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264


Tanise Vendruscolo Dalmolin et al


Table 1. Minimal Inhibitory Concentration (MIC)a of Several Antibiotics for Escherichia coli and Klebsiella pneumoniae Coharboring blaKPC/mcr-1 Genes Antibiotic


E. coli 3431F, MIC (mg/L)


Ertapenem Meropenem Imipenem


Ciprofloxacin Amikacin


Gentamicin Tigecycline Colistin


32 32


≥32 4 2 1


0.25 4


aPerformed by broth microdilution.


E. coli 5798F, MIC (mg/L)


16 8


16


≥64 8 2 1 4


E. coli 6699F, MIC (mg/L)


256 256 256 32 8 4


0.5 4


K. pneumoniae 3111F, MIC (mg/L)


256 256 256


≥64 16 32 1 4


128 128 16 64 8


0.5


0.25 0.25


K. pneumoniae 6701F, MIC (mg/L)


colistin, as already described in Shigella sonnei.8 Interestingly, the truncated mcr-1 gene could be reactivated after conjugation experiments, resulting in a colistin resistant phenotype.9 However, a truncated gene is not the only reason to justify the susceptibility; one study reported an E. coli colistin-susceptible mcr-1 positive isolate that presented an intact gene.10 Therefore, further studies are needed to elucidate the reason why the mcr-1gene of


the


K. pneumoniae 6701F in this study does not promote resistance to colistin. In fact, colistin-susceptible mcr-1 isolates may be con- tributing to a silent spread of the mcr-1 gene, which may be transferred to multidrug-resistant isolates such as the CPE described in this study. In conclusion, the current prevalence of mcr-1 is very low, but


the detection of 2 isolates in 2018 coharboring blaKPC/mcr-1 genes is a warning for a possible increase in the prevalence of these isolates in the coming years. Considering the association of mcr-1 with the broad-spectrum resistance mechanisms (eg, carbapenemases), this emergence is of great concern.


Acknowledgments. The authors would like to thank Luiza Castro for technical support.


Financial support. This work was supported by Fundo de Incentivo a Pesquisa e Eventos do Hospital de Clínicas de Porto Alegre (FIPE/HCPA project no. 16-0559) and by a grant from the Conselho Nacional de Desen- volvimento Científico e Tecnológico—Brazil (CNPq).


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


References


1. 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 2015;16:161–168.


2. Skov RL, Monnet DL. Plasmid-mediated colistin resistance (mcr-1 gene): three months later, the story unfolds. Euro Surveill 2016;21:30155.


3. Dalmolin TV, Castro L, Mayer FQ, et al. Co-occurrence of mcr-1 and KPC-2 in a clinical isolate of Escherichia coli in Brazil. J Antimicrob Chemother 2017;72:2404–2406.


4. Wang Y, Tian GB, Zhang R, et al. Prevalence, risk factors, outcomes, and molecular epidemiology of mcr-1–positive Enterobacteriaceae in patients and healthy adults from China: an epidemiological and clinical study. Lancet Infect Dis 2017;17:390–399.


5. Breakpoint tables for interpretation of MICs and zone diameters. Version 8.1. European Committee on Antimicrobial Susceptibility Testing (EUCAST) website. http://www.eucast.org/clinical_breakpoints/2018. Published 2018. Accessed October 30, 2018.


6. Mendes AC, Novais A, Campos J, et al. mcr-1 in carbapenemase- producing Klebsiella pneumoniae in hospitalized patients, Portugal, 2016– 2017. Emerg Infect Dis 2018;24:762–766.


7. Huang TD, Bogaerts P, Berhin C, et al. Increasing proportion of carbapenemase-producing Enterobacteriaceae and emergence of a MCR-1 producer through a multicentric study among hospital-based and private laboratories in Belgium from September to November 2015. Euro Surveill 2017;22: pii: 30530. doi: 10.2807/1560-7917.


8. Pham Thanh D, Thanh Tuyen H, Nguyen Thi Nguyen T, et al. Inducible colistin resistance via a disrupted plasmid-borne mcr-1 gene in a 2008 Vietnamese Shigella sonnei isolate. 2016;71:2314–2317.


J Antimicrob Chemother


9. TerveerEM, NijhuisRHT,Crobach MJT, et al.Prevalence of colistin resistance gene (mcr-1) containing Enterobacteriaceae in feces of patients attending a tertiary care hospital and detection of an mcr-1–containing, colistin-susceptible E. coli. PLoS One 2017;12: e0178598.


10. Liassine N, Assouvie L, Descombes MC, et al. Very low prevalence of MCR-1/MCR-2 plasmid-mediated colistin resistance in urinary tract Enterobacteriaceae in Switzerland. Int J Infect Dis 2016;51:4–5.


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