Loss in lung volume and changes in the immune response demonstrate disease progression in African green monkeys infected by small-particle aerosol and intratracheal exposure to Nipah virus

被引:32
作者
Cong, Yu [1 ]
Lentz, Margaret R. [1 ]
Lara, Abigail [1 ]
Alexander, Isis [1 ]
Bartos, Christopher [1 ]
Bohannon, J. Kyle [1 ]
Hammoud, Dima [2 ]
Huzella, Louis [1 ]
Jahrling, Peter B. [1 ,3 ]
Janosko, Krisztina [1 ]
Jett, Catherine [1 ,6 ]
Kollins, Erin [1 ]
Lackemeyer, Matthew [1 ]
Mollura, Daniel [2 ]
Ragland, Dan [1 ]
Rojas, Oscar [1 ]
Solomon, Jeffrey [3 ,4 ]
Xu, Ziyue [2 ]
Munster, Vincent [5 ]
Holbrook, Michael R. [1 ]
机构
[1] NIAID, Integrated Res Facil, Frederick, MD USA
[2] NIH, Ctr Infect Dis Imaging, Clin Ctr, Bldg 10, Bethesda, MD 20892 USA
[3] NIAID, Emerging Viral Pathogen Sect, Frederick, MD USA
[4] Leidos Biomed Res, Clin Monitoring Res Program, Clin Res Directorate, NCI Campus, Frederick, MD USA
[5] NIAID, Rocky Mt Labs, Lab Virol, Virus Ecol Unit, Hamilton, MT 59840 USA
[6] Texas Biomed Res Inst, San Antonio, TX USA
来源
PLOS NEGLECTED TROPICAL DISEASES | 2017年 / 11卷 / 04期
基金
美国国家卫生研究院;
关键词
HAMSTER MODEL; ENCEPHALITIS; BANGLADESH; MALAYSIA; TRANSMISSION; PATHOGENESIS; FEATURES; EVASION; MR;
D O I
10.1371/journal.pntd.0005532
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Nipah virus (NiV) is a paramyxovirus (genus Henipavirus) that emerged in the late 1990s in Malaysia and has since been identified as the cause of sporadic outbreaks of severe febrile disease in Bangladesh and India. NiV infection is frequently associated with severe respiratory or neurological disease in infected humans with transmission to humans through inhalation, contact or consumption of NiV contaminated foods. In the work presented here, the development of disease was investigated in the African Green Monkey (AGM) model following intratracheal (IT) and, for the first time, small-particle aerosol administration of NiV. This study utilized computed tomography (CT) and magnetic resonance imaging (MRI) to temporally assess disease progression. The host immune response and changes in immune cell populations over the course of disease were also evaluated. This study found that IT and small-particle administration of NiV caused similar disease progression, but that IT inoculation induced significant congestion in the lungs while disease following small-particle aerosol inoculation was largely confined to the lower respiratory tract. Quantitative assessment of changes in lung volume found up to a 45% loss in IT inoculated animals. None of the subjects in this study developed overt neurological disease, a finding that was supported by MRI analysis. The development of neutralizing antibodies was not apparent over the 8-10 day course of disease, but changes in cytokine response in all animals and activated CD8+ T cell numbers suggest the onset of cell-mediated immunity. These studies demonstrate that IT and small-particle aerosol infection with NiV in the AGM model leads to a severe respiratory disease devoid of neurological indications. This work also suggests that extending the disease course or minimizing the impact of the respiratory component is critical to developing a model that has a neurological component and more accurately reflects the human condition.
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页数:24
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共 44 条
  • [41] Relapsed and late-onset Nipah encephalitis
    Tan, CT
    Goh, KJ
    Wong, KT
    Sarji, SA
    Chua, KB
    Chew, NK
    Murugasu, P
    Loh, YL
    Chong, HT
    Tan, KS
    Thayaparan, T
    Kumar, S
    Jusoh, MR
    [J]. ANNALS OF NEUROLOGY, 2002, 51 (06) : 703 - 708
  • [42] Nosocomial transmissibility of Nipah virus
    Tan, CT
    Tan, KS
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2001, 184 (10) : 1367 - 1367
  • [43] A golden hamster model for human acute Nipah virus infection
    Wong, KT
    Grosjean, I
    Brisson, C
    Blanquier, B
    Fevre-Montange, M
    Bernard, A
    Loth, P
    Georges-Courbot, MC
    Chevallier, M
    Akaoka, H
    Marianneau, P
    Lam, SK
    Wild, TF
    Deubel, V
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) : 2127 - 2137
  • [44] Recombinant Measles Virus Vaccine Expressing the Nipah Virus Glycoprotein Protects against Lethal Nipah Virus Challenge
    Yoneda, Misako
    Georges-Courbot, Marie-Claude
    Ikeda, Fusako
    Ishii, Miho
    Nagata, Noriyo
    Jacquot, Frederic
    Raoul, Herve
    Sato, Hiroki
    Kai, Chieko
    [J]. PLOS ONE, 2013, 8 (03):