Changes in antennal gene expression underlying sensory system maturation in Rhodnius prolixus

Insect Biochem Mol Biol. 2022 Jan:140:103704. doi: 10.1016/j.ibmb.2021.103704. Epub 2021 Dec 20.

Abstract

Triatomine bugs are the blood feeding insect vectors transmitting Chagas disease to humans, a neglected tropical disease that affects over 8 million people, mainly in Latin America. The behavioral responses to host cues and bug signals in Rhodnius prolixus are state dependent, i.e., they vary as a function of post-ecdysis age. At the molecular level, these changes in behavior are probably due to a modulation of peripheral and central processes. In the present study, we report a significant modulation of the expression of a large set of sensory-related genes. Results were generated by means of antennal transcriptomes of 5th instar larvae along the first week (days 0, 2, 4, 6 and 8) after ecdysis sequenced using the Illumina HiSeq platform. Significant age-induced changes in transcript abundance were established for more than 6120 genes (54,7% of 11,186 genes expressed) in the antenna of R. prolixus. This was especially true between the first two days after ecdysis when more than 2500 genes had their expression significantly altered. In contrast, expression profiles were almost identical between day 6 and 8, with only a few genes showing significant modulation of their expression. A total of 86 sensory receptors, odorant carriers and odorant degrading enzymes were significantly modulated across age points and clustered into three distinct expression profiles. The set of sensory genes whose expression increased with age (profile 3) may include candidates underlying the increased responsiveness to host cues shown by R. prolixus during the first days after molting. For the first time, we describe the maturation process undergone at the molecular level by the peripheral sensory system of a hemimetabolous insect.

Keywords: Age; Antennae; Rhodnius prolixus; Sensory genes; Transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthropod Antennae*
  • Chagas Disease / transmission
  • Gene Expression Profiling
  • Genes, Insect*
  • Insect Vectors / genetics
  • Insect Vectors / metabolism
  • Larva / genetics
  • Larva / metabolism
  • Odorants
  • Receptors, Odorant / genetics
  • Receptors, Odorant / metabolism
  • Rhodnius* / genetics
  • Rhodnius* / metabolism
  • Sense Organs* / embryology
  • Sense Organs* / physiology
  • Smell / genetics
  • Transcriptome

Substances

  • Receptors, Odorant