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2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants

BACKGROUND: Differential expression of selected immunity genes may have a role in susceptibility to Respiratory Syncytial Virus (RSV). There are few data about some candidate gene single nucleotide polymorphisms (SNPs) associated with the severity of respiratory infections (e.g., Toll-like receptor...

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Autores principales: Ferolla, Fausto Martin, Acosta, Patricio, Toledano, Analia, Yfran, Eduardo Walter, Giordano, Ana Clara, Carrizo, Barbara, Anselmino, Cecilia, Feldman, Florencia, Chiormi, Agustina, Visingardi, Gabriela, Retta, Alejandra, Reyero, Mariana, Dastugue, Monica, Mascardi, Normando, Neira, Pablo, Caratozzolo, Ana, Marta Contrini, Maria, Lopez, Eduardo Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810930/
http://dx.doi.org/10.1093/ofid/ofz360.2294
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author Ferolla, Fausto Martin
Acosta, Patricio
Toledano, Analia
Yfran, Eduardo Walter
Giordano, Ana Clara
Carrizo, Barbara
Anselmino, Cecilia
Feldman, Florencia
Chiormi, Agustina
Visingardi, Gabriela
Retta, Alejandra
Reyero, Mariana
Dastugue, Monica
Mascardi, Normando
Neira, Pablo
Caratozzolo, Ana
Marta Contrini, Maria
Lopez, Eduardo Luis
author_facet Ferolla, Fausto Martin
Acosta, Patricio
Toledano, Analia
Yfran, Eduardo Walter
Giordano, Ana Clara
Carrizo, Barbara
Anselmino, Cecilia
Feldman, Florencia
Chiormi, Agustina
Visingardi, Gabriela
Retta, Alejandra
Reyero, Mariana
Dastugue, Monica
Mascardi, Normando
Neira, Pablo
Caratozzolo, Ana
Marta Contrini, Maria
Lopez, Eduardo Luis
author_sort Ferolla, Fausto Martin
collection PubMed
description BACKGROUND: Differential expression of selected immunity genes may have a role in susceptibility to Respiratory Syncytial Virus (RSV). There are few data about some candidate gene single nucleotide polymorphisms (SNPs) associated with the severity of respiratory infections (e.g., Toll-like receptor 4 [TLR4], Toll-like receptor 8 [TLR8], macrophage receptor with colagenous structure [MARCO], myxovirus resistance 1 [MX1]). The aims of this study were to detect the presence of SNPs in selected genes of previously healthy infants infected with RSV, to assess viral load (VL) and to analyze their relationship with life-threatening disease (LTD) METHODS: Prospective cohort study including previously healthy full-term infants < 12 months, hospitalized with a first RSV infection during 2017–2018. RSV diagnosis, virus quantification and genotyping for SNPs (TLR4 rs4986790, TLR4 rs4986791, MARCO rs1318645, MX1 rs469390, TLR8 rs3761624) were performed by qRT–PCR in nasopharyngeal aspirates obtained on admission. Patients with LTD were those admitted to the intensive care unit needing mechanical or non invasive ventilation RESULTS: 75 patients, mean age 3.9 months (±2.8), 41 (54.7%) male. Fifteen developed LTD. Infants who were homozygous (−/−) or heterozygous (+/−) for MX1rs469390 and TLR8rs3761624 or MARCOrs1318645 and TLR8rs3761624 had significantly more risk of developing LTD (OR 3.45, P = 0.042; OR 3.63, P = 0.048, respectively). Multivariable logistic regression analysis showed that concurrent MARCOrs1318645, MX1rs469390 and TLR8rs3761624 SNPs increased the risk of LTD (aOR 4.7, P = 0.018), fig 1. These SNPs also associated with prolonged length of stay (LOS) (P = 0.026) and > 7 days of hypoxemia (P = 0.031). No differences were seen in VL of patients with LTD compared with those with better outcome (P = 0.737). No differences in VL were seen in patients with SNPs. VL did not correlate with LOS or days of hypoxemia. No other socioeconomic, pregnancy or infant variables associated with LTD CONCLUSION: To the best of our knowledge, this is the first study assessing the presence of concurrent SNPs and their association with life-threatening disease in previously healthy infants with RSV infection. These findings provide evidence on the importance of the host and its immune response for the severity of RSV infection. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68109302019-10-28 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants Ferolla, Fausto Martin Acosta, Patricio Toledano, Analia Yfran, Eduardo Walter Giordano, Ana Clara Carrizo, Barbara Anselmino, Cecilia Feldman, Florencia Chiormi, Agustina Visingardi, Gabriela Retta, Alejandra Reyero, Mariana Dastugue, Monica Mascardi, Normando Neira, Pablo Caratozzolo, Ana Marta Contrini, Maria Lopez, Eduardo Luis Open Forum Infect Dis Abstracts BACKGROUND: Differential expression of selected immunity genes may have a role in susceptibility to Respiratory Syncytial Virus (RSV). There are few data about some candidate gene single nucleotide polymorphisms (SNPs) associated with the severity of respiratory infections (e.g., Toll-like receptor 4 [TLR4], Toll-like receptor 8 [TLR8], macrophage receptor with colagenous structure [MARCO], myxovirus resistance 1 [MX1]). The aims of this study were to detect the presence of SNPs in selected genes of previously healthy infants infected with RSV, to assess viral load (VL) and to analyze their relationship with life-threatening disease (LTD) METHODS: Prospective cohort study including previously healthy full-term infants < 12 months, hospitalized with a first RSV infection during 2017–2018. RSV diagnosis, virus quantification and genotyping for SNPs (TLR4 rs4986790, TLR4 rs4986791, MARCO rs1318645, MX1 rs469390, TLR8 rs3761624) were performed by qRT–PCR in nasopharyngeal aspirates obtained on admission. Patients with LTD were those admitted to the intensive care unit needing mechanical or non invasive ventilation RESULTS: 75 patients, mean age 3.9 months (±2.8), 41 (54.7%) male. Fifteen developed LTD. Infants who were homozygous (−/−) or heterozygous (+/−) for MX1rs469390 and TLR8rs3761624 or MARCOrs1318645 and TLR8rs3761624 had significantly more risk of developing LTD (OR 3.45, P = 0.042; OR 3.63, P = 0.048, respectively). Multivariable logistic regression analysis showed that concurrent MARCOrs1318645, MX1rs469390 and TLR8rs3761624 SNPs increased the risk of LTD (aOR 4.7, P = 0.018), fig 1. These SNPs also associated with prolonged length of stay (LOS) (P = 0.026) and > 7 days of hypoxemia (P = 0.031). No differences were seen in VL of patients with LTD compared with those with better outcome (P = 0.737). No differences in VL were seen in patients with SNPs. VL did not correlate with LOS or days of hypoxemia. No other socioeconomic, pregnancy or infant variables associated with LTD CONCLUSION: To the best of our knowledge, this is the first study assessing the presence of concurrent SNPs and their association with life-threatening disease in previously healthy infants with RSV infection. These findings provide evidence on the importance of the host and its immune response for the severity of RSV infection. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6810930/ http://dx.doi.org/10.1093/ofid/ofz360.2294 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Ferolla, Fausto Martin
Acosta, Patricio
Toledano, Analia
Yfran, Eduardo Walter
Giordano, Ana Clara
Carrizo, Barbara
Anselmino, Cecilia
Feldman, Florencia
Chiormi, Agustina
Visingardi, Gabriela
Retta, Alejandra
Reyero, Mariana
Dastugue, Monica
Mascardi, Normando
Neira, Pablo
Caratozzolo, Ana
Marta Contrini, Maria
Lopez, Eduardo Luis
2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title_full 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title_fullStr 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title_full_unstemmed 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title_short 2616. Genetic Susceptibility to Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants
title_sort 2616. genetic susceptibility to life-threatening respiratory syncytial virus infection in previously healthy infants
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810930/
http://dx.doi.org/10.1093/ofid/ofz360.2294
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