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. 2017 Mar 6;6:222. [Version 1] doi: 10.12688/f1000research.10970.1

Mitogenomes of Giant-Skipper Butterflies reveal an ancient split between deep and shallow root feeders

Jing Zhang 1, Qian Cong 1, Xiao-Ling Fan 2, Rongjiang Wang 3, Min Wang 2, Nick V Grishin 1,4,a
PMCID: PMC5373422  PMID: 28408977

Abstract

Background: Giant-Skipper butterflies from the genus Megathymus are North American endemics. These large and thick-bodied Skippers resemble moths and are unique in their life cycles. Grub-like at the later stages of development, caterpillars of these species feed and live inside yucca roots. Adults do not feed and are mostly local, not straying far from the patches of yucca plants.

Methods: Pieces of muscle were dissected from the thorax of specimens and genomic DNA was extracted (also from the abdomen of a specimen collected nearly 60 years ago). Paired-end libraries were prepared and sequenced for 150bp from both ends. The mitogenomes were assembled from the reads followed by a manual gap-closing procedure and a phylogenetic tree was constructed using a maximum likelihood method from an alignment of the mitogenomes.

Results: We determined mitogenome sequences of nominal subspecies of all five known species of Megathymus and Agathymus mariae to confidently root the phylogenetic tree. Pairwise sequence identity indicates the high similarity, ranging from 88-96% among coding regions for 13 proteins, 22 tRNAs and 2 rRNA, with a gene order typical for mitogenomes of Lepidoptera. Phylogenetic analysis confirms that Giant-Skippers (Megathymini) originate within the subfamily Hesperiinae and do not warrant a subfamily rank. Genus Megathymus is monophyletic and splits into two species groups. M. streckeri and M. cofaqui caterpillars feed deep in the main root system of yucca plants and deposit frass underground. M. ursus, M. beulahae and M. yuccae feed in the yucca caudex and roots near the ground, and deposit frass outside through a "tent" (a silk tube projecting from the center of yucca plant). M. yuccae and M. beulahae are sister species consistently with morphological similarities between them.

Conclusions: We constructed the first DNA-based phylogeny of the genus Megathymus from their mitogenomes. The phylogeny agrees with morphological considerations.

Keywords: phylogeny, mitochondria, sequence assembly, Hesperiidae, Megathymini


Giant-Skippers (Lepidoptera: Hesperiidae: Megathymini) are large, fat-bodied butterflies endemic to the North American continent 13. Their caterpillars adapted to feeding inside large roots and fleshy leaves of Yucca and Agave plants and relatives. Protected from many predators living within their nutrition-rich food sources, Megathymini are larger in size than most other skippers, and don't feed as adults. Genus Megathymus is characterized by root-feeding caterpillars, mostly in Yucca plants, that build a "tent" (a silk tube projecting above the ground) at least prior to pupation. Caterpillars of the genus Agathymus live inside Agave leaves and make a "trap-door" (a round, hardened disk of silk) to close the entrance to their leaf chamber before pupation.

To better understand the evolution and phylogeny of Megathymus, we sequenced complete mitogenomes of all five known species from the genus: M. yuccae, M. beulahae, M. ursus, M. streckeri, and M. cofaqui ( http://www.butterfliesofamerica.com/L/Hesperiidae.htm). For most species, nominotypical subspecies from or near the type localities were used (see Figure 1 for specimen data; collected under the permit #08-02Rev). M. beulahae specimen, male paratype, was from the National Museum of Natural History collection (Smithsonian Institution, Washington, DC, USA). To confidently root the Megathymus tree, we also sequenced a complete mitogenome of Agathymus mariae as an outgroup. Methods for genomic DNA extraction, library construction, next-generation sequencing, and computational procedures followed those we reported previously 414. The sequences have been deposited in GenBank and received accessions KY630500–KY630505.

Figure 1. Maximum likelihood tree of complete mitogenomes of 24 Hesperiidae species rooted with Pterourus glaucus (Papilionidae).

Figure 1.

Species names for mitogenome reported here are colored red. Numbers by the nodes show bootstrap support values and branches; bootstraps less than 70% are collapsed. GenBank accessions for sequences and data for specimens with mitogenomes reported here are: Achalarus lyciades NC_030602.1; Agathymus mariae mariae KY630504, voucher NVG-1647, female, USA: New Mexico, Eddy County, 22-Sep-2013; Ampittia dioscorides KM102732.1; Burara striata KY524446; Carterocephalus silvicola NC_024646.1; Celaenorrhinus maculosa NC_022853.1; Choaspes benjaminii NC_024647.1; Ctenoptilum vasava NC_016704.1; Daimio tethys NC_024648.1; Euschemon rafflesia KY513288; Erynnis montanus NC_021427.1; Hasora anura NC_027263.1; Hasora vitta NC_027170.1; Heteropterus morpheus NC_028506.1; Lerema accius NC_029826.1; Lobocla bifasciatus NC_024649.1; Megathymus beulahae beulahae KY630505, voucher 11-BOA-13385G05, paratype, male, Mexico, Hidalgo, near Ixmiquilpan, highway 85, klm. 176, 19-Aug-1957; Megathymus cofaqui cofaqui KY630503, voucher NVG-1536, female, USA: Georgia, Burke County, 2-Aug-2013; Megathymus streckeri streckeri KY630501, voucher NVG-1461, male, USA: Arizona, Apache County, southeast of Holbrook, 19-May-2013; Megathymus ursus violae KY630502, voucher NVG-1504, male, USA: Texas, Pecos County, Glass Mountains, 7-Jun-2013; Megathymus yuccae yuccae KY630500, voucher NVG-1185, male, USA: South Carolina, Aiken County, 25-Feb-2013; Papilio glaucus NC_027252; Parnara guttata NC_029136.1; Potanthus flavus NC_024650.1; Pyrgus maculatus NC_030192.1.

All specimens, but one, were collected in 2013 and pieces of their muscles cut out of the thorax were preserved in 100% ethanol to ensure best DNA quality. However, M. beulahae paratype specimen was collected in 1957 15 and stored pinned, spread and dry in a museum drawer for 60 years. DNA was extracted from its abdomen prior to genitalia dissection and produced good quality genomic reads resulting in a complete mitogenome assembly. Similarly to the results reported previously 16, we see that dry insect collections are an invaluable source of specimens for DNA studies; DNA can be extracted from Lepidoptera without damaging specimens beyond standard genitalia dissection procedure; and good quality DNA sequences can be obtained from specimens collected many decades ago.

Sequence comparison revealed that mitogenomes of all six species of Megathymini were very similar, about 15K base pairs in length, coding for 13 proteins, 22 transfer RNAs and 2 ribosomal RNA with gene order typical for mitogenomes of Lepidoptera. The A+T-rich control region is most variable in sequence and length and contains several direct repeats of about 360 bp present in all six species. Among Hesperiidae with available mitogenomes 6, 10, 11, 13, 14, 1724 these repeats are unique to Megathymini. The repeats cause difficulty with mitogenome assembly and their number remains uncertain.

To obtain the first DNA-based phylogeny of Megathymus, we constructed RAxML 25 (version 8.2.8, model GTRGAMMA, 100 bootstrap replicates) maximum likelihood tree from available high-quality mitogenomes of Hesperiidae 6, 10, 11, 13, 14, 1724 rooted with Pterourus glaucus (Papilionidae) sequence 10 ( Figure 1). While not giving confident resolution to the relationships between subfamilies Eudaminae and Pyrginae, the tree confirms the placement of Megathymini within the subfamily Hesperiinae 2628 and argues against historical treatment of Giant-Skippers at subfamily level. The tree resolves the Megathymini phylogeny with 100% bootstrap, supports monophyly of the genus Megathymus and suggests a split between the two species groups. The first group is formed by M. streckeri and M. cofaqui. Caterpillars of these species feed deep in the main root system of yucca plants and deposit frass underground 2, 3. They build a tent only prior to pupation and the tent usually projects from the ground surface. Males of these two species possess hair-like scales, particularly prominent on dorsal hindwing. M. streckeri and M. cofaqui are the closest sister species among Megathymus ( Figure 1). Due to their apparently close relationship and allopatric distribution, Scott has suggested that M. streckeri and M. cofaqui may be subspecies of the same biological species 2. However, the COI barcode sequences we obtained show about 4% divergence between them, revealing significant differences and supporting the two taxa as distinct species. COI barcode divergence in different populations of the same species mostly falls within 2% 29.

The second species group consists of M. yuccae, M. beulahae and M. ursus. Caterpillars of these species feed in Yucca caudex and in roots close to the ground, maintaining the tent throughout development and depositing frass outside the tent 2, 3. Males of these three species lack hair-like scales. M. yuccae and M. beulahae are sister species, as expected from their close morphological similarities. However, their COI barcodes show a very large divergence of 9%. This pronounced divergence was unexpected, because the two species are quite similar in appearance and some males are difficult to tell apart ( http://www.butterfliesofamerica.com/L/t/Megathymus_a.htm). The most noticeable difference between M. yuccae and M. beulahae is the larger white ventral hindwing spots in the latter species, frequently fused to form a bad, especially in females. However, these spots may be significantly reduced in males, frequently in the northern populations. Interestingly, M. beulahae is the only Megathymus species that feeds in yucca-like Agave plant 1, 15, but it is a confident sister of Yucca-feeding M. yuccae. M. ursus is a sister to these two Megathymus. M. ursus has rather different wing shape and patterns. The wings are narrower with more extended apex, forewing spots well-separated in M. yuccae form a band-like arrangement, and hindwings lack spots that females M. yuccae and M. beulahae possess.

In conclusion, we sequenced mitochondrial genomes of all five known species of Megathymus and one species of Agathymus as an outgroup, and constructed the first DNA-based phylogeny of Megathymus. The phylogeny is fully consistent with morphological and behavioral similarities between species. Our results support phylogenetic placement of Megathymini within the subfamily Hesperiinae and clarify the relationships between Megathymus species. In particular, the major phylogenetic split is between the shallow and deep yucca root feeders, and significant mitochondrial DNA divergences between M. yuccae and M. beulahae and between M. streckeri and M. cofaqui support the species status of these allopatric and similar in appearance taxa.

Acknowledgements

We acknowledge Texas Parks and Wildlife Department (Natural Resources Program Director David H. Riskind) for the permit #08-02Rev that makes research based on material collected in Texas State Parks possible. We are grateful to Robert K. Robbins, John M. Burns, and Brian Harris (National Museum of Natural History, Smithsonian Institution, Washington, DC) for granting access to the collections under their care. We thank Lisa N. Kinch for critical suggestions and proofreading of the manuscript. This work was supported in part by the National Institutes of Health (GM094575 to NVG) and the Welch Foundation (I-1505 to NVG).

Funding Statement

This work was supported by National Institutes of Health [GM094575] and the Welch Foundation [I-1505].

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

[version 1; referees: 2 approved]

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F1000Res. 2017 Mar 27. doi: 10.5256/f1000research.11826.r21272

Referee response for version 1

Jiasheng Hao 1

  1. This work determined mitogenome sequences of nominal subspecies of all five known species of Megathymus and Agathymus mariae and constructed the phylogenetic trees of the main Hesperiinae groups, the results confirms that  Giant-Skippers (Megathymini) should not warrant a subfamily rank and that the monophyletic Megathymus  splits into two species groups. In addition, the reconstructed mitogenomic phylogeny is fully consistent with morphological and behavioral similarities between the closely related species of the genus Megathymus. Overall this interesting work deserves to be published and indexed.

  2. The manuscript’s writing is good with an appropriate title and other content; the design, method and analysis is generally correct though some phylogenetic analyses should be more robust.

  3. If the work considers the molecular dating of the Megatheymus divergence by molecular clock method, and incorporates the analysis of relevant earth environmental factors, the results and significance will be more remarkable.

I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

F1000Res. 2017 Mar 23. doi: 10.5256/f1000research.11826.r21230

Referee response for version 1

John A Shuey 1

This paper is an interesting contribution to our understanding of the evolution of Megathymini and the phylogentic placement of the tribe within the Hesperiidae.   Using mitogenomes of all recognized species of Megathymus, the authors confirm morphologically-based  species and species groups.  Moreover – they identify a deep mitogenomic divergence between lineages that correspond with important life history traits that define species groups.

I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.


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