2010
DOI: 10.1016/j.funbio.2010.05.005
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Comparative analysis of the Metarhizium anisopliae secretome in response to exposure to the greyback cane grub and grub cuticles

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Cited by 10 publications
(12 citation statements)
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References 39 publications
(40 reference statements)
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“…The strategy of applying synthetic media to induce the activation of the infection systems has been applied with success, revealing genes and proteins involved in different stages of Metarhizium anisopliae ’s infection process. 7,12,43,44 Several articles have been reporting poor correlation between mRNA and protein levels. 4547 Most of the work in M. anisopliae has analyzed gene expression, which makes the identification of secreted proteins difficult.…”
Section: Discussionmentioning
confidence: 99%
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“…The strategy of applying synthetic media to induce the activation of the infection systems has been applied with success, revealing genes and proteins involved in different stages of Metarhizium anisopliae ’s infection process. 7,12,43,44 Several articles have been reporting poor correlation between mRNA and protein levels. 4547 Most of the work in M. anisopliae has analyzed gene expression, which makes the identification of secreted proteins difficult.…”
Section: Discussionmentioning
confidence: 99%
“…49 Only a few proteomic studies have been published on M. anisopliae and all applied low-throughput techniques. 12,43,5054 By applying shotgun proteomics, 21 we were able to identify 71 proteins differentially expressed under infection conditions. Most of these proteins were not detected in other proteomic experiments about insect infection.…”
Section: Discussionmentioning
confidence: 99%
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“…The cuticles were introduced to the fungal hyphae as a powder as described earlier (e.g., Fang et al, 2009; Manalil et al, 2010) to gain enough fungus material even though it may cause biases. However, using an in vivo system (fungus developing on whole ticks) might result in inadequate fungus material but also in masking fungus sequences due to higher abundance of host sequences.…”
Section: Methodsmentioning
confidence: 99%
“…Cleared supernatants were then aliquoted in 1.5 ml Eppendorf tubes and stored at -80°C. Fungal protease inhibitor cocktail (0.05% v/v, Sigma-Aldrich, Australia) was added in the culture supernatant samples used for proteomic analysis [36]. …”
Section: Methodsmentioning
confidence: 99%