Identification of genomic differences between Campylobacter jejuni subsp. jejuni and C. jejuni subsp. doylei at the nap locus leads to the development of a C. jejuni subspeciation multiplex PCR method

doi:10.1186/1471-2180-7-11

BMC Microbiology

Volume 7

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Miller WG
Parker CT
Heath S
Lastovica AJ

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Heath S
Lastovica AJ
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Methodology article

Identification of genomic differences between Campylobacter jejuni subsp. jejuni and C. jejuni subsp. doylei at the nap locus leads to the development of a C. jejuni subspeciation multiplex PCR method

William G Miller¹ , Craig T Parker¹ , Sekou Heath¹ and Albert J Lastovica²

¹Produce Safety and Microbiology Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Albany, CA 94710, USA

²Department of Biotechnology, University of the Western Cape, Bellville, South Africa

author email corresponding author email

BMC Microbiology 2007, 7:11doi:10.1186/1471-2180-7-11


Published:	28 February 2007

Additional files

Additional File 1:

Table S1. Campylobacter strains used to validate the nap multiplex PCR assay. The 321 Campylobacter strains used in the nap multiplex PCR validation are briefly described, including source/location of isolation and serotype, where available. Additionally, for each strain, the amplicon sizes (in bp, when present) for the nap and lpxA multiplex PCRs are provided.

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