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Field evaluation of a novel oral reservoir-targeted vaccine against Borrelia burgdorferi utilizing an inactivated whole-cell bacterial antigen expression vehicle
Blacklegged ticks ( Ixodes scapularis ) are the principal vector for Borrelia burgdorferi, among other infectious agents, in the northeastern, mid-Atlantic, and upper midwestern USA. White-footed mice ( Peromyscus leucopus ) are the primary and most competent reservoir host of B. burgdorferi in the...
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Published in: | Experimental & applied acarology 2020-02, Vol.80 (2), p.257-268 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Blacklegged ticks (
Ixodes scapularis
) are the principal vector for
Borrelia burgdorferi,
among other infectious agents, in the northeastern, mid-Atlantic, and upper midwestern USA. White-footed mice (
Peromyscus leucopus
) are the primary and most competent reservoir host of
B. burgdorferi
in the Northeast. Live reservoir-targeted vaccines (RTVs) to limit enzootic transmission of
B. burgdorferi
were previously developed and successfully evaluated in laboratory and controlled field trials. A novel, inactivated RTV was developed to minimize regulatory and market challenges facing previous RTVs based on live bacterial or viral vehicles. Thirty-two residential properties in Redding, Connecticut, participated in a field trial of an orally delivered, inactivated RTV efficacy study (2015–2016). During the two-year vaccination period, a significant decrease in the percentage of
B. burgdorferi-
infected
I. scapularis
larvae parasitizing
P. leucopus
was observed, as was a significant reduction in the percentage of infected
P. leucopus
on RTV-treated properties when compared to control properties. This novel inactivated RTV was effective in reducing numbers of
B. burgdorferi
-infected
I. scapularis
and
B. burgdorferi
-infected
P. leucopus
on properties where it was distributed. |
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ISSN: | 0168-8162 1572-9702 |
DOI: | 10.1007/s10493-019-00458-1 |