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Bruzzese, D. J.

Publications and source records attributed to Bruzzese, D. J..

3 recordsLinked to original sources

Endosymbiont hijacking of acylcarnitines regulates insect vector fecundity by suppressing the viability of stored sperm

Competition between insects and their endosymbiotic bacteria for environmentally limited nutrients can compromise the fitness of both organisms. Tsetse flies, the vectors of pathogenic African trypanosomes, harbor a species and population-specific consortium of vertically transmitted endosymbiotic bacteria that range on the functional spectrum from mutualistic to parasitic. Tsetses indigenous microbiota can include a member of the genus Spiroplasma, and infection with this bacterium causes fecundity-reducing phenotypes in the fly that include a prolonged gonotrophic cycle and a reduction in the motility of stored spermatozoa post-copulation. Herein we demonstrate that Spiroplasma and tsetse spermatozoa compete for fly-derived acylcarnitines, which in other bacteria and animals are used to maintain cell membranes and produce energy. The fat body of mated female flies increases acylcarnitine production in response to infection with Spiroplasma. Additionally, their spermathecae (sperm storage organs), and likely the sperm within, up-regulate expression of carnitine O-palmitoyltransferase-1, which is indicative of increased acylcarnitine metabolism and thus increased energy demand and energy production in this organ. These compensatory measures are insufficient to rescue the motility defect of spermatozoa stored in the spermathecae of Spiroplasma-infected females and thus results in reduced fly fecundity. Tsetses taxonomically simple and highly tractable indigenous microbiota make the fly an efficient model system for studying the biological processes that facilitate the maintenance of bacterial endosymbioses, and how these relationships impact conserved mechanisms (mammalian spermatozoa also use acylcarnitines as an energy source) that regulated animal host fecundity. In the case of insect pests and vectors, a better understanding of the metabolic mechanisms that underlie these associations can lead to the development of novel control strategies. Author SummaryAnimals and the endosymbiotic bacteria that live inside them often compete for nutrients that both organisms require in order to survive. Tsetse flies, which transmit pathogenic African trypanosomes, can house several endosymbionts that have different impacts on their hosts physiological well-being. Female tsetse flies that are infected with one of these bacteria, Spiroplasma, produce fewer offspring than do their uninfected counterparts. In this study we demonstrate that the bacterium and the flys sperm cells (spermatozoa) compete for a specific type of lipid called acylcarnitines. When mated female tsetse flies are experimentally manipulated to produce less acylcarnitine Spiroplasma density decreases. Additionally, spermatozoa stored in the sperm storage organs of acylcarnitine depleted females lose motility and are eventually resorbed, thus rendering the females reproductively sterile. These findings mechanistically demonstrate how endosymbiotic bacteria can manipulate their hosts reproductive potential. In the case of arthropods that transmit pathogenic microbes, this relationship has significant implications for disease transmission and epidemiology.

microbiology↗

Rapid evolution of Wolbachia in cherry fruit flies

Wolbachia is a widespread bacterial endosymbiont in arthropods known for its ability to manipulate host reproduction through cytoplasmic incompatibility (CI), thereby promoting its spread. However, Wolbachia harbors an array of mobile genetic elements (MGEs) that can rapidly alter its genomic structure and content, including the cif loci responsible for CI. At the phylogenetic scale, Wolbachia genomes are shown to be dynamic with MGEs causing widespread genome rearrangements. But on ecological time scales, the evolution of Wolbachia remains largely unknown. In this study, we leverage the natural history of Wolbachia in cherry-infesting fruit flies in the Rhagoletis cingulata sibling species group. Members of this species group share a common Wolbachia strain, wCin2, and their divergence spans from 1,000 to 150,000 years ago. We utilized Nanopore sequencing to characterize wCin2 Wolbachia genome divergence across recent to more distant evolutionary timescales. We report rapid evolution of population-level differences in gene content (including cif loci and MGEs) and genome structure, with differentiation increasing with time since host divergence. Notably, structural variants were the first to appear both between and among wCin2 populations. Our results also indicated that the CI phenotype previously attributed to a distinct Wolbachia strain, wCin3, that coinfects flies in the southwestern USA and Mexico, may instead be caused by cif genes that were horizontally transferred into wCin2. Finally, we discovered a novel Wolbachia strain, wInd, which appears to have been recently horizontally acquired by cherry fly populations in the Pacific Northwest of the USA. Our findings underscore the fluidity and rapid genome evolution of Wolbachia, with significant implications for cif gene dynamics and potential impacts on host evolutionary trajectories. Author SummaryIn our study, we explore the genome evolution of Wolbachia, a common bacterial endosymbiont found in many insects that can manipulate its hosts reproduction to help it spread more effectively. Wolbachias genome is shown to change dramatically over long evolutionary periods due to mobile genetic elements. However, little is known about how Wolbachias genome evolves over shorter ecological timeframes. Here, we utilized cherry-infesting fruit flies and their Wolbachia strain known as wCin2, both of which have spread across North America for the past 150,000 years. Using long-read sequencing, we assembled multiple wCin2 Wolbachia genomes from across North America and made comparisons between wCin2 Wolbachia genomes that have recently diverged and comparisons to those that have been isolated for over 150,000 years. Our findings reveal that Wolbachias genome can evolve swiftly, with differences in gene content and most prominently genome structure arising between recently separated Wolbachia populations and increasing as populations diverge over time. Interestingly, these changes also impact the key genes responsible for Wolbachias reproductive manipulation. This research highlights the rapid and dynamic nature of Wolbachia genome evolution across different evolutionary timescales and offers insights into endosymbiont-host relationships as well as their potential impact on host speciation and vector control.

evolutionary biology↗

Diversification in the microlepidopteran genus Mompha (Lepidoptera: Gelechioidea: Momphidae) is explained more by tissue specificity than host plant family.

Insect herbivores and their hostplants constitute much of Earths described diversity, but how these often-specialized associations evolve and generate biodiversity is still not fully understood. We combined detailed hostplant data and comparative phylogenetic analyses of the lepidopteran family Momphidae to explore how shifts in the use of hostplant resources, not just hostplant taxonomy, contribute to the diversification of phytophagous insect lineages. We generated two phylogenies primarily from momphid species in the nominate genus, Mompha Hubner. A six-gene phylogeny was constructed with exemplars from Onagraceae hosts in western and southwestern USA and a cytochrome c oxidase subunit 1 (COI) phylogeny utilized both our collected sequences and publicly available accessions from the Barcode of Life Data System. Coalescent-based analyses combined with morphological data revealed ca. 56 undescribed Mompha species-level taxa, many of which are hostplant specialists on southwestern USA Onagraceae. Our phylogenetic reconstructions identified four major momphid clades: 1) an Onagraceae flower- and fruit-feeding clade, 2) a Melastomataceae galling clade, 3) an Onagraceae and Rubiaceae leafmining clade, and 4) a heterogeneous clade associated with multiple hostplant families, plant tissues, and larval feeding modes. Ancestral trait reconstructions on the COI tree identified leafmining on Onagraceae as the ancestral state for Momphidae. Cophylogenetic analyses detected loose phylogenetic tracking of hostplant taxa. Our study finds that shifts along three hostplant resource axes (hostplant taxon, plant tissue type, and larval feeding mode) contributed to the evolutionary success and diversification of Mompha. More transitions between exploited host tissue types than between hostplant families indicated that exploited host tissue (without a change in host) played an unexpectedly large role in the diversification of these moths.

evolutionary biology↗