Affiliation:
1. Vector Ecology Laboratory, Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, Connecticut
2. Parasitology Institute
3. Institute of Zoology, Slovak Academy of Science, 04001 Košice, Slovak Republic
Abstract
ABSTRACT
In Europe the
Borrelia burgdorferi
sensu lato complex is represented by five distinct genospecies:
Borrelia burgdorferi
sensu stricto,
Borrelia afzelii
,
Borrelia garinii
,
Borrelia valaisiana
, and
Borrelia lusitaniae.
These taxonomic entities are known to differ in their specific associations with vertebrate hosts and to provoke distinct clinical manifestations in human patients. However, exceptions to these rules have often been observed, indicating that strains belonging to a single genospecies may be more heterogeneous than expected. It is, therefore, important to develop alternative identification tools which are able to distinguish
Borrelia
strains not only at the specific level but also at the intraspecific level. DNA from a sample of 370
Ixodes ricinus
ticks collected in the Czech Republic was analyzed by PCR for the presence of a ∼230-bp fragment of the
rrfA-rrlB
intergenic spacer of
Borrelia
spp. A total of 20.5% of the ticks were found to be positive. The infecting genospecies were identified by analyzing the amplified products by the restriction fragment length polymorphism (RFLP) method with restriction enzyme
Mse
I and by single-strand conformation polymorphism (SSCP) analysis. The two methods were compared, and PCR-SSCP analysis appeared to be a valuable tool for rapid identification of spirochetes at the intraspecific level, particularly when large samples are examined. Furthermore, by using PCR-SSCP analysis we identified a previously unknown
Borrelia
genotype, genotype I-77, which would have gone unnoticed if RFLP analysis alone had been used.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology