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Spread of Tst-positive Staphylococcus aureus strains belonging to ST30 clone among patients and healthcareworkers in two intensive care units

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Autor
Papadimitriou-Olivgeris M., Drougka E., Fligou F., Dodou V., Kolonitsiou F., Filos K.S., Anastassiou E.D., Petinaki E., Marangos M., Spiliopoulou I.
Fecha
2017
Language
en
DOI
10.3390/toxins9090270
Materia
Panton Valentine leukocidin
pseudomonic acid
toxic shock syndrome toxin 1
antiinfective agent
bacterial protein
bacterial toxin
enterotoxin
enterotoxin F, Staphylococcal
exotoxin
leukocidin
mecA protein, Staphylococcus aureus
Panton-Valentine leukocidin
penicillin binding protein
superantigen
adult
antibiotic resistance
antibiotic sensitivity
Article
bacterial clearance
bacterial colonization
bacterium carrier
bacterium isolation
controlled study
disease transmission
disk diffusion
gene frequency
gene sequence
health care personnel
hospital infection
human
infection control
intensive care unit
major clinical study
methicillin resistant Staphylococcus aureus infection
minimum inhibitory concentration
molecular cloning
nonhuman
polymerase chain reaction
Staphylococcus aureus
cross infection
drug effect
genetics
Greece
health care personnel
intensive care unit
isolation and purification
methicillin resistance
microbial sensitivity test
microbiology
multilocus sequence typing
pulsed field gel electrophoresis
Staphylococcus aureus
Staphylococcus infection
university hospital
Anti-Bacterial Agents
Bacterial Proteins
Bacterial Toxins
Cross Infection
Electrophoresis, Gel, Pulsed-Field
Enterotoxins
Exotoxins
Greece
Health Personnel
Hospitals, University
Humans
Intensive Care Units
Leukocidins
Methicillin Resistance
Microbial Sensitivity Tests
Multilocus Sequence Typing
Penicillin-Binding Proteins
Staphylococcal Infections
Staphylococcus aureus
Superantigens
MDPI AG
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Resumen
Staphylococcus aureus is a major cause of infections. Toxic shock syndrome toxin (TSST-1) and Panton-Valentine leukocidin (PVL) are associated with severe clinical syndromes. S. aureus colonizing isolates recovered from healthcare workers and patients in the intensive care unit (ICU) of a university hospital comprising Group A were compared with those from adult non-ICU carriers (Group B). mecA, lukS/lukF-PV (Panton-Valentine leukocidin, PVL), and tst (toxic shock syndrome toxin) gene carriage was detected by PCR. Clones were identified in all methicillin-resistant S. aureus (MRSA) and toxin-positive methicillin-susceptible strains (MSSA) by pulsed-field gel electrophoresis (PFGE), agr groups, and multi locus sequencing typing (MLST). Group A included 90 S. aureus isolates, whereas Group B 53. PVL was more frequently found among MRSA vs. MSSA (p < 0.001) and in strains of Group B as compared to Group A (p < 0.001), consistent with the spread of ST80-IV. Higher incidence of tst gene carriage was identified among MSSA vs. MRSA (P 0.005) belonging mainly to ST30, and Group A vs. Group B (P 0.002). The wide dissemination of ST80-IV mainly in the community is responsible for a high percentage of PVL-positive MRSA, while silent spread of tst-positive S. aureus clones among ICU patients and personnel poses a threat of hospital transmission and possible severe infections. © 2017 by the authors.
URI
http://hdl.handle.net/11615/77600
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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