Abstract:
:A polymerase chain reaction (PCR) amplification of 16S rDNA was developed to identify spirochaetes recovered from cases of intestinal spirochaetosis in humans and pigs; these bacteria belong to a distinct genetic group of spirochaetes, with the proposed name 'Anguillina coli'. The PCR incorporated a universal eubacterial 16S rDNA sequencing primer (1492r), and a 21-base forward primer designed to include a nucleotide sequence specific for 'A. coli'. The PCR was used to correctly identify DNA extracted from 43 isolates of 'A. coli' from humans and pigs, whilst no product was produced from Escherichia coli, or from other intestinal spirochaetes, including 38 isolates of Serpulina spp., and one each of Treponema succinifaciens and Brachyspira aalborgi. The amplification provided a rapid and simple means of identifying DNA from isolates of 'A. coli', and could be used on boiled whole 'A. coli' cells, with a detection limit equivalent to 2.5 x 10(2) cells. The reaction was used to detect and identify these spirochaetes from selective agar plates inoculated with stool specimens from infected pigs.
journal_name
FEMS Microbiol Lettjournal_title
FEMS microbiology lettersauthors
Park NY,Chung CY,McLaren AJ,Atyeo RF,Hampson DJdoi
10.1111/j.1574-6968.1995.tb07362.xsubject
Has Abstractpub_date
1995-01-15 00:00:00pages
225-9issue
2-3eissn
0378-1097issn
1574-6968pii
0378-1097(94)00502-Ijournal_volume
125pub_type
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