4.6 Review

Exaptation of Retroviral Syncytin for Development of Syncytialized Placenta, Its Limited Homology to the SARS-CoV-2 Spike Protein and Arguments against Disturbing Narrative in the Context of COVID-19 Vaccination

Journal

BIOLOGY-BASEL
Volume 10, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/biology10030238

Keywords

placenta; syncytin; spike protein; retrovirus; SARS-CoV-2; COVID-19 vaccine

Categories

Funding

  1. William Stamps Farish Fund
  2. Novartis
  3. Polish Ministry of National Defense [508/2017/DA]

Ask authors/readers for more resources

The alleged similarity between syncytin and the SARS-CoV-2 spike protein is unlikely to cause fertility and pregnancy issues with SARS-CoV-2 vaccines, due to low sequence similarity. More evaluation is needed on potential impacts of COVID-19 vaccines on fertility, placental formation, pregnancy, and overall health of mothers and newborns. The evolution of syncytin and its role in placenta formation through exaptation is also discussed.
Simple Summary The anti-vaccination movement claims an alleged danger of the COVID-19 vaccine based on the presupposed similarity between syncytin, which plays a role in human placentation and the SARS-CoV-2 spike protein. We argue that because of very low sequence similarity between human syncytin-1 and the SARS-CoV-2 S protein, it is unlikely that any S protein-specific SARS-CoV-2 vaccine would generate an immune response which would affect fertility and pregnancy. However, further evaluation of potential impacts of COVID-19 vaccines on fertility, placentation, pregnancy and general health of mother and newborn is required. Human placenta formation relies on the interaction between fused trophoblast cells of the embryo with uterine endometrium. The fusion between trophoblast cells, first into cytotrophoblast and then into syncytiotrophoblast, is facilitated by the fusogenic protein syncytin. Syncytin derives from an envelope glycoprotein (ENV) of retroviral origin. In exogenous retroviruses, the envelope glycoproteins coded by env genes allow fusion of the viral envelope with the host cell membrane and entry of the virus into a host cell. During mammalian evolution, the env genes have been repeatedly, and independently, captured by various mammalian species to facilitate the formation of the placenta. Such a shift in the function of a gene, or a trait, for a different purpose during evolution is called an exaptation (co-option). We discuss the structure and origin of the placenta, the fusogenic and non-fusogenic functions of syncytin, and the mechanism of cell fusion. We also comment on an alleged danger of the COVID-19 vaccine based on the presupposed similarity between syncytin and the SARS-CoV-2 spike protein.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available