White-nose syndrome initiates a cascade of physiologic disturbances in the hibernating bat host.

Q1 Biochemistry, Genetics and Molecular Biology
Michelle L Verant, Carol U Meteyer, John R Speakman, Paul M Cryan, Jeffrey M Lorch, David S Blehert
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引用次数: 185

Abstract

Background: The physiological effects of white-nose syndrome (WNS) in hibernating bats and ultimate causes of mortality from infection with Pseudogymnoascus (formerly Geomyces) destructans are not fully understood. Increased frequency of arousal from torpor described among hibernating bats with late-stage WNS is thought to accelerate depletion of fat reserves, but the physiological mechanisms that lead to these alterations in hibernation behavior have not been elucidated. We used the doubly labeled water (DLW) method and clinical chemistry to evaluate energy use, body composition changes, and blood chemistry perturbations in hibernating little brown bats (Myotis lucifugus) experimentally infected with P. destructans to better understand the physiological processes that underlie mortality from WNS.

Results: These data indicated that fat energy utilization, as demonstrated by changes in body composition, was two-fold higher for bats with WNS compared to negative controls. These differences were apparent in early stages of infection when torpor-arousal patterns were equivalent between infected and non-infected animals, suggesting that P. destructans has complex physiological impacts on its host prior to onset of clinical signs indicative of late-stage infections. Additionally, bats with mild to moderate skin lesions associated with early-stage WNS demonstrated a chronic respiratory acidosis characterized by significantly elevated dissolved carbon dioxide, acidemia, and elevated bicarbonate. Potassium concentrations were also significantly higher among infected bats, but sodium, chloride, and other hydration parameters were equivalent to controls.

Conclusions: Integrating these novel findings on the physiological changes that occur in early-stage WNS with those previously documented in late-stage infections, we propose a multi-stage disease progression model that mechanistically describes the pathologic and physiologic effects underlying mortality of WNS in hibernating bats. This model identifies testable hypotheses for better understanding this disease, knowledge that will be critical for defining effective disease mitigation strategies aimed at reducing morbidity and mortality that results from WNS.

Abstract Image

Abstract Image

白鼻综合征在冬眠的蝙蝠宿主中引发一连串的生理紊乱。
背景:冬眠蝙蝠感染白鼻综合征(WNS)的生理影响和破坏假裸鼠(原地霉菌)感染死亡的最终原因尚不完全清楚。在患有晚期WNS的冬眠蝙蝠中,从冬眠中唤醒的频率增加被认为会加速脂肪储备的消耗,但导致这些冬眠行为改变的生理机制尚未阐明。为了更好地了解WNS死亡的生理过程,我们采用双标记水(DLW)法和临床化学方法评估了实验感染了破坏性单胞菌的冬眠小棕蝙蝠(Myotis lucifugus)的能量使用、身体成分变化和血液化学扰动。结果:这些数据表明,与阴性对照相比,患有WNS的蝙蝠的脂肪能量利用率(由身体组成的变化所证明)高出两倍。这些差异在感染的早期阶段很明显,感染动物和未感染动物之间的休眠唤醒模式是相同的,这表明在出现晚期感染的临床症状之前,destructans对其宿主有复杂的生理影响。此外,与早期WNS相关的轻度至中度皮肤病变的蝙蝠表现出慢性呼吸性酸中毒,其特征是溶解二氧化碳显著升高、酸血症和碳酸氢盐升高。感染蝙蝠的钾浓度也明显较高,但钠、氯化物和其他水合参数与对照组相当。结论:将这些关于早期WNS发生的生理变化的新发现与先前在晚期感染中记录的生理变化相结合,我们提出了一个多阶段疾病进展模型,该模型从机制上描述了冬眠蝙蝠WNS死亡的病理和生理效应。该模型确定了可测试的假设,以更好地了解这种疾病,这些知识对于确定旨在降低WNS导致的发病率和死亡率的有效疾病缓解策略至关重要。
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来源期刊
BMC Physiology
BMC Physiology Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
9.60
自引率
0.00%
发文量
0
期刊介绍: BMC Physiology is an open access journal publishing original peer-reviewed research articles in cellular, tissue-level, organismal, functional, and developmental aspects of physiological processes. BMC Physiology (ISSN 1472-6793) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record and Google Scholar.
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