1975
DOI: 10.1016/0009-2797(75)90055-1
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Insecticidal and larvicidal activities of the mycotoxins aflatoxin B1, rubratoxin B, patulin and diacetoxyscirpenol towards Drosophila melanogaster

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Cited by 34 publications
(19 citation statements)
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“…At the 0.88 ppm concentration, both A-9 and A-11 strains showed significant mortality rates for first instar larvae, but the A-9 larvae died at higher rates than the A-11 larvae. Similar results were also obtained after the application of mycotoxins such as rubratoxin B, patulin and diacetoxyscirpenol (Reis, 1975). The total number of offsprings (for F1 progeny) of aflatoxin B 1 treated D.melanogaster were affected by all application groups ( Medium II, III and IV) of toxin ( Table 3).…”
Section: Resultssupporting
confidence: 71%
“…At the 0.88 ppm concentration, both A-9 and A-11 strains showed significant mortality rates for first instar larvae, but the A-9 larvae died at higher rates than the A-11 larvae. Similar results were also obtained after the application of mycotoxins such as rubratoxin B, patulin and diacetoxyscirpenol (Reis, 1975). The total number of offsprings (for F1 progeny) of aflatoxin B 1 treated D.melanogaster were affected by all application groups ( Medium II, III and IV) of toxin ( Table 3).…”
Section: Resultssupporting
confidence: 71%
“…This mechanism could function because mycotoxins are effective against Drosophila larvae in pharmaceutical tests [23]. Moreover, deleting a gene encoding a regulatory protein involved in positively influencing secondary metabolite expression in various filamentous fungi competing with Drosophila larvae was beneficial to the insects and detrimental to the fungi [15].…”
Section: Introductionmentioning
confidence: 99%
“…By using a knock-out mutant of A. nidulans that is unable to express the transcription factor LaeA and hence lacks the ability to synthesise a large number of secondary metabolites (Bok and Keller 2004), including mycotoxins, a recent study demonstrated that fungal secondary chemicals may operate as a shield against fungivores (Rohlfs et al 2007). It is likely that secondary metabolites also play a central role in insect-fungus competition, because many fungal compounds have insecticidal properties (Reiss 1975;Melone and Chinnici 1986;Rohlfs and Obmann 2009); yet a causal relationship between impaired saprophagous insect development and microbial secondary metabolite production remains to be demonstrated. In order to understand the rapid evolution of resistance to a noxious fungus, two main hypotheses are subject to current investigations: Wrst, Drosophila might have been selected for resistance against the chemical arsenal fungi secrete into the larval feeding substrate, an anti-microbial strategy that would allow them to use mould-laden resources.…”
Section: Discussionmentioning
confidence: 99%
“…In this context, the beneWt of larval grouping becomes especially pronounced (Rohlfs 2005a), and might explain why aggregative behaviour is widespread in saprophagous insect communities (Rohlfs and HoVmeister 2003). It remains to be demonstrated whether toxic secondary metabolites (so-called mycotoxins) produced by the fungus are the underlying mechanism causing high larval and post-emergence adult mortality (Reiss 1975;Melone and Chinnici 1986;Rohlfs and Obmann 2009).…”
Section: Introductionmentioning
confidence: 99%