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. 2012;6(11):e1797.
doi: 10.1371/journal.pntd.0001797. Epub 2012 Nov 15.

Open release of male mosquitoes infected with a wolbachia biopesticide: field performance and infection containment

Affiliations

Open release of male mosquitoes infected with a wolbachia biopesticide: field performance and infection containment

Linda O'Connor et al. PLoS Negl Trop Dis. 2012.

Abstract

Background: Lymphatic filariasis (LF) is a globally significant disease, with 1.3 billion persons in 83 countries at risk. A coordinated effort of administering annual macrofilaricidal prophylactics to the entire at-risk population has succeeded in impacting and eliminating LF transmission in multiple regions. However, some areas in the South Pacific are predicted to persist as transmission sites, due in part to the biology of the mosquito vector, which has led to a call for additional tools to augment drug treatments. Autocidal strategies against mosquitoes are resurging in the effort against invasive mosquitoes and vector borne disease, with examples that include field trials of genetically modified mosquitoes and Wolbachia population replacement. However, critical questions must be addressed in anticipation of full field trials, including assessments of field competitiveness of transfected males and the risk of unintended population replacement.

Methodology/principal findings: We report the outcome of field experiments testing a strategy that employs Wolbachia as a biopesticide. The strategy is based upon Wolbachia-induced conditional sterility, known as cytoplasmic incompatibility, and the repeated release of incompatible males to suppress a population. A criticism of the Wolbachia biopesticide approach is that unintended female release or horizontal Wolbachia transmission can result in population replacement instead of suppression. We present the outcome of laboratory and field experiments assessing the competitiveness of transfected males and their ability to transmit Wolbachia via horizontal transmission.

Conclusions/significance: The results demonstrate that Wolbachia-transfected Aedes polynesiensis males are competitive under field conditions during a thirty-week open release period, as indicated by mark, release, recapture and brood-hatch failure among females at the release site. Experiments demonstrate the males to be 'dead end hosts' for Wolbachia and that methods were adequate to prevent population replacement at the field site. The findings encourage the continued development and extension of a Wolbachia autocidal approach to additional medically important mosquito species.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. A. polynesiensis population dynamics.
Collection data is shown for the A) Tiano (ANO), B) Horea (HOR) and C) Toamaro (TOA) study sites, as measured by BG trap collections of adult females. Lines show moving averages across four collection periods. Time is shown as the relative week number, with ‘Week 0’ as the start of releases. The grey shaded box indicates the release period on TOA, with CP releases ending on Week 30.
Figure 2
Figure 2. Box plots of delta values used in the BACIPS statistical analysis.
Each of the three possible combinations of site pairs is shown. For each pair, delta values are of collections within the thirty-week period immediately prior to the start of CP male release (‘Before’) and the thirty-week period during CP male release (‘During’). Delta values are calculated as the difference between population numbers at the sites, with population number indicated as ln(Female Number +1). Sites are the release site Toamaro (TOA), which received releases of CP males, and the two no-release sites Tiano (ANO) and Horea (HOR), which did not receive CP male releases. Asterisks indicate a significant difference in comparisons of the ‘Before’ and ‘During’ release periods (p<0.0001).

Comment in

  • Male mosquitoes make waves in paradise.
    Benedict MQ. Benedict MQ. Pathog Glob Health. 2013 Jun;107(4):161. doi: 10.1179/2047772413Z.000000000134. Pathog Glob Health. 2013. PMID: 23816506 Free PMC article. No abstract available.

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