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The contaminated mosquitoes or control mosquitoes were maintained on a 10% glucose diet in plastic containers at 25 °C.
All mosquitoes, including larval and adult mosquitoes, were maintained in humidified incubators at 25 ± 1 °C on a 12-h light: dark photocycle.
Mice and mosquitoes were maintained as previously described [42], [43].
Mosquitoes were maintained on glucose water soaked sterile cotton balls and changed daily, until dissection.
SF mosquitoes were maintained (glucose pad) under appropriate conditions and were treated as controls.
Mosquitoes were maintained on sugar cubes and distilled water containing 0.05% PABA without an available oviposition site.
Similar(6)
This is consistent with field and laboratory studies that report failure to obtain virus from salivary glands when mosquitoes are maintained at 20°C and failure for larvae to reach adult stage below 14°C.
On the contrary, a longer 2 h light pulse resulted in an immediate inhibition (~50%) of the blood feeding propensity along with a phase-advance (by ~3 4 h) in mosquitoes that were maintained at both the LD and DD conditions (for 48 h), compared to the non-light pulse stimulated mosquitoes.
The mosquito cells were maintained as described in [61].
Anopheles stephensi mosquito colonies were maintained under standard insectary conditions of 27 ± 1°C, 70% humidity and 12 12 light:dark cycle.
C6/36 Aedes albopictus mosquito cells were maintained in RPMI medium supplemented with 10% FBS, and BHK21 cells were maintained in DMEM containing 5% FBS.
More suggestions(15)
mosquitoes were tested
mosquitoes were transferred
mosquitoes were offered
mosquitoes were reared
mosquitoes were counted
mosquitoes were released
mosquitoes were embedded
mosquitoes were found
mosquitoes were held
mosquitoes were blown
mosquitoes were discarded
mosquitoes were examined
mosquitoes were controlled
mosquitoes were killed
mosquitoes were used
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