2008
DOI: 10.1099/jmm.0.47663-0
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Presence of pathogenic Borrelia burgdorferi sensu lato in ticks and rodents in Zhejiang, south-east China

Abstract: A molecular epidemiological survey was conducted to investigate the presence of pathogenic Borrelia burgdorferi sensu lato (s.l.) species in the forest areas of Zhejiang province, south-east China. A total of 182 ticks of 6 species and 200 rodents of 8 species were collected and individually examined for the presence of B. burgdorferi s.l. DNA by nested PCR targeting the 5S-23S rRNA intergenic spacer. Forty-one ticks of four species, Haemaphysalis concinna, Haemaphysalis longicornis, Rhipicephalus microplus an… Show more

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Cited by 56 publications
(37 citation statements)
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References 24 publications
(23 reference statements)
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“…These data suggest that Apodemus agrarius may contribute to the maintenance of a natural cycle of Anaplasma phagocytophilum in China. Apodemus agrarius is distributed over an extensive area in mainland China and is also known to be a major reservoir host for B. burgdorferi sensu lato (Chu et al, 2008). Our results further demonstrate the role of Apodemus agrarius as a reservoir of Anaplasma phagocytophilum in the Gannan Tibetan Autonomous Prefecture in north-western China.…”
Section: Resultssupporting
confidence: 72%
“…These data suggest that Apodemus agrarius may contribute to the maintenance of a natural cycle of Anaplasma phagocytophilum in China. Apodemus agrarius is distributed over an extensive area in mainland China and is also known to be a major reservoir host for B. burgdorferi sensu lato (Chu et al, 2008). Our results further demonstrate the role of Apodemus agrarius as a reservoir of Anaplasma phagocytophilum in the Gannan Tibetan Autonomous Prefecture in north-western China.…”
Section: Resultssupporting
confidence: 72%
“…and Leptospira spp., serum samples were also tested using the SNAP® 4Dx test kit (IDEXX Laboratories, Westbrook, ME, U.S.A.), a qualitative in-clinic rapid ELISA test that specifically detects antibodies against the invariable domain IR6 of the variable surface antigen VlsE of B.burgdorferi, commonly known as the "C6 antigen". DNA was extracted from the blood samples containing EDTA using the QIAamp DNA Mini Kit (QIAGEN S.p.A., Milan, Italy) in accordance with the manufacturer's guidelines and then subjected to PCR assays previously described in veterinary literature: A. phagocytophilum DNA was detected using a nested-PCR protocol that amplifies a specific 928 bp fragment of the 16S-rRNA gene as described by Barlough et al [2]; a specific nested PCR protocol [12] amplifying a 226-266 bp fragment (depending on the strains) encompassing the 5S-23S intergenic spacer region of the rRNA was used for B. burddorferi DNA detection; in order to identify the presence of babesial parasite DNA, PCR was performed using the CRYPTO F [22] and RLB-R2 [8] that amplifies a fragment of the 18S-rRNA approximately 800 bp in size.…”
Section: Methodsmentioning
confidence: 99%
“…In conclusion, Borrelia strains obtained in Taiwan appear to be genetically similar to the B. valaisiana-related group found in eastern Asia and southwestern and southeastern China (Masuzawa et al, 2004;Chu et al, 2008aChu et al, , 2008bChao et al, 2010). We provide the first evidence of B. valaisiana-related genospecies in vector ticks and a rodent host, suggesting that B. valaisiana-related strains circulate between rodent reservoir hosts and tick vectors in Taiwan.…”
mentioning
confidence: 88%