Screening in Planarians Identifies MORN2 as a Key Component in LC3-Associated Phagocytosis and Resistance to Bacterial Infection

Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance...

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Published inCell host & microbe Vol. 16; no. 3; pp. 338 - 350
Main Authors Abnave, Prasad, Mottola, Giovanna, Gimenez, Gregory, Boucherit, Nicolas, Trouplin, Virginie, Torre, Cedric, Conti, Filippo, Ben Amara, Amira, Lepolard, Catherine, Djian, Benjamin, Hamaoui, Daniel, Mettouchi, Amel, Kumar, Atul, Pagnotta, Sophie, Bonatti, Stefano, Lepidi, Hubert, Salvetti, Alessandra, Abi-Rached, Laurent, Lemichez, Emmanuel, Mege, Jean-Louis, Ghigo, Eric
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 10.09.2014
Elsevier
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Abstract Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance mechanisms. Whole-transcriptome analysis coupled with RNAi screening of worms infected with Staphylococcus aureus or Legionella pneumophila identified 18 resistance genes with nine human orthologs, of which we examined the function of MORN2. Human MORN2 facilitates phagocytosis-mediated restriction of Mycobacterium tuberculosis, L. pneumophila, and S. aureus in macrophages. MORN2 promotes the recruitment of LC3, an autophagy protein also involved in phagocytosis, to M. tuberculosis-containing phagosomes and subsequent maturation to degradative phagolysosomes. MORN2-driven trafficking of M. tuberculosis to single-membrane, LC3-positive compartments requires autophagy-related proteins Atg5 and Beclin-1, but not Ulk-1 and Atg13, highlighting the importance of MORN2 in LC3-associated phagocytosis. These findings underscore the value of studying planarian defenses to identify immune factors. [Display omitted] •Dugesia japonica planarian flatworms eliminate a spectrum of ingested pathogenic bacteria•Transcriptomic and RNAi analyses reveal planarian genes promoting resistance to bacteria•MORN2 restricts the growth of all bacterial strains tested in planarians•MORN2 promotes lipidation of LC3-I and LC3-associated phagocytosis of M. tuberculosis Dugesia japonica planarian flatworms are resistant to various bacteria that are pathogenic in humans. Abnave et al. use planarians as a model to identify antibacterial immune factors and determine that MORN2, conserved in Homo sapiens, restricts intracellular bacterial growth by promoting LC3-associated phagocytosis of invading bacteria.
AbstractList Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance mechanisms. Whole-transcriptome analysis coupled with RNAi screening of worms infected with Staphylococcus aureus or Legionella pneumophila identified 18 resistance genes with nine human orthologs, of which we examined the function of MORN2. Human MORN2 facilitates phagocytosis-mediated restriction of Mycobacterium tuberculosis, L. pneumophila, and S. aureus in macrophages. MORN2 promotes the recruitment of LC3, an autophagy protein also involved in phagocytosis, to M. tuberculosis-containing phagosomes and subsequent maturation to degradative phagolysosomes. MORN2-driven trafficking of M. tuberculosis to single-membrane, LC3-positive compartments requires autophagy-related proteins Atg5 and Beclin-1, but not Ulk-1 and Atg13, highlighting the importance of MORN2 in LC3-associated phagocytosis. These findings underscore the value of studying planarian defenses to identify immune factors.
Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance mechanisms. Whole-transcriptome analysis coupled with RNAi screening of worms infected with Staphylococcus aureus or Legionella pneumophila identified 18 resistance genes with nine human orthologs, of which we examined the function of MORN2. Human MORN2 facilitates phagocytosis-mediated restriction of Mycobacterium tuberculosis, L. pneumophila, and S. aureus in macrophages. MORN2 promotes the recruitment of LC3, an autophagy protein also involved in phagocytosis, to M. tuberculosis-containing phagosomes and subsequent maturation to degradative phagolysosomes. MORN2-driven trafficking of M. tuberculosis to single-membrane, LC3-positive compartments requires autophagy-related proteins Atg5 and Beclin-1, but not Ulk-1 and Atg13, highlighting the importance of MORN2 in LC3-associated phagocytosis. These findings underscore the value of studying planarian defenses to identify immune factors.Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance mechanisms. Whole-transcriptome analysis coupled with RNAi screening of worms infected with Staphylococcus aureus or Legionella pneumophila identified 18 resistance genes with nine human orthologs, of which we examined the function of MORN2. Human MORN2 facilitates phagocytosis-mediated restriction of Mycobacterium tuberculosis, L. pneumophila, and S. aureus in macrophages. MORN2 promotes the recruitment of LC3, an autophagy protein also involved in phagocytosis, to M. tuberculosis-containing phagosomes and subsequent maturation to degradative phagolysosomes. MORN2-driven trafficking of M. tuberculosis to single-membrane, LC3-positive compartments requires autophagy-related proteins Atg5 and Beclin-1, but not Ulk-1 and Atg13, highlighting the importance of MORN2 in LC3-associated phagocytosis. These findings underscore the value of studying planarian defenses to identify immune factors.
Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria pathogenic to Homo sapiens, Caenorhabditis elegans, and/or Drosophila melanogaster and thus represent a model to identify innate resistance mechanisms. Whole-transcriptome analysis coupled with RNAi screening of worms infected with Staphylococcus aureus or Legionella pneumophila identified 18 resistance genes with nine human orthologs, of which we examined the function of MORN2. Human MORN2 facilitates phagocytosis-mediated restriction of Mycobacterium tuberculosis, L. pneumophila, and S. aureus in macrophages. MORN2 promotes the recruitment of LC3, an autophagy protein also involved in phagocytosis, to M. tuberculosis-containing phagosomes and subsequent maturation to degradative phagolysosomes. MORN2-driven trafficking of M. tuberculosis to single-membrane, LC3-positive compartments requires autophagy-related proteins Atg5 and Beclin-1, but not Ulk-1 and Atg13, highlighting the importance of MORN2 in LC3-associated phagocytosis. These findings underscore the value of studying planarian defenses to identify immune factors. [Display omitted] •Dugesia japonica planarian flatworms eliminate a spectrum of ingested pathogenic bacteria•Transcriptomic and RNAi analyses reveal planarian genes promoting resistance to bacteria•MORN2 restricts the growth of all bacterial strains tested in planarians•MORN2 promotes lipidation of LC3-I and LC3-associated phagocytosis of M. tuberculosis Dugesia japonica planarian flatworms are resistant to various bacteria that are pathogenic in humans. Abnave et al. use planarians as a model to identify antibacterial immune factors and determine that MORN2, conserved in Homo sapiens, restricts intracellular bacterial growth by promoting LC3-associated phagocytosis of invading bacteria.
Author Abi-Rached, Laurent
Gimenez, Gregory
Trouplin, Virginie
Ben Amara, Amira
Pagnotta, Sophie
Mettouchi, Amel
Mege, Jean-Louis
Abnave, Prasad
Djian, Benjamin
Bonatti, Stefano
Mottola, Giovanna
Ghigo, Eric
Torre, Cedric
Kumar, Atul
Boucherit, Nicolas
Conti, Filippo
Hamaoui, Daniel
Lepidi, Hubert
Lepolard, Catherine
Lemichez, Emmanuel
Salvetti, Alessandra
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  surname: Pagnotta
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  organization: Centre Commun de Microscopie Appliquée (CCMA) Université de Nice Sophia Antipolis, Faculté des Sciences, Parc Valrose, 06108 Nice Cedex 2, France
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  email: eric.ghigo@univ-amu.fr
  organization: CNRS UMR 7278, IRD198, INSERM U1095, Aix-Marseille Université, 27 Bd Jean Moulin 13385 Marseille Cedex 05, France
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Snippet Dugesia japonica planarian flatworms are naturally exposed to various microbes but typically survive this challenge. We show that planarians eliminate bacteria...
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StartPage 338
SubjectTerms Animals
Bacterial Infections - genetics
Bacterial Infections - immunology
Bacterial Infections - microbiology
Disease Models, Animal
Helminth Proteins - genetics
Helminth Proteins - immunology
Humans
Legionella pneumophila - immunology
Legionella pneumophila - physiology
Life Sciences
Microtubule-Associated Proteins - genetics
Microtubule-Associated Proteins - immunology
Phagocytosis
Planarians - genetics
Planarians - immunology
Planarians - microbiology
Staphylococcus aureus - immunology
Staphylococcus aureus - physiology
Title Screening in Planarians Identifies MORN2 as a Key Component in LC3-Associated Phagocytosis and Resistance to Bacterial Infection
URI https://dx.doi.org/10.1016/j.chom.2014.08.002
https://www.ncbi.nlm.nih.gov/pubmed/25211076
https://www.proquest.com/docview/1561968886
https://hal.science/hal-02111891
Volume 16
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