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Effect of Aspergillus fumigatus on infection in immunosuppressed rats
BACKGROUND: Immunosuppression is believed to increase the risk of invasive pulmonary aspergillosis (IPA), but information on the mechanism is limited. Therefore, we analyze the effect and mechanism of the pathogenesis and disease progression of IPA in a combined immunosuppressed rat model. METHODS:...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929786/ https://www.ncbi.nlm.nih.gov/pubmed/36819534 http://dx.doi.org/10.21037/atm-22-6600 |
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author | Huang, Wanhong Mo, Lida Yang, Yanfang Chen, Songlin Liu, Zeduan Ma, Qiuying Luo, Xiaolu |
author_facet | Huang, Wanhong Mo, Lida Yang, Yanfang Chen, Songlin Liu, Zeduan Ma, Qiuying Luo, Xiaolu |
author_sort | Huang, Wanhong |
collection | PubMed |
description | BACKGROUND: Immunosuppression is believed to increase the risk of invasive pulmonary aspergillosis (IPA), but information on the mechanism is limited. Therefore, we analyze the effect and mechanism of the pathogenesis and disease progression of IPA in a combined immunosuppressed rat model. METHODS: The immunosuppressed rat model was established by intraperitoneal injection of cyclophosphamide (CTX) and dexamethasone (DXM). IPA was established by nasal inoculation of Aspergillus fumigatus spore suspension. Pathological sections and tissue homogenate culture were used to evaluate the lung tissue. Routine blood and inflammatory indexes were dynamically observed. The expressions of NLRP3/caspase-1/GSDMD protein and gene were determined using western blot and quantitative polymerase chain reaction (q-PCR) respectively. T-test or one-way repeated measures analysis were used to do statistical analysis on the groups. RESULTS: Following intraperitoneal of CTX and DXM injections, the rats showed depression, weight loss, and significant decreases in the numbers of leukocytes and classified cells. Pathological sections revealed more severe lung lesions in the immunosuppressed rats infected with Aspergillus fumigatus. The expression of NLRP3/caspase-1/GSDMD protein increased significantly in both the aspergillosis and immunosuppressed plus aspergillosis groups. CONCLUSIONS: The pathological development of IPA in the immunosuppressed rats had the most serious effects, and the findings strongly implicated NLRP3/caspase-1/GSDMD pathway involvement. |
format | Online Article Text |
id | pubmed-9929786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-99297862023-02-16 Effect of Aspergillus fumigatus on infection in immunosuppressed rats Huang, Wanhong Mo, Lida Yang, Yanfang Chen, Songlin Liu, Zeduan Ma, Qiuying Luo, Xiaolu Ann Transl Med Original Article BACKGROUND: Immunosuppression is believed to increase the risk of invasive pulmonary aspergillosis (IPA), but information on the mechanism is limited. Therefore, we analyze the effect and mechanism of the pathogenesis and disease progression of IPA in a combined immunosuppressed rat model. METHODS: The immunosuppressed rat model was established by intraperitoneal injection of cyclophosphamide (CTX) and dexamethasone (DXM). IPA was established by nasal inoculation of Aspergillus fumigatus spore suspension. Pathological sections and tissue homogenate culture were used to evaluate the lung tissue. Routine blood and inflammatory indexes were dynamically observed. The expressions of NLRP3/caspase-1/GSDMD protein and gene were determined using western blot and quantitative polymerase chain reaction (q-PCR) respectively. T-test or one-way repeated measures analysis were used to do statistical analysis on the groups. RESULTS: Following intraperitoneal of CTX and DXM injections, the rats showed depression, weight loss, and significant decreases in the numbers of leukocytes and classified cells. Pathological sections revealed more severe lung lesions in the immunosuppressed rats infected with Aspergillus fumigatus. The expression of NLRP3/caspase-1/GSDMD protein increased significantly in both the aspergillosis and immunosuppressed plus aspergillosis groups. CONCLUSIONS: The pathological development of IPA in the immunosuppressed rats had the most serious effects, and the findings strongly implicated NLRP3/caspase-1/GSDMD pathway involvement. AME Publishing Company 2023-01-31 2023-01-31 /pmc/articles/PMC9929786/ /pubmed/36819534 http://dx.doi.org/10.21037/atm-22-6600 Text en 2023 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Huang, Wanhong Mo, Lida Yang, Yanfang Chen, Songlin Liu, Zeduan Ma, Qiuying Luo, Xiaolu Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title | Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title_full | Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title_fullStr | Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title_full_unstemmed | Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title_short | Effect of Aspergillus fumigatus on infection in immunosuppressed rats |
title_sort | effect of aspergillus fumigatus on infection in immunosuppressed rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929786/ https://www.ncbi.nlm.nih.gov/pubmed/36819534 http://dx.doi.org/10.21037/atm-22-6600 |
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