2010
DOI: 10.1128/jcm.00373-10
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Axillary Abscess Complicated by Venous Thrombosis: Identification ofStreptococcus pyogenesby 16S PCR

Abstract: We report a case of an axillary abscess with Streptococcus pyogenes complicated by venous thrombosis. Bacterial etiology and typing were obtained by PCR and sequencing of the 16S rRNA and M-protein genes from abscess material. The bacterium was of serotype M41, and serology indicated that it had expressed procoagulant factors. CASE REPORTA 62-year-old woman presented at our department with a 7-day history of fever, chills, and nausea. She was previously healthy, apart from having atopic eczema, and she worked … Show more

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Cited by 11 publications
(9 citation statements)
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“…Sequence analysis of an approximately 900 base pair fragment of the 16S rRNA-gene was essentially performed as described previously [20]. Because A. urinae is easily mistaken for an a-haemolytic streptococcus, all isolates classified as 'a-haemolytic streptococcus' (Lund laboratory) or 'streptococcal species' (Malmö laboratory) between 2005 and 2010 were reviewed.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Sequence analysis of an approximately 900 base pair fragment of the 16S rRNA-gene was essentially performed as described previously [20]. Because A. urinae is easily mistaken for an a-haemolytic streptococcus, all isolates classified as 'a-haemolytic streptococcus' (Lund laboratory) or 'streptococcal species' (Malmö laboratory) between 2005 and 2010 were reviewed.…”
Section: Methodsmentioning
confidence: 99%
“…Of the remaining isolates, those with a zone for cotrimoxazole <12 mm were subjected to sequencing of the 16S rRNA gene. Sequence analysis of an approximately 900 base pair fragment of the 16S rRNA-gene was essentially performed as described previously [20]. The primers BAK11w (5¢-AGA GTT TGA TCM TGG CTC AG -3¢) and p91E-Revers (5¢-CCC GTC AAT TCH TTT GAG T -3¢) were used [21].…”
Section: Methodsmentioning
confidence: 99%
“…SF was subjected to 16S rRNA gene PCR. The analysis was performed as previously described [ 36 ]. DNA was extracted from 200 µL fluid using a Bio Robot EZ-1 with DNA Tissue Kit (Qiagen, Hilden, Germany) after treatment with Proteinase K according to instructions by the manufacturer.…”
Section: Methodsmentioning
confidence: 99%
“…The laboratories used blood culture systems and MALDI-TOF MS, as previously described [ 23 ]. We performed species determination with 16S rRNA gene sequencing with fD1 mod and P911 primers, as previously described [ 24 ], on all isolates where both the initial and renewed MALDI-TOF MS analysis gave a score below 2.0.…”
Section: Methodsmentioning
confidence: 99%