Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19

SARS-CoV-2 uses the ACE2 receptor and the cellular protease TMPRSS2 for entry into target cells. The present study aimed to establish if the TMPRSS2 polymorphisms are associated with COVID-19 disease. The study included 609 patients with COVID-19 confirmed by RT-PCR test and 291 individuals negative...

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Main Authors: Rosalinda Posadas-Sánchez, José Manuel Fragoso, Fausto Sánchez-Muñoz, Gustavo Rojas-Velasco, Julian Ramírez-Bello, Alberto López-Reyes, Laura E. Martínez-Gómez, Carlos Sierra-Fernández, Tatiana Rodríguez-Reyna, Nora Elemi Regino-Zamarripa, Gustavo Ramírez-Martínez, Joaquín Zuñiga-Ramos, Gilberto Vargas-Alarcón
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/14/9/1976
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author Rosalinda Posadas-Sánchez
José Manuel Fragoso
Fausto Sánchez-Muñoz
Gustavo Rojas-Velasco
Julian Ramírez-Bello
Alberto López-Reyes
Laura E. Martínez-Gómez
Carlos Sierra-Fernández
Tatiana Rodríguez-Reyna
Nora Elemi Regino-Zamarripa
Gustavo Ramírez-Martínez
Joaquín Zuñiga-Ramos
Gilberto Vargas-Alarcón
author_facet Rosalinda Posadas-Sánchez
José Manuel Fragoso
Fausto Sánchez-Muñoz
Gustavo Rojas-Velasco
Julian Ramírez-Bello
Alberto López-Reyes
Laura E. Martínez-Gómez
Carlos Sierra-Fernández
Tatiana Rodríguez-Reyna
Nora Elemi Regino-Zamarripa
Gustavo Ramírez-Martínez
Joaquín Zuñiga-Ramos
Gilberto Vargas-Alarcón
author_sort Rosalinda Posadas-Sánchez
collection DOAJ
description SARS-CoV-2 uses the ACE2 receptor and the cellular protease TMPRSS2 for entry into target cells. The present study aimed to establish if the TMPRSS2 polymorphisms are associated with COVID-19 disease. The study included 609 patients with COVID-19 confirmed by RT-PCR test and 291 individuals negative for the SARS-CoV-2 infection confirmed by RT-PCR test and without antibodies anti-SARS-CoV-2. Four TMPRSS2 polymorphisms (rs12329760, rs2298659, rs456298, and rs462574) were determined using the 5′exonuclease TaqMan assays. Under different inheritance models, the rs2298659 (<i>p</i><sub>codominant2</sub> = 0.018, <i>p</i><sub>recessive</sub> = 0.006, <i>p</i><sub>additive</sub> = 0.019), rs456298 (<i>p</i><sub>codominant1</sub> = 0.014, <i>p</i><sub>codominant2</sub> = 0.004; <i>p</i><sub>dominant</sub> = 0.009, <i>p</i><sub>recessive</sub> = 0.004, <i>p</i><sub>additive</sub> = 0.0009), and rs462574 (<i>p</i><sub>codominant1</sub> = 0.017, <i>p</i><sub>codominant2</sub> = 0.004, <i>p</i><sub>dominant</sub> = 0.041, <i>p</i><sub>recessive</sub> = 0.002, <i>p</i><sub>additive</sub> = 0.003) polymorphisms were associated with high risk of developing COVID-19. Two risks (<i>ATGC</i> and <i>GAAC</i>) and two protectives (<i>GAGC</i> and <i>GAGT</i>) haplotypes were detected. High levels of lactic acid dehydrogenase (LDH) were observed in patients with the rs462574<i>AA</i> and rs456298<i>TT</i> genotypes (<i>p</i> = 0.005 and <i>p</i> = 0.020, respectively), whereas, high heart rate was present in patients with the rs462574<i>AA</i> genotype (<i>p</i> = 0.028). Our data suggest that the rs2298659, rs456298, and rs462574 polymorphisms independently and as haplotypes are associated with the risk of COVID-19. The rs456298 and rs462574 genotypes are related to high levels of LDH and heart rate.
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spelling doaj.art-8cd116bcdb7c4f28aa976ef645fae09f2023-11-23T19:27:25ZengMDPI AGViruses1999-49152022-09-01149197610.3390/v14091976Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19Rosalinda Posadas-Sánchez0José Manuel Fragoso1Fausto Sánchez-Muñoz2Gustavo Rojas-Velasco3Julian Ramírez-Bello4Alberto López-Reyes5Laura E. Martínez-Gómez6Carlos Sierra-Fernández7Tatiana Rodríguez-Reyna8Nora Elemi Regino-Zamarripa9Gustavo Ramírez-Martínez10Joaquín Zuñiga-Ramos11Gilberto Vargas-Alarcón12Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, MexicoDepartment of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano No. 1, Sección XVI, Tlalpan, Mexico City 14080, MexicoDepartament of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, MexicoIntensive Care Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, MexicoDepartment of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, MexicoLaboratorio de Gerociencias, Instituto Nacional de Rehabilitación “Luis Guillermo Ibarra Ibarra”, Mexico City 14080, MexicoLaboratorio de Gerociencias, Instituto Nacional de Rehabilitación “Luis Guillermo Ibarra Ibarra”, Mexico City 14080, MexicoDirección de Enseñanza, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, MexicoDepartment or Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutrición Salvador Zubirán, Mexico City 14080, MexicoTecnologico de Monterrey, Monterrey 64849, MexicoImmunology and Genetics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, MexicoTecnologico de Monterrey, Monterrey 64849, MexicoDepartment of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano No. 1, Sección XVI, Tlalpan, Mexico City 14080, MexicoSARS-CoV-2 uses the ACE2 receptor and the cellular protease TMPRSS2 for entry into target cells. The present study aimed to establish if the TMPRSS2 polymorphisms are associated with COVID-19 disease. The study included 609 patients with COVID-19 confirmed by RT-PCR test and 291 individuals negative for the SARS-CoV-2 infection confirmed by RT-PCR test and without antibodies anti-SARS-CoV-2. Four TMPRSS2 polymorphisms (rs12329760, rs2298659, rs456298, and rs462574) were determined using the 5′exonuclease TaqMan assays. Under different inheritance models, the rs2298659 (<i>p</i><sub>codominant2</sub> = 0.018, <i>p</i><sub>recessive</sub> = 0.006, <i>p</i><sub>additive</sub> = 0.019), rs456298 (<i>p</i><sub>codominant1</sub> = 0.014, <i>p</i><sub>codominant2</sub> = 0.004; <i>p</i><sub>dominant</sub> = 0.009, <i>p</i><sub>recessive</sub> = 0.004, <i>p</i><sub>additive</sub> = 0.0009), and rs462574 (<i>p</i><sub>codominant1</sub> = 0.017, <i>p</i><sub>codominant2</sub> = 0.004, <i>p</i><sub>dominant</sub> = 0.041, <i>p</i><sub>recessive</sub> = 0.002, <i>p</i><sub>additive</sub> = 0.003) polymorphisms were associated with high risk of developing COVID-19. Two risks (<i>ATGC</i> and <i>GAAC</i>) and two protectives (<i>GAGC</i> and <i>GAGT</i>) haplotypes were detected. High levels of lactic acid dehydrogenase (LDH) were observed in patients with the rs462574<i>AA</i> and rs456298<i>TT</i> genotypes (<i>p</i> = 0.005 and <i>p</i> = 0.020, respectively), whereas, high heart rate was present in patients with the rs462574<i>AA</i> genotype (<i>p</i> = 0.028). Our data suggest that the rs2298659, rs456298, and rs462574 polymorphisms independently and as haplotypes are associated with the risk of COVID-19. The rs456298 and rs462574 genotypes are related to high levels of LDH and heart rate.https://www.mdpi.com/1999-4915/14/9/1976COVID-19 diseasegenetic susceptibilitypolymorphismsSARS-CoV-2 infectiontransmembrane serine protease-2 (TMPRSS2)
spellingShingle Rosalinda Posadas-Sánchez
José Manuel Fragoso
Fausto Sánchez-Muñoz
Gustavo Rojas-Velasco
Julian Ramírez-Bello
Alberto López-Reyes
Laura E. Martínez-Gómez
Carlos Sierra-Fernández
Tatiana Rodríguez-Reyna
Nora Elemi Regino-Zamarripa
Gustavo Ramírez-Martínez
Joaquín Zuñiga-Ramos
Gilberto Vargas-Alarcón
Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
Viruses
COVID-19 disease
genetic susceptibility
polymorphisms
SARS-CoV-2 infection
transmembrane serine protease-2 (TMPRSS2)
title Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
title_full Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
title_fullStr Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
title_full_unstemmed Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
title_short Association of the Transmembrane Serine Protease-2 (TMPRSS2) Polymorphisms with COVID-19
title_sort association of the transmembrane serine protease 2 tmprss2 polymorphisms with covid 19
topic COVID-19 disease
genetic susceptibility
polymorphisms
SARS-CoV-2 infection
transmembrane serine protease-2 (TMPRSS2)
url https://www.mdpi.com/1999-4915/14/9/1976
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