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Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis

Commensal organisms are frequent causes of pneumonia. However, the detection of these organisms in the airway does not mean that they are the causative pathogens; they may exist merely as colonizers. In up to 50% cases of pneumonia, the causative pathogens remain unidentified, thereby hampering targ...

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Autores principales: Hirama, Takashi, Yamaguchi, Takefumi, Miyazawa, Hitoshi, Tanaka, Tomoaki, Hashikita, Giichi, Kishi, Etsuko, Tachi, Yoshimi, Takahashi, Shun, Kodama, Keiji, Egashira, Hiroshi, Yokote, Akemi, Kobayashi, Kunihiko, Nagata, Makoto, Ishii, Toshiaki, Nemoto, Manabu, Tanaka, Masahiko, Fukunaga, Koichi, Morita, Satoshi, Kanazawa, Minoru, Hagiwara, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164732/
https://www.ncbi.nlm.nih.gov/pubmed/21909436
http://dx.doi.org/10.1371/journal.pone.0024474
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author Hirama, Takashi
Yamaguchi, Takefumi
Miyazawa, Hitoshi
Tanaka, Tomoaki
Hashikita, Giichi
Kishi, Etsuko
Tachi, Yoshimi
Takahashi, Shun
Kodama, Keiji
Egashira, Hiroshi
Yokote, Akemi
Kobayashi, Kunihiko
Nagata, Makoto
Ishii, Toshiaki
Nemoto, Manabu
Tanaka, Masahiko
Fukunaga, Koichi
Morita, Satoshi
Kanazawa, Minoru
Hagiwara, Koichi
author_facet Hirama, Takashi
Yamaguchi, Takefumi
Miyazawa, Hitoshi
Tanaka, Tomoaki
Hashikita, Giichi
Kishi, Etsuko
Tachi, Yoshimi
Takahashi, Shun
Kodama, Keiji
Egashira, Hiroshi
Yokote, Akemi
Kobayashi, Kunihiko
Nagata, Makoto
Ishii, Toshiaki
Nemoto, Manabu
Tanaka, Masahiko
Fukunaga, Koichi
Morita, Satoshi
Kanazawa, Minoru
Hagiwara, Koichi
author_sort Hirama, Takashi
collection PubMed
description Commensal organisms are frequent causes of pneumonia. However, the detection of these organisms in the airway does not mean that they are the causative pathogens; they may exist merely as colonizers. In up to 50% cases of pneumonia, the causative pathogens remain unidentified, thereby hampering targeting therapies. In speculating on the role of a commensal organism in pneumonia, we devised the battlefield hypothesis. In the “pneumonia battlefield,” the organism-to-human cell number ratio may be an index for the pathogenic role of the organism. Using real-time PCR reactions for sputum samples, we tested whether the hypothesis predicts the results of bacteriological clinical tests for 4 representative commensal organisms: Streptococcus pneumoniae, Haemophilus influenzae, Pseudomonas spp., and Moraxella catarrhalis. The cutoff value for the organism-to-human cell number ratio, above which the pathogenic role of the organism was suspected, was set up for each organism using 224 sputum samples. The validity of the cutoff value was then tested in a prospective study that included 153 samples; the samples were classified into 3 groups, and each group contained 93%, 7%, and 0% of the samples from pneumonia, in which the pathogenic role of Streptococcus pneumoniae was suggested by the clinical tests. The results for Haemophilus influenzae, Pseudomonas spp., and Moraxella catarrhalis were 100%, 0%, and 0%, respectively. The battlefield hypothesis enabled legitimate interpretation of the PCR results and predicted pneumonia in which the pathogenic role of the organism was suggested by the clinical test. The PCR reactions based on the battlefield hypothesis may help to promote targeted therapies for pneumonia. The prospective observatory study described in the current report had been registered to the University Hospital Medical Information Network (UMIN) registry before its initiation, where the UMIN is a registry approved by the International Committee of Medical Journal Editors (ICMJE). The UMIN registry number was UMIN000001118: A prospective study for the investigation of the validity of cutoff values established for the HIRA-TAN system (April 9, 2008).
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spelling pubmed-31647322011-09-09 Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis Hirama, Takashi Yamaguchi, Takefumi Miyazawa, Hitoshi Tanaka, Tomoaki Hashikita, Giichi Kishi, Etsuko Tachi, Yoshimi Takahashi, Shun Kodama, Keiji Egashira, Hiroshi Yokote, Akemi Kobayashi, Kunihiko Nagata, Makoto Ishii, Toshiaki Nemoto, Manabu Tanaka, Masahiko Fukunaga, Koichi Morita, Satoshi Kanazawa, Minoru Hagiwara, Koichi PLoS One Research Article Commensal organisms are frequent causes of pneumonia. However, the detection of these organisms in the airway does not mean that they are the causative pathogens; they may exist merely as colonizers. In up to 50% cases of pneumonia, the causative pathogens remain unidentified, thereby hampering targeting therapies. In speculating on the role of a commensal organism in pneumonia, we devised the battlefield hypothesis. In the “pneumonia battlefield,” the organism-to-human cell number ratio may be an index for the pathogenic role of the organism. Using real-time PCR reactions for sputum samples, we tested whether the hypothesis predicts the results of bacteriological clinical tests for 4 representative commensal organisms: Streptococcus pneumoniae, Haemophilus influenzae, Pseudomonas spp., and Moraxella catarrhalis. The cutoff value for the organism-to-human cell number ratio, above which the pathogenic role of the organism was suspected, was set up for each organism using 224 sputum samples. The validity of the cutoff value was then tested in a prospective study that included 153 samples; the samples were classified into 3 groups, and each group contained 93%, 7%, and 0% of the samples from pneumonia, in which the pathogenic role of Streptococcus pneumoniae was suggested by the clinical tests. The results for Haemophilus influenzae, Pseudomonas spp., and Moraxella catarrhalis were 100%, 0%, and 0%, respectively. The battlefield hypothesis enabled legitimate interpretation of the PCR results and predicted pneumonia in which the pathogenic role of the organism was suggested by the clinical test. The PCR reactions based on the battlefield hypothesis may help to promote targeted therapies for pneumonia. The prospective observatory study described in the current report had been registered to the University Hospital Medical Information Network (UMIN) registry before its initiation, where the UMIN is a registry approved by the International Committee of Medical Journal Editors (ICMJE). The UMIN registry number was UMIN000001118: A prospective study for the investigation of the validity of cutoff values established for the HIRA-TAN system (April 9, 2008). Public Library of Science 2011-09-01 /pmc/articles/PMC3164732/ /pubmed/21909436 http://dx.doi.org/10.1371/journal.pone.0024474 Text en Hirama et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hirama, Takashi
Yamaguchi, Takefumi
Miyazawa, Hitoshi
Tanaka, Tomoaki
Hashikita, Giichi
Kishi, Etsuko
Tachi, Yoshimi
Takahashi, Shun
Kodama, Keiji
Egashira, Hiroshi
Yokote, Akemi
Kobayashi, Kunihiko
Nagata, Makoto
Ishii, Toshiaki
Nemoto, Manabu
Tanaka, Masahiko
Fukunaga, Koichi
Morita, Satoshi
Kanazawa, Minoru
Hagiwara, Koichi
Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title_full Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title_fullStr Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title_full_unstemmed Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title_short Prediction of the Pathogens That Are the Cause of Pneumonia by the Battlefield Hypothesis
title_sort prediction of the pathogens that are the cause of pneumonia by the battlefield hypothesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164732/
https://www.ncbi.nlm.nih.gov/pubmed/21909436
http://dx.doi.org/10.1371/journal.pone.0024474
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