The effect of relative humidity (43%, 75%, 86% and > 98%) Aedes aegypti is the principal vector of dengue viruses in tropical and subtropical regions throughout the world. This closely human-associated mosquito uses a great variety of large to small sized breeding sites and occurs year round even in semi-arid regions. Females oviposit mainly above the waterline on damp surfaces, and unhatched larvae have to hold out until immersion of eggs in water will permit eclosion and further development. Populations decline during the dryer and colder season but mosquitoes never disappear completely using subterranean and other breeding sites resulting from watering behavior by local residents (Varejão et al. 2005, Maciel-de-Freitas et al. 2007). Moreover, eggs out of water resist prolonged desiccation during distinct dry seasons, and the surviving larvae contribute to a reestablishment of vector populations at the beginning of the rainy season, thus increasing the risk of dengue epidemics (Sota & Mogi 1992, Silva & Silva 1999. Inside eggs, diapausing larvae are exposed to predation and infection by pathogens, particularly fungi that may invade eggs actively through the egg shell or affect larvae with toxic metabolites produced on the egg surface (Russell et al. 2001, Luz et al. 2007). Moisture is a limiting factor for both egg survival and fungal activity but there is still little information about the impact of relative humidity (RH) on the survival of larvae inside eggs or a possible effect of entomopathogenic fungi.We report here on the impact of RH on egg survival and an ovicidal activity of M. anisopliae under laboratory conditions. This fungal species is pathogenic to larvae and adults of A. aegypti (Scholte et al. 2004, Silva et al. 2004, and recent studies indicated that it is also effective against eggs of this vector (Luz et al. 2007). The fungal isolate tested here, IP 46, originated from a soil sample collected in 2001 in the Cerrado of Central Brazil and was stored at the IPTSP, UFG, Goiânia, Brazil. Conidia were collected from 15 days old sporulating cultures grown in Petri dishes (100 x 20 mm) at 25°C and 12 h photophase on potato-dextrose-agar; hyphal bodies were produced in liquid Sabouraud-dextrose-yeast extract medium (Goettel & Inglis 1997) for five days on a rotary shaker at 25°C and 240 rpm.The population of A. aegypti originated from virusfree larvae, collected in 1991 in Goiânia, Brazil. Mosquitoes were reared under laboratory conditions as described by Silva et al. (1998). Eggs were prepared using the method related by Luz et al. (2007), and then topically treated with 50 µl water-suspended conidia or hyphal bodies, at 5x10 6 propagules/cm 2 or with water only for the controls and incubated for up to six months at 25°C and 43%, 75%, 86% or > 98% RH regulated in the test chambers with saturated solutions of K 2 CO 3 , NaCl, KCl and K 2 SO 4 , respectively (Winston & Bates 1960). Each month, fungal development on eggs and egg viability were tested. Eggs were submerged in water and quantitative ecl...