Corrigendum: Off-target capture data, endosymbiont genes and morphology reveal a relict lineage that is sister to all other singing cicadas

Simon, Chris; Gordon, Eric R. L.; Moulds, Maxwell S.; Cole, Jeffrey A.; Haji, Diler; Lemmon, Alan R.; Lemmon, Emily Moriarty; Kortyna, Michelle L; Nazario, Katherine; Wade, Elizabeth J.; Meister, Russell C.; Goemans, Geert; Chiswell, Stephen M.; Pessacq, Pablo; Veloso, Claudio; McCutcheon, John P.; Łukasik, Piotr

doi:10.1093/biolinnean/blz177

Cited by 6 publications

(11 citation statements)

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“…4). The results are consistent with the hypothesis of Simon et al (2019), which inferred the date of origin of Cicadidae to be 99-60 Ma during the time of the main Angiosperm radiation. Hill et al (2021) estimated that the age of the Asian subclade of the subfamily Cicadinae [Clade 9 in Marshall et al (2018)] is at approximately 38-31 Ma.…”

Section: Co-diversification Of Cicadas and Ylssupporting

confidence: 91%

“…Matsuura et al (2018) reported that the phylogeny of Sulcia constructed based on genome sequences was highly congruent with the phylogeny of host cicadas, whereas the clade of Sulcia associated with Cicadettinae was embedded inside the clade associated with Cicadinae in the phylogenetic tree constructed based on 16S rRNA. Simon et al (2019) also reported that the phylogeny of Sulcia constructed based on 10 protein-coding genes supports or strengthens the phylogenetic relationships Host-symbiont connections are shown by dashed lines. Sequences of cicadas and YLS obtained in this study are indicated in boldface.…”

Section: Co-evolution Between Sulcia and Host Insectsmentioning

confidence: 79%

“…Simon et al . (2019) also reported that the phylogeny of Sulcia constructed based on 10 protein‐coding genes supports or strengthens the phylogenetic relationships of related host cicadas, but the monophyly of Cicadinae, Cicadettinae and Tettigomyiinae was not well supported. In our present study, the relationships of Sulcia lineages constructed based on 16S rRNA generally mirror the topology of the phylogenetic tree of related host cicadas, except that the clade associated with Cicadettinae is embedded inside the clade associated with Cicadinae, and that Sulcia of Hyalessa formed a sister group of the lineage associated with some other taxa of Cicadinae (Fig.…”

Section: Discussionmentioning

confidence: 99%

“…The results are consistent with the hypothesis of Simon et al . (2019), which inferred the date of origin of Cicadidae to be 99–60 Ma during the time of the main Angiosperm radiation. Hill et al .…”

Section: Discussionmentioning

confidence: 99%

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Complex co‐evolutionary relationships between cicadas and their symbionts

Wang

Huang

Billen

et al. 2021

Environmental Microbiology

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Summary Previous evidence suggests that cicadas lacking Hodgkinia may harbour the yeast‐like fungal symbionts (YLS). Here, we reinforce an earlier conclusion that the pathogenic ancestor of YLS independently infected different cicada lineages instead of the common ancestor of Cicadidae. Five independent replacement events in the loss of Hodgkinia/acquisition of YLS and seven other replacement events of YLS (from an Ophiocordyceps fungus to another Ophiocordyceps fungus) are hypothesised to have occurred within the sampled cicada taxa. The divergence time of YLS lineages was later than that of corresponding cicada lineages. The rapid shift of diversification rates of YLS and related cicada‐parasitizing Ophiocordyceps began at approximately 32.94 Ma, and the diversification rate reached the highest value at approximately 24.82 Ma, which corresponds to the cooling climate changes at the Eocene–Oligocene boundary and the Oligocene–Miocene transition respectively. Combined with related acquisition/replacement events of YLS occurred during the cooling‐climate periods, we hypothesise that the cooling‐climate changes impacted the interactions between cicadas and related Ophiocordyceps, which coupled with the unusual life cycle and the differentiation of cicadas may finally led to the diversification of YLS in Cicadidae. Our results contribute to a better understanding of the evolutionary transition of YLS from entomopathogenic fungi in insects.

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Section: Co-diversification Of Cicadas and Ylssupporting

confidence: 91%

Section: Co-evolution Between Sulcia and Host Insectsmentioning

confidence: 79%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

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Complex co‐evolutionary relationships between cicadas and their symbionts

Wang

Huang

Billen

et al. 2021

Environmental Microbiology

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“…A phylogenetic tree of worldwide cicada was recently constructed by Marshall et al (2018) and Simon et al (2019) applying five concatenated sequences of mitochondrial COI and COII, and nuclear ARD1, EF-1a, and 18S rRNA, and by Łukasik et al (2019) applying whole mitochondrial sequences for representative species in Marshall et al (2018), and family level phylogenetic relation has been clarified. Although Tettigarctinae is an old diverged lineage and Derotettiginae may be next, their worldwide phylogenetic trees were not dated trees.…”

Section: Introductionmentioning

confidence: 99%

Cicada minimum age tree: Cryptic speciation and exponentially increasing base substitution rates in recent geologic time

Osozawa,

Wakabayashi

2024

F1000Res

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We developed a new time-calibrated tree incorporating primarily endemic along with some cryptic Ryukyu islands cicada data, following the recent publication of global cicada data by Marshall et al. (2018), Łukasik et al. (2018), Simon et al. (2019), Price et al. (2019), and Hill et al. (2021). A total of 352 specimens were analyzed using BEAST v1. X software with a relaxed clock model. Fossil calibrations as old as Triassic were adopted largely following Johnson et al. (2018) and Moulds (2018), and a Quaternary geological event calibration was adopted following Osozawa et al. (2012, 2021b) and input into BEAST v1. X. Our timetree suggests that Tettigarctidae had a cicada basal lineage as old as 200.63 Ma, with Derotettiginae the next oldest lineage at 99.2 Ma. Tibicininae is a sister of the remaining subfamilies of Tettigomyiinae, Cicadettinae, and Cicadidae, and their species level differentiation and radiation began at 40.57 Ma. The Cicadinae clade consists of specific tribes with paraphyletic relationship, and the vicariance and adaptive radiation generated many cryptic species in each tribe. We estimated base substitution rate as a function of age, and the result strongly indicates an exponential increase of base substitution rate in recent geologic time. The consequent increase in cicada biodiversity, including generation of cryptic species in the Ryukyu Islands and surroundings, may have been driven by the generation and spreading of C4 grasses and coeval Quaternary climate change.

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Host-associated microbial diversity in New Zealand cicadas uncovers elevational structure and replacement of obligate bacterial endosymbionts byOphiocordycepsfungal pathogens

Haji

Vailionis

Stukel

et al. 2021

Preprint

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Host-microbe interactions influence eukaryotic evolution, particularly in the sap-sucking insects that often rely on obligate microbial symbionts to provision deficient nutrients in their diets. Cicadas (Hemiptera: Auchenorrhyncha: Cicadidae) specialize on xylem fluid and derive many essential amino acids and vitamins from intracellular bacteria or fungi (Hodgkinia, Sulcia, and Ophiocordyceps) that are propagated via transmission from mothers to offspring. Despite the beneficial role of these symbionts in nutrient provisioning, they are generally not considered to function within the gut where microbiota may play an important dietary role during insect diversification. Here, we investigate the relative impact of host phylogeny and ecology on gut microbial diversity in cicadas by sequencing 16S ribosomal RNA gene amplicons from 197 wild-collected cicadas and new mitochondrial genomes across 38 New Zealand cicada species, including natural hybrids between one species pair. We find a lack of phylogenetic structure and hybrid effects but a significant role of elevation in explaining variation in gut microbiota. Additionally, we provide evidence of Hodgkinia loss with gains of Ophiocordyceps fungal pathogens in all New Zealand cicadas examined that suggests convergent domestications of fungal pathogens. This highlights the macroevolutionary instability of obligate symbiosis and the relative importance of ecology rather than phylogeny for structuring gut microbial diversity in cicadas.

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Corrigendum: Off-target capture data, endosymbiont genes and morphology reveal a relict lineage that is sister to all other singing cicadas

Cited by 6 publications

References 0 publications

Complex co‐evolutionary relationships between cicadas and their symbionts

Complex co‐evolutionary relationships between cicadas and their symbionts

Cicada minimum age tree: Cryptic speciation and exponentially increasing base substitution rates in recent geologic time

Host-associated microbial diversity in New Zealand cicadas uncovers elevational structure and replacement of obligate bacterial endosymbionts byOphiocordycepsfungal pathogens

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