Evidence map›Paper›PMID 33118022›Full record

ReviewFEMS microbiology reviews2021

Molecular diversity of coronavirus host cell entry receptors.

Jean K Millet, Javier A Jaimes, Gary R Whittaker

Open access · bronzeAbstract readReview
In one paragraph

Review in FEMS microbiology reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

90 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

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30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Jean K MilletUniversité Paris-Saclay, INRAE, UVSQ, Virologie et Immunologie Moléculaires, 78352 Jouy-en-Josas, France.
Javier A JaimesDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0001-6706-092X
Gary R WhittakerDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY 14853, USA.
Cornell University · USUniversité de Versailles Saint-Quentin-en-Yvelines · FR

Funding

JHK VIRUSR01AI032710 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI GROSSBERG, SIDNEY E · 1993 to 1997
–
NIAID NIH HHS R01 AI032710
6 · The paper itself

Abstract

Coronaviruses are a group of viruses causing disease in a wide range of animals, and humans. Since 2002, the successive emergence of bat-borne severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), swine acute diarrhea syndrome coronavirus (SADS-CoV) and SARS-CoV-2 has reinforced efforts in uncovering the molecular and evolutionary mechanisms governing coronavirus cell tropism and interspecies transmission. Decades of studies have led to the discovery of a broad set of carbohydrate and protein receptors for many animal and human coronaviruses. As the main determinant of coronavirus entry, the spike protein binds to these receptors and mediates membrane fusion. Prone to mutations and recombination, spike evolution has been studied extensively. The interactions between spike proteins and their receptors are often complex and despite many advances in the field, there remains many unresolved questions concerning coronavirus tropism modification and cross-species transmission, potentially leading to delays in outbreak responses. The emergence of SARS-CoV-2 underscores the need to address these outstanding issues in order to better anticipate new outbreaks. In this review, we discuss the latest advances in the field of coronavirus receptors emphasizing on the molecular and evolutionary processes that underlie coronavirus receptor usage and host range expansion.

Indexed as

Host-Pathogen InteractionsAnimalsBiodiversityCoronavirusCoronavirus InfectionsCOVID-19GenotypeHost SpecificityHumansPhylogenyReceptors, CoronavirusSARS-CoV-2Spike Glycoprotein, CoronavirusViral TropismReceptors, CoronavirusSpike Glycoprotein, Coronaviruscoronavirushost cell receptorhost tropismpathogenesissevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2)virus entry

Identifiers

PMID33118022
PMCPMC7665467
OpenAlexW3096829897

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.