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.
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.