2018
DOI: 10.1099/jmm.0.000764
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Stenotrophomonas maltophilia isolated from patients exposed to invasive devices in a university hospital in Argentina: molecular typing, susceptibility and detection of potential virulence factors

Abstract: This is the first epidemiological study of the clonal relatedness of S. maltophilia clinical isolates in Argentina. Great genomic diversity was observed, and only two small clusters of related S. maltophilia types were found. Minocycline and trimethoprim-sulfamethoxazole were the most active agents. S. maltophilia virulence in the G. mellonella model is multifactorial, and further studies are needed to elucidate the role of each potential virulence factor.

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Cited by 20 publications
(17 citation statements)
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“…S. maltophilia has high genetic diversity, as demonstrated with various typing methods (Gherardi et al, 2015;Pompilio et al, 2016;Alcaraz et al, 2018;Guvenir et al, 2018). However, in Mexico, 75-100% similarity has been obtained among strains collected from the same hospital source over a period of 7 years (Flores-Trevino et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
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“…S. maltophilia has high genetic diversity, as demonstrated with various typing methods (Gherardi et al, 2015;Pompilio et al, 2016;Alcaraz et al, 2018;Guvenir et al, 2018). However, in Mexico, 75-100% similarity has been obtained among strains collected from the same hospital source over a period of 7 years (Flores-Trevino et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
“…Among these genes, dihydropteroate synthase (sul1 and sul2), and dihydrofolate reductase (drfA) are the main mechanisms of SXT resistance in S. maltophilia (Toleman et al, 2007). Some virulence factors have been described in S. maltophilia, including Smf1-fimbrial operon, proteases, hemolysins, exopolysaccharides (EPSs), lipopolysaccharides (LPSs), siderophores, flagella, lipases, putative virulence genes in a pathogenicity island encoding proteins from the RTX (repeats-in-toxin) family, and transmembrane secretion system components (Brooke, 2012;Adamek et al, 2014;Sanchez, 2015;Pompilio et al, 2016;Alcaraz et al, 2018;Trifonova and Strateva, 2019). A few studies have described the colonization of S. maltophilia in cultures of HEp-2 and IB3-1 cells as well as A/J, DBA/2, BALB/c, and C57BL/6 mice (De Vidipo et al, 2001;De Oliveira-Garcia et al, 2003;Pompilio et al, 2008;Lin et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…Phenotypic typing of the isolates was performed using API20NE test kits (bioMérieux, France) according to the manufacturer's instructions. Genotypic typing was assessed by RAPD-PCR as described previously [36]. Briefly, amplification reactions were performed in a 25 µl final volume containing 2 U of GoTaq DNA polymerase (Promega) in 5× GoTaq reaction buffer, 4 mM MgCl 2 , dimethyl sulfoxide 10 %, 0.4 mM of each dNTP, 50 pmol of primer ERIC-2 (5′-AAGT AAGT GACT GGGG TGAGCG-3′) and 3 µl of The antimicrobial susceptibility for minocycline, trimethoprim-sulfamethoxazole (SXT) and levofloxacin (LEV) was assessed using the disc diffusion method according to CLSI recommendations.…”
Section: Phenotypic and Genotypic Typingmentioning
confidence: 99%
“…PCR product patterns were considered identical when the positions of all bands matched, regardless of band intensity [37]. Isolates were also genotyped by PFGE using the restriction enzyme XbaI (Thermo Fisher Scientific) as reported previously [36]. Gels were stained with ethidium bromide and digitized (Molecular Imager Gel Doc XR, Bio-Rad).…”
Section: Phenotypic and Genotypic Typingmentioning
confidence: 99%
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