Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-25T13:50:44.991Z Has data issue: false hasContentIssue false

Detection of the emergence of mcr-1–mediated colistin-resistant Escherichia coli and Klebsiella pneumoniae through a hospital-based surveillance in an oncology center in eastern India

Published online by Cambridge University Press:  09 January 2020

Samadrita Roy
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Parijat Das
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Surojit Das
Affiliation:
Department of Biomedical Laboratory Science and Management, Vidyasagar University, West Bengal, India
Subhanita Roy
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Soumik Pal
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Vinitha Mary Joy
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Sudipta Mukherjee
Affiliation:
Department of Anaesthesia & Critical Care Medicine, Tata Medical Center, Kolkata, India
Arpita Bhattacharyya
Affiliation:
Department of Paediatric Hematology and Oncology, Tata Medical Center, Kolkata, India
Gaurav Goel
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Sanjay Bhattacharya*
Affiliation:
Department of Microbiology, Tata Medical Center, Kolkata, India
Purva Mathur
Affiliation:
Department of Laboratory Medicine, JPNA Trauma Centre, All India Institute of Medical Sciences, New Delhi, India
Kamini Walia
Affiliation:
Indian Council of Medical Research, New Delhi, India
Mammen Chandy
Affiliation:
Department of Clinical Hematology, Tata Medical Center, Kolkata, India
*
Author for correspondence: Sanjay Bhattacharya, MD, Tata Medical Center, Kolkata, India. E-mail: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Type
Letter to the Editor
Copyright
© 2020 by The Society for Healthcare Epidemiology of America. All rights reserved.

To the Editor—The global emergence of colistin-resistant Enterobacteriaceae through the plasmid-mediated mcr gene has raised concerns with regard to spread of antimicrobial resistance and infection control.Reference Liu, Wang and Walsh1 There are several mechanisms of colistin resistance.Reference Aghapour, Gholizadeh and Ganbarov2 However, the molecular epidemiology of colistin resistance in clinically relevant gram-negative isolates is poorly defined in India, a country that is large and populous and is also a major trading center and an international tourism destination.Reference Singh, Pathak and Kumar3,Reference Pragasam, Shankar and Veeraraghavan4 Here, we document 2 cases of mcr-gene–mediated colistin resistance in Enterobacteriaceae from an oncology center in eastern India.

Case 1

In June 2018, we isolated Escherichia coli in the urine of a 51-year-old woman from West Bengal, India, with metastatic carcinoma of lung. The E. coli isolate (detected while she was in the community) was positive for bla OXA-48 and mcr-1 (confirmed by PCR and DNA sequencing).The minimum inhibitory concentration (MIC) for colistin was 4 µg/mL. In September 2019, while she was in the hospital, we detected Klebsiella pneumoniae from endotracheal aspirate which was bla OXA-48 and mcr-1 positive (colistin MIC, 16 µg/mL). The patient was treated with fosfomycin. The patient had a diagnosis of diabetes mellitus and had several medical devices (urinary catheter, tracheostomy, central line). Carbapenemase-resistant isolates were detected previously, and she had received treatment in the past with meropenem and colistin.

Case 2

In an 8-year-old girl from Bangladesh with acute lymphoblastic leukemia, we detected, from left buttock wound swab, a carbapenem-sensitive but colistin-resistant Escherichia coli (positive for mcr-1) with an MIC of 8 µg/mL.

These 2 cases were part of a prospective surveillance for mcr-1–5 genes conducted in Tata Medical Center, Kolkata, India, a 183-bed oncology center where patients are mainly from the state of West Bengal in India but also from neighboring states in India and countries such as Bangladesh and Bhutan. The inclusion criteria for testing of mcr-1–5 genes by polymerase chain reaction (PCR) was the detection of colistin resistance (MIC ≥ 2 µg/mL) using the microbroth dilution method according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) and Clinical Laboratory Standards Institute (CLSI) guidelines. If found to be carbapenem resistant, the isolates were also screened for the presence of the following carbapenemase-associated genes: bla NDM-1, bla VIM, bla IMP, bla OXA48-like,23,24,58, bla KPC. Identification of the isolates was performed using the Vitek2 system (bioMèrieux, Marcy-l'Étoile, France), and mcr-1–5 genes were tested using in-house end-point multiplex PCR. If positive, they were confirmed by Sanger-based DNA sequencing. The results of this surveillance (conducted between August 2017 to October 2019) are presented in online Fig. 1 and Table 1.

Table 1. Distribution of Carbapenemase- and Colistin-Resistant mcr-1 Gene in the Samples Studied (N = 198)

Note: carbapenemase genes tested included: bla NDM, bla KPC, bla IMP, bla VIM, blaOXA-48, 23,24,58.

Among colistin-resistant mechanisms, plasmid-mediated resistance is a major cause of global concern because of the potential for transfer of colistin-resistance genes to susceptible strains. These genes were first reported in E. coli isolated in China.Reference Liu, Wang and Walsh1 The mechanism of mcr-mediated colistin resistance is as follows. Encoded mcr-1 protein is a member of the phosphoethanolamine transferase enzyme family; mcr acquisition results in the addition of phosphoethanolamine to lipid A, and thereby to a more cationic lipopolysaccharide, which contributes to acquired colistin resistance in Enterobacteriaceae.Reference Poirel, Jayol and Nordmann5 Isolates carrying the mcr-1 gene demonstrate resistance to colistin displaying 4–8-fold increase in colistin MIC.Reference Poirel, Jayol and Nordmann5 Some plasmids containing the mcr-1 gene carry other genes that are resistant to antibiotics, such as β-lactams, aminoglycosides, quinolones, sulfonamides, tetracyclines, and fosfomycin.Reference Poirel, Jayol and Nordmann5 The mcr gene has also been identified in Enterobacteriaceae isolates, which carry such carbapenemase genes as bla NDM1, bla NDM5, bla NDM9, bla OXA48, bla KPC2, and bla VIM1.Reference Du, Chen, Tang and Kreiswirth6 Studies have shown mcr-2–mediated colistin resistance in E. coli isolates from European countries, whereas mcr-3 has been widely identified in Enterobacteriaceae (mainly E. coli) and Aeromonas spp from Asia, Europe, and North America.Reference Xavier, Lammens and Ruhal7,Reference Yin, Li and Shen8 The mcr-4 and mcr-5 genes were first characterized in Salmonella and E. coli from European countries.Reference Carattoli, Villa and Feudi9,Reference Borowiak, Fischer, Hammerl, Hendriksen, Szabo and Malorny10 Currently from India, only 1 report of mcr-mediated colistin resistance in Klebsiella pneumoniae has been published.Reference Singh, Pathak and Kumar3 In 2017, Borowiak et alReference Borowiak, Fischer, Hammerl, Hendriksen, Szabo and Malorny10 reported a new gene of the mcr family from Salmonella paratyphi B that were carried in transposons instead of plasmids.

The emergence of colistin resistance is a cause for concern for both clinicians and patients, particularly in countries with high rates of carbapenem- and/or colistin-resistant Enterobacteriaceae such as China and India. We are not aware of any report of the prevalence of mcr-mediated colistin resistance in the immunocompromised cancer patient population in India.

Because the mcr gene is plasmid mediated, the infection prevention and control challenges are significant. Using the PCR-based method, we have tried to develop a relatively low cost and feasible system to detect mcr-mediated mechanisms of colistin resistance. The cost of mcr gene detection is USD $7 for the multiplex screening PCR and USD $20 for Sanger-based DNA sequencing per isolate.

This study is important in several aspects. We have shown that mcr-1–mediated colistin resistance may occur independent of carbapenem resistance (i.e. case 2). The occurrence of these resistance mechanisms in immunocompromised cancer patients who have extensive healthcare and antibiotic exposure as well as hospital admission episodes increases the risk of infection spread in healthcare settings as well as in community (case 1). The second case shows that this resistance phenomenon can be found even in children. These cases are, to the best of our knowledge, the first reports of such infections from eastern India. Because of the proximity of this region to highly populous areas and to international trade, tourism, and travel, the likelihood of international dissemination may be high. Surveillance of mcr-mediated colistin resistance may reveal more cases and facilitate better infection control.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/ice.2019.363

Acknowledgments

We thank the Indian Council of Medical Research for supporting the study.

Financial support

This study was supported by the Indian Council of Medical Research.

Conflicts of interest

All authors report no conflicts of interest relevant to this article.

References

Liu, YY, Wang, Y, Walsh, TR, et al.Emergence of plasmid-mediated colistin resistance mechanism mcr-1 in animals and human beings in China: a microbiological and molecular biological study. Lancet Infect Dis 2016;16:161168.CrossRefGoogle ScholarPubMed
Aghapour, Z, Gholizadeh, P, Ganbarov, K, et al.Molecular mechanisms related to colistin resistance in Enterobacteriaceae. Infect Drug Resist 2019;12:965975.CrossRefGoogle ScholarPubMed
Singh, S, Pathak, A, Kumar, A, et al.Emergence of chromosome-borne colistin resistance gene mcr-1 in clinical isolates of Klebsiella pneumoniae from India. Antimicrob Agents Chemother 2018;62:pii:e01885-17.Google ScholarPubMed
Pragasam, AK, Shankar, C, Veeraraghavan, B, et al.Molecular mechanisms of colistin resistance in Klebsiella pneumoniae–causing bacteremia from India—a first report. Front Microbiol 2017;7:21352143.CrossRefGoogle ScholarPubMed
Poirel, L, Jayol, A, Nordmann, P.Polymyxins: antibacterial activity, susceptibility testing, and resistance mechanisms encoded by plasmids or chromosomes. Clin Microbiol Rev 2017;30:557596.CrossRefGoogle ScholarPubMed
Du, H, Chen, L, Tang, YW, Kreiswirth, BN.Emergence of the mcr-1 colistin resistance gene in carbapenem-resistant Enterobacteriaceae. Lancet Infect Dis 2016;16:287288.CrossRefGoogle ScholarPubMed
Xavier, BB, Lammens, C, Ruhal, Ret al.Identification of a novel plasmid-mediated colistin-resistance gene, mcr-2, in Escherichia coli, Belgium, June 2016. Euro Surveill 2016;21:30280.CrossRefGoogle Scholar
Yin, W, Li, H, Shen, Y, et al.Novel plasmid-mediated colistin resistance gene mcr-3 in Escherichia coli. MBio 2017;8:pii:e00543-17.Google ScholarPubMed
Carattoli, A, Villa, L, Feudi, C, et al.Novel plasmid-mediated colistin resistance mcr-4 gene in Salmonella and Escherichia coli, Italy 2013, Spain and Belgium, 2015 to 2016. Euro Surveill 2017;22:pii:30589.CrossRefGoogle Scholar
Borowiak, M, Fischer, J, Hammerl, JA, Hendriksen, RS, Szabo, I, Malorny, B.Identification of a novel transposon-associated phosphoethanolamine transferase gene, mcr-5, conferring colistin resistance in d-tartrate fermenting Salmonella enterica subsp. enterica serovar Paratyphi B. J Antimicrob Chemother 2017;72:33173324.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Distribution of Carbapenemase- and Colistin-Resistant mcr-1 Gene in the Samples Studied (N = 198)

Supplementary material: File

Roy et al. supplementary material

Roy et al. supplementary material

Download Roy et al. supplementary material(File)
File 18.2 KB