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棉鼠呼吸道合胞病毒感染后的肺功能分析。

Pulmonary function analysis in cotton rats after respiratory syncytial virus infection.

机构信息

Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, Ohio, United States of America.

出版信息

PLoS One. 2020 Aug 10;15(8):e0237404. doi: 10.1371/journal.pone.0237404. eCollection 2020.


DOI:10.1371/journal.pone.0237404
PMID:32776985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7416943/
Abstract

The cotton rat (Sigmodon hispidus) is an excellent small animal model for human respiratory viral infections such as human respiratory syncytial virus (RSV) and human metapneumovirus (HMPV). These respiratory viral infections, as well as other pulmonary inflammatory diseases such as asthma, are associated with lung mechanic disturbances. So far, the pathophysiological effects of viral infection and allergy on cotton rat lungs have not been measured, although this information might be an important tool to determine the efficacy of vaccine and drug candidates. To characterize pulmonary function in the cotton rat, we established forced oscillation technique in uninfected, RSV infected and HDM sensitized cotton rats, and characterized pulmonary inflammation, mucus production, pulmonary edema, and oxygenation. There was a gender difference after RSV infection, with females demonstrating airway hyper-responsiveness while males did not. Female cotton rats 2dpi had a mild increase in pulmonary edema (wet: dry weight ratios). At day 4 post infection, female cotton rats demonstrated mild pulmonary inflammation, no increase in mucus production or reduction in oxygenation. Pulmonary function was not significantly impaired after RSV infection. In contrast, cotton rats sensitized to HDM demonstrated airway hyper-responsiveness with a significant increase in pulmonary inflammation, increase in baseline tissue damping, and a decrease in baseline pulmonary compliance. In summary, we established baseline data for forced oscillation technique and other respiratory measures in the cotton rat and used it to analyze respiratory diseases in cotton rats.

摘要

棉鼠(Sigmodon hispidus)是人类呼吸道病毒感染(如呼吸道合胞病毒[RSV]和人偏肺病毒[HMPV])的优秀小动物模型。这些呼吸道病毒感染以及哮喘等其他肺部炎症性疾病与肺力学障碍有关。尽管这些信息可能是确定疫苗和药物候选物疗效的重要工具,但迄今为止,尚未测量病毒感染和过敏对棉鼠肺部的病理生理影响。为了描述棉鼠的肺功能,我们在未感染、RSV 感染和 HDM 致敏的棉鼠中建立了强迫振荡技术,并对肺部炎症、黏液产生、肺水肿和氧合进行了特征描述。RSV 感染后存在性别差异,女性表现出气道高反应性,而男性则没有。感染后 2dpi 的雌性棉鼠出现轻度肺水肿(湿重/干重比增加)。在感染后第 4 天,雌性棉鼠表现出轻度肺部炎症,黏液产生无增加,氧合无降低。RSV 感染后肺功能未明显受损。相比之下,对 HDM 致敏的棉鼠表现出气道高反应性,肺部炎症明显增加,基础组织阻尼增加,基础肺顺应性降低。总之,我们建立了棉鼠强迫振荡技术和其他呼吸测量的基础数据,并将其用于分析棉鼠的呼吸疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/c5c0f74ae1d1/pone.0237404.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/f8c769c2a764/pone.0237404.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/70df725f76a5/pone.0237404.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/ad68c6b0bd22/pone.0237404.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/c5c0f74ae1d1/pone.0237404.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/f8c769c2a764/pone.0237404.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/70df725f76a5/pone.0237404.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/ad68c6b0bd22/pone.0237404.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/7416943/c5c0f74ae1d1/pone.0237404.g004.jpg

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[8]
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本文引用的文献

[1]
Mathematical modelling identifies the role of adaptive immunity as a key controller of respiratory syncytial virus in cotton rats.

J R Soc Interface. 2019-11-27

[2]
Characterization of Cotton Rat () Eosinophils, Including Their Response to Respiratory Syncytial Virus Infection.

Comp Med. 2018-2-1

[3]
Assessing Structure-Function Relations in Mice Using the Forced Oscillation Technique and Quantitative Histology.

Methods Mol Biol. 2017

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Respiratory syncytial virus hospitalization and mortality: Systematic review and meta-analysis.

Pediatr Pulmonol. 2017-4

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Pneumonol Alergol Pol. 2016

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Paediatr Respir Rev. 2016-6

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Paediatr Respir Rev. 2015-11-10

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Respiratory Syncytial Virus Disease Is Mediated by Age-Variable IL-33.

PLoS Pathog. 2015-10-16

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Mouse Models of Acute Respiratory Distress Syndrome: A Review of Analytical Approaches, Pathologic Features, and Common Measurements.

Toxicol Pathol. 2015-12

[10]
Respiratory syncytial virus infection increases chlorine-induced airway hyperresponsiveness.

Am J Physiol Lung Cell Mol Physiol. 2015-8-1

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