2009
DOI: 10.1128/jcm.01590-08
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Oral Abscess Caused by Campylobacter rectus : Case Report and Literature Review

Abstract: Campylobacter rectus was isolated under routine anaerobic conditions (no additional hydrogen gas in the atmosphere) from an oral, nonperiodontal abscess from a patient with gastroesophageal adenocarcinoma. We report the first case of a palate abscess caused by C. rectus and review the literature and atmospheric requirements of this organism.

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Cited by 34 publications
(34 citation statements)
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References 19 publications
(15 reference statements)
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“…Primers VAB1 (TGGAGAGTTTGATCCTGGCTCA), VAB2 (GTATTACCGCGGCTGCTGG), VAB3 (CCAGCAGCCG CGGTAATAC), VAB4 (CGGGACTTAACCCAACATCTC AC), VAB5 (GTGAGATGTTGGGTTAAGTCCCG), and VAB6 (AAGGAGGTGATCCAGCCGCA) were utilized to sequence a large portion of the 16S rRNA gene in five separate reactions in the following pair subsets: VAB-1/2, VAB-3/4, VAB-5/6, VAB-1/4, and VAB-3/6. PCR assays were performed as previously described (23). The resulting PCR products were cleaned with ExoSAP-IT (USB Products, Cleveland, OH) and sent to a core sequencing lab for cycle sequencing.…”
Section: Case Reportmentioning
confidence: 99%
“…Primers VAB1 (TGGAGAGTTTGATCCTGGCTCA), VAB2 (GTATTACCGCGGCTGCTGG), VAB3 (CCAGCAGCCG CGGTAATAC), VAB4 (CGGGACTTAACCCAACATCTC AC), VAB5 (GTGAGATGTTGGGTTAAGTCCCG), and VAB6 (AAGGAGGTGATCCAGCCGCA) were utilized to sequence a large portion of the 16S rRNA gene in five separate reactions in the following pair subsets: VAB-1/2, VAB-3/4, VAB-5/6, VAB-1/4, and VAB-3/6. PCR assays were performed as previously described (23). The resulting PCR products were cleaned with ExoSAP-IT (USB Products, Cleveland, OH) and sent to a core sequencing lab for cycle sequencing.…”
Section: Case Reportmentioning
confidence: 99%
“…The NCBI, Microseq, and BIBI databases were all used to search for comparison sequences, with all confirming the identification. Sequence analysis was performed using Microseq software as previously described (3,10).…”
mentioning
confidence: 99%
“…Primers (synthesized by TIB Molbiol, Adelphia, NJ) VAB1 (5=-TGGAGAGTTTGATC CTGGCTCAG-3=) and VAB2 (5=-GTATTACCGCGGCTGCTGG-3=) were used to generate a 543-bp amplicon of the 16S rRNA gene. PCR was performed as previously described (9), and sequencing reactions were performed using the ABI Prism BigDye Terminator cycle sequencing kit (Applied Biosystems, Foster City, CA, USA), with sequences generated using the Biosystems 3500 genetic analyzer, according to the manufacturer's instructions. The sequences were analyzed and compared to information in the BIBI and GenBank databases (10).…”
Section: Methodsmentioning
confidence: 99%