Literature DB >> 21615665

Revisiting the extracellular lifestyle.

Guillaume Dumenil1.   

Abstract

In microbiology textbooks infectious agents are traditionally classified as intracellular or extracellular pathogens depending on whether they multiply inside or outside host cells. In recent literature an increasing number of extracellular pathogens are described in close apposition with the host cell surface embedded in plasma membrane folds, making it difficult to classify them as strictly extracellular pathogens. This review further explores this emerging new lifestyle category tentatively named 'epicellular' in reference to earlier work describing the location of the parasite Cryptosporidium parvum. The lifestyles of three diverse such pathogens were examined: the parasite Cryptosporidium parvum, the Gram-negative bacterium Neisseria meningitidis and the human T cell leukaemia virus type 1 (HTLV-1). The specific cellular location, the mechanisms of adhesion, the induction of plasma membrane folds and the subsequent functional consequences will be compared. Although current knowledge suggests different underlying mechanisms, a concept that emerges is that the particular location of these pathogens has important functional consequences for the pathogens in terms of nutrient acquisition, immune escape, resistance to mechanical stress and transmission. Re-examining the lifestyle of other classically extracellular pathogens might thus shed a new light on the way pathogens interact with cells and point to new areas of investigation.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21615665     DOI: 10.1111/j.1462-5822.2011.01613.x

Source DB:  PubMed          Journal:  Cell Microbiol        ISSN: 1462-5814            Impact factor:   3.715


  6 in total

1.  Apicomplexan lineage-specific polytopic membrane proteins in Cryptosporidium parvum.

Authors:  Thavamani Rajapandi
Journal:  J Parasit Dis       Date:  2020-03-13

2.  Intestinal coccidiosis of anadromous and landlocked alewives, Alosa pseudoharengus, caused by Goussia ameliae n. sp. and G. alosii n. sp. (Apicomplexa: Eimeriidae).

Authors:  Jan Lovy; Sarah E Friend
Journal:  Int J Parasitol Parasites Wildl       Date:  2015-02-28       Impact factor: 2.674

3.  Adhesion to nanofibers drives cell membrane remodeling through one-dimensional wetting.

Authors:  Arthur Charles-Orszag; Feng-Ching Tsai; Daria Bonazzi; Valeria Manriquez; Martin Sachse; Adeline Mallet; Audrey Salles; Keira Melican; Ralitza Staneva; Aurélie Bertin; Corinne Millien; Sylvie Goussard; Pierre Lafaye; Spencer Shorte; Matthieu Piel; Jacomine Krijnse-Locker; Françoise Brochard-Wyart; Patricia Bassereau; Guillaume Duménil
Journal:  Nat Commun       Date:  2018-10-25       Impact factor: 14.919

4.  Neisseria gonorrhoeae subverts formin-dependent actin polymerization to colonize human macrophages.

Authors:  Stanimir S Ivanov; Reneau Castore; Maria Dolores Juarez Rodriguez; Magdalena Circu; Ana-Maria Dragoi
Journal:  PLoS Pathog       Date:  2021-12-28       Impact factor: 6.823

Review 5.  The Host-Pathogen Interactions and Epicellular Lifestyle of Neisseria meningitidis.

Authors:  August Mikucki; Nicolie R McCluskey; Charlene M Kahler
Journal:  Front Cell Infect Microbiol       Date:  2022-04-22       Impact factor: 6.073

6.  Cryptosporidium parvum scavenges LDL-derived cholesterol and micellar cholesterol internalized into enterocytes.

Authors:  Karen Ehrenman; Jane W Wanyiri; Najma Bhat; Honorine D Ward; Isabelle Coppens
Journal:  Cell Microbiol       Date:  2013-01-28       Impact factor: 3.715

  6 in total

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