Literature DB >> 31591148

Distinct Host-Mycobacterial Pathogen Interactions between Resistant Adult and Tolerant Tadpole Life Stages of Xenopus laevis.

Kun Hyoe Rhoo1, Eva-Stina Edholm2, María J Forzán3, Adil Khan1, Anthony W Waddle1,4, Martin S Pavelka1, Jacques Robert5.   

Abstract

Mycobacterium marinum is a promiscuous pathogen infecting many vertebrates, including humans, whose persistent infections are problematic for aquaculture and public health. Among unsettled aspects of host-pathogen interactions, the respective roles of conventional and innate-like T (iT) cells in host defenses against M. marinum remain unclear. In this study, we developed an infection model system in the amphibian Xenopus laevis to study host responses to M. marinum at two distinct life stages, tadpole and adult. Adult frogs possess efficient conventional T cell-mediated immunity, whereas tadpoles predominantly rely on iT cells. We hypothesized that tadpoles are more susceptible and elicit weaker immune responses to M. marinum than adults. However, our results show that, although anti-M. marinum immune responses between tadpoles and adults are different, tadpoles are as resistant to M. marinum inoculation as adult frogs. M. marinum inoculation triggered a robust proinflammatory CD8+ T cell response in adults, whereas tadpoles elicited only a noninflammatory CD8 negative- and iT cell-mediated response. Furthermore, adult anti-M. marinum responses induced active granuloma formation with abundant T cell infiltration and were associated with significantly reduced M. marinum loads. This is reminiscent of local CD8+ T cell response in lung granulomas of human tuberculosis patients. In contrast, tadpoles rarely exhibited granulomas and tolerated persistent M. marinum accumulation. Gene expression profiling confirmed poor tadpole CD8+ T cell response, contrasting with the marked increase in transcript levels of the anti-M. marinum invariant TCR rearrangement (iVα45-Jα1.14) and of CD4. These data provide novel insights into the critical roles of iT cells in vertebrate antimycobacterial immune response and tolerance to pathogens.
Copyright © 2019 by The American Association of Immunologists, Inc.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 31591148      PMCID: PMC6832864          DOI: 10.4049/jimmunol.1900459

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  23 in total

1.  Phylogenetic and developmental study of CD4, CD8 α and β T cell co-receptor homologs in two amphibian species, Xenopus tropicalis and Xenopus laevis.

Authors:  Asiya Seema Chida; Ana Goyos; Jacques Robert
Journal:  Dev Comp Immunol       Date:  2010-11-21       Impact factor: 3.636

Review 2.  Disease tolerance: concept and mechanisms.

Authors:  J L McCarville; J S Ayres
Journal:  Curr Opin Immunol       Date:  2017-12-15       Impact factor: 7.486

3.  Antimicrobial activity of mucosal-associated invariant T cells.

Authors:  Lionel Le Bourhis; Emmanuel Martin; Isabelle Péguillet; Amélie Guihot; Nathalie Froux; Maxime Coré; Eva Lévy; Mathilde Dusseaux; Vanina Meyssonnier; Virginie Premel; Charlotte Ngo; Béatrice Riteau; Livine Duban; Delphine Robert; Shouxiong Huang; Martin Rottman; Claire Soudais; Olivier Lantz
Journal:  Nat Immunol       Date:  2010-06-27       Impact factor: 25.606

4.  Nonclassical MHC-Restricted Invariant Vα6 T Cells Are Critical for Efficient Early Innate Antiviral Immunity in the Amphibian Xenopus laevis.

Authors:  Eva-Stina Edholm; Leon Grayfer; Francisco De Jesús Andino; Jacques Robert
Journal:  J Immunol       Date:  2015-06-10       Impact factor: 5.422

Review 5.  CD8 T cells and Mycobacterium tuberculosis infection.

Authors:  Philana Ling Lin; JoAnne L Flynn
Journal:  Semin Immunopathol       Date:  2015-04-28       Impact factor: 9.623

6.  Identification of a candidate CD5 homologue in the amphibian Xenopus laevis.

Authors:  J B Jürgens; L A Gartland; L Du Pasquier; J D Horton; T W Göbel; M D Cooper
Journal:  J Immunol       Date:  1995-11-01       Impact factor: 5.422

Review 7.  Comparative pathogenesis of Mycobacterium marinum and Mycobacterium tuberculosis.

Authors:  David M Tobin; Lalita Ramakrishnan
Journal:  Cell Microbiol       Date:  2008-02-20       Impact factor: 3.715

8.  Nonclassical MHC class I-dependent invariant T cells are evolutionarily conserved and prominent from early development in amphibians.

Authors:  Eva-Stina Edholm; Liz-Marie Albertorio Saez; Ann L Gill; Steven R Gill; Leon Grayfer; Nikesha Haynes; Jason R Myers; Jacques Robert
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-12       Impact factor: 11.205

Review 9.  Comparative and developmental study of the immune system in Xenopus.

Authors:  Jacques Robert; Yuko Ohta
Journal:  Dev Dyn       Date:  2009-06       Impact factor: 3.780

Review 10.  Unravelling the networks dictating host resistance versus tolerance during pulmonary infections.

Authors:  Isabelle Meunier; Eva Kaufmann; Jeffrey Downey; Maziar Divangahi
Journal:  Cell Tissue Res       Date:  2017-02-06       Impact factor: 5.249

View more
  3 in total

Review 1.  γδ T, NKT, and MAIT Cells During Evolution: Redundancy or Specialized Functions?

Authors:  Christelle Harly; Jacques Robert; Francois Legoux; Olivier Lantz
Journal:  J Immunol       Date:  2022-07-15       Impact factor: 5.426

2.  Developing Tadpole Xenopus laevis as a Comparative Animal Model to Study Mycobacterium abscessus Pathogenicity.

Authors:  Arianna Lopez; Carolyn Shoen; Michael Cynamon; Dionysia Dimitrakopoulou; Matthieu Paiola; Martin S Pavelka; Jacques Robert
Journal:  Int J Mol Sci       Date:  2021-01-15       Impact factor: 5.923

3.  Enhancers of Host Immune Tolerance to Bacterial Infection Discovered Using Linked Computational and Experimental Approaches.

Authors:  Megan M Sperry; Richard Novak; Vishal Keshari; Alexandre L M Dinis; Mark J Cartwright; Diogo M Camacho; Jean-François Paré; Michael Super; Michael Levin; Donald E Ingber
Journal:  Adv Sci (Weinh)       Date:  2022-06-15       Impact factor: 17.521

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.