AI Article Synopsis

  • The study examines the fat body of the mosquito Aedes aegypti to understand its role in metabolism and protein synthesis, focusing on changes before and after blood feeding.
  • Researchers created two libraries from mosquito fat bodies: one non-blood fed (NBF) and one 24 hours post-blood meal (PBM), resulting in significant data with over 200,000 usable reads from each sample.
  • The analysis showed distinct differences in transcript expression between NBF and PBM, highlighting a shift towards vitellogenic gene expression after feeding, with key proteins like yolk proteins being highly expressed in response to the blood meal.

Article Abstract

Background: The fat body is the main organ of intermediary metabolism in insects and the principal source of hemolymph proteins. As part of our ongoing efforts to understand mosquito fat body physiology and to identify novel targets for insect control, we have conducted a transcriptome analysis of the fat body of Aedes aegypti before and in response to blood feeding.

Results: We created two fat body non-normalized EST libraries, one from mosquito fat bodies non-blood fed (NBF) and another from mosquitoes 24 hrs post-blood meal (PBM). 454 pyrosequencing of the non-normalized libraries resulted in 204,578 useable reads from the NBF sample and 323,474 useable reads from the PBM sample. Alignment of reads to the existing reference Ae. aegypti transcript libraries for analysis of differential expression between NBF and PBM samples revealed 116,912 and 115,051 matches, respectively. De novo assembly of the reads from the NBF sample resulted in 15,456 contigs, and assembly of the reads from the PBM sample resulted in 15,010 contigs. Collectively, 123 novel transcripts were identified within these contigs. Prominently expressed transcripts in the NBF fat body library were represented by transcripts encoding ribosomal proteins. Thirty-five point four percent of all reads in the PBM library were represented by transcripts that encode yolk proteins. The most highly expressed were transcripts encoding members of the cathepsin b, vitellogenin, vitellogenic carboxypeptidase, and vitelline membrane protein families.

Conclusion: The two fat body transcriptomes were considerably different from each other in terms of transcript expression in terms of abundances of transcripts and genes expressed. They reflect the physiological shift of the pre-feeding fat body from a resting state to vitellogenic gene expression after feeding.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144915PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0022573PLOS

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