BACKGROUND: Controlled blood-feeding is essential for
maintaining laboratory colonies of disease-transmitting
mosquitoes and investigating pathogen transmission. We evaluated
a low-cost artificial feeding (AF) method, as an alternative to
direct human feeding (DHF), commonly used in mosquito
laboratories. METHODS: We applied thinly-stretched pieces of
polytetrafluoroethylene (PTFE) membranes cut from locally
available seal tape (i.e. plumbers tape, commonly used for
sealing pipe threads in gasworks or waterworks). Approximately 4
ml of bovine blood was placed on the bottom surfaces of inverted
Styrofoam cups and then the PTFE membranes were thinly stretched
over the surfaces. The cups were filled with boiled water to
keep the blood warm (~37 degrees C), and held over netting cages
containing 3-4 day-old inseminated adults of female Aedes
aegypti, Anopheles gambiae (s.s.) or Anopheles arabiensis.
Blood-feeding success, fecundity and survival of mosquitoes
maintained by this system were compared against DHF. RESULTS:
Aedes aegypti achieved 100% feeding success on both AF and DHF,
and also similar fecundity rates (13.1 +/- 1.7 and 12.8 +/- 1.0
eggs/mosquito respectively; P > 0.05). An. arabiensis had
slightly lower feeding success on AF (85.83 +/- 16.28%) than DHF
(98.83 +/- 2.29%) though these were not statistically different
(P > 0.05), and also comparable fecundity between AF (8.82
+/- 7.02) and DHF (8.02 +/- 5.81). Similarly, for An. gambiae
(s.s.), we observed a marginal difference in feeding success
between AF (86.00 +/- 10.86%) and DHF (98.92 +/- 2.65%), but
similar fecundity by either method. Compared to DHF, mosquitoes
fed using AF survived a similar number of days [Hazard Ratios
(HR) for Ae. aegypti = 0.99 (0.75-1.34), P > 0.05; An.
arabiensis = 0.96 (0.75-1.22), P > 0.05; and An. gambiae
(s.s.) = 1.03 (0.79-1.35), P > 0.05]. CONCLUSIONS: Mosquitoes
fed via this simple AF method had similar feeding success,
fecundity and longevity. The method could potentially be used
for laboratory colonization of mosquitoes, where DHF is
unfeasible. If improved (e.g. minimizing temperature
fluctuations), the approach could possibly also support studies
where vectors are artificially infected with blood-borne
pathogens