 
          Journal of Mosquito Research 2015, Vol.5, No.14, 1-8
        
        
        
          6
        
        
          Table 5
        
        
          Plasmodium falciparum
        
        
          infection in
        
        
          Anopheles
        
        
          mosquitoes in Mwea and Ahero rice study sites
        
        
          Village
        
        
          An. species
        
        
          Indoor collected and Sporozoite positive (%) Outdoor collected and Sporozoite positive (%)
        
        
          Mbuinjeru
        
        
          Ndindiruku
        
        
          Murinduko
        
        
          An. arabiensis
        
        
          (n=200)
        
        
          An. arabiensis
        
        
          (n=200)
        
        
          An. arabiensis
        
        
          (n=200)
        
        
          0.00
        
        
          0.00
        
        
          3
        
        
          0.00
        
        
          0.00
        
        
          0.00
        
        
          Kamagaga
        
        
          Kobura
        
        
          Wagai
        
        
          An. arabiensis
        
        
          (n=52)
        
        
          An. funestus
        
        
          (n=148)
        
        
          An. arabiensis
        
        
          (n=180)
        
        
          An. funestus
        
        
          (n=20)
        
        
          An. arabiensis
        
        
          (n=18)
        
        
          An. funestus
        
        
          (n=182)
        
        
          0.00
        
        
          3
        
        
          0.00
        
        
          0.00
        
        
          0.00
        
        
          1
        
        
          0.00
        
        
          4
        
        
          0.00
        
        
          0.00
        
        
          0.00
        
        
          3
        
        
          et al., (1975) where
        
        
          An. gambiae
        
        
          s.l. was present in a
        
        
          higher proportion than members of
        
        
          An. funestus
        
        
          complex. This variation may be attributed to a gradual
        
        
          change in malaria vector composition since 1975 with
        
        
          unclear causes (Githeko et al., 2003).
        
        
          Anopheles
        
        
          rivulorum, An. leesoni
        
        
          and
        
        
          An. parensis,
        
        
          which are
        
        
          members of the
        
        
          An. funestus
        
        
          complex, had not been
        
        
          reported in Ahero in earlier studies, mostly likely due
        
        
          to the lack of molecular assays to differentiate
        
        
          between members of the species complex.
        
        
          In terms of resistance to insecticides, there was
        
        
          evidence of reduced susceptibility of
        
        
          An. arabiensis
        
        
          to
        
        
          insecticides in Mwea, especially to pyrethroids when
        
        
          compared to studies of Kamau and Vulule (2006).
        
        
          This indicates that resistance is spreading and is likely
        
        
          to increase further with the continued use of
        
        
          insecticide-based vector interventions.
        
        
          An. arabiensis
        
        
          sampled from Ahero were susceptible to the test
        
        
          insecticides except for fenitrothion which indicated
        
        
          reduced activity. Similarly, the use of permethrin and
        
        
          bendiocarb in Ahero should be monitored as reduced
        
        
          insecticidal activity has been demonstrated in Kamagaga
        
        
          and Kobura villages. Therefore, insecticides based
        
        
          malaria control programs can be effectively used in
        
        
          this ecosystem with close monitoring for resistance
        
        
          development or in integrated vector control programs.
        
        
          In Mwea, only mosquitoes collected from one of the
        
        
          three villages were positive for
        
        
          P. falciparum
        
        
          . In the
        
        
          said village, Murinduko, malaria parasite rates were
        
        
          much lower than those reported earlier, which were
        
        
          three-fold higher (Muturi et al., 2008). The lower
        
        
          malaria parasite rates in the current study are likely
        
        
          due to the use of bed nets as reported by Kamau and
        
        
          Vulule (2006) in which 93% of the 42 households they
        
        
          surveyed used bed nets and also due to high zoophilic
        
        
          behaviour of
        
        
          An. arabiensis
        
        
          (Muturi et al., 2009). In
        
        
          Ahero, only members of
        
        
          An. funestus
        
        
          complex were
        
        
          reported to be positive for
        
        
          P. falciparum
        
        
          . This
        
        
          indicates the potential of these members to transmit
        
        
          malaria parasites in this region.
        
        
          In Mwea study site, assessment on the feeding pattern
        
        
          indicated mixed feeding for a blood meal. These
        
        
          findings compare well with those published earlier by
        
        
          Muturi et al.
        
        
          ,
        
        
          (2008). This phenomenon can be utilised
        
        
          by individuals to keep animals around their homesteads
        
        
          while themselves sleep under a treated mosquito net.
        
        
          This is because; the vector in this site can still obtain a
        
        
          blood meal from animals, especially bovines, as the
        
        
          preferred host, and this will reduce malaria parasite
        
        
          transmission to humans.
        
        
          In Ahero, we found lower human blood indices for
        
        
          both
        
        
          An. arabiensis
        
        
          and
        
        
          An. funestus
        
        
          mosquitoes
        
        
          sampled compared to those reported by Githeko et al.
        
        
          ,
        
        
          (1994). The entire mosquito samples from Kamagaga
        
        
          showed animal preference. This should be further
        
        
          investigated to determine if it is due to human
        
        
          inaccessibility or intrinsic behaviour of the vectors. In
        
        
          Kobura and Wagai villages,
        
        
          An. funestus
        
        
          obtained
        
        
          their blood meal from both humans and animals thus a
        
        
          potential vector for malaria parasite while
        
        
          An.
        
        
          arabiensis
        
        
          from the same villages obtained their blood
        
        
          meal from none of the test hosts. This calls for
        
        
          investigations to determine the source of blood meal
        
        
          by
        
        
          An. arabiensis
        
        
          in these villages.
        
        
          Feeding on multiple hosts, including non-human hosts
        
        
          in
        
        
          Anopheles
        
        
          populations, has been suggested as one
        
        
          of the factors responsible for lower levels of malaria
        
        
          transmission despite higher vector densities (Lincithicum
        
        
          et al., 1999; Maria et al., 2005). However, because
        
        
          An.