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SP-A1, SP-A2 and SP-D gene polymorphisms in severe acute respiratory syncytial infection in Chilean infants

► In this work, polymorphisms of SP-A1, SP-A2 and SP-D genes, was performed in Chilean infants with RSV-ALRI. ► Infants- SNP comparison was done according to their clinical severity and with general population. ► This is a study of genetic susceptibility for RSV infection in South-American populatio...

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Published in:Infection, genetics and evolution genetics and evolution, 2011-08, Vol.11 (6), p.1368-1377
Main Authors: Ampuero, Sandra, Luchsinger, Vivian, Tapia, Lorena, Palomino, María Angélica, Larrañaga, Carmen E.
Format: Article
Language:English
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Summary:► In this work, polymorphisms of SP-A1, SP-A2 and SP-D genes, was performed in Chilean infants with RSV-ALRI. ► Infants- SNP comparison was done according to their clinical severity and with general population. ► This is a study of genetic susceptibility for RSV infection in South-American population. ► Differences found with other authors, indicates the need to identify local biomarkers of severity. Respiratory syncytial virus (RSV) is the principal pathogen that causes acute lower respiratory tract infection (ALRI) in infants. Severe RSV-ALRI has been associated with the host genetic susceptibility. To assess whether severe RSV disease in infants is associated with certain single nucleotide polymorphism (SNP) into the gene of SP-A1, SP-A2 and SP-D, a prospective study was performed among blood donors and RSV-infected infants aged
ISSN:1567-1348
1567-7257
DOI:10.1016/j.meegid.2011.04.033