Literature DB >> 9391960

Duration of Borrelia burgdorferi infectivity in white-footed mice for the tick vector Ixodes scapularis under laboratory and field conditions in Ontario.

L R Lindsay1, I K Barker, G A Surgeoner, S A McEwen, G D Campbell.   

Abstract

The duration of Borrelia burgdorferi infectivity in white-footed mice (Peromyscus leucopus) experimentally inoculated or infested with infected Ixodes scapularis nymphs was evaluated. Infectivity was assessed by infesting these mice with unfed I. scapularis larvae at 7, 21, 35 and 49 days post-inoculation (DPI) or post-infestation (PI). At 7 DPI, B. burgdorferi was transmitted from 18 of 24 syringe-inoculated mice and all three tick-infected mice to I. scapularis larvae which fed upon them. However, at 21, 35 and 49 DPI, significantly fewer mice were infective. Borrelia burgdorferi was isolated from tissues of 14 of 22 syringe-inoculated mice about 56 DPI, and from all three tick-infected mice. However, the level of agreement between xenodiagnosis and bacterial culture was no greater than would be expected by chance alone. We also determined if B. burgdorferi infectivity of mice varied in relation to periods of tick feeding in the field. White-footed mice were trapped during April, July and August 1993 from two habitats on Long Point peninsula (Ontario, Canada), where B. burgdorferi is endemic. Mice from each habitat were infested with laboratory-reared I. scapularis larvae. Ticks from each mouse were subsequently examined by immunofluorescent assay for B. burgdorferi infection and mice were cultured for B. burgdorferi. None of 3577 I. scapularis larvae fed on 62 mice captured within the cottonwood dune habitat were infected with B. burgdorferi, although it was isolated from six of these mice. Within the maple forest habitat, 0/24, 8/21 (38%) and 1/21 (5%) mice transmitted B. burgdorferi to I. scapularis larvae during April, July and August, respectively. Most mice from the maple forest with B. burgdorferi-positive tissues (14/21) were collected during July, although the level of agreement between xenodiagnosis and tissue culture was poor. Because B. burgdorferi infectivity in mice appears to be of short duration, overwintered I. scapularis larvae and nymphs may have to feed upon infected hosts at the same time of year in order for a cycle of B. burgdorferi infection to be maintained on Long Point. Infected I. scapularis nymphs, rather than persistently infected vertebrate hosts, likely serve as the overwintering "reservoir" for B. burgdorferi on Long Point.

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Year:  1997        PMID: 9391960     DOI: 10.7589/0090-3558-33.4.766

Source DB:  PubMed          Journal:  J Wildl Dis        ISSN: 0090-3558            Impact factor:   1.535


  21 in total

Review 1.  The emergence of Lyme disease in Canada.

Authors:  Nicholas H Ogden; L Robbin Lindsay; Muhammad Morshed; Paul N Sockett; Harvey Artsob
Journal:  CMAJ       Date:  2009-06-09       Impact factor: 8.262

2.  Long-term survival of Borrelia burgdorferi lacking the hibernation promotion factor homolog in the unfed tick vector.

Authors:  Lisa Fazzino; Kit Tilly; Daniel P Dulebohn; Patricia A Rosa
Journal:  Infect Immun       Date:  2015-10-05       Impact factor: 3.441

3.  Analysis of Borrelia burgdorferi vlsE gene expression and recombination in the tick vector.

Authors:  K J Indest; J K Howell; M B Jacobs; D Scholl-Meeker; S J Norris; M T Philipp
Journal:  Infect Immun       Date:  2001-11       Impact factor: 3.441

4.  Experimental Demonstration of Reservoir Competence of the White-Footed Mouse, Peromyscus leucopus (Rodentia: Cricetidae), for the Lyme Disease Spirochete, Borrelia mayonii (Spirochaetales: Spirochaetaceae).

Authors:  Christina M Parise; Nicole E Breuner; Andrias Hojgaard; Lynn M Osikowicz; Adam J Replogle; Rebecca J Eisen; Lars Eisen
Journal:  J Med Entomol       Date:  2020-05-04       Impact factor: 2.278

5.  Fitness variation of Borrelia burgdorferi sensu stricto strains in mice.

Authors:  Klára Hanincová; Nicholas H Ogden; Maria Diuk-Wasser; Christopher J Pappas; Radha Iyer; Durland Fish; Ira Schwartz; Klaus Kurtenbach
Journal:  Appl Environ Microbiol       Date:  2007-11-02       Impact factor: 4.792

Review 6.  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

7.  Active and passive surveillance and phylogenetic analysis of Borrelia burgdorferi elucidate the process of Lyme disease risk emergence in Canada.

Authors:  Nicholas H Ogden; Catherine Bouchard; Klaus Kurtenbach; Gabriele Margos; L Robbin Lindsay; Louise Trudel; Soulyvane Nguon; François Milord
Journal:  Environ Health Perspect       Date:  2010-03-25       Impact factor: 9.031

8.  Identifying the reservoir hosts of the Lyme disease spirochete Borrelia burgdorferi in California: the role of the western gray squirrel (Sciurus griseus).

Authors:  Daniel J Salkeld; Sarah Leonhard; Yvette A Girard; Nina Hahn; Jeomhee Mun; Kerry A Padgett; Robert S Lane
Journal:  Am J Trop Med Hyg       Date:  2008-10       Impact factor: 2.345

9.  Serum antibodies to Borrelia burgdorferi, Anaplasma phagocytophilum, and Babesia microti in recaptured white-footed mice.

Authors:  Louis A Magnarelli; Scott C Williams; Steven J Norris; Erol Fikrig
Journal:  J Wildl Dis       Date:  2013-04       Impact factor: 1.535

Review 10.  Infection resistance and tolerance in Peromyscus spp., natural reservoirs of microbes that are virulent for humans.

Authors:  Alan G Barbour
Journal:  Semin Cell Dev Biol       Date:  2016-07-02       Impact factor: 7.727

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