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viruses can be grown in mammalian cells and the viruses produced can infect either
mosquitoes or mosquito cell cultures. Infection is sustained and Sindbis infection
was used to express an antisense form of a dengue protein in Ae. aegypti adults,
making the mosquitoes unable to transmit the viral disease ( Olson et  al. 1996,
Olson 2000 ). The Sindbis virus can be fed to mosquitoes, allowing expression of
transgenes in the midgut ( Olson et al. 2000 ). No arthropods that have been geneti-
cally modified using these viruses have been released into the environment.
14.5.4 Transfer of Wolbachia from Another Arthropod
Transfer of Wolbachia into a novel arthropod host can result in unstable or
stable infections ( Werren and Bartos 2001 ). For example, Kawai et  al. (2009)
introduced Wolbachia into planthoppers by injecting cultured Wolbachia into
nymphs. One line of Laodelphax striatellus lost its infection within several gen-
erations. In the second line, the infection was present for > 7 years, but the
frequency of infection declined from 80% to < 10% after 40-60 generations.
Heath et al. (1999) found that Wolbachia can be transmitted to a parasitic wasp
( Leptopilina boulardi ) from its host, Drosophila simulans , although the infection
was lost after three generations.
Some strains of Wolbachia reduce the rate of transmission of diseases by
mosquitoes, either by reducing lifespan or by inhibiting the replication of mos-
quito-borne pathogens such as filarial worms, dengue, or chikungunya viruses
in Aedes aegypti and of Plasmodium parasites in Ae. aegypti and An. gambiae
( Min and Benzer 1997 , Cook et al. 2008 , Kambris et al. 2009, McMeniman et al.
2009, Moreira et  al. 2009a,b, Bian et  al. 2010, Hussain et  al. 2011 ). One of the
most-advanced efforts to use Wolbachia to control disease transmission by the
mosquito Aedes aegypti has been studied by Scott O'Neill's group in Australia,
as described in Box 14.3 in Section 14.13.
Hancock et  al. (2011) discuss methods for introducing Wolbachia into wild
mosquito populations for control of mosquito-borne diseases. They modeled
different introduction scenarios involving the releases of infected mosquitoes,
included seasonal fluctuations in the size of populations, and concluded that
releases of mostly males allow the infection to spread after the introduction of a
few females. This strategy was expected to cause substantial reductions in trans-
mission without increasing risk of disease.
14.5.5 Site-Specific Modifications
The ability to introduce cloned genes into the germ line at a predictable chromo-
somal site is especially desirable, because it should reduce the likelihood of position
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