Partial characterization of the extracellular keratinase from Microsporum canis

The extracellular keratinase of Microsporum canis released peptides from alpha-type fibrous protein and the membranous fraction isolated from human stratum corneum. Inhibition of the enzyme by phenylmethyl-sulfonylfluoride and its weak inhibition by N-ethylmaleimide and etheneglycol tetra-acetic acid indicated that it is probably a serine proteinase.     

Can lantana seeds be utilized in lamb rations?

Lantana seeds contain 70.6 g crude protein, 12.8 g ether extract, 103.1 g crude fibre, 761.0 g nitrogen-free extract, 52.5 g total ash, 8.4 g calcium and 2.5 g phosphorus/kg dry matter. The replacement, by lantana seeds, of 200 g maize/kg of concentrate mixture for lambs was studied in two experiments lasting 3–4 months. The crude protein concentration in the lantana ration was lower than in the maize, and significantly (P<0.01) so in the second experiment. In the first experiment, the digestibility and intakes of dietary crude protein (DCP) and total dietary nitrogen (TDN) of the lantana group were not significantly lower. In the second experiment, dry matter and crude protein digestibility and intakes of DCP and TDN of the lantana group were significantly (P<0.01) lower than the maize group. Even after adjustment for mean protein concentration in the diets, the intakes of DCP (P<0.01) and TDN (P<0.05) in the lantana group were significantly lower. In a repeat metabolic trial also, the adjusted intakes of both DCP and TDN (P<0.01) of the lantana group were significantly lower. In spite of the depression in feed utilization, the biochemical and haematological parameters of the blood of animals in the lantana group were within the normal range. The apparent non-toxicity of lantana seeds to lambs over long-term feeding trials calls for further work on their possible utilization as a feed ingredient.     

Induction of autophagy through CLEC4E in combination with TLR4: an innovative strategy to restrict the survival of Mycobacterium tuberculosis

ABSTRACT

Host-directed therapies are gaining considerable impetus because of the emergence of drug-resistant strains of pathogens due to antibiotic therapy. Therefore, there is an urgent need to exploit alternative and novel strategies directed at host molecules to successfully restrict infections. The C-type lectin receptor CLEC4E and Toll-like receptor TLR4 expressed by host cells are among the first line of defense in encountering pathogens. Therefore, we exploited signaling of macrophages through CLEC4E in association with TLR4 agonists (C₄.T₄) to control the growth of Mycobacterium tuberculosis (Mtb). We observed significant improvement in host immunity and reduced bacterial load in the lungs of Mtb-infected mice and guinea pigs treated with C₄.T₄ agonists. Further, intracellular killing of Mtb was achieved with a 10-fold lower dose of isoniazid or rifampicin in conjunction with C₄.T₄ than the drugs alone. C₄.T₄ activated MYD88, PtdIns3K, STAT1 and RELA/NFKB, increased lysosome biogenesis, decreased Il10 and Il4 gene expression and enhanced macroautophagy/autophagy. Macrophages from autophagy-deficient (atg5 knockout or Becn1 knockdown) mice showed elevated survival of Mtb. The present findings also unveiled the novel role of CLEC4E in inducing autophagy through MYD88, which is required for control of Mtb growth. This study suggests a unique immunotherapeutic approach involving CLEC4E in conjunction with TLR4 to restrict the survival of Mtb through autophagy.