Fluoroquinolone Resistance in Relation to Phylogenetic Background and Iron Uptake Associated Virulence Profile among Urinary Escherichia coli Isolates from HIV and Non-HIV Patients | Chapter 9 | Innovations in Medicine and Medical Research Vol.2
Introduction:
Urinary tract infection is a major cause of morbidity among HIV patients and is
more often underestimated in developing countries. Urinary Escherichia coli
isolated from HIV and non-HIV patients in South India were analyzed to
determine the virulence profile and phylogenetic distribution and their
correlation with fluoroquinolone (FQ) resistance. Methods: This study aimed to
assess the difference in the incidence of iron uptake associated virulence
genes among urinary E. coli isolated from HIV (n= 76) and non-HIV antenatal
patients (n=42). We compared the incidence of virulence associated genes (VAGs)
among the E. coli isolates in relation to FQ resistance, phylogeny and host
immunocompromise. Results: fyuA was
higher among the isolates from HIV than from non-HIV patients (P=0.00024). E. coli isolates from HIV,
non-HIV patients primarily belonged to the phylogroups D and B2 respectively. Q
and FQ resistance were higher among isolates from HIV patients compared to
nonHIV patients (P=0.000414, P<0.0001 respectively). PhylogroupB2 strains
were predominant among the FQ susceptible than FQ-resistant strains
(P=0.000652). fyuA and iutA was higher among the Qresistant isolates than their
susceptible counterparts (P<0.0001; P=0.000132). FQ resistant isolates
harboured fyuA, iutA than the susceptible isolates (P=0.0063; P=0.000478). Hly+
phenotype was significantly associated with FQ-susceptible isolates
(P=0.003253). Discussion: Our results
establish the relative predominance of non-hemolytic, fyuA+, Q, FQ resistant E.
coli isolates primarily of phylogroup-D among the HIV patients and there by
suggests that non-B2 strains with lower virulence but with increased antibiotic
resistance establish infection in HIV patients.
Author(s) Details
Dr. Kesavaram Padmavathy
Department of Microbiology, Research Laboratory for Oral and Systemic Health, Sree Balaji Dental College and Hospital, Bharath Institute of Higher Education and Research, Chennai, India and Department of Microbiology, Dr. ALM PGIBMS, University of Madras, Chennai, India.
Dr. Krishnan Padma
Department of Microbiology, Dr. ALM PGIBMS, University of Madras, Chennai, India.
Dr. Sikhamani Rajasekaran
Government Hospital of Thoracic Medicine, Chennai, India.
View Book: - http://bp.bookpi.org/index.php/bpi/catalog/book/161
Author(s) Details
Dr. Kesavaram Padmavathy
Department of Microbiology, Research Laboratory for Oral and Systemic Health, Sree Balaji Dental College and Hospital, Bharath Institute of Higher Education and Research, Chennai, India and Department of Microbiology, Dr. ALM PGIBMS, University of Madras, Chennai, India.
Dr. Krishnan Padma
Department of Microbiology, Dr. ALM PGIBMS, University of Madras, Chennai, India.
Dr. Sikhamani Rajasekaran
Government Hospital of Thoracic Medicine, Chennai, India.
View Book: - http://bp.bookpi.org/index.php/bpi/catalog/book/161
Comments
Post a Comment