2007
DOI: 10.1111/j.1348-0421.2007.tb04015.x
|View full text |Cite
|
Sign up to set email alerts
|

First Molecular Detection of Borrelia afzelii in Clinical Samples in Korea

Abstract: Borrelia afzelii nucleic acids were detected in the sera of febrile disease patients by a nested PCR that targeted the rrf (5S)‐rrl (23S) spacer of B. burgdorferi sensu lato. The B. afzelii‐specific DNA fragment was detected in 8 out of 283 sera which were proven to have immunoglobulin G or M antibodies against B. burgdorferi antigens through IFA. The results were further confirmed through restriction fragment length polymorphism and sequencing analysis of the DNA fragments. The results indicated for the first… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
19
1

Year Published

2009
2009
2021
2021

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 17 publications
(20 citation statements)
references
References 32 publications
0
19
1
Order By: Relevance
“…The purified PCR products were confirmed by direct sequencing using the CEQ 2000 Dye Terminator Cycle Sequencing method with the Quick Start kit (Beckman Coulter, Inc., Fullerton, CA, U.S.A.) and the CEQ 2000 DNA analysis system (Beckman Coulter, Inc.) according to the manufacturer's instructions. PCR targeting borrelia rrf(5S)-rrl(23S) intergenic spacer gene and RFLP were then performed as previously described [3,23]. The reaction mixture contained 1.5 µl of DNA (approximately 100 ng) sample as template in a total reaction volume of 30 µl.…”
Section: ©2013mentioning
confidence: 99%
“…The purified PCR products were confirmed by direct sequencing using the CEQ 2000 Dye Terminator Cycle Sequencing method with the Quick Start kit (Beckman Coulter, Inc., Fullerton, CA, U.S.A.) and the CEQ 2000 DNA analysis system (Beckman Coulter, Inc.) according to the manufacturer's instructions. PCR targeting borrelia rrf(5S)-rrl(23S) intergenic spacer gene and RFLP were then performed as previously described [3,23]. The reaction mixture contained 1.5 µl of DNA (approximately 100 ng) sample as template in a total reaction volume of 30 µl.…”
Section: ©2013mentioning
confidence: 99%
“…Since then, the number of cases has gradually increased; 23 cases have been reported in 2019, including 11 imported cases [11]. To date, various molecular and serological studies have identified the pathogenic cause of LD in ticks and animals including wild rodents, migratory birds, water deer, and dogs [12][13][14][15][16][17][18][19][20]. Borrelia afzelii and B. garinii were first identified in I. persulcatus and wild rodents, respectively, from the Gangwon province.…”
Section: Introductionmentioning
confidence: 99%
“…Subsequent technological advances enabled the development of diagnostic molecular tests, which were shown to be more sensitive than cultures . Molecular epidemiology of human isolates of Lyme Borrelia (LB) has clarified the global prevalence of the B. burgdorferi sensu lato complex, which now also includes Europe ( B. burgdorferi sensu stricto (ss), Borrelia afzelii and Borrelia garinii ), eastern Russia ( B. burgdorferi ss, B. afzelii and B. garinii ), China ( B. afzelii and B. garinii ), Japan ( B. afzelii and B. garinii ), South Korea ( B. afzelii ) and Taiwan ( B. burgdorferi ss, B. afzelii and B. garinii ) and extends into South America ( B. burgdorferi ss, Borrelia chilensis and B. garinii ) …”
Section: Diagnostics/pathogenesismentioning
confidence: 99%