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1.
J Med Microbiol ; 57(Pt 8): 986-991, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18628500

ABSTRACT

Human granulocytic anaplasmosis (HGA) and Lyme borreliosis (LB) are tick-borne infectious diseases caused by Anaplasma phagocytophilum and Borrelia burgdorferi sensu lato species, respectively. In this study, p44/msp2 paralogues specific to A. phagocytophilum and 5S-23S rRNA gene-intergenic spacers specific to B. burgdorferi sensu lato species were detected by PCR in ticks collected in two regions, Tver (Kalinin) and Konakovo, of the Tver (Kalinin) Province located 150 km north-west of Moscow. The PCR amplicons obtained were further characterized by sequencing and RFLP analysis. In the total of 199 ticks collected, 8.8 % (7/80) and 33.8 % (27/80) of Ixodes ricinus, and 2.5 % (3/119) and 45.4 % (54/119) of Ixodes persulcatus, were found to be infected with A. phagocytophilum and B. burgdorferi sensu lato spp., respectively. Of those 199 ticks, 5 (2.5 %) were coinfected with A. phagocytophilum and Borrelia afzelii. Phylogenetic analysis revealed unique p44/msp2 paralogous genes in A. phagocytophilum-infected Russian ticks. The sequence similarities with those of A. phagocytophilum in the United States, UK and Japan ranged from 42 % to 80.4 %, and there were no sequences showing more than 90 % similarity with those sequences from the other countries. The results showed that the p44/msp2 sequence similarity groups may provide an index of adaptation of A. phagocytophilum strains to specific vector ticks or reservoir hosts in different countries and areas. These findings suggest that there is a public health threat from HGA and LB in Tver Province surrounding Moscow.


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Ehrlichiosis/complications , Ehrlichiosis/epidemiology , Ixodes/microbiology , Tick Infestations/complications , Tick Infestations/epidemiology , Anaplasma phagocytophilum/classification , Anaplasma phagocytophilum/genetics , Animals , DNA/genetics , DNA/isolation & purification , DNA, Bacterial/genetics , DNA, Bacterial/isolation & purification , Genotype , Humans , Ixodes/classification , Ixodes/genetics , Molecular Sequence Data , Phylogeny , Prevalence , Russia/epidemiology
2.
Int J Med Microbiol ; 294(7): 455-64, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15715174

ABSTRACT

The relationships between Borrelia species and the vector ticks, Ixodes persulcatus and Ixodes ricinus were examined in a molecular epidemiological study. We conducted a survey in the Moscow region which is a sympatric region for both species of tick. We examined 630 unfed I. ricinus and I. persulcatus, ticks collected from four different regions around Moscow within an area of 250 km2. Eighty-four ticks were culture positive (13.3%) and the prevalence rate varied in each region from 5.7% to 42.3%. No difference was found between the total prevalence rate for both species. Eight Borrelia afzelii-like variant isolates from I. ricinus and Clethrionomys glareolus were identified as B. afzelii by flagellin gene and 16S rDNA sequence analyses. Most isolates from I. ricinus were identified as Borrelia garinii type 20047 and B. afzelii. Two isolates were identified as Borrelia burgdorferi sensu stricto (s.s.) and Borrelia valaisiana, respectively, but no B. garinii type NT29 was found. In contrast, isolates from I. persulcatus were identified as both types 20047 and NT29 of B. garinii, and B. afzelii. No B. burgdorferi s.s. isolate was found among isolates from I. persulcatus.


Subject(s)
Arvicolinae/microbiology , Borrelia burgdorferi Group/classification , Ixodes/microbiology , Lyme Disease/veterinary , Rodent Diseases/microbiology , Animals , Arachnid Vectors/microbiology , Base Sequence , Borrelia burgdorferi Group/genetics , Borrelia burgdorferi Group/isolation & purification , DNA, Bacterial/analysis , DNA, Ribosomal/analysis , DNA, Ribosomal Spacer/analysis , Flagellin/genetics , Ixodes/classification , Lyme Disease/microbiology , Molecular Sequence Data , Moscow , Phylogeny , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Species Specificity
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