Author:
Brisson Dustin,Zhou Wei,Jutras Brandon L.,Casjens Sherwood,Stevenson Brian
Abstract
ABSTRACTLyme disease spirochetes possess complex genomes, consisting of a main chromosome and 20 or more smaller replicons. Among those small DNAs are the cp32 elements, a family of prophages that replicate as circular episomes. All complete cp32s contain anerplocus, which encodes surface-exposed proteins. Sequences were compared for all 193erpalleles carried by 22 different strains of Lyme disease-causing spirochete to investigate their natural diversity and evolutionary histories. These included multiple isolates from a focus where Lyme disease is endemic in the northeastern United States and isolates from across North America and Europe. Bacteria were derived from diseased humans and from vector ticks and included members of 5 differentBorreliagenospecies. Allerpoperon 5′-noncoding regions were found to be highly conserved, as were the initial 70 to 80 bp of allerpopen reading frames, traits indicative of a common evolutionary origin. However, the majority of the protein-coding regions are highly diverse, due to numerous intra- and intergenic recombination events. Mosterpalleles are chimeras derived from sequences of closely related and distantly relatederpsequences and from unknown origins. Since known functions of Erp surface proteins involve interactions with various host tissue components, this diversity may reflect both their multiple functions and the abilities of Lyme disease-causing spirochetes to successfully infect a wide variety of vertebrate host species.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
33 articles.
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