First Indian report on genome-wide comparison of multidrug-resistant Escherichia coli from blood stream infections.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 20 07 2019
accepted: 07 02 2020
entrez: 27 2 2020
pubmed: 27 2 2020
medline: 28 4 2020
Statut: epublish

Résumé

Multidrug-resistant (MDR) E. coli with extended-spectrum β-lactamases (ESBLs) is becoming endemic in health care settings around the world. Baseline data on virulence and antimicrobial resistance (AMR) of specific lineages of E. coli circulating in developing countries like India is currently lacking. Whole-genome sequencing was performed for 60 MDR E. coli isolates. The analysis was performed at single nucleotide polymorphism (SNP) level resolution to identify the presence of their virulence and AMR genes. Genome comparison revealed the presence of ST-131 global MDR and ST410 as emerging-MDR clades of E. coli in India. AMR gene profile for cephalosporin and carbapenem resistance differed between the clades. Genotypes blaCTX-M-15 and blaNDM-5 were common among cephalosporinases and carbapenemases, respectively. For aminoglycoside resistance, rmtB was positive for 31.7% of the isolates, of which 95% were co-harboring carbapenemases. In addition, the FimH types and virulence gene profile positively correlated with the SNP based phylogeny, and also revealed the evolution of MDR clones among the study population with temporal accumulation of SNPs. The predominant clone was ST167 (blaNDM lineage) followed by ST405 (global clone ST131 equivalent) and ST410 (fast spreading high risk clone). This is the first report on the whole genome analysis of MDR E. coli lineages circulating in India. Data from this study will provide public health agencies with baseline information on AMR and virulent genes in pathogenic E. coli in the region.

Sections du résumé

BACKGROUND
Multidrug-resistant (MDR) E. coli with extended-spectrum β-lactamases (ESBLs) is becoming endemic in health care settings around the world. Baseline data on virulence and antimicrobial resistance (AMR) of specific lineages of E. coli circulating in developing countries like India is currently lacking.
METHODS
Whole-genome sequencing was performed for 60 MDR E. coli isolates. The analysis was performed at single nucleotide polymorphism (SNP) level resolution to identify the presence of their virulence and AMR genes.
RESULTS
Genome comparison revealed the presence of ST-131 global MDR and ST410 as emerging-MDR clades of E. coli in India. AMR gene profile for cephalosporin and carbapenem resistance differed between the clades. Genotypes blaCTX-M-15 and blaNDM-5 were common among cephalosporinases and carbapenemases, respectively. For aminoglycoside resistance, rmtB was positive for 31.7% of the isolates, of which 95% were co-harboring carbapenemases. In addition, the FimH types and virulence gene profile positively correlated with the SNP based phylogeny, and also revealed the evolution of MDR clones among the study population with temporal accumulation of SNPs. The predominant clone was ST167 (blaNDM lineage) followed by ST405 (global clone ST131 equivalent) and ST410 (fast spreading high risk clone).
CONCLUSIONS
This is the first report on the whole genome analysis of MDR E. coli lineages circulating in India. Data from this study will provide public health agencies with baseline information on AMR and virulent genes in pathogenic E. coli in the region.

Identifiants

pubmed: 32101543
doi: 10.1371/journal.pone.0220428
pii: PONE-D-19-19739
pmc: PMC7043739
doi:

Substances chimiques

Carbapenems 0
Cephalosporins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0220428

Subventions

Organisme : Department of Health
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Naveen Kumar Devanga Ragupathi (NK)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.
Department of Chemical and Biological Engineering, The University of Sheffield, Sheffield, United Kingdom.

Balaji Veeraraghavan (B)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Dhiviya Prabaa Muthuirulandi Sethuvel (DP)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Shalini Anandan (S)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Karthick Vasudevan (K)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Ayyan Raj Neeravi (AR)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Jones Lionel Kumar Daniel (JLK)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Sowmya Sathyendra (S)

Department of Medicine, Christian Medical College, Vellore, India.

Ramya Iyadurai (R)

Department of Medicine, Christian Medical College, Vellore, India.

Ankur Mutreja (A)

Department of Medicine, Addenbrookes Hospital, University of Cambridge, Cambridge, United Kingdom.
Translational Health Science and Technology Institute (THSTI), Delhi-NCR, India.

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