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ACE2, TMPRSS2, and Furin variants and SARS-CoV-2 infection in Madrid, Spain.
Torre-Fuentes, Laura; Matías-Guiu, Jorge; Hernández-Lorenzo, Laura; Montero-Escribano, Paloma; Pytel, Vanesa; Porta-Etessam, Jesús; Gómez-Pinedo, Ulises; Matías-Guiu, Jordi A.
  • Torre-Fuentes L; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Matías-Guiu J; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Hernández-Lorenzo L; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Montero-Escribano P; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Pytel V; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Porta-Etessam J; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Gómez-Pinedo U; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
  • Matías-Guiu JA; Department of Neurology, Instituto de Neurociencias IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
J Med Virol ; 93(2): 863-869, 2021 02.
Article in English | MEDLINE | ID: covidwho-1196406
ABSTRACT
It has been suggested that some individuals may present genetic susceptibility to SARS-CoV-2 infection, with particular research interest in variants of the ACE2 and TMPRSS2 genes, involved in viral penetration into cells, in different populations and geographic regions, although insufficient information is currently available. This study addresses the apparently reasonable hypothesis that variants of these genes may modulate viral infectivity, making some individuals more vulnerable than others. Through whole-exome sequencing, the frequency of exonic variants of the ACE2, TMPRSS2, and Furin genes was analyzed in relation to presence or absence of SARS-CoV-2 infection in a familial multiple sclerosis cohort including 120 individuals from Madrid. The ACE2 gene showed a low level of polymorphism, and none variant was significantly associated with SARS-CoV-2 infection. These variants have previously been detected in Italy. While TMPRSS2 is highly polymorphic, the variants found do not coincide with those described in other studies, with the exception of rs75603675, which may be associated with SARS-CoV-2 infection. The synonymous variants rs61735792 and rs61735794 showed a significant association with infection. Despite the limited number of patients with SARS-CoV-2 infection, some variants, especially in TMPRSS2, may be associated with COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Receptors, Virus / Serine Endopeptidases / Furin / Angiotensin-Converting Enzyme 2 / COVID-19 / Multiple Sclerosis Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Country/Region as subject: Europa Language: English Journal: J Med Virol Year: 2021 Document Type: Article Affiliation country: Jmv.26319

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Receptors, Virus / Serine Endopeptidases / Furin / Angiotensin-Converting Enzyme 2 / COVID-19 / Multiple Sclerosis Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Country/Region as subject: Europa Language: English Journal: J Med Virol Year: 2021 Document Type: Article Affiliation country: Jmv.26319