Biochemical and Functional Characterization of Glycoside Hydrolase Family 16 Genes in Aedes aegypti Larvae: Identification of the Major Digestive β-1,3-Glucanase

Insect β-1,3-glucanases belong to Glycoside Hydrolase Family 16 (GHF16) and are involved in digestion of detritus and plant hemicellulose. In this work, we investigated the role of GHF16 genes in larvae, due to their detritivore diet. genome has six genes belonging to GHF16 (Aae GH16.1 - Aae GH16.6)...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in physiology Vol. 10; p. 122
Main Authors Souza, Raquel Santos, Gama, Maiara do Valle Faria, Schama, Renata, Lima, José Bento Pereira, Diaz-Albiter, Hector Manuel, Genta, Fernando Ariel
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 28.02.2019
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Insect β-1,3-glucanases belong to Glycoside Hydrolase Family 16 (GHF16) and are involved in digestion of detritus and plant hemicellulose. In this work, we investigated the role of GHF16 genes in larvae, due to their detritivore diet. genome has six genes belonging to GHF16 (Aae GH16.1 - Aae GH16.6), containing two to six exons. Sequence analysis suggests that five of these GHF16 sequences (Aae GH16.1, 2, 3, 5, and 6) contain the conserved catalytic residues of this family and correspond to glucanases. All genomes of Nematocera analyzed showed putative gene duplications corresponding to these sequences. Aae GH16.4 has no conserved catalytic residues and is probably a β-1,3-glucan binding protein involved in the activation of innate immune responses. Additionally, larvae contain significant β-1,3-glucanase activities in the head, gut and rest of body. These activities have optimum pH about 5-6 and molecular masses between 41 and 150 kDa. All GHF16 genes above showed different levels of expression in the larval head, gut or rest of the body. Knock-down of AeGH16.5 resulted in survival and pupation rates lower than controls (dsGFP and water treated). However, under stress conditions, severe mortalities were observed in AeGH16.1 and AeGH16.6 knocked-down larvae. Enzymatic assays of β-1,3-glucanase in AeGH16.5 silenced larvae exhibited lower activity in the gut and no change in the rest of the body. Chromatographic activity profiles from gut samples after GH16.5 silencing showed suppression of enzymatic activity, suggesting that this gene codes for the digestive larval β-1,3-glucanase of . This gene and enzyme are attractive targets for new control strategies, based on the impairment of normal gut physiology.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Reviewed by: Marcela Barbosa Figueiredo, Swansea University, United Kingdom; Najmeh Sahebzadeh, Zabol University, Iran; Muthugounder S. Shivakumar, Periyar University, India
This article was submitted to Invertebrate Physiology, a section of the journal Frontiers in Physiology
Present address: Hector Manuel Diaz-Albiter, El Colegio de la Frontera Sur, Villahermosa, Tabasco, Mexico
Edited by: Senthil-Nathan Sengottayan, Manonmaniam Sundaranar University, India
ISSN:1664-042X
1664-042X
DOI:10.3389/fphys.2019.00122