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(18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging disease that causes fever, enteritis, thrombocytopenia, and leucopenia and can be fatal in up to 30% of cases. However, the mechanism of severe disease is not fully understood. Molecular imaging approaches, such as positron-emission t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807988/ https://www.ncbi.nlm.nih.gov/pubmed/26700962 |
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author | Hayasaka, Daisuke Nishi, Kodai Fuchigami, Takeshi Shiogama, Kazuya Onouchi, Takanori Shimada, Satoshi Tsutsumi, Yutaka Morita, Kouichi |
author_facet | Hayasaka, Daisuke Nishi, Kodai Fuchigami, Takeshi Shiogama, Kazuya Onouchi, Takanori Shimada, Satoshi Tsutsumi, Yutaka Morita, Kouichi |
author_sort | Hayasaka, Daisuke |
collection | PubMed |
description | Severe fever with thrombocytopenia syndrome (SFTS) is an emerging disease that causes fever, enteritis, thrombocytopenia, and leucopenia and can be fatal in up to 30% of cases. However, the mechanism of severe disease is not fully understood. Molecular imaging approaches, such as positron-emission tomography (PET), are functional in vivo imaging techniques that provide real-time dynamics of disease progression, assessments of pharmacokinetics, and diagnoses for disease progression. Molecular imaging also potentially provides useful approaches to explore the pathogenesis of viral infections. Thus, the purpose of this study was to image the pathological features of SFTSV infection in vivo by PET imaging. In a mouse model, we showed that (18)F-FDG accumulations clearly identified the intestinal tract site as a pathological site. We also demonstrated that (18)F-FDG PET imaging can assess disease progression and response to antiserum therapy within the same individual. This is the first report demonstrating a molecular imaging strategy for SFTSV infection. Our results provide potentially useful information for preclinical studies such as the elucidation of the mechanism of SFTSV infection in vivo and the assessment of drugs for SFTS treatment. |
format | Online Article Text |
id | pubmed-4807988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-48079882016-04-19 (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model Hayasaka, Daisuke Nishi, Kodai Fuchigami, Takeshi Shiogama, Kazuya Onouchi, Takanori Shimada, Satoshi Tsutsumi, Yutaka Morita, Kouichi Oncotarget Research Paper: Immunology Severe fever with thrombocytopenia syndrome (SFTS) is an emerging disease that causes fever, enteritis, thrombocytopenia, and leucopenia and can be fatal in up to 30% of cases. However, the mechanism of severe disease is not fully understood. Molecular imaging approaches, such as positron-emission tomography (PET), are functional in vivo imaging techniques that provide real-time dynamics of disease progression, assessments of pharmacokinetics, and diagnoses for disease progression. Molecular imaging also potentially provides useful approaches to explore the pathogenesis of viral infections. Thus, the purpose of this study was to image the pathological features of SFTSV infection in vivo by PET imaging. In a mouse model, we showed that (18)F-FDG accumulations clearly identified the intestinal tract site as a pathological site. We also demonstrated that (18)F-FDG PET imaging can assess disease progression and response to antiserum therapy within the same individual. This is the first report demonstrating a molecular imaging strategy for SFTSV infection. Our results provide potentially useful information for preclinical studies such as the elucidation of the mechanism of SFTSV infection in vivo and the assessment of drugs for SFTS treatment. Impact Journals LLC 2015-12-17 /pmc/articles/PMC4807988/ /pubmed/26700962 Text en Copyright: © 2016 Hayasaka et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper: Immunology Hayasaka, Daisuke Nishi, Kodai Fuchigami, Takeshi Shiogama, Kazuya Onouchi, Takanori Shimada, Satoshi Tsutsumi, Yutaka Morita, Kouichi (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title | (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title_full | (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title_fullStr | (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title_full_unstemmed | (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title_short | (18)F-FDG PET imaging for identifying the dynamics of intestinal disease caused by SFTSV infection in a mouse model |
title_sort | (18)f-fdg pet imaging for identifying the dynamics of intestinal disease caused by sftsv infection in a mouse model |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807988/ https://www.ncbi.nlm.nih.gov/pubmed/26700962 |
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