistance in the environment under real-world scenarios.

Entities:  

Keywords:  antibiotics resistance genes; azithromycin; biosolids; ciprofloxacin

Mesh:

Substances:

Year:  2021        PMID: 34085858      PMCID: PMC8315170          DOI: 10.1128/AEM.00373-21

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  56 in total

Review 1.  Gene flow, mobile genetic elements and the recruitment of antibiotic resistance genes into Gram-negative pathogens.

Authors:  Hatch W Stokes; Michael R Gillings
Journal:  FEMS Microbiol Rev       Date:  2011-05-20       Impact factor: 16.408

2.  Distribution of macrolide resistance genes erm(B) and mef(A) among 160 penicillin-intermediate clinical isolates of Streptococcus pneumoniae isolated in southern France.

Authors:  H Marchandin; H Jean-Pierre; E Jumas-Bilak; L Isson; B Drouillard; H Darbas; C Carrière
Journal:  Pathol Biol (Paris)       Date:  2001-09

3.  Fate of antibiotic resistance genes and class 1 integrons in soil microcosms following the application of treated residual municipal wastewater solids.

Authors:  Tucker R Burch; Michael J Sadowsky; Timothy M LaPara
Journal:  Environ Sci Technol       Date:  2014-05-05       Impact factor: 9.028

4.  Toward a Comprehensive Strategy to Mitigate Dissemination of Environmental Sources of Antibiotic Resistance.

Authors:  Peter J Vikesland; Amy Pruden; Pedro J J Alvarez; Diana Aga; Helmut Bürgmann; Xiang-Dong Li; Celia M Manaia; Indumathi Nambi; Krista Wigginton; Tong Zhang; Yong-Guan Zhu
Journal:  Environ Sci Technol       Date:  2017-10-30       Impact factor: 9.028

5.  Quantitative multiplex real-time PCR for detecting class 1, 2 and 3 integrons.

Authors:  O Barraud; M C Baclet; F Denis; M C Ploy
Journal:  J Antimicrob Chemother       Date:  2010-06-11       Impact factor: 5.790

Review 6.  DNA topoisomerases.

Authors:  M Gellert
Journal:  Annu Rev Biochem       Date:  1981       Impact factor: 23.643

7.  Effects of ofloxacin on nitrogen removal and microbial community structure in constructed wetland.

Authors:  Xinnan Tong; Xinze Wang; Xiaojuan He; Kaiqin Xu; Feijian Mao
Journal:  Sci Total Environ       Date:  2018-11-27       Impact factor: 7.963

8.  Detection of erythromycin-resistant determinants by PCR.

Authors:  J Sutcliffe; T Grebe; A Tait-Kamradt; L Wondrack
Journal:  Antimicrob Agents Chemother       Date:  1996-11       Impact factor: 5.191

Review 9.  Mobile gene cassettes and integrons: capture and spread of genes by site-specific recombination.

Authors:  R M Hall; C M Collis
Journal:  Mol Microbiol       Date:  1995-02       Impact factor: 3.501

Review 10.  Review of Antimicrobial Resistance in the Environment and Its Relevance to Environmental Regulators.

Authors:  Andrew C Singer; Helen Shaw; Vicki Rhodes; Alwyn Hart
Journal:  Front Microbiol       Date:  2016-11-01       Impact factor: 5.640

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  1 in total

1.  Midecamycin Is Inactivated by Several Different Sugar Moieties at Its Inactivation Site.

Authors:  Ru Lin; Li-Li Hong; Zhong-Ke Jiang; Ke-Meng Li; Wei-Qing He; Jian-Qiang Kong
Journal:  Int J Mol Sci       Date:  2021-11-23       Impact factor: 5.923

  1 in total

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