HIV-1 lentivirus with VSV-G envelope: Complex N glycosylation governs shifts in aggregation and infectivity state at close to physiological pH, serum, and Ca2+ levels.

Authors

Tzu-Lan Chang, Ayobami I Ogundiran, Andrey Ivanov, Gabrielle Torain, Sergei Nekhai, Preethi L Chandran

Published in

PloS one. Volume 21. Issue 9. Pages e0357567. Epub Sep 09, 2026.

Abstract

The goal of the study is to determine if the N-glycosylation on a virus affects its diffusion or solution state in different environmental conditions, and if the nature of the solution states has any consequence for the virus infectivity. HIV-1 lentivirus is frequently pseudo-typed with the envelope protein of Vesicular Stomatitis Virus, VSV-G, for gene and cell therapy applications. VSV-G proteins have complex type N-glycans. The diffusion profile of the lentivirus having VSV-G envelope proteins was monitored in different solution conditions using Dynamic Light Scattering, and inferences checked by AFM, filtration, antibody, and p24 ELISA experiments. The virus switched between one of three solution states in response to changes in its environment: (a) a self-aggregated state when serum to virus ratio was low, and Ca2+ and pH levels were below 2 mM and 7.4, respectively, (b) a dispersed state when serum to virus ratio was high, but Ca2+ and pH levels were still below 2mM and 7.4, respectively, and (c) a Ca-induced aggregated state when Ca2+ and pH levels exceeded 2mM and 7.4 respectively. The diffusion peak of the aggregated virus can be pulled out by antibodies against VSV-G or can be filtered out with attendant loss in p24 count and infectivity. The three solution states exhibited significantly different infectivity levels. Interestingly, the trigger conditions for switching the virus solution state occur at physiological levels of pH, Ca2+, and serum, implying that small deviations from the homeostatic conditions can induce large changes in virus infectivity. The ability to exist and switch between three solution states was lost when the terminal sialic acid and galactose residues on the virus envelope protein were cleaved. It appears that the complex N-glycans on a virus allow the latter to respond to deviations from homeostatic environmental conditions by switching solution states.

PMID:
42715248
Bibliographic data and abstract were imported from PubMed on 10 Sep 2026.

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