HISTOPATHOLOGICAL AND ULTRASTRUCTURAL STUDIES OF LUNG TISSUE OF MICE REINFECTED WITH DENGUE VIRUS SEROTYPES 1 OR 2

D. Barreto, H. Schatzmayr, C. Takiya, F. C. Jácome, M. Silva, N. Faria, R. Nogueira, O. Barth
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引用次数: 2

Abstract

Histological and ultrastructural alterations in lung of BALB/c mice reinfected with heterologous DENV by the intravenous route with non-neuroadapted dengue viruses serotypes 1 and 2 were analyzed. The lung samples were processed following the standard techniques of photonic and transmission electron microscopy. Morphological studies showed breakdown of alveolocapilar barrier leading to alveolitis, focal zones of collapse, and intraalveolar hemorrhage. Inside alveolar septa, congested capillaries exhibited neutrophils and platelets. Alveolar capillary endothelial cells exhibited aspects of activation with exuberant phylopodia and intracytoplasmic vesicles and vacuoles. Morphometrical analyses demonstrated an increase of the surface density of interalveolar septa in all reinfected mice while alveolar space density was decreased. All these morphometrical data corroborated the histological features emphasizing the alveolocapilar breakdrown in dengue infected animals. Important is the fact that reinfection leads to intraalveolar fibrogenesis as demonstrated by histomorphometry and ultrastructural studies. DENV particles, antigens and RNA were observed 72 hours post-reinfection in mosquito cells (C6/36) inoculated with sera of the animals. The morphological alterations observed in lungs were similar to the observed in human cases of dengue fever and dengue hemorrhagic fever. The present study demonstrates that the BALB/c mice, during the secondary infection by a heterologous serotype of DENV, develop morphological alterations in lung tissue more severe than those observed in the primary infection.
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登革病毒1型或2型再感染小鼠肺组织的组织病理学和超微结构研究
采用非神经适应性1型和2型登革病毒经静脉途径再次感染外源DENV的BALB/c小鼠,观察其肺组织和超微结构的变化。肺样品按照标准的光子显微镜和透射电镜技术进行处理。形态学研究显示肺泡毛细血管屏障的破坏导致肺泡炎、局灶性塌陷和肺泡内出血。肺泡间隔内充血毛细血管内可见中性粒细胞和血小板。肺泡毛细血管内皮细胞表现出丰富的门足和胞浆内囊泡和液泡的激活。形态计量学分析表明,所有再感染小鼠的肺泡间隔表面密度增加,而肺泡间隙密度降低。所有这些形态学数据证实了登革热感染动物的肺泡毛细血管断裂的组织学特征。重要的是,组织形态学和超微结构研究表明,再感染导致肺泡内纤维形成。接种动物血清的蚊子细胞(C6/36)再感染72 h后,观察DENV颗粒、抗原和RNA的变化。在肺部观察到的形态学改变与在登革热和登革出血热病例中观察到的相似。本研究表明,BALB/c小鼠继发性感染DENV时,肺组织的形态学改变比原发性感染时更为严重。
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