Literature DB >> 23880551

Early lesions following aerosol infection of rhesus macaques (Macaca mulatta) with Mycobacterium tuberculosis strain H37RV.

E L Rayner1, G R Pearson, G A Hall, R J Basaraba, F Gleeson, A McIntyre, S Clark, A Williams, M J Dennis, S A Sharpe.   

Abstract

As part of a study to investigate early changes following exposure to aerosols of Mycobacterium tuberculosis (Mtb), 10 rhesus macaques (Macaca mulatta) were infected with high (731 colony forming units [cfu]), medium (70 cfu) or low (7 cfu) doses of Mtb, and tissues were examined at 2 and 3 weeks post infection (wpi). Clinical disease was not observed. Results of advanced imaging and pathological findings were compared with respect to the delivered dose and time post infection. Magnetic resonance imaging revealed lesions in the lungs at these early time points ex vivo immediately prior to detailed post-mortem examination in the absence of clinical disease. In animals exposed to high and medium doses of Mtb that were studied at 2 and 3 wpi, a range of lesions including small foci of mainly mononuclear cells, primarily macrophages (granulomatous lesions), as well as obvious granulomas, were observed microscopically in the lungs, including lymphatics and hilar lymph nodes. In the low-dose group at 3 weeks, small lesions were identified in the lung and hilar lymph nodes of one animal, and the remaining two animals in this group had lesions in either lung or hilar lymph node. Acid fast bacilli were demonstrated in the lung and lymph nodes in all animals that received high and medium doses, and the lymph nodes of two animals at the low dose. A dose-dependent effect was observed with increasing dose and time post infection. Furthermore, early dissemination of bacilli to the draining, hilar lymph nodes with concomitant granulomatous lesion formation was observed. By contributing to the recognition of early lesion development due to aerosol challenge of Mtb in the rhesus macaque, this study forms a basis for further investigation of early lesions and may inform the design of future vaccine and therapeutic studies involving early time points in this species. Crown
Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  early granuloma; lung; macaque; tuberculosis

Mesh:

Substances:

Year:  2013        PMID: 23880551     DOI: 10.1016/j.jcpa.2013.05.005

Source DB:  PubMed          Journal:  J Comp Pathol        ISSN: 0021-9975            Impact factor:   1.311


  8 in total

1.  Aerosol vaccination with AERAS-402 elicits robust cellular immune responses in the lungs of rhesus macaques but fails to protect against high-dose Mycobacterium tuberculosis challenge.

Authors:  Patricia A Darrah; Diane L Bolton; Andrew A Lackner; Deepak Kaushal; Pyone Pyone Aye; Smriti Mehra; James L Blanchard; Peter J Didier; Chad J Roy; Srinivas S Rao; David A Hokey; Charles A Scanga; Donata R Sizemore; Jerald C Sadoff; Mario Roederer; Robert A Seder
Journal:  J Immunol       Date:  2014-07-14       Impact factor: 5.422

Review 2.  Modeling tuberculosis in nonhuman primates.

Authors:  Charles A Scanga; JoAnne L Flynn
Journal:  Cold Spring Harb Perspect Med       Date:  2014-09-11       Impact factor: 6.915

3.  Prevention of tuberculosis in rhesus macaques by a cytomegalovirus-based vaccine.

Authors:  Scott G Hansen; Daniel E Zak; Guangwu Xu; Julia C Ford; Emily E Marshall; Daniel Malouli; Roxanne M Gilbride; Colette M Hughes; Abigail B Ventura; Emily Ainslie; Kurt T Randall; Andrea N Selseth; Parker Rundstrom; Lauren Herlache; Matthew S Lewis; Haesun Park; Shannon L Planer; John M Turner; Miranda Fischer; Christina Armstrong; Robert C Zweig; Joseph Valvo; Jackie M Braun; Smitha Shankar; Lenette Lu; Andrew W Sylwester; Alfred W Legasse; Martin Messerle; Michael A Jarvis; Lynn M Amon; Alan Aderem; Galit Alter; Dominick J Laddy; Michele Stone; Aurelio Bonavia; Thomas G Evans; Michael K Axthelm; Klaus Früh; Paul T Edlefsen; Louis J Picker
Journal:  Nat Med       Date:  2018-01-15       Impact factor: 53.440

4.  Presence of multiple lesion types with vastly different microenvironments in C3HeB/FeJ mice following aerosol infection with Mycobacterium tuberculosis.

Authors:  Scott M Irwin; Emily Driver; Edward Lyon; Christopher Schrupp; Gavin Ryan; Mercedes Gonzalez-Juarrero; Randall J Basaraba; Eric L Nuermberger; Anne J Lenaerts
Journal:  Dis Model Mech       Date:  2015-03-30       Impact factor: 5.758

5.  Protective Efficacy of Inhaled BCG Vaccination Against Ultra-Low Dose Aerosol M. tuberculosis Challenge in Rhesus Macaques.

Authors:  Andrew D White; Charlotte Sarfas; Laura S Sibley; Jennie Gullick; Simon Clark; Emma Rayner; Fergus Gleeson; Martí Català; Isabel Nogueira; Pere-Joan Cardona; Cristina Vilaplana; Mike J Dennis; Ann Williams; Sally A Sharpe
Journal:  Pharmaceutics       Date:  2020-04-25       Impact factor: 6.321

6.  X-ray-based virtual slicing of TB-infected lungs.

Authors:  Ana Ortega-Gil; Juan José Vaquero; Mario Gonzalez-Arjona; Joaquín Rullas; Arrate Muñoz-Barrutia
Journal:  Sci Rep       Date:  2019-12-18       Impact factor: 4.379

Review 7.  One Size Fits All? Not in In Vivo Modeling of Tuberculosis Chemotherapeutics.

Authors:  Hee-Jeong Yang; Decheng Wang; Xin Wen; Danielle M Weiner; Laura E Via
Journal:  Front Cell Infect Microbiol       Date:  2021-03-16       Impact factor: 5.293

8.  Dynamics of Macrophage, T and B Cell Infiltration Within Pulmonary Granulomas Induced by Mycobacterium tuberculosis in Two Non-Human Primate Models of Aerosol Infection.

Authors:  Laura Hunter; Suzie Hingley-Wilson; Graham R Stewart; Sally A Sharpe; Francisco Javier Salguero
Journal:  Front Immunol       Date:  2022-01-06       Impact factor: 8.786

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.