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Loss of cytoplasmic incompatibility and minimal fecundity effects explain relatively low Wolbachia frequencies in Drosophila mauritiana
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ece3.3449openalex-snapshot
Genome comparisons indicate recent transfer of w R i‐like Wolbachia between sister species Drosophila suzukii and D. subpulchrella
inferredcites →https://doi.org/10.1007/978-1-4899-4541-9openalex-snapshot
An Introduction to the Bootstrap
inferredcites →https://doi.org/10.1007/bf02111283openalex-snapshot
Evolution in bacteria: Evidence for a universal substitution rate in cellular genomes
inferredcites →https://doi.org/10.1007/s002390010067openalex-snapshot
Comparative Genomics of Mitochondrial DNA in Drosophila simulans
inferredcites →https://doi.org/10.1016/j.cub.2018.02.015openalex-snapshot
Rapid Global Spread of wRi-like Wolbachia across Multiple Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2018.07.005openalex-snapshot
A Maladaptive Combination of Traits Contributes to the Maintenance of a Drosophila Hybrid Zone
inferredcites →https://doi.org/10.1016/j.ibmb.2013.07.002openalex-snapshot
Detection of the Wolbachia protein WPIP0282 in mosquito spermathecae: Implications for cytoplasmic incompatibility
inferredcites →https://doi.org/10.1016/j.tig.2018.12.004openalex-snapshot
The Toxin–Antidote Model of Cytoplasmic Incompatibility: Genetics and Evolutionary Implications
inferredcites →https://doi.org/10.1016/j.tpb.2017.03.003openalex-snapshot
Deploying dengue-suppressing Wolbachia : Robust models predict slow but effective spatial spread in Aedes aegypti
inferredcites →https://doi.org/10.1016/j.ympev.2004.03.013openalex-snapshot
Linking phylogenetics with population genetics to reconstruct the geographic origin of a species
inferredcites →https://doi.org/10.1017/s0016672302005827openalex-snapshot
Male age, host effects and the weak expression or non-expression of cytoplasmic incompatibility in Drosophila strains infected by maternally transmitted Wolbachia
inferredcites →https://doi.org/10.1038/232657a0openalex-snapshot
New Hypothesis of the Cause of Cytoplasmic Incompatibility in Culex pipiens L.
inferredcites →https://doi.org/10.1038/348178a0openalex-snapshot
Bidirectional incompatibility between conspecific populations of Drosophila simulans
inferredcites →https://doi.org/10.1038/36017openalex-snapshot
Rescuing Wolbachia have been overlooked
inferredcites →https://doi.org/10.1038/hdy.1996.1openalex-snapshot
Naturally-occurring Wolbachia infection in Drosophila simulans that does not cause cytoplasmic incompatibility
inferredcites →https://doi.org/10.1038/nature10356openalex-snapshot
Successful establishment of Wolbachia in Aedes populations to suppress dengue transmission
inferredcites →https://doi.org/10.1038/nature21391openalex-snapshot
Prophage WO genes recapitulate and enhance Wolbachia-induced cytoplasmic incompatibility
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.241openalex-snapshot
Comparative genomics provides a timeframe for Wolbachia evolution and exposes a recent biotin synthesis operon transfer
inferredcites →https://doi.org/10.1038/nmicrobiol.2017.7openalex-snapshot
A Wolbachia deubiquitylating enzyme induces cytoplasmic incompatibility
inferredcites →https://doi.org/10.1038/sj.hdy.6800025openalex-snapshot
Dynamics of double and single Wolbachia infections in Drosophila simulans from New Caledonia
inferredcites →https://doi.org/10.1046/j.1365-2583.2000.00203.xopenalex-snapshot
Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty‐three arthropod species
inferredcites →https://doi.org/10.1046/j.1570-7458.1998.00269.xopenalex-snapshot
Wolbachia transmission in a naturally bi‐infected Drosophila simulans strain from New‐Caledonia
inferredcites →https://doi.org/10.1073/pnas.0810753106openalex-snapshot
The mosaic genome structure of the Wolbachia w Ri strain infecting Drosophila simulans
inferredcites →https://doi.org/10.1073/pnas.1301524110openalex-snapshot
Evolutionarily conserved Wolbachia -encoded factors control pattern of stem-cell niche tropism in Drosophila ovaries and favor infection
inferredcites →https://doi.org/10.1073/pnas.1800650115openalex-snapshot
One prophage WO gene rescues cytoplasmic incompatibility in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.87.24.9558openalex-snapshot
Evolution of Drosophila mitochondrial DNA and the history of the melanogaster subgroup.
inferredcites →https://doi.org/10.1073/pnas.89.7.2699openalex-snapshot
16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects.
inferredcites →https://doi.org/10.1073/pnas.92.14.6389openalex-snapshot
Evolution of single and double Wolbachia symbioses during speciation in the Drosophila simulans complex.
inferredcites →https://doi.org/10.1086/282991openalex-snapshot
Necessary and Sufficient Conditions for Multiple-Niche Polymorphism in Haploids
inferredcites →https://doi.org/10.1086/661246openalex-snapshot
Spatial Waves of Advance with Bistable Dynamics: Cytoplasmic and Genetic Analogues of Allee Effects
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btr670openalex-snapshot
Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/btu153openalex-snapshot
Prokka: rapid prokaryotic genome annotation
inferredcites →https://doi.org/10.1093/bioinformatics/btv351openalex-snapshot
BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs
inferredcites →https://doi.org/10.1093/gbe/evr007openalex-snapshot
Complete Bacteriophage Transfer in a Bacterial Endosymbiont (Wolbachia) Determined by Targeted Genome Capture
inferredcites →https://doi.org/10.1093/gbe/evu198openalex-snapshot
Genome Diversity and Divergence in Drosophila mauritiana : Multiple Signatures of Faster X Evolution
inferredcites →https://doi.org/10.1093/gbe/evy012openalex-snapshot
Evolutionary Genetics of Cytoplasmic Incompatibility Genes cifA and cifB in Prophage WO of Wolbachia
inferredcites →https://doi.org/10.1093/genetics/119.2.435openalex-snapshot
Unidirectional incompatibility in Drosophila simulans: inheritance, geographic variation and fitness effects.
inferredcites →https://doi.org/10.1093/genetics/126.4.933openalex-snapshot
Factors affecting the distribution of cytoplasmic incompatibility in Drosophila simulans.
inferredcites →https://doi.org/10.1093/genetics/132.3.713openalex-snapshot
Dynamics of cytoplasmic incompatibility and mtDNA variation in natural Drosophila simulans populations.
inferredcites →https://doi.org/10.1093/genetics/135.1.81openalex-snapshot
Type I repressors of P element mobility.
inferredcites →https://doi.org/10.1093/genetics/140.4.1307openalex-snapshot
Wolbachia infections and the expression of cytoplasmic incompatibility in Drosophila sechellia and D. mauritiana.
inferredcites →https://doi.org/10.1093/genetics/140.4.1319openalex-snapshot
Cytoplasmic incompatibility in Drosophila simulans: dynamics and parameter estimates from natural populations.
inferredcites →https://doi.org/10.1093/genetics/141.3.1015openalex-snapshot
Variability within the Seychelles cytoplasmic incompatibility system in Drosophila simulans.
inferredcites →https://doi.org/10.1093/genetics/148.1.221openalex-snapshot
Population Dynamics of the Wolbachia Infection Causing Cytoplasmic Incompatibility in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/150.1.227openalex-snapshot
Wolbachia Transfer from Drosophila melanogaster into D. simulans: Host Effect and Cytoplasmic Incompatibility Relationships
inferredcites →https://doi.org/10.1093/genetics/156.4.1913openalex-snapshot
The Population Genetics of the Origin and Divergence of the Drosophila simulans Complex Species
inferredcites →https://doi.org/10.1093/jtm/tay084openalex-snapshot
Wolbachia and the near cessation of dengue outbreaks in Northern Australia despite continued dengue importations via travellers
inferredcites →https://doi.org/10.1093/molbev/msh028openalex-snapshot
Sequential Evolution of a Symbiont Inferred From the Host: Wolbachia and Drosophila simulans
inferredcites →https://doi.org/10.1093/molbev/msn133openalex-snapshot
Genome Evolution of Wolbachia Strain wPip from the Culex pipiens Group
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/mst123openalex-snapshot
A Selective Sweep across Species Boundaries in Drosophila
inferredcites →https://doi.org/10.1093/oso/9780198577867.003.0002openalex-snapshot
Cytoplasmic incompatibility in insects
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026394openalex-snapshot
When One Is Not Enough: Introgression of Mitochondrial DNA in Drosophila
inferredcites →https://doi.org/10.1093/sysbio/syw021openalex-snapshot
RevBayes: Bayesian Phylogenetic Inference Using Graphical Models and an Interactive Model-Specification Language
inferredcites →https://doi.org/10.1098/rspb.1995.0117openalex-snapshot
Evolution and phylogeny of Wolbachia : reproductive parasites of arthropods
inferredcites →https://doi.org/10.1098/rspb.2000.1139openalex-snapshot
Wolbachiainfection frequencies in insects: evidence of a global equilibrium?
inferredcites →https://doi.org/10.1098/rspb.2003.2640openalex-snapshot
Natural interspecific and intraspecific horizontal transfer of parthenogenesis–inducingWolbachiainTrichogrammawasps
inferredcites →https://doi.org/10.1098/rspb.2015.0249openalex-snapshot
The incidence of bacterial endosymbionts in terrestrial arthropods
inferredcites →https://doi.org/10.1098/rspb.2017.0809openalex-snapshot
The route of infection determines Wolbachia antibacterial protection in Drosophila
inferredcites →https://doi.org/10.1098/rspb.2018.1165openalex-snapshot
No detectable effect of Wolbachia w Mel on the prevalence and abundance of the RNA virome of Drosophila melanogaster
inferredcites →https://doi.org/10.1101/551036openalex-snapshot
Introgressive and horizontal acquisition of Wolbachia by Drosophila yakuba -clade hosts and horizontal transfer of incompatibility loci between distantly related Wolbachia
inferredcites →https://doi.org/10.1101/gr.130922.111openalex-snapshot
Genome sequencing reveals complex speciation in the Drosophila simulans clade
inferredcites →https://doi.org/10.1101/gr.214346.116openalex-snapshot
ABySS 2.0: resource-efficient assembly of large genomes using a Bloom filter
inferredcites →https://doi.org/10.1111/1365-2435.12264openalex-snapshot
Thermal adaptation of cellular membranes in natural populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1111/1365-2664.13101openalex-snapshot
Back and forth Wolbachia transfers reveal efficient strains to control spotted wing drosophila populations
inferredcites →https://doi.org/10.1111/evo.12923openalex-snapshot
Persistence of a Wolbachia infection frequency cline in Drosophila melanogaster and the possible role of reproductive dormancy
inferredcites →https://doi.org/10.1111/evo.13506openalex-snapshot
Rapid spread of aWolbachiainfection that does not affect host reproduction inDrosophila simulanscage populations
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00710.xopenalex-snapshot
EXPRESSION OF CYTOPLASMIC INCOMPATIBILITY IN DROSOPHILA SIMULANS AND ITS IMPACT ON INFECTION FREQUENCIES AND DISTRIBUTION OF WOLBACHIA PIPIENTIS
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00760.xopenalex-snapshot
Tetracycline treatment influences mitochondrial metabolism and mtDNA density two generations after treatment in Drosophila
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03608.xopenalex-snapshot
Insight into the routes of Wolbachia invasion: high levels of horizontal transfer in the spider genus Agelenopsis revealed by Wolbachia strain and mitochondrial DNA diversity
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04838.xopenalex-snapshot
Multiple hybridization events between Drosophila simulans and Drosophila mauritiana are supported by mtDNA introgression
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05127.xopenalex-snapshot
Inter-island divergence within Drosophila mauritiana, a species of the D. simulans complex: Past history and/or speciation in progress?
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THE WAVE OF ADVANCE OF ADVANTAGEOUS GENES
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CROSSING EXPERIMENTS WITHCULEXSTRAINS
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ON THE EVOLUTIONARY IMPORTANCE OF CYTOPLASMIC STERILITY IN MOSQUITOES
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00468.xopenalex-snapshot
THE REPRODUCTIVE RELATIONSHIPS OFDROSOPHILA SECHELLIAWITHD. MAURITIANA, D. SIMULANS, ANDD. MELANOGASTERFROM THE AFROTROPICAL REGION
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00505.xopenalex-snapshot
RACE FORMATION, SPECIATION, AND INTROGRESSION WITHINDROSOPHILA SIMULANS, D. MAURITIANA, ANDD. SECHELLIAINFERRED FROM MITOCHONDRIAL DNA ANALYSIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00531.xopenalex-snapshot
UNIDIRECTIONAL INCOMPATIBILITY BETWEEN POPULATIONS OF DROSOPHILA SIMULANS
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb01371.xopenalex-snapshot
SOME EVOLUTIONARY POSSIBILITIES FOR A MICROBE THAT CAUSES INCOMPATIBILITY IN ITS HOST
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb02192.xopenalex-snapshot
EVOLUTION OF INCOMPATIBILITY‐INDUCING MICROBES AND THEIR HOSTS
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00533.xopenalex-snapshot
MODES OF ACQUISITION OFWOLBACHIA: HORIZONTAL TRANSFER, HYBRID INTROGRESSION, AND CODIVERGENCE IN THENASONIASPECIES COMPLEX
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00550.xopenalex-snapshot
EVOLUTION OF INCOMPATIBILITY-INDUCING MICROBES IN SUBDIVIDED HOST POPULATIONS
inferredcites →https://doi.org/10.1111/j.1574-6968.2008.01110.xopenalex-snapshot
How many species are infected with Wolbachia? – a statistical analysis of current data
inferredcites →https://doi.org/10.1111/jeb.12391openalex-snapshot
Hybridization occurs between Drosophila simulans and D. sechellia in the Seychelles archipelago
inferredcites →https://doi.org/10.1111/jeb.12861openalex-snapshot
Hidden suppression of sex ratio distortion suggests Red queen dynamics between Wolbachia and its dwarf spider host
inferredcites →https://doi.org/10.1111/mec.12901openalex-snapshot
Wolbachiado not live by reproductive manipulation alone: infection polymorphism inDrosophila suzukiiandD. subpulchrella
inferredcites →https://doi.org/10.1111/mec.13571openalex-snapshot
The hitchhiker's guide to Europe: the infection dynamics of an ongoing Wolbachia invasion and mitochondrial selective sweep in Rhagoletis cerasi
inferredcites →https://doi.org/10.1126/science.1162418openalex-snapshot
Wolbachia and Virus Protection in Insects
inferredcites →https://doi.org/10.1126/science.1209609openalex-snapshot
Wolbachia Enhance Drosophila Stem Cell Proliferation and Target the Germline Stem Cell Niche
inferredcites →https://doi.org/10.1128/aem.02987-14openalex-snapshot
Passage of Wolbachia pipientis through Mutant Drosophila melanogaster Induces Phenotypic and Genomic Changes
inferredcites →https://doi.org/10.1128/genomea.00032-13openalex-snapshot
Draft Genome Sequence of the Wolbachia Endosymbiont of Drosophila suzukii
inferredcites →https://doi.org/10.1128/jb.00036-12openalex-snapshot
Whole-Genome Sequence of Wolbachia Strain w AlbB, an Endosymbiont of Tiger Mosquito Vector Aedes albopictus
inferredcites →https://doi.org/10.1128/jb.180.9.2373-2378.1998openalex-snapshot
Cloning and Characterization of a Gene Encoding the Major Surface Protein of the Bacterial EndosymbiontWolbachia pipientis
inferredcites →https://doi.org/10.1186/1471-2164-15-928openalex-snapshot
Comparative genome analysis of Wolbachia strain wAu
inferredcites →https://doi.org/10.1371/journal.pbio.0020069openalex-snapshot
Phylogenomics of the Reproductive Parasite Wolbachia pipientis wMel: A Streamlined Genome Overrun by Mobile Genetic Elements
inferredcites →https://doi.org/10.1371/journal.pbio.0040283openalex-snapshot
Evolution of Male-Killer Suppression in a Natural Population
inferredcites →https://doi.org/10.1371/journal.pbio.0050114openalex-snapshot
From Parasite to Mutualist: Rapid Evolution of Wolbachia in Natural Populations of Drosophila
inferredcites →https://doi.org/10.1371/journal.pbio.1000002openalex-snapshot
The Bacterial Symbiont Wolbachia Induces Resistance to RNA Viral Infections in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pbio.1002210openalex-snapshot
The Discovery, Distribution, and Evolution of Viruses Associated with Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pbio.2001894openalex-snapshot
Local introduction and heterogeneous spatial spread of dengue-suppressing Wolbachia through an urban population of Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pgen.1003129openalex-snapshot
Population Genomics of the Wolbachia Endosymbiont in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1003381openalex-snapshot
Comparative Genomics of Wolbachia and the Bacterial Species Concept
inferredcites →https://doi.org/10.1371/journal.pgen.1007341openalex-snapshot
Supervised machine learning reveals introgressed loci in the genomes of Drosophila simulans and D. sechellia
inferredcites →https://doi.org/10.1371/journal.pone.0002442openalex-snapshot
Estimation of Isolation Times of the Island Species in the Drosophila simulans Complex from Multilocus DNA Sequence Data
inferredcites →https://doi.org/10.1371/journal.pone.0022565openalex-snapshot
A Re-Examination of Wolbachia-Induced Cytoplasmic Incompatibility in California Drosophila simulans
inferredcites →https://doi.org/10.1371/journal.pone.0038544openalex-snapshot
Still a Host of Hosts for Wolbachia: Analysis of Recent Data Suggests That 40% of Terrestrial Arthropod Species Are Infected
inferredcites →https://doi.org/10.1371/journal.ppat.1000368openalex-snapshot
Evidence for Metabolic Provisioning by a Common Invertebrate Endosymbiont, Wolbachia pipientis, during Periods of Nutritional Stress
inferredcites →https://doi.org/10.1371/journal.ppat.1003607openalex-snapshot
Rapid Sequential Spread of Two Wolbachia Variants in Drosophila simulans
inferredcites →https://doi.org/10.1371/journal.ppat.1003647openalex-snapshot
Transcriptional Regulation of Culex pipiens Mosquitoes by Wolbachia Influences Cytoplasmic Incompatibility
inferredcites →https://doi.org/10.1371/journal.ppat.1004369openalex-snapshot
Symbionts Commonly Provide Broad Spectrum Resistance to Viruses in Insects: A Comparative Analysis of Wolbachia Strains
inferredcites →https://doi.org/10.1534/g3.116.028449openalex-snapshot
Comparative Genomics of a Parthenogenesis-Inducing Wolbachia Symbiont
inferredcites →https://doi.org/10.1534/genetics.107.086488openalex-snapshot
Multiple Rescue Factors Within a Wolbachia Strain
inferredcites →https://doi.org/10.1534/genetics.116.196238openalex-snapshot
Wolbachia in the Drosophila yakuba Complex: Pervasive Frequency Variation and Weak Cytoplasmic Incompatibility, but No Apparent Effect on Reproductive Isolation
inferredcites →https://doi.org/10.1534/genetics.119.302349openalex-snapshot
Wolbachia Acquisition by Drosophila yakuba -Clade Hosts and Transfer of Incompatibility Loci Between Distantly Related Wolbachia
inferredcites →https://doi.org/10.1554/0014-3820(2000)054[1661:eociid]2.0.co;2openalex-snapshot
EXPRESSION OF CYTOPLASMIC INCOMPATIBILITY IN DROSOPHILA SIMULANS AND ITS IMPACT ON INFECTION FREQUENCIES AND DISTRIBUTION OF WOLBACHIA PIPIENTIS
inferredcites →https://doi.org/10.2307/2405682openalex-snapshot
Crossing Experiments with Culex Strains
inferredcites →https://doi.org/10.2307/2408456openalex-snapshot
Unidirectional Incompatibility between Populations of Drosophila simulans
inferredcites →https://doi.org/10.2307/2408575openalex-snapshot
Race Formation, Speciation, and Introgression Within Drosophila simulans, D. mauritiana, and D. schellia Inferred from Mitochondrial DNA Analysis
inferredcites →https://doi.org/10.2307/2408806openalex-snapshot
The Reproductive Relationships of Drosophila sechellia with D. mauritiana, D. simulans, and D. melanogaster from the Afrotropical Region
inferredcites →https://doi.org/10.3201/eid0604.000402openalex-snapshot
Male-Killing Bacteria in Insects: Mechanisms, Incidence, and Implications
inferredcites →https://doi.org/10.5281/zenodo.10741511openalex-snapshot
Drosophila communities on Mauritius and the ecological niche of D. mauritiana (Diptera, Drosophilidae).
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.11705openalex-snapshot
Describing endosymbiont–host interactions within the parasitism–mutualism continuum
inferred← citeshttps://doi.org/10.1002/ece3.71989openalex-snapshot
Stochastic Fluctuations of the Facultative Endosymbiont Wolbachia due to Finite Host Population Size
inferred← citeshttps://doi.org/10.1002/ece3.7782openalex-snapshot
Wolbachia in the spittlebug Prosapia ignipectus : Variable infection frequencies, but no apparent effect on host reproductive isolation
inferred← citeshttps://doi.org/10.1002/evl3.270openalex-snapshot
Why did the Wolbachia transinfection cross the road? drift, deterministic dynamics, and disease control
inferred← citeshttps://doi.org/10.1007/978-1-0716-3553-7_19openalex-snapshot
Using Baker’s Yeast to Determine Functions of Novel Wolbachia (and Other Prokaryotic) Effectors
inferred← citeshttps://doi.org/10.1007/978-3-031-22028-9_5openalex-snapshot
The Creativity of Natural Selection and the Creativity of Organisms: Their Roles in Traditional Evolutionary Theory and Some Proposed Extensions
inferred← citeshttps://doi.org/10.1007/s00248-023-02198-7openalex-snapshot
Two Complete Genomes of Male-Killing Wolbachia Infecting Ostrinia Moth Species Illuminate Their Evolutionary Dynamics and Association with Hosts
inferred← citeshttps://doi.org/10.1007/s00248-024-02444-6openalex-snapshot
Symbiotic Bacteria: Wolbachia, Midgut Microbiota in Mosquitoes and Their Importance for Vector Prevention Strategies
inferred← citeshttps://doi.org/10.1007/s42690-021-00623-3openalex-snapshot
Impact of native Wolbachia on reproductive fitness and bacterial pathogens in Aedes aegypti mosquitoes
inferred← citeshttps://doi.org/10.1016/j.cois.2019.10.001openalex-snapshot
Impact of Wolbachia infection on Drosophila female germline stem cells
inferred← citeshttps://doi.org/10.1016/j.cub.2021.11.065openalex-snapshot
Temperature effects on cellular host-microbe interactions explain continent-wide endosymbiont prevalence
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.107061openalex-snapshot
A phylogeny for the Drosophila montium species group: A model clade for comparative analyses
inferred← citeshttps://doi.org/10.1038/s41467-020-19016-0openalex-snapshot
Large scale genome reconstructions illuminate Wolbachia evolution
inferred← citeshttps://doi.org/10.1038/s41467-024-55779-6openalex-snapshot
Double trouble: two retrotransposons triggered a cascade of invasions in Drosophila species within the last 50 years
inferred← citeshttps://doi.org/10.1038/s41564-021-00998-6openalex-snapshot
Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector
inferred← citeshttps://doi.org/10.1038/s42003-024-06431-yopenalex-snapshot
Comparative analysis of Wolbachia maternal transmission and localization in host ovaries
inferred← citeshttps://doi.org/10.1073/pnas.1914571116openalex-snapshot
A Wolbachia nuclease and its binding partner provide a distinct mechanism for cytoplasmic incompatibility
inferred← citeshttps://doi.org/10.1073/pnas.2113271118openalex-snapshot
A single mutation weakens symbiont-induced reproductive manipulation through reductions in deubiquitylation efficiency
inferred← citeshttps://doi.org/10.1073/pnas.2211637119openalex-snapshot
Why Wolbachia -induced cytoplasmic incompatibility is so common
inferred← citeshttps://doi.org/10.1093/evolut/qpad131openalex-snapshot
Evolution under a model of functionally buffered deleterious mutations can lead to positive selection in protein-coding genes
inferred← citeshttps://doi.org/10.1093/g3journal/jkab221openalex-snapshot
Horizontal transmission and recombination of Wolbachia in the butterfly tribe Aeromachini Tutt, 1906 (Lepidoptera: Hesperiidae)
inferred← citeshttps://doi.org/10.1093/genetics/iyad038openalex-snapshot
Distinct Wolbachia localization patterns in oocytes of diverse host species reveal multiple strategies of maternal transmission
inferred← citeshttps://doi.org/10.1093/genetics/iyae019openalex-snapshot
Enrichment of hard sweeps on the X chromosome compared to autosomes in six Drosophila species
inferred← citeshttps://doi.org/10.1093/jisesa/ieab106openalex-snapshot
Effect of Quorum Sensing Inducers and Inhibitors on Cytoplasmic Incompatibility Induced by Wolbachia (Rickettsiales: Anaplasmataceae) in American Serpentine Leafminer (Diptera: Agromyzidae): Potential Tool for the Incompatible Insect Technique.
inferred← citeshttps://doi.org/10.1093/molbev/msaa209openalex-snapshot
Life and Death of Selfish Genes: Comparative Genomics Reveals the Dynamic Evolution of Cytoplasmic Incompatibility
inferred← citeshttps://doi.org/10.1093/molbev/msaa308openalex-snapshot
Tirant Stealthily Invaded Natural Drosophila melanogaster Populations during the Last Century
inferred← citeshttps://doi.org/10.1093/molbev/msad258openalex-snapshot
Historic Museum Samples Provide Evidence for a Recent Replacement of Wolbachia Types in European Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/molbev/msag186openalex-snapshot
Temperature-sensitive cytoplasmic incompatibility across divergent Wolbachia partly reflects cifB transcription, not endosymbiont density
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgac099openalex-snapshot
cifB- transcript levels largely explain cytoplasmic incompatibility variation across divergent Wolbachia
inferred← citeshttps://doi.org/10.1098/rsbl.2021.0052openalex-snapshot
Pervasive effects of Wolbachia on host activity
inferred← citeshttps://doi.org/10.1098/rsos.250545openalex-snapshot
Male-dependent resistance to Spiroplasma -induced cytoplasmic incompatibility
inferred← citeshttps://doi.org/10.1098/rstb.2019.0809openalex-snapshot
Wolbachia strain w AlbB maintains high density and dengue inhibition following introduction into a field population of Aedes aegypti
inferred← citeshttps://doi.org/10.1099/mgen.0.000805openalex-snapshot
Wolbachia endosymbionts in two Anopheles species indicates independent acquisitions and lack of prophage elements
inferred← citeshttps://doi.org/10.1101/2022.02.14.480440openalex-snapshot
A model of functionally buffered deleterious mutations can lead to signatures of positive selection
inferred← citeshttps://doi.org/10.1101/2023.03.23.533954openalex-snapshot
Modelling Emergence of Wolbachia Toxin-Antidote Protein Functions with an Evolutionary Algorithm
inferred← citeshttps://doi.org/10.1101/2023.12.04.569981openalex-snapshot
Rapid host switching of Wolbachia and even more rapid turnover of their phages and incompatibility-causing loci
inferred← citeshttps://doi.org/10.1101/2025.01.13.632697openalex-snapshot
Rapid evolution of Wolbachia in cherry fruit flies
inferred← citeshttps://doi.org/10.1101/551036openalex-snapshot
Introgressive and horizontal acquisition of Wolbachia by Drosophila yakuba -clade hosts and horizontal transfer of incompatibility loci between distantly related Wolbachia
inferred← citeshttps://doi.org/10.1101/gr.263442.120openalex-snapshot
Evolution of genome structure in the Drosophila simulans species complex
inferred← citeshttps://doi.org/10.1111/eva.70138openalex-snapshot
Reciprocal Host– Wolbachia Interactions Shape Infection Persistence Upon Loss of Cytoplasmic Incompatibility in Haplodiploids
inferred← citeshttps://doi.org/10.1111/evo.14259openalex-snapshot
Pure species discriminate against hybrids in the Drosophila melanogaster species subgroup
inferred← citeshttps://doi.org/10.1111/jeb.14016openalex-snapshot
Complex effects of environment and Wolbachia infections on the life history of Drosophila melanogaster hosts
inferred← citeshttps://doi.org/10.1111/mec.70125openalex-snapshot
Wolbachia Host Shifts and Widespread Occurrence of Reproductive Manipulation Loci in European Butterflies
inferred← citeshttps://doi.org/10.1128/aem.03071-18openalex-snapshot
Symbiosis Comes of Age at the 10th Biennial Meeting of Wolbachia Researchers
inferred← citeshttps://doi.org/10.1128/mbio.01768-20openalex-snapshot
Pervasive Effects of Wolbachia on Host Temperature Preference
inferred← citeshttps://doi.org/10.1128/mbio.02998-21openalex-snapshot
Male Age and Wolbachia Dynamics: Investigating How Fast and Why Bacterial Densities and Cytoplasmic Incompatibility Strengths Vary
inferred← citeshttps://doi.org/10.1139/cjz-2020-0260openalex-snapshot
Next generation sequencing, insect microbiomes, and the confounding effect of Wolbachia: a case study using spotted-wing drosophila (Drosophila suzukii) (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1146/annurev-genet-112618-043609openalex-snapshot
Evolutionary Ecology ofWolbachiaReleases for Disease Control
inferred← citeshttps://doi.org/10.11606/d.41.2021.tde-30092021-131343openalex-snapshot
Prevalência da bactéria endossimbionte Wolbachia em comunidades de drosofilídeos neotropicais
inferred← citeshttps://doi.org/10.1186/s12862-021-01822-9openalex-snapshot
Prevalence and relationship of endosymbiotic Wolbachia in the butterfly genus Erebia
inferred← citeshttps://doi.org/10.1186/s12862-022-01995-xopenalex-snapshot
Remnants of horizontal transfers of Wolbachia genes in a Wolbachia-free woodwasp
inferred← citeshttps://doi.org/10.1186/s12915-025-02130-0openalex-snapshot
Wolbachia enhances the survival of Drosophila infected with fungal pathogens
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001879openalex-snapshot
A male-killing Wolbachia endosymbiont is concealed by another endosymbiont and a nuclear suppressor
inferred← citeshttps://doi.org/10.1534/genetics.119.302349openalex-snapshot
Wolbachia Acquisition by Drosophila yakuba -Clade Hosts and Transfer of Incompatibility Loci Between Distantly Related Wolbachia
inferred← citeshttps://doi.org/10.1534/genetics.120.303330openalex-snapshot
Environmental and Genetic Contributions to Imperfect w Mel-Like Wolbachia Transmission and Frequency Variation
inferred← citeshttps://doi.org/10.3389/fgene.2021.669045openalex-snapshot
Hybrid Sterility, Genetic Conflict and Complex Speciation: Lessons From the Drosophila simulans Clade Species
inferred← citeshttps://doi.org/10.3389/fmicb.2020.576844openalex-snapshot
A Role for Maternal Factors in Suppressing Cytoplasmic Incompatibility
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1116766openalex-snapshot
Modeling emergence of Wolbachia toxin-antidote protein functions with an evolutionary algorithm
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1304401openalex-snapshot
Bacterial community and genome analysis of cytoplasmic incompatibility-inducing Wolbachia in American serpentine leafminer, Liriomyza trifolii
inferred← citeshttps://doi.org/10.3390/genes11080852openalex-snapshot
The Biochemistry of Cytoplasmic Incompatibility Caused by Endosymbiotic Bacteria
inferred← citeshttps://doi.org/10.3390/vaccines9010032openalex-snapshot
A Review: Aedes-Borne Arboviral Infections, Controls and Wolbachia-Based Strategies
inferred← citeshttps://doi.org/10.4103/0972-9062.364760openalex-snapshot
Distribution and phenotypic effect of Wolbachia in natural population of Indian Drosophila
inferred← citeshttps://doi.org/10.53846/goediss-9301openalex-snapshot
The confused flour beetle, Tribolium confusum A model for investigating Wolbachia-host interactions
inferred← citeshttps://doi.org/10.6084/m9.figshare.14642995openalex-snapshot
Additional file 1 of Prevalence and relationship of endosymbiotic Wolbachia in the butterfly genus Erebia
inferred← citeshttps://doi.org/10.7554/elife.50026openalex-snapshot
The Wolbachia cytoplasmic incompatibility enzyme CidB targets nuclear import and protamine-histone exchange factors
inferred← citeshttps://doi.org/10.7554/elife.61989openalex-snapshot
Symbiont-mediated cytoplasmic incompatibility: What have we learned in 50 years?
inferred← citeshttps://doi.org/10.7717/peerj.10646openalex-snapshot
Evolution of Wolbachia mutualism and reproductive parasitism: insight from two novel strains that co-infect cat fleas
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