Autosomal interactions and mechanisms of pyrethroid resistance in house flies, Musca domestica

Five BC? lines and 16 house fly mass-cross homozygous lines were generated from crosses of the pyrethroid resistant ALHF (wild-type) and susceptible aabys (bearing recessive morphological markers on each of five autosomes) strains. Each of the resulting homozygous lines had different combinations of autosomes from the resistant ALHF strain. Levels of resistance to permethrin were measured for each line to determine the autosomal linkage, interaction and, possibly, regulation in pyrethroid resistance of house flies. Results indicated that factors on autosome 4 are not involved in the development of resistance in house flies, while factors on autosomes 1, 2, 3 and 5 play important roles in pyrethroid resistance. The sodium channel gene has been mapped on autosome 3 and multiple cytochrome P450 genes overexpressed in resistant ALHF house flies have been genetically mapped on autosome 5, suggesting that P450 mediated detoxification and sodium channel-mediated target site insensitivity located on autosomes 3 and 5, respectively, are major factors related to resistance development in house flies. However, neither the factors on autosome 3 or 5 alone, nor the factors from both autosomes 3 and 5 combined could confer high levels of resistance to pyrethroid. In addition, strong synergistic effects on resistance was obtained when autosomes 1 and 2 interact with autosome 3 and/or 5, suggesting that the trans factors on autosomes 1 and 2 may interact with factors on autosomes 3 and 5, therefore, playing regulatory roles in the development of sodium channel insensitivity- and P450 detoxification-mediated resistance.     

Potential for biocontrol of house flies,Musca domestica,using fungal biopesticides

Chemical control of house flies in poultry production facilities is becoming increasingly difficult due to insecticide resistance and regulatory constraints. Biopesticides based on entomopathogenic fungi could provide an alternative approach. Here we evaluated population control potential of two fungal pathogens, Beauveria bassiana and Metarhizium anisopliae. Cohorts of adult flies were established in large plastic boxes in the laboratory and were exposed to residues of oil-formulated fungal conidia sprayed on strips of plastic sheeting attached to the box walls. Exposure to the biopesticide barrier treatments caused 100% mortality in adult populations within 8–16 days, depending on the fungal species. In contrast, control flies survived until 96–110 days. Additionally, fungal infections caused 13–20% reduction in egg viability and >70% reduction in fecundity of flies prior to death. The combined lethal and pre-lethal impacts resulted in 21- to 26-fold reduction in basic reproductive rate in the fungus-exposed populations relative to controls. Based on these promising proof-of-principle results, further research is currently under way to determine the feasibility of developing a biopesticide product for operational use.     

Kinetic mechanism of cytochrome P450 reductase from the house fly (Musca domestica).

Recombinant house fly (Musca domestica) cytochrome P450 reductase has been purified by anion exchange and affinity chromatography. Steady-state kinetics of cytochrome c reductase activity revealed a random Bi-Bi mechanism with formation of a ternary P450 reductase-NADPH-electron acceptor complex as catalytic intermediate. NADP(H) binding is essential for fast hydride ion transfer to FAD, as well as for electron transfer from FMN to cytochrome c. Reduced cytochrome c had no effect on the enzyme activity, while NADP+ and 2'-AMP inhibited P450 reductase competitively with respect to NADPH and noncompetitively with respect to cytochrome c. The affinity of the P450 reductase to NADPH is 10 times higher than to NADP+ (Kd of 0.31 and 3.3 microM, respectively). Such an affinity change during catalysis could account for a +30 mV shift of the redox potential of FAD. Cys560 was substituted for Tyr by site-directed mutagenesis. This mutation decreased enzyme affinity to NADPH 35-fold by decreasing the bimolecular rate constant of nucleotide binding with no detectable effect on the kinetic mechanism. The affinity of the C560Y mutant enzyme to NADP+ decreased 9-fold compared to the wild-type enzyme, while the affinity to 2'-AMP was not significantly affected, suggesting that Cys560 is located in the nicotinamide binding site of the active, full-size enzyme in solution.     

Visual targets for capture and management of house flies, Musca domestica L.

House flies and stable flies were collected on a Florida dairy farm using a commercial Alsynite sticky cylinder trap that was either used alone or covered with white, blue, or black outdoor awning fabric. Collections of both species of flies were highest on exposed Alsynite (house flies, 506.2 flies/day; stable flies, 19.1) followed by blue fabric (house flies, 308.1 flies/day; stable flies 12.5). Responses of both species to white and black fabric were 70% lower than to either of the former materials. When blue fabric was used to cover 50% of the surface area of Alsynite cylinders, house fly responses were significantly higher (290.2 flies/day) than to blue fabric alone (165.2); stable fly responses to the bi-colored target were significantly higher (152.6) than to Alsynite alone (93.8). Comparison of fly counts in the blue-covered versus uncovered Alsynite with traps of a single material indicated that house fly attraction to blue fabric was enhanced by the presence of clear Alsynite, whereas stable fly attraction to Alsynite was enhanced by the presence of blue fabric. The presence of blue+Alsynite visual targets increased collections of house flies in pans of dry fly bait but not in baited jug traps. Visual targets treated with 1.2% bifenthrin controlled >50% and 90% of house flies in large cages by days two and four after placement, respectively.     

Characterization of NADPH-cytochrome P-450 reductase from house flies (Musca domestica,L.) susceptible and resistant to insecticides,and the blow fly (Phormia regina,meigen)

NADPH-cytochrome $\text{c}$ reductase was purified by affinity chromatographic techniques from microsomes prepared from the abdomens of insecticide-resistant (R) and -susceptible (S) house flies Musca domestica and of the black blow fly Phormia regina. Data are presented which describe (1) the ability of the purified enzymes to support an in vitro reconstitution of mono-oxygenase activity, (2) the changes in activity of these preparations observed in buffers of varying ionic strength, (3) comparative kinetic behaviour between microsomal and purified forms of the enzymes, (4) the immunochemical characteristics of these preparations, and (5) their amino acid composition. The reductases from the three sources were found to be very similar in all of these tests. Substrate binding constants were 5 μM for NADPH, 12 μM for cytochrome $\text{c}$, and the catalytic mechanism was interpreted as ordered Bi Bi. The inhibitory constant of the reductase from the resistant fly for 2′-AMP, an analogue of NADP⁺, was 187 μM; whereas no assciation of the inhibitor was observed below concentrations of 400 μM for the enzyme of either the susceptible house fly or the blow fly. However, the data are insufficient to suggest that the reductase is a significant factor in insecticide resistance. Compared to the same enzymes from rat and rabbit liver, the insect reductases show a different ionic strength optimum (0.14), have distinct antigenic determinants, and have different levels of acidic and basic amino acids in the membrane-binding peptide.     

拟除虫菊酯对家蝇Ca—ATPase和Ca—Mg—ATPase的抑制作用

通过对家蝇神经系统的Ca-ATPase、Ca-Mg-ATPase性质的研究,表明Ca-ATPase、Ca-Mg-AT-Pase反应的适宜pH值分别为7.0-8.5和6.5。适温皆为35-40℃;底物（ATP）最适浓度均为0.5mmol/L。比较测定了家蝇三个品系中两种ATPase的活性及拟除虫菊酯对该酶的抑制作用,实验证明,敏感与Del-R、2Cl-R品系间Ca-ATPase、Ca-Mg-ATPase活力无明显的差异。溴氰菊酯、氯菊酯可部分地抑制敏感品系家蝇Ca-ATPase活性,而对拟除虫菊酯抗性品系Ca-ATPase无抑制作用,从而证明,Del-R、2Cl-B品系Ca-ATPase对拟除虫菊酯的敏感性已明显降低,这可能能是击倒抗性机制之一。实验还表明,拟除虫菊酯对Ca-Mg-ATPase基本上无抑制作用,这说明在家蝇中,Ca-Mg-ATPase并不是拟除虫菊酯的一个靶标位点。     

Phylogenetic characterization of bacteria in the gut of house flies (Musca domestica L.)

House flies (Musca domestica L.) are cosmopolitan, ubiquitous, synanthropic insects that serve as mechanical or biological vectors for various microorganisms. To fully assess the role of house flies in the epidemiology of human diseases, it is essential to understand the diversity of microbiota harbored by natural fly populations. This study aimed to identify the diversity of house fly gut bacteria by both culture-dependent and culture-independent approaches. A total of 102 bacterial strains were isolated from the gut of 65 house flies collected from various public places including a garden, public park, garbage/dump area, public toilet, hospital, restaurant/canteen, mutton shop/market, and house/human habitation. Molecular phylogenetic analyses placed these isolates into 22 different genera. The majority of bacteria identified were known potential pathogens of the genera Klebsiella, Aeromonas, Shigella, Morganella, Providencia, and Staphylococcus. Culture-independent methods involved the construction of a 16S rRNA gene clone library, and sequence analyses supported culture recovery results. However, additional bacterial taxa not determined via culture recovery were revealed using this methodology and included members of the classes Alphaproteobacteria, Deltaproteobacteria, and the phylum Bacteroidetes. Here, we show that the house fly gut is an environmental reservoir for a vast number of bacterial species, which may have impacts on vector potential and pathogen transmission.     

Ecdysteroidostatin from the house fly,Musca domestica

Ovaries from house flies maintained on sucrose secrete large amounts of ecdysteroid when they are cultured with ovarian ecdysteroidogenic hormone, OEH. However, ovarian ecdysteroid secretion is reduced by incubation with both OEH and the ovarian ecdysteroidostatin (OES). A partially purified OES fraction from a semi-preparative reverse phase HPLC C₁₈ column caused a 98% inhibition of ovarian ecdysteroid secretion in vitro at a concentration of 0.8 equivalents per μl. Ovaries can be activated to produce ecdysteroid in vivo by feeding diet containing protein to flies maintained on sucrose. Ecdysteroid secretion was inhibited when the in vivo stimulated ovaries were cultured with OES. This suggests that OES does not interfere with the OEH activation mechanism, but blocks ovarian ecdysteroid synthesis or release. Furthermore, OES inhibition is reversible and ecdysteroid secretion resumes when OES is removed. Musca OES could explain the decrease in ecdysteroid levels found in flies after mid-vitellogenesis. Both adult male and female abdomens contain OES, but OES was not transferred to females during mating. Evidence is presented that OES is not a trypsin modulating oostatic factor. Arch. Insect Biochem. Physiol. 38:166–176, 1998. © 1998 Wiley-Liss, Inc.     

Methods for monitoring outdoor populations of house flies, Musca domestica L. (Diptera: Muscidae).

Relative collections of house flies were compared on two Florida dairy farms using several monitoring methods: sticky cylinders, baited jug traps (Farnam Terminator and Victor Fly Magnet), and bait strips (Wellmark QuikStrike). Bait strips were placed over collecting pans and under 61 cm square plywood roofs to protect the toxicant from sunlight ("sheltered QuikStrike traps"). Sticky cylinders collected the fewest flies (515-679 flies/trap/day) and sheltered QuikStrike traps the most (5,659-8,814 flies/trap/day). The sheltered QuikStrike traps are promising tools for disease surveillance programs. The two baited jugs collected a similar and intermediate number of flies, with collections highest during the first 2 days after placement (2,920-5,462 flies/trap/day). Jug trap collections were low after 4 days of use in the field, apparently due to deterioration in the attractiveness of the bait over time. Jug traps collected mostly females, whereas sticky cylinders and sheltered QuikStrike traps collected mostly males. Exposure of jug trap bait (Farnam) to fly cadavers for 3 days did not increase attractiveness of the bait. Combinations of the Farnam and Victor attractants were more attractive than either attractant alone and 25-43% more attractive than expected based on the sum of collections in the single-attractant jug traps. A 25% solution of farm-grade blackstrap molasses was as effective as either of the two proprietary baits tested, offering a low-cost alternative for fly population monitoring.     

Multiple Cytochrome P450 genes: their constitutive overexpression and permethrin induction in insecticide resistant mosquitoes, Culex quinquefasciatus

Four cytochrome P450 cDNAs, CYP6AA7, CYP9J40, CYP9J34, and CYP9M10, were isolated from mosquitoes, Culex quinquefasciatus. The P450 gene expression and induction by permethrin were compared for three different mosquito populations bearing different resistance phenotypes, ranging from susceptible (S-Lab), through intermediate (HAmCq(G0), the field parental population) to highly resistant (HAmCq(G8), the 8(th) generation of permethrin selected offspring of HAmCq(G0)). A strong correlation was found for P450 gene expression with the levels of resistance and following permethrin selection at the larval stage of mosquitoes, with the highest expression levels identified in HAmCq(G8), suggesting the importance of CYP6AA7, CYP9J40, CYP9J34, and CYP9M10 in the permethrin resistance of larva mosquitoes. Only CYP6AA7 showed a significant overexpression in HAmCq(G8) adult mosquitoes. Other P450 genes had similar expression levels among the mosquito populations tested, suggesting different P450 genes may be involved in the response to insecticide pressure in different developmental stages. The expression of CYP6AA7, CYP9J34, and CYP9M10 was further induced by permethrin in resistant mosquitoes. Taken together, these results indicate that multiple P450 genes are up-regulated in insecticide resistant mosquitoes through both constitutive overexpression and induction mechanisms, thus increasing the overall expression levels of P450 genes.