Literature DB >> 12201601

Chemotactic migration of the Lyme disease spirochete (Borrelia burgdorferi) to salivary gland extracts of vector ticks.

Chien-Ming Shih1, Li-Lian Chao, Chia-Pan Yu.   

Abstract

The migration of Lyme disease spirochetes (Borrelia burgdorferi) toward salivary gland extracts (SGEs) of vector ticks was determined by a modified U-tube chemotaxis assay. Responses of cultured spirochetes to the SGEs were measured by dark-field microscopy at intervals after the initial inoculation. The average numbers of spirochetes that migrated were compared between U-tubes containing either SGEs or phosphate-buffered saline (PBS). Spirochetes showed increased migration in tubes containing SGE, and migration was approximately 10-20-fold higher than that for spirochetes observed in tubes containing PBS. In addition, the span of migration showed no significant difference relative to the origin of spirochete isolation. These results demonstrate that spirochete migration can be enhanced by SGEs from fed vector ticks. This mechanism may contribute to the novel transmission of Lyme disease spirochetes between cofeeding infected and uninfected ticks in nature.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12201601     DOI: 10.4269/ajtmh.2002.66.616

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  22 in total

1.  Rrp1, a cyclic-di-GMP-producing response regulator, is an important regulator of Borrelia burgdorferi core cellular functions.

Authors:  Elizabeth A Rogers; Darya Terekhova; Hong-Ming Zhang; Kelley M Hovis; Ira Schwartz; Richard T Marconi
Journal:  Mol Microbiol       Date:  2009-01-23       Impact factor: 3.501

2.  Identification of specific chemoattractants and genetic complementation of a Borrelia burgdorferi chemotaxis mutant: flow cytometry-based capillary tube chemotaxis assay.

Authors:  Richard G Bakker; Chunhao Li; Michael R Miller; Cynthia Cunningham; Nyles W Charon
Journal:  Appl Environ Microbiol       Date:  2006-12-15       Impact factor: 4.792

Review 3.  Spirochetal motility and chemotaxis in the natural enzootic cycle and development of Lyme disease.

Authors:  Md A Motaleb; Jun Liu; R Mark Wooten
Journal:  Curr Opin Microbiol       Date:  2015-11-02       Impact factor: 7.934

Review 4.  Evolutionary aspects of emerging Lyme disease in Canada.

Authors:  N H Ogden; E J Feil; P A Leighton; L R Lindsay; G Margos; S Mechai; P Michel; T J Moriarty
Journal:  Appl Environ Microbiol       Date:  2015-08-21       Impact factor: 4.792

5.  Borrelia burgdorferi chemotaxis toward tick protein Salp12 contributes to acquisition.

Authors:  Kristen E Murfin; Ruby Kleinbard; Merve Aydin; Samuel A Salazar; Erol Fikrig
Journal:  Ticks Tick Borne Dis       Date:  2019-06-08       Impact factor: 3.744

6.  Borrelia burgdorferi needs chemotaxis to establish infection in mammals and to accomplish its enzootic cycle.

Authors:  Ching Wooen Sze; Kai Zhang; Toru Kariu; Utpal Pal; Chunhao Li
Journal:  Infect Immun       Date:  2012-04-16       Impact factor: 3.441

Review 7.  The unique paradigm of spirochete motility and chemotaxis.

Authors:  Nyles W Charon; Andrew Cockburn; Chunhao Li; Jun Liu; Kelly A Miller; Michael R Miller; Md A Motaleb; Charles W Wolgemuth
Journal:  Annu Rev Microbiol       Date:  2012       Impact factor: 15.500

Review 8.  Update on persistent symptoms associated with Lyme disease.

Authors:  Carlos R Oliveira; Eugene D Shapiro
Journal:  Curr Opin Pediatr       Date:  2015-02       Impact factor: 2.856

9.  Molecular analysis of Ixodes granulatus, a possible vector tick for Borrelia burgdorferi sensu lato in Taiwan.

Authors:  Li-Lian Chao; Wen-Jer Wu; Chien-Ming Shih
Journal:  Exp Appl Acarol       Date:  2009-01-31       Impact factor: 2.132

Review 10.  Reviewing molecular adaptations of Lyme borreliosis spirochetes in the context of reproductive fitness in natural transmission cycles.

Authors:  Jean I Tsao
Journal:  Vet Res       Date:  2009-04-16       Impact factor: 3.683

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.