1997
DOI: 10.1016/s0934-8840(97)80059-x
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Typing of Staphylococcus aureus Isolated from Nasal Carriers

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Cited by 15 publications
(13 citation statements)
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References 19 publications
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“…As shown for patient L this nasal carriage appeared to be stable at least for a 2-year period. These ¢ndings correspond to data presented previously [27]. The identity of the S. aureus isolates in each pair could be demonstrated phenotypically by hemolysin production, their antibiotic resistances, the secreted enterotoxins and by phage-typing.…”
Section: Discussionsupporting
confidence: 89%
“…As shown for patient L this nasal carriage appeared to be stable at least for a 2-year period. These ¢ndings correspond to data presented previously [27]. The identity of the S. aureus isolates in each pair could be demonstrated phenotypically by hemolysin production, their antibiotic resistances, the secreted enterotoxins and by phage-typing.…”
Section: Discussionsupporting
confidence: 89%
“…Additionally, PFGE analysis also demonstrated the same patterns within different carriers (PT C and D) at different times, suggesting that there occurred transference of microorganisms among food workers through direct or indirect contact and consequently this is a potential source of diet contamination. This fact was previously demonstrated by other researchers in healthy person, including personnel staff (Toshkova and others 1997). According to Kennedy and others (2000), the strains that are present in the nose can be transmitted to the hands and skin and may contaminate the air, water, soil, food, and any area or object that has come into contact with the carrier increasing risks of food poisoning.…”
Section: Resultssupporting
confidence: 78%
“…Ten differentsized amplicons of approximately 90,110,140,170,190,220,240,270,290, and 320 bp and calculated numbers of 2, 3, 4, 5, 6, 7, 8, 9, 10, and 11 repeats, respectively, were observed. Comparable differences in the number of repeats of the X region of the protein A (spa) gene had already been used for genotyping isolates of this species (14,15,46,48).…”
Section: Discussionmentioning
confidence: 99%
“…The isolates were also investigated by digestion of their chromosomal DNAs with the restriction enzyme SmaI and subsequent separation of the fragments by pulsed-field gel electrophoresis (PFGE) using the Chef-Dr II pulsed-field electrophoresis system (Bio-Rad, Munich, Germany). The preparation of the DNA and the program for PFGE were described previously (46). In accordance with the method of Tenover et al (45), restriction patterns with no fragment difference were recorded as indistinguishable, restriction patterns with two to three fragments difference were recorded as closely related, and those with four and more differences were recorded as not related.…”
Section: Methodsmentioning
confidence: 99%