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1 ing seven TPSs from six species in the genus Metarhizium.
2                                              Metarhizium acridum, a fungal pathogen that specifically
3 tG1, in the locust-specific fungal pathogen, Metarhizium acridum, functions as a ROS detoxification m
4 es infected with the entomopathogenic fungus Metarhizium acridum.
5 tion by the locust-specific fungal pathogen, Metarhizium acridum.
6 odified Metarhizium Deployment of transgenic Metarhizium against mosquitoes could (subject to appropr
7 for their ability to improve the efficacy of Metarhizium against wild-caught, insecticide-resistant a
8 ws that two generalist isolates of the genus Metarhizium and Beauveria, commonly used as biological p
9  We focus primarily on species in the genera Metarhizium and Beauveria, traditionally recognized as i
10 e broad host range ascomycete entomopathogen Metarhizium anisopliae (Ma549), indicative of generalist
11 usceptibility to the natural insect pathogen Metarhizium anisopliae (Ma549).
12 insecticides and the entomopathogenic fungi, Metarhizium anisopliae (Metschin.) against the cotton ap
13 bility to the broad-spectrum entomopathogen, Metarhizium anisopliae (strain Ma549).
14 secticidal properties of Beauveria bassiana, Metarhizium anisopliae and Heterorhabditis bacteriophora
15                                   The fungus Metarhizium anisopliae has potential as a biopesticide a
16 d sequence tag analysis of the deuteromycete Metarhizium anisopliae identified two trypsins (family S
17                                              Metarhizium anisopliae infects mosquitoes through the cu
18                The insect pathogenic fungus, Metarhizium anisopliae is a commercialized microbial age
19               The ubiquitous fungal pathogen Metarhizium anisopliae kills a wide range of insects.
20                                          The Metarhizium anisopliae nrr1 (nitrogen response regulator
21 development of effective oil formulations of Metarhizium anisopliae spores in Africa, Australia, and
22 tary locusts to the entomopathogenic fungus, Metarhizium anisopliae var. acridum, a key natural disea
23 ulated cuticle-degrading protease (Pr1) from Metarhizium anisopliae were inserted into the genome of
24 ify genes that are specifically expressed by Metarhizium anisopliae when it contacts the host insect
25  entomopathogenic fungi (Beauveria bassiana, Metarhizium anisopliae) and entomopathogenic nematodes (
26     A cDNA clone (MeCPA) for a novel fungal (Metarhizium anisopliae) carboxypeptidase (MeCPA) was obt
27 ns, EAS from Neurospora crassa and ssgA from Metarhizium anisopliae) could partially complement each
28 gen Metarhizium robertsii (formerly known as Metarhizium anisopliae).
29 istic inhibition of a fungal entomopathogen, Metarhizium anisopliae, and multiple streptomycete isola
30 enge exposure to the entomopathogenic fungus Metarhizium anisopliae, dampwood termites Zootermopsis a
31 n A, a mycotoxin of entomopathogenic fungus, Metarhizium anisopliae, has broad-spectrum insecticidal
32 chlorantraniliprole and the fungal pathogen, Metarhizium anisopliae.
33 tion and the virulence of the entomopathogen Metarhizium anisopliae.
34 ersity of subtilisins in the insect pathogen Metarhizium anisopliae.
35 ases secreted by an entomopathogenic fungus, Metarhizium anisopliae.
36 ially sequenced from the filamentous fungus, Metarhizium anisopliae.
37 fter exposure to the entomopathogenic fungus Metarhizium anisopliae.
38                           Fungi in the genus Metarhizium are insect pathogens able to function in oth
39                                              Metarhizium biopesticide kills 70%-90% of treated locust
40  cv. Castello L.) with and without the R-AEF Metarhizium brunneum (Petch).
41 es developed for this system, new strains of Metarhizium brunneum were created that survived, germina
42 combination with the entomopathogenic fungus Metarhizium brunneum, in the non-target ant species Lasi
43  via chisel-till harboured higher numbers of Metarhizium cfu than no-till plots.
44                            Here we show that Metarhizium-colonized insect cadavers release the volati
45 ybean cultivation produced higher numbers of Metarhizium colony-forming units (cfu) than corn or alfa
46 ia to fungi and functional divergence within Metarhizium could be traced.
47 cy lasted longer than that of the unmodified Metarhizium Deployment of transgenic Metarhizium against
48 These findings illuminate multiple levels of Metarhizium diversity that can be used to inform strateg
49 tides when encountering live insect tissues, Metarhizium employed them primarily on dead tissue.
50 te that all seven BTPSL genes from the genus Metarhizium encode active enzymes with sesquiterpene syn
51 chanism in broad-host-range entomopathogenic Metarhizium, enhancing mosquito control efficacy.
52 podoptera litura in response to infection by Metarhizium flavoviride. At 48 h following exposure to M
53                                              Metarhizium fungi are emerging as promising alternatives
54 tsii and another congeneric insect pathogen, Metarhizium guizhouense.
55 ort results from a selective media survey of Metarhizium in soils sampled from a long-term experiment
56                           Sequence typing of Metarhizium isolates revealed four species, with M. robe
57  larger seven-gene PPZ cluster in M. rileyi, Metarhizium majus and the stalked-cup lichen fungus Clad
58                      Entomopathogenic fungus Metarhizium majus contains the nine-gene PPZ cluster, wi
59 ed sporozoite counts by 98%, suggesting that Metarhizium-mediated inhibition of Plasmodium developmen
60                                              Metarhizium pingshaense provides an effective, mosquito-
61               The virulent mosquito pathogen Metarhizium pingshaense was engineered to express pine l
62 n be used to inform strategies by which soil Metarhizium populations may be manipulated to exert down
63                 We identified mutants in the Metarhizium raffinose transporter (Mrt) gene of M. rober
64               Entomopathogenic fungi such as Metarhizium rileyi and Beauveria bassiana are widely use
65 n the genome of the insect-pathogenic fungus Metarhizium rileyi.
66 a exempta NPV (SpexNPV); the fungal pathogen Metarhizium rileyi; and the bacterium Wolbachia.
67 hizosphere competence in the insect pathogen Metarhizium robertsii (formerly known as Metarhizium ani
68 osed colonies to the entomopathogenic fungus Metarhizium robertsii by exposing two individuals from t
69 rains of the asexual entomopathogenic fungus Metarhizium robertsii during experimental co-infection o
70 a green fluorescent protein tagged strain of Metarhizium robertsii following transfer from a semitrop
71 rotia- or blastospores-based formulations of Metarhizium robertsii for R. microplus control under sem
72                                              Metarhizium robertsii is a versatile fungus with saproph
73                                              Metarhizium robertsii occupies a wide array of ecologica
74 ive bacterium Bacillus cereus and the fungus Metarhizium robertsii) in male and female Gryllodes sigi
75 , during infection with the fungal pathogen, Metarhizium robertsii, and the consequence of temperatur
76 olog of BI-1, in the entomopathogenic fungus Metarhizium robertsii.
77                                              Metarhizium-root colonization ranged from 25 to 66.7% de
78                         Genetically modified Metarhizium spp represent a major new arsenal for combat
79                                   Strains of Metarhizium spp., a well-known group of entomopathogenic
80 , U. virens is close to the entomopathogenic Metarhizium spp., suggesting potential host jumping acro
81 cation has continued during the evolution of Metarhizium subtilisins with evidence of gene duplicatio
82 ent strategy, with an emphasis on the use of Metarhizium, that incorporates rational use of chemical
83  with unknown effects on the distribution of Metarhizium, whose presence can reduce populations of cr