Evidence of a hemolymph-born factor that induces onset of maturation in Manduca sexta larvae

•The factors responsible for metamorphic commitment in larval insects are unresolved.•Hemolymph transfused from post-CW larvae caused a significant reduction in growth duration.•Hemolymph transfused from pre-CW larvae resulted in no change in the duration of growth.•Shortened growth duration after post-CW hemolymph transfusion did not change in pupal size.•These results suggest there may be a circulating hemolymph factor responsible for induction of CW.

Insect metamorphosis is a complex developmental transition determined and coordinated by hormonal signaling that begins at a critical weight late in the larval phase of life. Even though this hormonal signaling is well understood in insects, the internal factors that are assessed at the critical weight and that drive commitment to metamorphosis have remained unresolved in most species. The critical weight may represent either an autonomous decision by the neuroendocrine system without input from other developing larval tissues, or an assessment of developmental thresholds occurring throughout the body that are then integrated by the neuroendocrine tissues. The latter hypothesis predicts that there could be one or more developmental threshold signals that originate from developing tissues and ultimately induce the onset of metamorphosis. However, there is no evidence for such a signal in the organisms for which the critical weight is well described. Here we test for the evidence of this factor in Manduca sexta (Lepidoptera: Sphingidae) by transferring hemolymph from individuals that are either post- or pre-critical weight into pre-critical weight 5th instar larvae. We found that hemolymph from a post-critical weight donor induces a shortening of development time, though the mass at pupation is unaffected. This suggests that metamorphic commitment occurring at the critical weight is at least partially coordinated by signaling from developing tissues via a hemolymph-borne signaling factor.

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