The occurrence of deuteromycetous entomopathogenic fungi was determined by examining 224 soil samples from 19 locations in three climatic zones of Mauritius. Three sites were sampled per location: one site under vegetables cultivation, one site under sugar cane plantation and one natural site each within 1 km of each other. Soil samples were baited with the waxmoth larvae Galleria mellonella L. and incubated in the dark at 15, 20, 25 or 30°C for 7, 14 and 21 days. Entomopathogenic fungi were isolated from 77 out of 224 (38.6%) soil samples. Metarhizium anisopliae was isolated from 42 (18.8%) samples, Beauveria bassiana from 24 (10.7%), Metarhizium spp. and Paecilomyces fumosoroseus from 5 (2.2%) each and Beauveria spp. from 1 (0.4%). It was observed that M. anisopliae was isolated more frequently from soils under vegetables as compared to soils under sugarcane or habitat with natural vegetation. Beauveria bassiana was isolated more frequently at the lowest incubation temperature (15°C) while M. anisopliae isolates were recovered more frequently at higher temperatures (25 and 30°C). The pathogenicity of seven isolates of M. anisopliae, five isolates of B. bassiana and two isolates of P. fumosoroseus towards the adults of Bactrocera zonata and Bactrocera cucurbitae was tested by topical application of conidial suspension of 1 × 106 conidia/ml. All the isolates tested were pathogenic to the two fruit fly species. Mortality of B. zonata varied between 12.0 and 98.0% and between 2.0 and 94.0% in B. cucurbitae at 5 days post‐treatment. Our results suggest that entomopathogenic fungi present locally, could be integrated for the control of B. zonata and B. cucurbitae.
Furanoterpenoid accumulation in response
to microbial attack in
rotting sweetpotatoes has long been linked to deaths and lung edema
of cattle in the world. However, it is not known whether furanoterpenoid
ipomeamarone accumulates in the healthy-looking parts of infected
sweetpotato storage roots. This is critical for effective utilization
as animal feed and assessment of the potential negative impact on
human health. Therefore, we first identified the fungus from infected
sweetpotatoes as a Rhizopus stolonifer strain and then used it to infect healthy sweetpotato storage roots
for characterization of furanoterpenoid content. Ipomeamarone and
its precursor, dehydroipomeamarone, were identified through spectroscopic
analyses, and detected in all samples and controls at varying concentrations.
Ipomeamarone concentration was at toxic levels in healthy-looking
parts of some samples. Our study provides fundamental information
on furanoterpenoids in relation to high levels reported that could
subsequently affect cattle on consumption and high ipomeamarone levels
in healthy-looking parts.
Ouna (2008) Susceptibility of immature stages of the locusts Schistocerca gregaria and Locusta migratoria migratorioides to the microsporidium Johenrea locustae and effects of infection on feeding and fertility in the laboratory, Biocontrol Science and Technology, 18:9, 913-920, Second instar nymphs of African migratory locust, Locusta migratoria migratorioides, and desert locust, Schistocerca gregaria, were tested for their susceptibility to the microsporidium pathogen Johenrea locustae (Lange et al. 1996, Journal of Invertebrate Pathology, 68, 28) in the laboratory. Spores of J. locustae were produced from live L.m. migratorioides, a conspecific to L. migratoria capito. Locusta m. migratorioides and S. gregaria were exposed to wheat seedlings sprayed with 20 mL of three concentrations (10 6 , 10 7 and 10 8 spores mL (1 ). Both second-instar nymphs of L.m. migratorioides and S. gregaria were susceptible to J. locustae infection at the three concentrations. There was no effect of concentration of the microsporidium on mortalities of S. gregaria (92Á98%) 19 days postinfection. Adjusted mortality in L.m. migratorioides at 19 days postexposure was 24, 43 and 80% at the corresponding treatment concentrations. The effect of infection on fecundity was tested on both L.m. migratorioides and S. gregaria. Spinach leaf discs were treated with different concentrations (0, 10 4 , 10 5 and 10 6 spores mL (1 ) of J. locustae and presented to female insects for 24 h. Female L.m. migratorioides surviving infection as nymphs laid significantly fewer egg pods than untreated controls at all levels of exposure. The number of eggs per female was also significantly lower in treated lots than in the controls. Higher spore concentrations also adversely affected egg hatching rate. The effect of J. locustae infection on feeding was tested on S. gregaria. There was a significant decrease in food intake among S. gregaria nymphs treated only at the high concentration (10 6 spores mL (1 ).
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