Rajaram S et al. (2000) Genesis "The sequence and associated null phenotype of a C. elegans neurocalcin-like gene."

Sedensky MM, Rajaram S, Morgan PG

[Genesis, 2000]

The neuronal calcium sensor (NCS) proteins belong to a subfamily of the EF-hand calcium binding proteins. These proteins are primarily expressed in the nervous system and currently include more than 20 members across species [Nakayama et al., J Mol Evol 34:416-448, 1992]. Two homologues of the ncs genes, Ce-ncs-1 and Ce-ncs-2, have recently been identified in the nematode C. elegans. Here we report the cDNA sequence of a third C. elegans ncs homologue, Ce-ncs-3. We demonstrate that a null mutation in this gene caused by a large deletion in the locus does not confer a visible phenotype in C. elegans. This, in addition to the strong homology between Ce-NCS-3 and the other C. elegans NCS proteins, may indicate functional redundancy between the three genes.

Skrdla PJ (2005) Biophys Chem "Statistical kinetic approach for modeling lifespan."

Skrdla PJ

[Biophys Chem, 2005]

Lifespan regulation through gene expression involves complex biochemical processes. Unfortunately, current mathematical models for treating lifespan data afford little insight into the mechanisms that control longevity. In this work, we demonstrate the use of a novel kinetic model to successfully fit the lifespan curves of the nematode, Caenorhabditis elegans. Our findings show that population aging may be treated analogously to a dispersive chemical process [P.J. Skrdla, R.T. Robertson., J. Phys. Chem. B 109 10611 (2005)]. Much like the Gompertz model, only two fit parameters, alpha and beta, are needed to adequately describe the entire data set for each nematode population. These parameters relate a ''global first-order time constant'' and a ''global second-order rate constant'', with units of (time) and (time)(-2), respectively. In C. elegans, the increased longevity resulting from DAF-16 (a transcription factor) activity in the intestinal tissue correlates with a larger alpha value and a smaller beta value; the opposite is true for animals with shorter lifespans. A basic physical interpretation of the two parameters is provided.

Thomas R et al. (2013) J Med Microbiol "Stenotrophomonas maltophilia: pathogenesis model using Caenorhabditis elegans."

Neela V, Thomas R, Hamat RA

[J Med Microbiol, 2013]

Stenotrophomonas maltophilia plays an important role as an opportunistic pathogen in immunocompromised individuals. Despite its clinical implication, the true knowledge regarding the pathogenicity of these bacteria remains unclear. Various methods have been employed to prove this bacterium to be pathogenic. However, the debate whether S. maltophilia is a true pathogen or a colonizer still remains unanswered as effective killing was not seen in earlier experiments with different animal models of infection (Denton et al., 1998; Adamak et al., 2011; Pompilo et al., 2011). Study by Rouf et al. (2011) on murine lung infection model illustrated that different strains of mice exhibited different outcome for S. maltophilia infection. Strains such as A/J and DBA/2 were permissive for clinical isolates of S. maltophilia and showed higher levels of pro-inflammatory cytokines. In contrast, BALB/c and C57BL/6 strains were non-permissive for S. maltophilia. While Huang et al. (2009) showed nematotoxic activity by environmental S. maltophilia strain against free-living nematode, Panagrellus redivivus, and plant-parasitic nematode, Bursaphelenchus xylophilus.