Sialic Acid Expression in the MosquitoAedes aegyptiand Its Possible Role in Dengue Virus-Vector Interactions

Author:

Cime-Castillo Jorge1,Delannoy Philippe2,Mendoza-Hernández Guillermo3,Monroy-Martínez Verónica1,Harduin-Lepers Anne2ORCID,Lanz-Mendoza Humberto4,Hernández-Hernández Fidel de la Cruz5,Zenteno Edgar3ORCID,Cabello-Gutiérrez Carlos6,Ruiz-Ordaz Blanca H.1

Affiliation:

1. Molecular Biology and Biotechnology Department, Biomedical Research Institute, National University of México (UNAM), 04510 México City, Mexico

2. Structural and Functional Glycobiology Unit, UMR 8576 CNRS, University of Sciences and Technologies of Lille, 59655 Villeneuve d’Ascq, France

3. Biochemistry Department, Faculty of Medicine, UNAM, 04510 México City, Mexico

4. CISEI, National Institute of Public Health, 62100 Cuernavaca, MOR, Mexico

5. Infectomics and Molecular Pathogenesis Department, CINVESTAV-IPN, 07360 México City, Mexico

6. Virology Department, National Respiratory Institute (INER), 14050 México City, Mexico

Abstract

Dengue fever (DF) is the most prevalent arthropod-borne viral disease which affects humans. DF is caused by the four dengue virus (DENV) serotypes, which are transmitted to the host by the mosquitoAedes aegyptithat has key roles in DENV infection, replication, and viral transmission (vector competence). Mosquito saliva also plays an important role during DENV transmission. In this study, we detected the presence of sialic acid (Sia) inAedes aegyptitissues, which may have an important role during DENV-vector competence. We also identified genome sequences encoding enzymes involved in Sia pathways. The cDNA forAedes aegyptiCMP-Sia synthase (CSAS) was amplified, cloned, and functionally evaluated via the complementation of LEC29.Lec32 CSAS-deficient CHO cells.AedesCSAS-transfected LEC29.Lec32 cells were able to express Sia moieties on the cell surface. Sequences related toα-2,6-sialyltransferase were detected in theAedes aegyptigenome. Likewise, we identified Sia-α-2,6-DENV interactions in different mosquito tissues. In addition, we evaluated the possible role of sialylated molecules in a salivary gland extract during DENV internalization in mammalian cells. The knowledge of early DENV-host interactions could facilitate a better understanding of viral tropism and pathogenesis to allow the development of new strategies for controlling DENV transmission.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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