Publications by authors named "Md Tafim Hossain Hrithik"

Upon immune challenge, recognition signals trigger insect immunity to remove the pathogens through cellular and humoral responses. Various immune mediators propagate the immune signals to nearby tissues, in which polyunsaturated fatty acid (PUFA) derivatives play crucial roles. However, little was known on how the insects terminate the activated immune responses after pathogen neutralization.

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  • Honeybees need a strong immune system to fight off pathogens, particularly the dangerous American foulbrood bacteria, which can lead to colony collapse.
  • The study found that both Apis mellifera and Apis cerana larvae experience high mortality when infected, but A. mellifera showed more tolerance compared to A. cerana.
  • Both species activated immune responses involving hemocyte behavior and antimicrobial peptides, but these responses were weakened by a specific enzyme inhibitor, highlighting the role of phospholipase A2 (PLA2) in honeybee immunity.
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An entomopathogenic bacterium, subsp. , is mutualistic to its host nematode, . The infective juvenile nematodes enter target insects through natural openings and release the symbiotic bacteria into the insect hemocoel.

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A nonmodel insect, Acrolepiopsis sapporensis, has been analyzed in immune responses. The total hemocytes in the fifth instar larvae were 2.33 × 10  cells/mL.

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Background: Eicosanoids are a group of the oxygenated C20 polyunsaturated fatty acids and play crucial roles in mediating various insect physiological processes. Catalytic activity of phospholipase A (PLA) provides an initial substrate, arachidonic acid (AA), for subsequent eicosanoid biosynthesis.

Results: This study identified four different secretory PLA (-) genes encoded in the Asian onion moth, .

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Insect immunity defends against the virulence of various entomopathogens, including (Bt). This study tested a hypothesis that any suppression of immune responses enhances Bt virulence. In a previous study, the entomopathogenic bacterium, (Xh), was shown to produce secondary metabolites to suppress insect immune responses.

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Article Synopsis
  • Insects have an immune response to the pathogenic bacterium Bacillus thuringiensis (Bt), but the mechanism of their recognition of Bt was not previously understood.
  • The study found that the dorsal switch protein 1 (DSP1) is crucial for insect immunity, as it is released in response to Bt infection and activates immune responses by interacting with specific receptors in the midgut.
  • The release of DSP1 triggers the expression of the Repat33 gene, which is important for immune responses, by activating phospholipase A and two other immune mediators, highlighting a complex immune signaling pathway in the insect midgut.
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Phurealipids (Photorhabdus urea lipids) are synthesized from Photorhabdus bacteria that are symbiotic to entomopathogenic nematodes. Their chemical structures are similar to that of juvenile hormone (JH) and have been suspected to mimic JH signaling in immunity and the development of insects. This study investigated the physiological roles of phurealipids with respect to their contribution to bacterial pathogenicity using four natural (HB13, HB69, HB416, and HB421) and one derivative (HB27) compound.

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Repat (=response to pathogen) is proposed for an immune-associated gene family from , a lepidopteran insect. In this gene family, 46 members (-) have been identified. They show marked variations in their inducible expression patterns in response to infections by different microbial pathogens.

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