Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
23 03 2022
Historique:
received: 25 01 2022
revised: 11 03 2022
accepted: 18 03 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 27 4 2022
Statut: epublish

Résumé

Chronic conditions like type II diabetes (T2DM) have long been known to exacerbate many infectious diseases. For many arboviruses, including Zika virus (ZIKV), severe outcomes, morbidity and mortality usually only occur in patients with such pre-existing conditions. However, the effects of T2DM and other pre-existing conditions on human blood (e.g., hypo/hyperinsulinemia, hyperglycemia and hyperlipidemia) that may impact infectivity of arboviruses for vectors is largely unexplored. We investigated whether the susceptibility of Aedes aegypti mosquitoes was affected when the mosquitoes fed on "diabetic" bloodmeals, such as bloodmeals composed of artificially glycosylated erythrocytes or those from viremic, diabetic mice (LEPRDB/DB). Increasing glycosylation of erythrocytes from hemoglobin A1c (HgbA1c) values of 5.5-5.9 to 6.2 increased the infection rate of a Galveston, Texas strain of Ae. aegypti to ZIKV strain PRVABC59 at a bloodmeal titer of 4.14 log10 FFU/mL from 0.0 to 40.9 and 42.9%, respectively. ZIKV was present in the blood of viremic LEPRDB/DB mice at similar levels as isogenic control C57BL/6J mice (3.3 log10 FFU/mL and 3.6 log10 FFU/mL, respectively. When mice sustained a higher ZIKV viremia of 4.6 log10 FFU/mL, LEPRDB/DB mice infected 36.3% of mosquitoes while control C57BL/6J mice with a viremia of 4.2 log10 FFU/mL infected only 4.1%. Additionally, when highly susceptible Ae. aegypti Rockefeller mosquitoes fed on homozygous LEPRDB/DB, heterozygous LEPRWT/DB, and control C57BL/6J mice with viremias of ≈ 4 log10 FFU/mL, 54%, 15%, and 33% were infected, respectively. In total, these data suggest that the prevalence of T2DM in a population may have a significant impact on ZIKV transmission and indicates the need for further investigation of the impacts of pre-existing metabolic conditions on arbovirus transmission.

Identifiants

pubmed: 35458395
pii: v14040665
doi: 10.3390/v14040665
pmc: PMC9024453
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI121452
Pays : United States
Organisme : NIH HHS
ID : 5R01AI121452-05
Pays : United States

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Auteurs

Sasha R Azar (SR)

Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.

Rafael K Campos (RK)

Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-0610, USA.

Ruimei Yun (R)

Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-0610, USA.

Taylor Strange (T)

Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.

Shannan L Rossi (SL)

Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Tropical Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555-0610, USA.

Kathryn A Hanley (KA)

Department of Biology, New Mexico State University, Las Cruces, NM 88003, USA.

Nikos Vasilakis (N)

Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Tropical Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555-0610, USA.
World Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Vector-Borne and Zoonotic Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Department of Preventive Medicine and Population Health, The University of Texas Medical Branch, Galveston, TX 77555, USA.

Scott C Weaver (SC)

Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-0610, USA.
Center for Tropical Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555-0610, USA.
World Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Center for Vector-Borne and Zoonotic Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA.

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