Transcriptome analysis of Nosema assamensis infecting muga silkworms (Antheraea assamensis) reveals insights into

Anupama Jagadish1,2, Himanshu Dubey1, Indumathi Kamatchi1

  • 1Genomic Division, Seri Biotech Research Laboratory, Carmelaram Post, Kodathi, Bengaluru-560035, India.

Annals of Parasitology
|March 15, 2022
PubMed

Insights

Researchers analyzed gene expression in muga silkworms infected with pebrine disease, caused by Microsporidia. They identified key virulence genes (PTP2, PTP3, SWP12, SWP26) involved in host-pathogen interactions, aiding potential early diagnostics.

Area of Science:

  • * Genomics and Bioinformatics
  • * Molecular Biology
  • * Pathogen-Host Interactions

Background:

  • * Muga silkworms, reared outdoors, are susceptible to diseases like pebrine, caused by Microsporidia.
  • * Understanding the molecular mechanisms of Microsporidia infection is crucial for silkworm health.

Purpose of the Study:

  • * To categorize transcript data of Nosema from infected muga silkworms.
  • * To identify potential virulence genes and understand host-pathogen interactions.

Main Methods:

  • * Gene ontology (GO) and KEGG pathway analysis of Nosema transcript data.
  • * Identification and comparison of unigenes and orthologous sequences.
  • * Analysis of virulence gene expression in infected silkworms.

Main Results:

  • * 2850 unigene sets identified; 2739 categorized by GO terms.
  • * Enrichment in organic metabolism, cyclic compound binding, and intracellular structures.
  • * KEGG analysis revealed enrichment in purine and thiamine metabolic pathways, suggesting increased energy metabolism during infection.
  • * Putative virulence genes (PTP2, PTP3, SWP12, SWP26) identified, showing conservation across Nosema species and detectable expression.

Conclusions:

  • * Identified virulence genes are likely conserved and play a role in host-pathogen interactions.
  • * These genes offer potential targets for developing early diagnostic tools for pebrine disease.
  • * Further bioassays are needed to validate the role of these genes in infection and spore propagation.

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