Challenge of drug resistance in Pseudomonas aeruginosa: clonal spread of NDM-1-positive ST-308 within a tertiary hospital

Author:

Chew Ka Lip1ORCID,Octavia Sophie2,Ng Oon Tek345,Marimuthu Kalisvar346ORCID,Venkatachalam Indumathi7,Cheng Bernadette1,Lin Raymond T P12,Teo Jeanette W P1

Affiliation:

1. Department of Laboratory Medicine, National University Hospital, Singapore

2. National Public Health Laboratory, Ministry of Health, Singapore

3. Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore

4. National Centre for Infectious Diseases, Singapore

5. Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore

6. Yong Loo Lin School of Medicine, National University of Singapore, Singapore

7. Department of Infectious Diseases, Singapore General Hospital, Singapore

Abstract

Abstract Objectives MDR Pseudomonas aeruginosa is a serious global threat to healthcare institutions. The mechanism by which drug resistance can be acquired is variable, but acquired carbapenemase production has been reported in P. aeruginosa. An investigation was performed to determine the rate and genomic epidemiology of New Delhi MBL (NDM) in β-lactam-non-susceptible isolates. Methods P. aeruginosa isolates from a tertiary hospital in Singapore between January 2015 and February 2018 were investigated for the presence of NDM genes. Results Out of 298 pan-β-lactam-non-susceptible isolates, 31 were found to be NDM positive (10.4%). WGS demonstrated that all 31 NDM-positive isolates were clonal, belonging to ST-308. blaNDM was chromosomally inserted within an integrative and conjugative element (ICE), ICETn43716385. The NDM-P. aeruginosa isolates possessed an extensive repertoire of both cell-associated [flagella, pili, alginate/biofilm, LPS, type III secretion system (T3SS) and type VI secretion system (T6SS)] and secreted virulence factors. Antibiograms revealed higher rates of drug resistance in NDM-positive isolates compared with their non-NDM counterparts. The NDM isolates remained 100% susceptible only to colistin. Conclusions The combination of chromosomal mutations, acquired resistance genes and virulence factors likely facilitated the persistent and ongoing spread of the ST-308 clade of P. aeruginosa within the hospital. Our study illustrates the particular threat of NDM-positive P. aeruginosa in a tertiary hospital setting in the era of antimicrobial resistance.

Funder

NMRC

Clinician-Scientist Individual Research Grant

MOE Tier 2: New Delhi Metallo-Beta-Lactamase:

Collaborative Solutions Targeting Antimicrobial Resistance Threats in Health Systems

Clinician Scientist Award

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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