For example, microcins H47 and M are active substances produced b

For example, PFT�� in vitro microcins H47 and M are active substances produced by the non-pathogenic, probiotic E. coli strain

Nissle 1917 [19]. At the same time, several studies have shown an association between the production of some types of bacteriocins and pathogenic E. coli strains [20–23]. Previous studies have found that genes encoding colicin E1, as well as microcins H47, M, I47, E492 and V were associated with extraintestinal pathogenic E. coli strains [20–23]. Colicin E1 is also Ricolinostat datasheet known to have toxic effects on eukaryotic cells and is considered to be a virulence factor in UPEC strains [21, 24, 25]. Microcins H47 and M are induced when iron is a limiting factor and are associated with competition for iron [22, 26]. Synthesis of microcin H47 and M could therefore be advantageous in bacteremia of urinary tract origin [22, 26]. Previously published studies have only provided partial insight into the association between bacteriocin production and bacterial virulence, as they were primarily focused upon UPEC strains and differed in the number of detected bacteriocin and virulence genes. Azpiroz et al. (2009) screened 5 microcin types in 125 UPEC strains and 9 virulence factors [20], while Budič et al. (2011) and Petkovšek et al. (2012) analyzed 14 virulence factors (primarily those associated with urinary tract infections)

and 19 bacteriocin types in 105 UPEC strains [22, 23]. Similarly, Abraham

et al. (2012) analyzed 16 bacteriocin types and 18 virulence factors in a collection of 159 UPEC strains [27]. Together, these studies selleck compound identified an association between microcins (M, H47, V, B17 and L) and several virulence genes [20, 22, 23, 27]. Studies by Gordon et al. (2005) and Gordon and O’Brien (2006) focused on 266 fecal E. coli strains and identified an association between strains encoding at least one microcin type, and four genes involved in iron acquisition (from a total of 29 tested virulence determinants) [26, 28]. The main aim of our study was to test the association Adenosine between bacteriocin production and bacterial virulence within a large collection of E. coli strains (n = 1181) isolated from human gut microflora. In this study, new associations between bacteriocin-encoding genes and virulence determinants were found in human fecal E. coli strains. Results Detection of virulence determinants and bacteriocin-encoding genes Altogether, 18 DNA determinants (pCVD432, α-hly, afaI, aer, cnf1, sfa, pap, ial, lt, st, bfpA, eaeA, ipaH, iucC, fimA and stx1, stx2 and ehly) encoding 17 different virulence factors were tested in each of 1181 E. coli strains (Additional file 1: Table S1). The vast majority of strains (94.7%) possessed at least one virulence factor. The most common virulence determinant was the fimA gene (encoding fimbriae type I), which was detected in 87.9% of all strains.

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