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2 tG1, in the locust-specific fungal pathogen, Metarhizium acridum, functions as a ROS detoxification m
5 for their ability to improve the efficacy of Metarhizium against wild-caught, insecticide-resistant a
6 ws that two generalist isolates of the genus Metarhizium and Beauveria, commonly used as biological p
7 We focus primarily on species in the genera Metarhizium and Beauveria, traditionally recognized as i
9 secticidal properties of Beauveria bassiana, Metarhizium anisopliae and Heterorhabditis bacteriophora
11 d sequence tag analysis of the deuteromycete Metarhizium anisopliae identified two trypsins (family S
15 development of effective oil formulations of Metarhizium anisopliae spores in Africa, Australia, and
16 tary locusts to the entomopathogenic fungus, Metarhizium anisopliae var. acridum, a key natural disea
17 ulated cuticle-degrading protease (Pr1) from Metarhizium anisopliae were inserted into the genome of
18 ify genes that are specifically expressed by Metarhizium anisopliae when it contacts the host insect
19 A cDNA clone (MeCPA) for a novel fungal (Metarhizium anisopliae) carboxypeptidase (MeCPA) was obt
20 ns, EAS from Neurospora crassa and ssgA from Metarhizium anisopliae) could partially complement each
22 enge exposure to the entomopathogenic fungus Metarhizium anisopliae, dampwood termites Zootermopsis a
23 n A, a mycotoxin of entomopathogenic fungus, Metarhizium anisopliae, has broad-spectrum insecticidal
32 ybean cultivation produced higher numbers of Metarhizium colony-forming units (cfu) than corn or alfa
33 These findings illuminate multiple levels of Metarhizium diversity that can be used to inform strateg
35 ort results from a selective media survey of Metarhizium in soils sampled from a long-term experiment
37 ed sporozoite counts by 98%, suggesting that Metarhizium-mediated inhibition of Plasmodium developmen
38 n be used to inform strategies by which soil Metarhizium populations may be manipulated to exert down
40 hizosphere competence in the insect pathogen Metarhizium robertsii (formerly known as Metarhizium ani
41 osed colonies to the entomopathogenic fungus Metarhizium robertsii by exposing two individuals from t
42 a green fluorescent protein tagged strain of Metarhizium robertsii following transfer from a semitrop
45 , during infection with the fungal pathogen, Metarhizium robertsii, and the consequence of temperatur
48 , U. virens is close to the entomopathogenic Metarhizium spp., suggesting potential host jumping acro
49 cation has continued during the evolution of Metarhizium subtilisins with evidence of gene duplicatio
50 ent strategy, with an emphasis on the use of Metarhizium, that incorporates rational use of chemical
51 with unknown effects on the distribution of Metarhizium, whose presence can reduce populations of cr
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