Abstract
Vectored immunocontraception is a novel technology and simple models are
described to help predict whether, and how, it might work. That is, given that
an effective immunocontraceptive agent can be produced, and given that it can
be inserted into a microparasitic or macroparasitic infective vector, would
the vector persist and reach a high prevalence in the host and, if so, would
it sterilize a sufficient proportion of the host breeding population to
significantly reduce its density? Both conditions are necessary for success.
The first question is an epidemiological one, relating solely to disseminating
systems and differing according to whether the vector itself is newly
introduced or pre-existing. If it is newly introduced, the assumption is that
it is present in some other geographical areas occupied by the same target
species, or is found in closely-related species. If the vector already exists
in the population, the issue is one of competition between the engineered and
wild-type vectors.
The second question is an ecological one, common to both non-disseminating and
disseminating systems. Whatever level of sterilization the immunocontraception
provides must translate into a significant reduction in population density,
having regard to the nature and extent of compensatory, density-dependence
mechanisms in the population.
These two questions, together with other more minor issues, are addressed in
turn with particular reference to models for immunocontraception of brushtail
possums (Trichosurus vulpecula)in New Zealand.
Subject
Developmental Biology,Endocrinology,Genetics,Molecular Biology,Animal Science and Zoology,Reproductive Medicine,Biotechnology
Cited by
29 articles.
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