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Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados

Hantavirus and dengue virus (DENV) infections are caused by RNA viruses which infect immune systems’ cells including monocytes, macrophages and dendritic cells and occur year-round in Barbados. A retrospective serological study (2008–2015) was conducted on hantavirus and dengue patient sera confirme...

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Autores principales: Douglas, Kirk Osmond, Samuels, Thelma Alafia, Gittens-St. Hilaire, Marquita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783883/
https://www.ncbi.nlm.nih.gov/pubmed/31505806
http://dx.doi.org/10.3390/v11090838
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author Douglas, Kirk Osmond
Samuels, Thelma Alafia
Gittens-St. Hilaire, Marquita
author_facet Douglas, Kirk Osmond
Samuels, Thelma Alafia
Gittens-St. Hilaire, Marquita
author_sort Douglas, Kirk Osmond
collection PubMed
description Hantavirus and dengue virus (DENV) infections are caused by RNA viruses which infect immune systems’ cells including monocytes, macrophages and dendritic cells and occur year-round in Barbados. A retrospective serological study (2008–2015) was conducted on hantavirus and dengue patient sera confirmed by IgM and IgG ELISA, NS1 and RT-PCR using Limulus amoebocyte lysate (LAL) kinetic turbidimetric method to determine serum endotoxin levels. Hantavirus patients were categorized into two groups, namely (a) hospitalized and (b) non-hospitalized. Dengue patients were categorized into 3 groups using 2009 WHO dengue guidelines (a) severe dengue (SD), (b) hospitalized non-severe dengue (non-SD) and (c) non-hospitalized non-SD. Statistical analyses were conducted to determine the association of endotoxin levels with hantavirus disease severity based on hospitalization and dengue disease severity. Serum endotoxin levels are associated with hantavirus disease severity and hospitalization and dengue disease severity (p < 0.01). Similar studies have found an association of serum endotoxin levels with dengue disease severity but never with hantavirus infection. Co-detection of hantavirus- and DENV-specific IgM in some patients were observed with elevated serum endotoxin levels. In addition, previous studies observed hantavirus replication in the gut of patients, gastrointestinal tract as a possible entry route of infection and evidence of microbial translocation and its impact on hantavirus disease severity. A significant correlation of serum endotoxin and hantavirus disease severity and hospitalization in hantavirus infected patients is reported for the first time ever. In addition, serum endotoxin levels correlated with dengue disease severity. This study adds further support to the role of endotoxin in both hantavirus and dengue virus infection and disease severity and its role as a possible therapeutic target for viral haemorrhagic fevers (VHFs).
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spelling pubmed-67838832019-10-16 Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados Douglas, Kirk Osmond Samuels, Thelma Alafia Gittens-St. Hilaire, Marquita Viruses Communication Hantavirus and dengue virus (DENV) infections are caused by RNA viruses which infect immune systems’ cells including monocytes, macrophages and dendritic cells and occur year-round in Barbados. A retrospective serological study (2008–2015) was conducted on hantavirus and dengue patient sera confirmed by IgM and IgG ELISA, NS1 and RT-PCR using Limulus amoebocyte lysate (LAL) kinetic turbidimetric method to determine serum endotoxin levels. Hantavirus patients were categorized into two groups, namely (a) hospitalized and (b) non-hospitalized. Dengue patients were categorized into 3 groups using 2009 WHO dengue guidelines (a) severe dengue (SD), (b) hospitalized non-severe dengue (non-SD) and (c) non-hospitalized non-SD. Statistical analyses were conducted to determine the association of endotoxin levels with hantavirus disease severity based on hospitalization and dengue disease severity. Serum endotoxin levels are associated with hantavirus disease severity and hospitalization and dengue disease severity (p < 0.01). Similar studies have found an association of serum endotoxin levels with dengue disease severity but never with hantavirus infection. Co-detection of hantavirus- and DENV-specific IgM in some patients were observed with elevated serum endotoxin levels. In addition, previous studies observed hantavirus replication in the gut of patients, gastrointestinal tract as a possible entry route of infection and evidence of microbial translocation and its impact on hantavirus disease severity. A significant correlation of serum endotoxin and hantavirus disease severity and hospitalization in hantavirus infected patients is reported for the first time ever. In addition, serum endotoxin levels correlated with dengue disease severity. This study adds further support to the role of endotoxin in both hantavirus and dengue virus infection and disease severity and its role as a possible therapeutic target for viral haemorrhagic fevers (VHFs). MDPI 2019-09-09 /pmc/articles/PMC6783883/ /pubmed/31505806 http://dx.doi.org/10.3390/v11090838 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Douglas, Kirk Osmond
Samuels, Thelma Alafia
Gittens-St. Hilaire, Marquita
Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title_full Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title_fullStr Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title_full_unstemmed Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title_short Serum LPS Associated with Hantavirus and Dengue Disease Severity in Barbados
title_sort serum lps associated with hantavirus and dengue disease severity in barbados
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783883/
https://www.ncbi.nlm.nih.gov/pubmed/31505806
http://dx.doi.org/10.3390/v11090838
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