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  1. TI=1918 pandemic influenza virus and Streptococcus pneumoniae coinfection results in activation of coagulation and widespread pulmonary thrombosis in mice and humans
  2. AU="Kapiotis, S"

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Artikel ; Online: 1918 pandemic influenza virus and Streptococcus pneumoniae co-infection results in activation of coagulation and widespread pulmonary thrombosis in mice and humans.

Walters, Kathie-Anne / D'Agnillo, Felice / Sheng, Zong-Mei / Kindrachuk, Jason / Schwartzman, Louis M / Kuestner, Rolf E / Chertow, Daniel S / Golding, Basil T / Taubenberger, Jeffery K / Kash, John C

The Journal of pathology

2015  Band 238, Heft 1, Seite(n) 85–97

Abstract: ... with the 1918 influenza virus, followed by Streptococcus pneumoniae (SP) 72 h later. Co-infected mice exhibited ... influenza virus and SP co-infection in mice and humans is extensive expression of tissue factor and activation ... To study bacterial co-infection following 1918 H1N1 influenza virus infection, mice were inoculated ...

Abstract To study bacterial co-infection following 1918 H1N1 influenza virus infection, mice were inoculated with the 1918 influenza virus, followed by Streptococcus pneumoniae (SP) 72 h later. Co-infected mice exhibited markedly more severe disease, shortened survival time and more severe lung pathology, including widespread thrombi. Transcriptional profiling revealed activation of coagulation only in co-infected mice, consistent with the extensive thrombogenesis observed. Immunohistochemistry showed extensive expression of tissue factor (F3) and prominent deposition of neutrophil elastase on endothelial and epithelial cells in co-infected mice. Lung sections of SP-positive 1918 autopsy cases showed extensive thrombi and prominent staining for F3 in alveolar macrophages, monocytes, neutrophils, endothelial and epithelial cells, in contrast to co-infection-positive 2009 pandemic H1N1 autopsy cases. This study reveals that a distinctive feature of 1918 influenza virus and SP co-infection in mice and humans is extensive expression of tissue factor and activation of the extrinsic coagulation pathway leading to widespread pulmonary thrombosis.
Mesh-Begriff(e) Animals ; Blood Coagulation ; Coinfection/complications ; Disease Models, Animal ; Female ; Humans ; Immunohistochemistry ; Influenza A Virus, H1N1 Subtype ; Influenza Pandemic, 1918-1919 ; Influenza, Human/complications ; Influenza, Human/microbiology ; Influenza, Human/pathology ; Mice ; Mice, Inbred BALB C ; Oligonucleotide Array Sequence Analysis ; Orthomyxoviridae Infections/complications ; Orthomyxoviridae Infections/microbiology ; Orthomyxoviridae Infections/pathology ; Pneumococcal Infections/complications ; Pneumococcal Infections/microbiology ; Pneumococcal Infections/pathology ; Pulmonary Embolism/microbiology ; Pulmonary Embolism/pathology ; Reverse Transcriptase Polymerase Chain Reaction ; Streptococcus pneumoniae
Sprache Englisch
Erscheinungsdatum 2015-10-14
Erscheinungsland England
Dokumenttyp Journal Article ; Research Support, N.I.H., Intramural ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID 3119-7
ISSN 1096-9896 ; 0022-3417
ISSN (online) 1096-9896
ISSN 0022-3417
DOI 10.1002/path.4638
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