Abstract

Adult females of stag beetles (Coleoptera: Lucanidae) possess an ovipositor-associated mycangium for conveying symbiotic microorganisms. In most lucanid species, their mycangium contains yeast symbionts of the genus Scheffersomyces Kurtzman and Suzuki that are known for their xylose-fermenting capability. The lucanid genus Platycerus Geoffroy, 1762 is a group of small blue stag beetles, in which ten Japanese species constitute a monophyletic clade. Here we examined the evolutionary relationships of these Japanese Platycerus species and their yeast symbionts, together with a Korean Platycerus species and other lucanid species as outgroup taxa. Based on the internal transcribed spacer (ITS) and the intergenic spacer (IGS) sequences, the yeast symbionts of all Platycerus species were closely related to each other and formed a monophyletic clade. There is no variation in ITS sequences of the yeast symbionts of the Japanese Platycerus species. Based on IGS sequences, the yeast symbionts formed clusters that largely reflected the geographic distribution of the host insects, being shared by sympatric Platycerus species except for P. delicatulus Lewis, 1883 and P. viridicuprus Kubota & Otobe, The symbiont phylogeny was globally not congruent with the host COI-based phylogeny, although some local congruences were observed. Statistically significant correlations were detected between the genetic distances of COI sequences of the host insects and those of IGS sequences of the yeast symbionts in Japan. These results suggest that, at least to some extent, the host insects and the yeast symbionts may have experienced co-evolutionary associations. While the Japanese Platycerus species formed a monophyletic clade in the COI phylogeny, the yeast symbionts of Japanese P. viridicuprus were very closely related to those of Korean P. hongwonpyoi Imura & Choe, 1989, suggesting the possibility that a recent secondary contact of the two beetle species during a marine withdrawal, e.g., in the last glacial period, might have resulted in an inter-specific horizontal transmission of the yeast symbiont.

Highlights

  • Symbiotic relationships with fungi are known in diverse insect taxa (Vega and Blackwell, 2005; Biedermann and Vega, 2020)

  • These sequences were completely identical to the sequences previously reported from two Japanese Platycerus species and seven Korean individuals of P. hongwonpyoi (Tanahashi et al, 2017) contained only two nucleotide substitutions compared with the sequence of the yeast symbiont from Prosmognathus angularis (Tanahashi et al, 2017) and were the most similar to the sequence of Scheffersomyces segobiensis (Tanahashi et al, 2017) among formally described yeast species

  • We first tested genetic variation of the yeast symbionts based on 2–8 colonies within a host female by using the primers IGS1 and IGS2

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Summary

Introduction

Symbiotic relationships with fungi are known in diverse insect taxa (Vega and Blackwell, 2005; Biedermann and Vega, 2020). Adult females of the Lucanidae possess a mycangium, constituted by an invaginated pouch of intersegmental membrane on the dorsal side of the abdominal tip, for conveying symbiotic microorganisms, which have been found in all the lucanid species representing 13 genera so far examined (Aegus Macleay, 1819; Dorcus Macleay, 1819; Prosopocoilus Hope & Westwood, 1845; Lucanus Scopoli, 1763; Neolucanus Thomson, 1862; Prismognathus Motschulsky, 1860; Figulus MacLeay, 1819; Nigidius MacLeay, 1819; Platycerus Geoffroy, 1762; Aesalus Fabricius, 1801; Nicagus LeConte, 1862; Ceruchus Macleay, 1819; Sinodendron Hellwig, 1792) (Tanahashi et al, 2010, 2017; Tanahashi and Hawes, 2016) They commonly harbor yeast symbionts in their mycangia (Tanahashi et al, 2010, 2017; Hawes, 2013) most of which belong to the genus Scheffersomyces Kurtzman & M. The yeast symbionts seem likely to be mutualistic to the host stag beetles, but so far, no proof for this has been found

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