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1.
Microb Drug Resist ; 26(12): 1546-1558, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32429830

ABSTRACT

Disinfection and antisepsis are of primary importance in controlling nosocomial infections and outbreaks by pathogens expressing multiple resistance to antimicrobial agents (multidrug-resistant [MDR]) used in therapy. Nowadays, infections related to health services (HAIs) due to MDR and multidrug-susceptible (MDS) Corynebacterium striatum should not be underestimated, including patients using invasive medical devices. The virulence potential of C. striatum needs further investigation. Currently, susceptibility profiles of planktonic and/or sessile forms of four C. striatum strains of different pulsed-field gel electrophoresis types were examined as biocides based on the manufacturer's recommendations: 2% glutaraldehyde (GA), 2% peracetic acid (PA), 1% potassium monopersulfate (Virkon®; VK), 1% sodium hypochlorite (SH), and 70% ethyl alcohol (ET). Time-kill assays using 2% bovine serum albumin (BSA) were performed for evaluation of influence of organic matter on biocides effects. Planktonic forms expressed GA resistance at different levels. C. striatum viability was observed until 2, 4, 20, and 30 min for MDR 2369/II, MDS 1954/IV, MDR 1987/I, and MDS 1961/III strains, respectively. In contrast to GA, the biocides PA, VK24h, SH, and ET had higher effective bacterial mortality. However, storage of VK (48 hr) reduced their biocide activities. Moreover, mature biofilms were produced on abiotic substrates, including steel surfaces. Post-treatment with GA (30 min), survival of sessile forms was ≥100% than planktonic forms of all C. striatum tested strains. Independent of biocides tested, BSA increased the survival of planktonic and sessile forms (p ≤ 0.005). Present data indicated that hospital staff should be aware of dissemination and eradication of HAIs by C. striatum presenting resistance to biocides, including high-level disinfectants, such as GA.


Subject(s)
Anti-Infective Agents, Local/pharmacology , Biofilms/drug effects , Corynebacterium/drug effects , Disinfectants/pharmacology , Drug Resistance, Multiple, Bacterial , Plankton/drug effects , Adult , Cross Infection/prevention & control , Electrophoresis, Gel, Pulsed-Field , Female , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Virulence
2.
Antonie Van Leeuwenhoek ; 112(9): 1331-1340, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31055716

ABSTRACT

Corynebacterium striatum strains have been increasingly reported as etiological agents of nosocomial infections and outbreaks in industrialized and developing countries. However, there are few studies focused on the virulence potential of C. striatum. A growing body of research supports the use of Caenorhabditis elegans as a model host for investigating the virulence potential of pathogenic bacteria, including corynebacteria. In the present study, chemotaxis behaviour, mortality, and morphological changes were investigated in nematodes infected by four C. striatum strains isolated from different clinical sites, and with different MDR profiles and PFGE types. The results showed chemotaxis of nematodes towards C. striatum. Nematode death (> 60%) was detected from the first day post-infection with all strains tested, but at different levels, independent of biofilm formation on catheter surfaces and differences in growth temperature between nematodes (20 °C) and mammals (37 °C). C. striatum 2369/II multidrug-resistant (MDR; from tracheal aspirate of a patient undergoing endotracheal intubation) and 1961/III multidrug-sensitive (MDS; urine) strains led to 100% mortality in worms. Survival of nematodes was observed until 4 days post-infection with the C. striatum 1954/IV MDS strain isolated from a surgical wound (13%) and 1987/I MDR strain isolated from a patient with a lower respiratory tract infection (39%). The Dar phenotype was observed post-infection with all MDS and MDR strains except 1954/IV. All strains showed the capacity for bagging formation. Star formation was observed only with strains that led to 100% nematode mortality. In conclusion, C. striatum was found to exert virulence for C. elegans. Variations in nematode morphological changes and levels of mortality indicate differences in the virulence potential of C. striatum independent of clinical isolation site, capacity for biofilm formation, and MDR and PFGE profiles.


Subject(s)
Caenorhabditis elegans/microbiology , Corynebacterium Infections/microbiology , Corynebacterium Infections/pathology , Corynebacterium/growth & development , Corynebacterium/pathogenicity , Animals , Caenorhabditis elegans/physiology , Corynebacterium/classification , Corynebacterium/isolation & purification , Disease Models, Animal , Drug Resistance, Multiple, Bacterial , Electrophoresis, Gel, Pulsed-Field , Humans , Survival Analysis , Virulence
3.
Mem Inst Oswaldo Cruz ; 108(1): 23-9, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23440110

ABSTRACT

Corynebacterium striatum is a potentially pathogenic microorganism with the ability to produce outbreaks of nosocomial infections. Here, we document a nosocomial outbreak caused by multidrug-resistant (MDR) C. striatum in Rio de Janeiro, Brazil. C. striatum identification was confirmed by 16S rRNA and rpoB gene sequencing. Fifteen C. striatum strains were isolated from adults (half of whom were 50 years of age and older). C. striatum was mostly isolated in pure culture from tracheal aspirates of patients undergoing endotracheal intubation procedures. The analysis by pulsed-field gel electrophoresis (PFGE) indicated the presence of four PFGE profiles, including two related clones of MDR strains (PFGE I and II). The data demonstrated the predominance of PFGE type I, comprising 11 MDR isolates that were mostly isolated from intensive care units and surgical wards. A potential causal link between death and MDR C. striatum (PFGE types I and II) infection was observed in five cases.


Subject(s)
Corynebacterium Infections/microbiology , Corynebacterium/drug effects , Cross Infection/microbiology , Disease Outbreaks , Drug Resistance, Multiple, Bacterial/genetics , Adult , Aged, 80 and over , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , Brazil , Cloning, Molecular , Corynebacterium/genetics , Corynebacterium Infections/epidemiology , Cross Infection/epidemiology , DNA, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Female , Genotype , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Phenotype , Young Adult
4.
Mem. Inst. Oswaldo Cruz ; 108(1): 23-29, Feb. 2013. ilus, graf, tab
Article in English | LILACS | ID: lil-666039

ABSTRACT

Corynebacterium striatum is a potentially pathogenic microorganism with the ability to produce outbreaks of nosocomial infections. Here, we document a nosocomial outbreak caused by multidrug-resistant (MDR) C. striatum in Rio de Janeiro, Brazil. C. striatum identification was confirmed by 16S rRNA and rpoB gene sequencing. Fifteen C. striatum strains were isolated from adults (half of whom were 50 years of age and older). C. striatum was mostly isolated in pure culture from tracheal aspirates of patients undergoing endotracheal intubation procedures. The analysis by pulsed-field gel electrophoresis (PFGE) indicated the presence of four PFGE profiles, including two related clones of MDR strains (PFGE I and II). The data demonstrated the predominance of PFGE type I, comprising 11 MDR isolates that were mostly isolated from intensive care units and surgical wards. A potential causal link between death and MDR C. striatum (PFGE types I and II) infection was observed in five cases.


Subject(s)
Adult , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult , Corynebacterium Infections/microbiology , Corynebacterium/drug effects , Cross Infection/microbiology , Disease Outbreaks , Drug Resistance, Multiple, Bacterial/genetics , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , Brazil , Cloning, Molecular , Corynebacterium Infections/epidemiology , Corynebacterium/genetics , Cross Infection/epidemiology , DNA, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Genotype , Microbial Sensitivity Tests , Phenotype
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