We evaluated 2 strategies to manage Aedes albopictus: 1) motorized backpack applications and 2) source reduction (coupled with hand-applied applications of larvicide). Backpack applications used a water-dispersible granular formulation (VectoBac WDG) of Bacillus thuringiensis var. israelensis (Bti), whereas source reduction used granular formulations of the insect growth regulator methoprene (Altosid) combined with a monomolecular film surfactant (Agnique). Six subplots (total 8.02 ha) were selected for backpack applications, source reduction, and control groups. The experiments were blind with applications conducted randomly and independently. Efficacy was determined through placement of bioassay cups with larvae within experimental plots 1 day before treatment. Backpack applications resulted in 76% (+/- 8.2% SE) and source reduction resulted in 92% (+/- 4.1% SE) larval mortality. Backpack applications required 50 times less labor than source reduction (0.25 versus 0.005 ha/h). The cost of backpack applications, including labor, was $159.88/ha, compared with $659.65/ha for source reduction. Although overall efficacy was slightly lower, motorized backpack applications of Bti were more efficient and cost-effective than source reduction methods to control Ae. albopictus in urban settings at the community level.

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Based on the conserved heme-binding region and the charge pair consensus of insect cytochrome P450s, two novel full-length P450 cDNAs, CYP6BB1 and CYP6P10, were cloned from the salt marsh mosquito Aedes sollicitans (Walker). CYP6BB1 and CYP6P10 had open reading frames of 1,518 and 1,521 nucleotides encoding 506 and 507 amino acid residue proteins, respectively. Several alleles with amino acid substitutions were found both in CYP6BB1 and CYP6P10. The deduced proteins are typical microsomal P450s sharing signature sequences with other insect CYP6 P450s. Sequence analysis showed that both CYP6BB1 and CYP6P10 shared highest sequence identities with P450 CYP6P4, 56% and 65%, respectively. Phylogenetic analysis showed both CYP6BB1 and CYP6P10 were grouped into the clade containing several P450s from subfamily CYP6P. Real-time RT-PCR analysis showed CYP6BB1 but not CYP6P10 transcription in females was significantly increased 24 h after a blood meal. Neither CYP6BB1 nor CYP6P10 were life stage or gender specific. Protein expression experiments are needed to determine the functions of these proteins.

An NADPH-cytochrome P450 reductase (CPR) gene was identiÞed in Aedes sollicitans Walker (Diptera: Culicidae). The open reading frame is 2,040 bp long, encoding a 679-residue polypeptide. Amino acid sequence analysis indicates that the Ae. sollicitans CPR carries conserved ligand-binding domains and belongs to the same phylogenetic group as CPRs in other mosquitoes. The cDNA of the CPR gene was cloned, and the recombinant protein was expressed in Escherichia coli. Cytochrome c reductase activity was detected in the bacterial cytosolic and membrane fractions and in larval microsomes from two New Jersey Ae. sollicitans populations, indicating that the Ae. sollicitans CPR is enzymatically functional and closely related to that in other dipterans.