Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

Users Online : 26179

Original article / research
Year : 2016 | Month : May | Volume : 10 | Issue : 5 | Page : DC27 - DC30

Global DNA Methylation Level among Ciprofloxacin-Resistant Clinical Isolates of Escherichia coli

Thiyagarajan Yugendran, Belgode Narasimha Harish

1. Research Scholar, Department of Microbiology, JIPMER, Puducherry, India. 2. Senior Professor and Head, Department of Microbiology, JIPMER, Puducherry, India.

Correspondence Address :
Dr. Belgode Narasimha Harish,
Department of Microbiology, Second Floor, Institute Block, JIPMER, Gorimedu, Puducherry - 605006, India.
E-mail: drbnharish@gmail.com

Abstract

Introduction: Fluoroquinolone resistant clinical isolates belonging to the family Enterobacteriaceae, is a major public health concern in India. Data analysis in JIPMER hospital revealed 10% rise in fluoroquinolone resistance within a span of three years suggestive of the possible involvement of mechanism/s other than QRDR capable of imparting fluoroquinolone resistance. DNA methylation regulates gene expression. Moreover, methylated cytosine is a mutational hotspot. Thus, DNA methylation can alter bacterial gene expression profile as well as facilitate the bacteria in accumulating mutations possibly leading to increased antimicrobial resistance. Therefore, the present study was carried out to identify the potential involvement of DNA methylation in ciprofloxacin resistance.

Aim: To elucidate and compare the methylation level of genomic and plasmid DNA among clinical isolates of E. coli sensitive and resistant to ciprofloxacin.

Materials and Methods: The study included 40 clinical E. coli isolates of which, 30 were ciprofloxacin-resistant and 10 were sensitive to ciprofloxacin. Genomic DNA (gDNA) and plasmid DNA were extracted and quantified. Methylation levels were elucidated using 5-mC DNA ELISA kit (Zymoresearch, California, USA) as per kit protocol and guidelines. Statistical Analysis: Spearman correlation 2-tailed test was used. A p-value <0.05 was considered significant.

Results: The MIC values of sensitive and resistant strains against ciprofloxacin ranged from 0.125 g/mL 0.75 g/mL and 8 g/mL - >256 g/mL respectively. No difference was found in plasmid DNA methylation level but, the gDNA methylation level of the resistant strains significantly differed from that of the sensitive strains. Based on Spearman correlation test gDNA methylation level of bacteria was found to be inversely proportional to its MIC against ciprofloxacin with p= -0.956 (p-value < 0.0001).

Conclusion: The influence of DNA methylation over plasmid-mediated quinolone resistance needs to be further confirmed by bisulphite DNA sequencing of the plasmid-borne genes. Extensive usage of ciprofloxacin has led to rise in ciprofloxacin resistance possibly induced by DNA methylation. Thus rational usage of ciprofloxacin in a clinical setting is essential to combat the further development of ciprofloxacin resistance. Hypomethylated genes and adenine methylation needs to be identified to fill up gaps in knowledge concerning the involvement of DNA methylation in fluoroquinolone resistance exhibited by E. coli.

Keywords

5-mC methylation, Bacterial epigenetics, Enterobacteriaceae, Fluoroquinolone resistance

How to cite this article :

Thiyagarajan Yugendran, Belgode Narasimha Harish. GLOBAL DNA METHYLATION LEVEL AMONG CIPROFLOXACIN-RESISTANT CLINICAL ISOLATES OF ESCHERICHIA COLI. Journal of Clinical and Diagnostic Research [serial online] 2016 May [cited: 2018 Jan 20 ]; 10:DC27-DC30. Available from
http://www.jcdr.net/back_issues.asp?issn=0973-709x&year=2016&month=May&volume=10&issue=5&page=DC27-DC30&id=7830

DOI and Others

DOI: 10.7860/JCDR/2016/19034.7830


Date of Submission: Jan 23, 2016
Date of Peer Review: Feb 08, 2016
Date of Acceptance: Apr 07, 2016
Date of Publishing: May 01, 2016

Financial OR OTHER COMPETING INTERESTS: As declared above.

JCDR is now Monthly and more widely Indexed .
  • Emerging Sources Citation Index (Web of Science, thomsonreuters)
  • Index Copernicus ICV 2016: 132.37
  • SCOPUS
  • Academic Search Complete Database
  • Directory of Open Access Journals (DOAJ)
  • EBSCOhost
  • Embase & EMbiology
  • Google Scholar
  • HINARI Access to Research in Health Programme
  • Indian Science Abstracts (ISA)
  • Journal seek Database
  • Google
  • Popline (reproductive health literature)
  • www.omnimedicalsearch.com