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Environmental induction and genetic control of surface antigen switching in the nematode Caenorhabditis elegans

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TLDR
It is demonstrated that wild-type C. elegans can be induced to display the M37 antigen on a later larval stage by altering the growth conditions, and the mechanisms of nematode surface antigen switching can now be investigated directly.
Abstract
Nematodes can alter their surface coat protein compositions at the molts between developmental stages or in response to environmental changes; such surface alterations may enable parasitic nematodes to evade host immune defenses during the course of infection. Surface antigen switching mechanisms are presently unknown. In a genetic study of surface antigen switching, we have used a monoclonal antibody, M37, that recognizes a surface antigen on the first larval stage of the free-living nematode Caenorhabditis elegans. We demonstrate that wild-type C. elegans can be induced to display the M37 antigen on a later larval stage by altering the growth conditions. Mutations that result in nonconditional display of this antigen on all four larval stages fall into two classes. One class defines the new gene srf-6 II. The other mutations are in previously identified dauer-constitutive genes involved in transducing environmental signals that modulate formation of the dauer larva, a developmentally arrested dispersal stage. Although surface antigen switching is affected by some of the genes that control dauer formation, these two process can be blocked separately by specific mutations or induced separately by environmental factors. Based on these results, the mechanisms of nematode surface antigen switching can now be investigated directly.

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daf-12 encodes a nuclear receptor that regulates the dauer diapause and developmental age in C. elegans

TL;DR: It is proposed that DAF-12 integrates hormonal signals in cellular targets to coordinate major life history traits in Caenorhabditis elegans, and is expressed widely in target tissues from embryo to adult, but is upregulated during midlarval stages.
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DAF-9, a cytochrome P450 regulating C. elegans larval development and adult longevity.

TL;DR: The surprising cellular specificity of daf-9 expression supports a previously unrecognized role for these cells in neuroendocrine control of larval development, reproduction and life span.
Journal ArticleDOI

Caenorhabditis elegans as a model for parasitic nematodes

TL;DR: Caenorhabditis elegans has become a popular model system for genetic and molecular research, since it is easy to maintain and has a very fast life-cycle, and it is expected that by 1998 the complete sequence will be available.
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A Caenorhabditis elegans model of Yersinia infection: biofilm formation on a biotic surface

TL;DR: To investigate Yersinia pathogenicity and the evolutionary divergence of the genus, the effect of pathogenic yersiniae on the model organism Caenorhabditis elegans was studied and electron microscope and cytochemical examination of infected worms indicated that the infection phenotype is a result of biofilm formation on the head of the worm.
Journal ArticleDOI

Cuticle surface coat of plant-parasitic nematodes.

TL;DR: Although Caenorhabditis elegans is a poor model for plant-parasitic nematodes, it is a useful starting point for investigations of the cuticle and its SC, especially in the light of recent work using this species as a model for innate immunity and the generic biology underpinning much host-Parasite biology.
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