Egg and fourth instar larvae gut of Aedes aegypti as a source of stem cells

Tissue Cell. 2016 Oct;48(5):558-65. doi: 10.1016/j.tice.2016.05.004. Epub 2016 May 18.

Abstract

According to the World Health Organization, 2015 registered more than 1.206.172 cases of Dengue in the Americas. Recently, the Aedes aegypti has been not only related to Dengue, but also with cases of Zika virus and Chikungunya. Due to its epidemiological importance, this study characterized the morphology of the embryonated eggs of A. aegypti and provided a protocol to culture stem cells from eggs and digestive tract of fourth instar larvae in order to examine cell biology and expression of markers in these vectors. Cells were isolated and cultured in DMEM-High at 28°C, and their morphology, cell cycle and immunophenotyping were examined. Morphologically, embryos were at the end of the embryonic period and showed: head, thorax, and abdomen with eight abdominal segments. The embryonic tissues expressed markers related to cell proliferation (PCNA), pluripotency (Sox2 and OCT3/4), neural cells (Nestin), mesenchymal cells (Vimentin and Stro-1), and endosomal cells (GM130 and RAB5). In culture, cells from both tissues (eggs and larvae gut) were composed by a heterogeneous population. The cells had a globoid shape and small size. Cell cycle analysis on passage 1 (P1) showed 27.5%±2.0% of cell debris, 68% of cells on G0-G1 phase, 30.2% on S phase, 1.9%±0.5% on G2-M phase. In addition, cells on passage 2 showed: 10% of cell debris, 92.4% of cells on G0-G1 phase, 6.8% on S phase, 0.6% on G2-M phase. Embryonated eggs expressed markers involved with pluripotency (Sox2 and Oct 3/4), mesenchymal cells (vimentin and Stro-1), neural cells (Nestin), and cellular death by apoptosis (Caspase 3). Specific endosomal markers for insect cells (GM130 and RAB5) were also highly expressed. In cell culture of A. aegypti larvae gut the same labeling pattern was observed, with a small decrease in the expression of mesenchymal (vimentin and Stro-1) and neural (Nestin) markers. In summary, we were able to establish a protocol to culture embryonated eggs and larvae gut of A. aegypti, describing the characteristics of undifferentiated cells, as well as the cell cycle and expression of markers, which can be used for biotechnology studies for the biological control of this vector.

Keywords: Cell culture; Dengue; Emerging diseases; Morphology.

MeSH terms

  • Aedes / cytology*
  • Aedes / virology
  • Animals
  • Chikungunya Fever / transmission
  • Chikungunya Fever / virology
  • Chikungunya virus / pathogenicity
  • Dengue / transmission
  • Dengue / virology
  • Gastrointestinal Tract / cytology*
  • Gastrointestinal Tract / virology
  • Larva / cytology
  • Larva / virology
  • Ovum / cytology*
  • Ovum / virology
  • Stem Cells / cytology*
  • Stem Cells / virology
  • Zika Virus / pathogenicity
  • Zika Virus Infection / transmission
  • Zika Virus Infection / virology