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Gerth, M.

Publications and source records attributed to Gerth, M..

10 recordsLinked to original sources

Rapid spread of nutritional Wolbachia symbionts across and within solitary bee species

Maternally inherited, intracellular Bacteria of the genus Wolbachia are extremely widespread among arthropods. Their evolutionary success is owed to frequent host shifts and rapid subsequent spread within host populations, often facilitated by Wolbachia-induced reproductive manipulations. Theory suggests that carrying Wolbachia must also be beneficial for a successful spread, however the nature of such benefits remains unclear. Here, we demonstrate that Wolbachias success in many solitary bee species is strongly associated with the presence of a gene cassette enabling Wolbachia to synthesize Biotin (vitamin B7). This ability is absent from almost all other Wolbachia strains but common among bee associated strains. We show that Wolbachia occurs in up to 70% of all bee species and that strains carrying this rare genomic element have independently spread into numerous bee hosts recently. We further demonstrate that the presence of the biotin operon is associated with specialised diets in several bee species, suggesting a previously overlooked nutritional role of Wolbachia in this group of important pollinators. Overall, our results suggest that nutritional benefits provided by symbionts may represent a more widespread and important mechanism by which reproductive manipulators spread into new host species than previously appreciated.

evolutionary biology↗

Rapid divergence in independent aspects of the compatibility phenotype in the Spiroplasma/Drosophila interaction.

Heritable symbionts represent important components of host biology, both as antagonistic reproductive parasites and as beneficial protective partners. An important component of heritable microbes biology is their ability to establish in new host species, a process equivalent to a host shift for an infectiously transmitted parasite or pathogen. For a host shift to occur, the symbiont must be compatible with the host: it must not cause excess pathology, must have good vertical transmission, and possess a drive phenotype that enables spread. Classically, compatibility has been considered a declining function of genetic distance between novel and ancestral host species. Here we investigate the evolutionary lability of compatibility to heritable microbes by comparing the capacity for a symbiont to establish in two novel host species equally related to the ancestral host. Compatibility of the protective Spiroplasma from D. hydei with D. simulans and D. melanogaster was tested. The Spiroplasma had contrasting compatibility in these two host species. The transinfection showed pathology and low vertical transmission in D. melanogaster but was asymptomatic and transmitted with high efficiency in D. simulans. These results were not affected by the presence/absence of Wolbachia in either of the two species. The pattern of protection was not congruent with that for pathology/transmission, with protection being weaker in the D. simulans, the host in which Spiroplasma was asymptomatic and transmitted well. Further work indicated pathological interactions occurred in D. sechellia and D. yakuba, indicating that D. simulans was unusual in being able to carry the symbiont without damage. The differing compatibility of the symbiont with these closely related host species emphasises first the rapidity with which host-symbiont compatibility evolves despite compatibility itself not being subject to direct selection, and second the independence of the different components of compatibility (pathology, transmission, protection). This requirement to fit three different independently evolving aspects of compatibility, if commonly observed, is likely to be a major feature limiting the rate of host shifts. Moving forward, the variation between sibling species pairs observed above provides an opportunity to identify the mechanisms behind variable compatibility between closely related host species, which will drive hypotheses as to the evolutionary drivers of compatibility variation.

evolutionary biology↗

Multiple colonisations and Wolbachia infections influence the fine-scale population structure of the widespread Common Blue butterfly (Polyomattus icarus) in the British Isles

The paradigm of differentiation in southern refugia during glacial periods followed by expansions during interglacials, producing limited genetic diversity and population sub-division in northern areas, dominates European phylogeography. However, the existence of complex structured populations in formerly glaciated areas, and on islands connected to mainland areas during glacial maxima, call for alternative explanations. Here, we reconstruct the mtDNA phylogeography of the widespread Polyommatus icarus butterfly over its native range, with an emphasis on the formerly glaciated and connected British Isles. We found distinct geographical structuring of CO1 mitotypes, with an ancient lineage restricted to the marginal European areas, including Northern Scotland and Outer Hebrides. We detected perfect mtDNA-Wolbachia associations in Northern Britain that support the possibility of at least two post-glacial Wolbachia-mediated sweeps, suggesting a series of sequential replacement of mtDNA in the British Isles and potentially in Europe. Population genomic analysis, using ddRADSeq genomic markers, also reveal unexpected genetic structuring within Britain. However, weak mito-nuclear concordance suggests the potential for independent histories of nuclear versus mitochondrial genomes. We found clustering of genomic SNPs of French samples, with respect to those in the British Isles, is not consistent with a scenario of a single recolonisation. Taken together our mtDNA and ddRADseq observations are consistent with a history of at least two distinct colonisations, a phylogeographic scenario previously put forth to explain diversity and structuring in other British flora and fauna. Additionally, we also present preliminary evidence that Wolbachia-induced feminization may be occurring in the isolated population in the Outer Hebrides.

evolutionary biology↗

Rapid molecular evolution of Spiroplasma symbionts of Drosophila

Spiroplasma are a group of Mollicutes whose members include plant pathogens, insect pathogens, and endosymbionts of animals. Spiroplasma phenotypes have been repeatedly observed to be spontaneously lost in Drosophila cultures, and several studies have documented a high genomic turnover in Spiroplasma symbionts and plant pathogens. These observations suggest that Spiroplasma evolves quickly in comparison to other insect symbionts. Here, we systematically assess evolutionary rates and patterns of Spiroplasma poulsonii, a natural symbiont of Drosophila. We analysed genomic evolution of sHy within flies, and sMel within in vitro culture over several years. We observed that S. poulsonii substitution rates are among the highest reported for any bacteria, and around two orders of magnitude higher compared with other inherited arthropod endosymbionts. The absence of mismatch repair loci mutS and mutL is conserved across Spiroplasma and likely contributes to elevated substitution rates. Further, the closely related strains sMel and sHy (>99.5% sequence identity in shared loci) show extensive structural genomic differences, which potentially indicates a higher degree of host adaptation in sHy, a protective symbiont of Drosophila hydei. Finally, comparison across diverse Spiroplasma lineages confirms previous reports of dynamic evolution of toxins, and identifies loci similar to the male-killing toxin Spaid in several Spiroplasma lineages and other endosymbionts. Overall, our results highlight the peculiar nature of Spiroplasma genome evolution, which may explain unusual features of its evolutionary ecology.

evolutionary biology↗

Neglecting model selection alters phylogenetic inference

Molecular phylogenetics is a standard tool in modern biology that informs the evolutionary history of genes, organisms, and traits, and as such is important in a wide range of disciplines from medicine to palaeontology. Maximum likelihood phylogenetic reconstruction involves assumptions about the evolutionary processes that underlie the dataset to be analysed. These assumptions must be specified in forms of an evolutionary model, and a number of criteria may be used to identify the best-fitting from a plethora of available models of DNA evolution. Using many empirical and simulated nucleotide sequence alignments, Abadi et al.1 have recently found that phylogenetic inferences using best models identified by six different model selection criteria are, on average, very similar to each other. They further claimed that using the model GTR+I+G4 without prior model-fitting results in similarly accurate phylogenetic estimates, and consequently that skipping model selection entirely has no negative impact on many phylogenetic applications. Focussing on this claim, I here revisit and re-analyse some of the data put forward by Abadi et al. I argue that while the presented analyses are sound, the results are misrepresented and in fact - in line with previous work - demonstrate that model selection consistently leads to different phylogenetic estimates compared with using fixed models.

evolutionary biology↗

Is Anopheles gambiae a natural host of Wolbachia?

Wolbachia (Alphaproteobacteria, Rickettsiales) is an intraovarially-transmitted symbiont of insects able to exert striking phenotypes, including reproductive manipulations and pathogen blocking. These phenotypes make Wolbachia a promising tool to combat mosquito-borne diseases. Although Wolbachia is present in the majority of terrestrial arthropods, including many disease vectors, it was considered absent from Anopheles gambiae mosquitos, the main vectors of malaria in sub-Saharan Africa. In 2014, Wolbachia sequences were detected in A. gambiae samples collected in Burkina Faso. Subsequently, similar evidence came from collections all over Africa, revealing a high Wolbachia 16S sequence diversity, low abundance, and a lack of congruence between host and symbiont phylogenies. Here, we reanalyze and discuss recent evidence on the presence of Wolbachia sequences in A. gambiae. We find that although detected at increasing frequencies, the unusual properties of these Wolbachia sequences render them insufficient to diagnose natural infections in A. gambiae. Future studies should focus on uncovering the origin of Wolbachia sequence variants in Anopheles and seeking sequence-independent evidence for this new symbiosis. Understanding the ecology of Anopheles mosquitos and their interactions with Wolbachia will be key in designing successful, integrative approaches to limit malaria spread. Although the prospect of using Wolbachia to fight malaria is intriguing, the newly discovered strains do not bring it closer to realization.\n\nSignificanceAnopheles gambiae mosquitos are the main vectors of malaria, threatening around half of the worlds population. The bacterial symbiont Wolbachia can interfere with disease transmission by other important insect vectors, but until recently it was thought to be absent from natural A. gambiae populations. Here, we critically analyze the genomic, metagenomic, PCR, imaging and phenotypic data presented in support of the presence of natural Wolbachia infections in A. gambiae. We find that they are insufficient to diagnose Wolbachia infections and argue for the need of obtaining robust data confirming basic Wolbachia characteristics in this system. Determining Wolbachia infection status of Anopheles is critical due to its potential to influence Anopheles population structure and Plasmodium transmission.

microbiology↗

Microbial composition of enigmatic bird parasites: Wolbachia and Spiroplasma are the most important bacterial associates of quill mites (Acari:Syringophilidae)

The microbiome is an integral component of many animal species, potentially affecting behaviour, physiology, and other biological properties. Despite this importance, bacterial communities remain vastly understudied in many groups of invertebrates, including mites. Quill mites (Acariformes: Syringophilidae) are a poorly known group of permanent bird ectoparasites that occupy quills of feathers and feed on bird subcutaneous tissue and fluids. Most species have strongly female biased sex ratios and it was hypothesized that this is caused by endosymbiotic bacteria. Their peculiar lifestyle further makes them potential vectors for bird diseases. Previously, Anaplasma phagocytophilum and a high diversity of Wolbachia strains were detected in quill mites via targeted PCR screens. Here, we use an unbiased 16S amplicon sequencing approach to determine other Bacteria that potentially impact quill mite biology.\n\nWe performed 16S V4 amplicon sequencing of 126 quill mite individuals from eleven species parasitizing twelve bird species (four families) of passeriform birds. In addition to Wolbachia, we found Spiroplasma as potential symbiont of quill mites. Interestingly, consistently high Spiroplasma titres were only found in individuals of two mite species associated with finches of the genus Cardfuelis, suggesting a history of horizontal transfers of Spiroplasma via the bird host. Furthermore, there was evidence for Spiroplasma negatively affecting Wolbachia titres. We found no evidence for the previously reported Anaplasma in quill mites, but detected the potential pathogens Brucella and Bartonella at low abundances. Other amplicon sequence variants (ASVs) could be assigned to a diverse number of bacterial taxa, including several that were previously isolated from bird skin. We observed a relatively uniform distribution of these ASVs across mite taxa and bird hosts, i.e, there was a lack of host-specificity for most detected ASVs. Further, many frequently found ASVs were assigned to taxa that show a very broad distribution with no strong prior evidence for symbiotic association with animals. We interpret these findings as evidence for a scarcity or lack of resident microbial associates (other than inherited symbionts) in quill mites, or for abundances of these taxa below our detection threshold.

evolutionary biology↗

Infections patterns and fitness effects of Rickettsia and Sodalis symbionts in the green lacewing Chrysoperla carnea

Endosymbionts are wide-spread among insects and can play an essential role in host ecology. The common green lacewing (Chrysoperla carnea s. str.) is a neuropteran insect species which is widely used as a biological pest control. We screened for endosymbionts in natural and laboratory populations of the green lacewing using diagnostic PCR amplicons. We found the endosymbiont Rickettsia to be very common in all screened populations, whereas a so far uncharacterized Sodalis strain was solely found in laboratory populations. The new Sodalis strain was characterized using a whole genome shotgun approach. Its draft genome revealed an approximate genome size of 4.3 Mbp and the presence of 5213 coding sequences. Phylogenomic analyses indicated that this bacterium is the sister taxon of S. praecaptivus. In an experimental approach, we found a negative impact of Sodalis on the reproduction success of the green lacewing. Co-infections with Rickettsia and Sodalis caused an even higher decrease of reproductive success than single Sodalis infections. In contrast, no significant fitness differences were found in Rickettsia infected green lacewings compared to uninfected lacewings. The Rickettsia/Sodalis/Ch. carnea system presents a promising model to study evolutionary endosymbiont-host interactions in Neuroptera and endosymbiont-endosymbiont interactions in general. The economic and ecological importance of green lacewings in biological pest control warrants a more profound understanding of its biology, which might be strongly influenced by symbionts.

evolutionary biology↗

Prot-SpaM: Fast alignment-free phylogeny reconstruction based on whole-proteome sequences

Word-based or alignment-free sequence comparison has become an active area of research in bioinformatics. While previous word-frequency approaches calculated rough measures of sequence similarity or dissimilarity, some new alignment-free methods are able to accurately estimate phylogenetic distances between genomic sequences. One of these approaches is Filtered Spaced Word Matches. Herein, we extend this approach to estimate evolutionary distances between complete or incomplete proteomes; our implementation of this approach is called Prot-SpaM. We compare the performance of Prot-SpaM to other alignment-free methods on simulated sequences and on various groups of eukaryotic and prokaryotic taxa. Prot-SpaM can be used to calculate high-quality phylogenetic trees from whole-proteome sequences in a matter of seconds or minutes and often outperforms other alignment-free approaches. The source code of our software is available through Github:\n\nhttps://github.com/jschellh/ProtSpaM

bioinformatics↗

Is It Time To Retire Wolbachia Multilocus Sequence Typing (MLST)?

Wolbachia (Alphaproteobacteria, Rickettsiales) is the most common, and arguably one of the most important inherited symbionts. Molecular differentiation of Wolbachia strains is routinely performed with a set of five multilocus sequence typing (MLST) markers. However, since its inception in 2006, the performance of MLST in Wolbachia strain typing has not been assessed objectively. Here, we evaluate the properties of Wolbachia MLST markers and compare it to 252 other single copy loci present in the genome of most Wolbachia strains. Specifically, we investigated how well MLST performs at strain differentiation, at reflecting genetic diversity of strains, and as phylogenetic marker. We find that MLST loci are outperformed by other loci at all tasks they are currently employed for, and thus that they do not reflect the properties of a Wolbachia strain very well. We argue that whole genome typing approaches should be used for Wolbachia typing in the future. Alternatively, if few-loci-approaches are necessary, we provide a characterization of 252 single copy loci for a number a criteria, which may assist in designing specific typing systems or phylogenetic studies.

evolutionary biology↗