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Molecular Diversity and Antimicrobial Susceptibility of Listeria Monocytogenes Isolates from Invasive Infections in Poland (1997-2013)

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Journal Sci Rep
Specialty Science
Date 2018 Sep 30
PMID 30267005
Citations 20
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Abstract

The epidemiology of invasive listeriosis in humans appears to be weakly characterized in Poland, the sixth most populous member state of the European Union. We obtained antimicrobial susceptibility data, PCR-serogroups and genotypic profiles for 344 invasive isolates of Listeria monocytogenes, collected between 1997 and 2013 in Poland. All isolates were susceptible to the 10 tested antimicrobials, except one that was resistant to tetracycline and minocycline and harbored the tet(M), tet(A) and tet(C) genes. Overall, no increasing MIC values were observed during the study period. Four PCR-serogroups were observed: IVb (55.8%), IIa (34.3%), IIb (8.1%) and IIc (1.8%). We identified clonal complexes (CCs) and epidemic clones (ECs) previously involved in outbreaks worldwide, with the most prevalent CCs/ECs being: CC6/ECII (32.6%), CC1/ECI (17.2%), CC8/ECV (6.1%) and CC2/ECIV (5.5%). The present study is the first extensive analysis of Polish L. monocytogenes isolates from invasive infections.

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References
1.
Scortti M, Lacharme-Lora L, Wagner M, Chico-Calero I, Losito P, Vazquez-Boland J . Coexpression of virulence and fosfomycin susceptibility in Listeria: molecular basis of an antimicrobial in vitro-in vivo paradox. Nat Med. 2006; 12(5):515-7. DOI: 10.1038/nm1396. View

2.
Borucki M, Call D . Listeria monocytogenes serotype identification by PCR. J Clin Microbiol. 2003; 41(12):5537-40. PMC: 309009. DOI: 10.1128/JCM.41.12.5537-5540.2003. View

3.
Gillespie I, McLauchlin J, Little C, Penman C, Mook P, Grant K . Disease presentation in relation to infection foci for non-pregnancy-associated human listeriosis in England and Wales, 2001 to 2007. J Clin Microbiol. 2009; 47(10):3301-7. PMC: 2756898. DOI: 10.1128/JCM.00969-09. View

4.
Moura A, Criscuolo A, Pouseele H, Maury M, Leclercq A, Tarr C . Whole genome-based population biology and epidemiological surveillance of Listeria monocytogenes. Nat Microbiol. 2016; 2:16185. PMC: 8903085. DOI: 10.1038/nmicrobiol.2016.185. View

5.
Ward T, Gorski L, Borucki M, Mandrell R, Hutchins J, Pupedis K . Intraspecific phylogeny and lineage group identification based on the prfA virulence gene cluster of Listeria monocytogenes. J Bacteriol. 2004; 186(15):4994-5002. PMC: 451661. DOI: 10.1128/JB.186.15.4994-5002.2004. View