| Literature DB >> 27932027 |
Jun Beom Lee1, Kyoung-Eun Park1, Seung Ah Lee1, Seong Han Jang1, Ho Jeong Eo1, Ho Am Jang1, Chan-Hee Kim1, Tsubasa Ohbayashi2, Yu Matsuura3, Yoshitomo Kikuchi4, Ryo Futahashi5, Takema Fukatsu5, Bok Luel Lee6.
Abstract
Recent studies have suggested that gut symbionts modulate insect development and reproduction. However, the mechanisms by which gut symbionts modulate host physiologies and the molecules involved in these changes are unclear. To address these questions, we prepared three different groups of the insect Riptortus pedestris: Burkholderia gut symbiont-colonized (Sym) insects, Burkholderia-non-colonized (Apo) insects, and Burkholderia-depleted (SymBurk-) insects, which were fed tetracycline. When the hemolymph proteins of three insects were analyzed by SDS-PAGE, the hexamerin-α, hexamerin-β and vitellogenin-1 proteins of Sym-adults were highly expressed compared to those of Apo- and SymBurk--insects. To investigate the expression patterns of these three genes during insect development, we measured the transcriptional levels of these genes. The hexamerin-β gene was specifically expressed at all nymphal stages, and its expression was detected 4-5 days earlier in Sym-insect nymphs than that in Apo- and SymBurk--insects. However, the hexamerin-α and vitellogenin-1 genes were only expressed in adult females, and they were also detected 6-7 days earlier and were 2-fold higher in Sym-adult females than those in the other insects. Depletion of hexamerin-β by RNA interference in 2nd instar Sym-nymphs delayed adult emergence, whereas hexamerin-α and vitellogenin-1 RNA interference in 5th instar nymphs caused loss of color of the eggs of Sym-insects. These results demonstrate that the Burkholderia gut symbiont modulates host development and egg production by regulating production of these three hemolymph storage proteins.Entities:
Keywords: Burkholderia; Hexamerin; Riptortus pedestris; Symbiosis; Symbiosis-affected host molecule; Vitellogenin
Mesh:
Substances:
Year: 2016 PMID: 27932027 DOI: 10.1016/j.dci.2016.11.019
Source DB: PubMed Journal: Dev Comp Immunol ISSN: 0145-305X Impact factor: 3.636