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Multiplex PCR as a tool for validating plasmid content of Borrelia burgdorferi.

Bunikis, Ignas (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Bergström
Bonde, Mari (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Bergström
Kutschan-Bunikis, Sabrina (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Bergström
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Bergström, Sven (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Bergström
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 (creator_code:org_t)
Elsevier BV, 2011
2011
English.
In: Journal of Microbiological Methods. - : Elsevier BV. - 0167-7012 .- 1872-8359. ; 86:2, s. 243-7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Borrelia burgdorferi has an unusual genomic structure containing 21 plasmids. These plasmids carry genes that are essential for infectivity and survival of the spirochetes in vivo. Several plasmids are lost during cultivation in vitro, which might lead to a heterogeneous population after multiple passages and loss of infectivity in laboratory animals. Herein, we present a simple and inexpensive multiplex PCR method that detects the complete plasmid profile of B. burgdorferi B31 in just two PCR tubes.

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