Effects of forest fragmentation on dipterofauna (Calliphoridae) at the Reserva Biológica do Tinguá, Nova Iguaçu, RJ.

Samples were collected every month in three different sites of the Reserva Biológica do Tinguá, Brazil: site A was located on the border of the forest and sites B and C were located 1,000 and 500 m, respectively, towards the forest interior. The objective was to determine edge effects on a fragment of the Atlantic Forest. The greatest species richness was observed in sites A and B (23 species), compared with site C (16 species). Site A showed the greatest abundance and constancy, independent of the degree of synanthropy. Asynanthropic species were more abundant and constant in sites B and C. Site B showed the greatest diversity; and sites A and B showed the greatest similarity of populations. There was no significant correlation between Calliphoridae richness and canopy openness except in site C. Richness and abundance were positively correlated with subwood density, except for richness in site B.

The main proteinases in Dermatobia hominis second and third instars larvae are serine-proteinases.

We performed a combination of proteinase assay, either in solution or immobilized in sodium dodecyl sulfate-polyacrylamide gel copolymerized with gelatin, to detect and quantify proteinases of Dermatobia hominis second (L2) and third (L3) instar larvae. In the quantitative assay, we examined proteinase activity by hydrolysis of a panel of peptide bonds specific for the main proteinase classes. We verified that the pGlu-Phe-Leu p-nitroanilide substrate was hydrolyzed by crude extracts of L2 (3.0+/-0.2 nmol h(-1)mg of protein(-1)) and L3 (7.7+/-0.1 nmol h(-1)mg of protein(-1)) and that both activities were partially inhibited by trans-epoxysuccinyl-l-leucylamido-(4-guanidino)butane, 15% and 3%, respectively. Also, we demonstrated that the Nalpha-p-Tosyl-l-Arg methyl ester substrate was hydrolyzed by crude extracts of L2 (117+/-24 nmol h(-1)mg of protein(-1)) and L3 (111+/-10 nmol h(-1)mg of protein(-1)), suggesting a predominance of esterase activity in the crude larval preparation. Interestingly, the specific activity of serine-proteinases was totally inhibited by phenylmethylsulphonyl fluoride in the L3 crude extract, while only 10% of this enzyme class activity was inhibited in the L2 crude extract. The results of the qualitative assays with substrate gels suggested that L2 and L3 larvae express serine-proteinases with similar (13 and 22 kDa) and distinct (50 kDa in L2 and 30 kDa in L3) relative molecular masses. These findings contribute to the biochemical characterization of D. hominis L2 and L3 larvae.

Protective efficacy of doramectin and ivermectin against Cochliomyia hominivorax.

Two studies were conducted in Brazil using induced infestations of the New World screwworm, Cochliomyia hominivorax, to investigate: a) the comparative prophylactic efficacy of doramectin and ivermectin at their recommended use levels (200 micrograms kg-1 s.c.), and b) the duration of protection of a single injection of doramectin. In the comparative efficacy study, two groups of six animals each were treated with ivermectin or doramectin. Two hours after treatment, four incisions were made. Each incision was infested with 30 first instar C. hominivorax larvae and their status evaluated daily for 7 days post-treatment (p.t.). Doramectin treatment was 100% effective in prevention of C. hominivorax infestations whereas ivermectin efficacy was incomplete. First instar larvae were eliminated in doramectin-treated calves by 48 h p.t., while in the ivermectin group, C. hominivorax developed in over 29% of the incisions. Healing began in wounds of doramectin-treated animals at 24 h p.t. and was in progress in 100% of all wounds at 2 days p.t., while 50% of ivermectin-treated calves showed incisions with active lesions. In the duration of protection study, 24 calves were allocated to six groups (T1-T6) of four animals each. Three groups (T1, T3 and T5) were treated with saline and three groups (T2, T4 and T6) with doramectin. Animals were infested as described previously according to the following schedule: T1 and T2 at day 14, T3 and T4 at day 21, and T5 and T6 at day 28 p.t. Incisions were evaluated daily for 8 days post-infestation. Screwworm infestations and viable third-instar larvae developed of all incisions of saline-treated calves, while doramectin was 100% effective preventing development of C. hominivorax for 21 days p.t. and showed partial activity at 28 days p.t.

Population genetics and gene variation in screwworms (Diptera: Calliphoridae) from Brazil.

Allozyme variation in New World screwworm, Cochliomyia hominivorax (Coquerel), populations from Brazil was examined. Variability was observed in 8 of 13 enzyme loci and the frequency of the most common allele was < 0.95 for seven loci. Observed and expected heterozygosities were 0.159 and 0.165, respectively. Comparisons of the Brazilian populations with previously studied populations from Costa Rica resulted in Nei's genetic distances of between 0.000 and 0.006, with the greatest distance being between populations within Brazil. Comparisons with Mexican populations using only three loci resulted in genetic distances < or = 0.031. Goodness-of-fit statistics for Hardy-Weinberg equilibrium and Wright's F statistics indicated small deviations from expected equilibrium genotype frequencies and low levels of differentiation between populations within Brazil. Differentiation among screwworm populations from Brazil, Costa Rica, and Mexico was minimal.

Therapeutic and persistent efficacy of doramectin against Dermatobia hominis in cattle.

One therapeutic and one persistent efficacy study were conducted in Brazil to evaluate doramectin at a dose rate of 200 micrograms/kg-1 against induced infestations of the tropical warble-fly, Dermatobia hominis. Doramectin was very effective in both the treatment of established infestations and also in the prevention of damage caused by the parasite. In the therapeutic trial, 12 calves were infested along the dorsal line with 25 first instar larvae of recent field isolates of D. hominis but in one calf nodules did not develop. Twenty-four days later animals were allocated to two groups on the basis of the number of parasite nodules present. Six calves were treated with doramectin, and five received saline solution. Animals were examined daily for 11 days post-treatment and the number of nodules mapped and recorded. Larvae that completed development were collected and incubated to evaluate viability. In the persistent efficacy study, 24 calves were allocated to six groups (T1-T6) of four animals each. On the day of treatment, three groups (T1, T3 and T5) were treated with saline and three groups (T2, T4 and T6) with doramectin. At 21 days, 28 days and 35 days post-treatment, 25 first instar D. hominis larvae were seeded along the dorsal line of each calf of T1 and T2, T3 and T4, and T5 and T6, respectively. Animals were examined daily for 18 days and the number of nodules mapped and recorded 6, 12 and 18 days post-infestation.(ABSTRACT TRUNCATED AT 250 WORDS)

Prophylactic and persistent efficacy of doramectin against Cochliomyia hominivorax in cattle.

Two prophylactic studies and one persistent efficacy study were conducted in Brazil to evaluate one injection of doramectin at a dose rate of 200 micrograms kg-1 against induced infestations of the New World screwworm, Cochliomyia hominivorax. In each prophylactic study, 12 calves were allocated to two groups of six animals. Six calves were treated with doramectin and six with saline. Two hours after treatment, animals were anesthetized and received two incisions, one in the shoulder and one in the rump. Each incision was then infested with 50 first instar larvae. In the persistent efficacy study, 24 calves were allocated to six groups (T1-T6) of four animals each. On the day of treatment, three groups (T1, T3 and T5) were treated with saline and three groups (T2, T4 and T6) with doramectin. All animals were anesthetized and received four incisions, one in the shoulder and one in the rump of each side. Each incision was then infested with 30 first instar larvae of C. hominivorax with the following schedule: T1 and T2 at Day 3, T3 and T4 at Day 7, and T5 and T6 at Day 14 post-treatment. Calves were observed daily and incisions evaluated for 8 days post-infection. Larvae that completed development and exited the wounds were collected and incubated to evaluate viability. In all experiments, doramectin was 100% efficacious in preventing screwworm infestation caused by field isolates of C. hominivorax. First instar larvae were eliminated from the incisions of doramectin-treated calves between 24 and 48 h post-treatment, and no third instar were recovered at any time. As a consequence, healing started at 24 h and was completed at 96-120 h post-infection. Screwworm infestations and viable third-instar larvae developed in all the incisions in non-treated calves, and healing did not begin until larvae had completed their normal life cycle and exited the wounds. The persistent efficacy of a single injection of doramectin extended beyond 14 days.