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Diversity and phylogenetic relationships of Wolbachia in Drosophila and other native Hawaiian insects
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00248-006-9036-xopenalex-snapshot
Closely Related Wolbachia Strains within the Pumpkin Arthropod Community and the Potential for Horizontal Transmission via the Plant
inferredcites →https://doi.org/10.1016/j.ympev.2007.12.021openalex-snapshot
Mitochondrial phylogeny of the endemic Hawaiian craneflies (Diptera, Limoniidae, Dicranomyia): Implications for biogeography and species formation
inferredcites →https://doi.org/10.1016/j.ympev.2010.11.022openalex-snapshot
Phylogenetic and ecological relationships of the Hawaiian Drosophila inferred by mitochondrial DNA analysis
inferredcites →https://doi.org/10.1016/s0022-2011(03)00106-xopenalex-snapshot
Infection density of Wolbachia and level of cytoplasmic incompatibility in the Mediterranean flour moth, Ephestia kuehniella
inferredcites →https://doi.org/10.1016/s0960-9822(01)00101-4openalex-snapshot
Recombination in Wolbachia
inferredcites →https://doi.org/10.1038/nature00843openalex-snapshot
A host–parasite interaction rescues Drosophila oogenesis defects
inferredcites →https://doi.org/10.1038/nature10355openalex-snapshot
The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations
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/nrmicro1969openalex-snapshot
Wolbachia: master manipulators of invertebrate biology
inferredcites →https://doi.org/10.1038/sj.hdy.6800739openalex-snapshot
Wolbachia requirement for oogenesis: occurrence within the genus Asobara (Hymenoptera, Braconidae) and evidence for intraspecific variation in A. tabida
inferredcites →https://doi.org/10.1046/j.1365-2540.2001.00920.xopenalex-snapshot
Wolbachia diversity in the Porcellionides pruinosus complex of species (Crustacea: Oniscidea): evidence for host-dependent patterns of infection
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.1420-9101.2001.00279.xopenalex-snapshot
Wolbachia infection in crustaceans: novel hosts and potential routes for horizontal transmission
inferredcites →https://doi.org/10.1073/pnas.0911476107openalex-snapshot
Wolbachia as a bacteriocyte-associated nutritional mutualist
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/10.1080/10635150802429642openalex-snapshot
A Rapid Bootstrap Algorithm for the RAxML Web Servers
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/molbev/msj049openalex-snapshot
Widespread Recombination Throughout Wolbachia Genomes
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkl042openalex-snapshot
ModelTest Server: a web-based tool for the statistical selection of models of nucleotide substitution online
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026084openalex-snapshot
Phylogenetic evidence for horizontal transmission of Wolbachia in host- parasitoid associations
inferredcites →https://doi.org/10.1098/rsbl.2007.0575openalex-snapshot
Out of Hawaii: the origin and biogeography of the genus Scaptomyza (Diptera: Drosophilidae)
inferredcites →https://doi.org/10.1098/rspb.1998.0324openalex-snapshot
Phylogeny and PCR–based classification of Wolbachia strains using wsp gene sequences
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.2001.1632openalex-snapshot
How many species are infected withWolbachia? Cryptic sex ratio distorters revealed to be common by intensive sampling
inferredcites →https://doi.org/10.1098/rspb.2002.2100openalex-snapshot
The distribution ofWolbachiain fig wasps: correlations with host phylogeny, ecology and population structure
inferredcites →https://doi.org/10.1098/rspb.2002.2175openalex-snapshot
How old is the Hawaiian biota? Geology and phylogeny suggest recent divergence
inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot
Creating the CIPRES Science Gateway for inference of large phylogenetic trees
inferredcites →https://doi.org/10.1111/j.0962-1075.2004.00492.xopenalex-snapshot
Distribution and prevalence of Wolbachia in Japanese populations of Lepidoptera
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.1365-3113.2007.00400.xopenalex-snapshot
Revision of the ‘nudidrosophila’ and ‘ateledrosophila’ species groups of Hawaiian Drosophila (Diptera: Drosophilidae), with descriptions of twenty‐two new species
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/10.1126/science.1060788openalex-snapshot
Infiltration of a Hawaiian Community by Introduced Biological Control Agents
inferredcites →https://doi.org/10.1128/aem.00731-06openalex-snapshot
Multilocus Sequence Typing System for the Endosymbiont Wolbachia pipientis
inferredcites →https://doi.org/10.1128/aem.01109-08openalex-snapshot
How Diverse Is the GenusWolbachia? Multiple-Gene Sequencing Reveals a Putatively NewWolbachiaSupergroup Recovered from Spider Mites (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1128/aem.02878-10openalex-snapshot
Variable Infection Frequency and High Diversity of Multiple Strains of Wolbachia pipientis in Perkinsiella Planthoppers
inferredcites →https://doi.org/10.1128/aem.69.10.6082-6090.2003openalex-snapshot
Diversity ofWolbachiaEndosymbionts in Heteropteran Bugs
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145244openalex-snapshot
Arthropods on Islands: Colonization, Speciation, and Conservation
inferredcites →https://doi.org/10.1146/annurev.es.15.110184.000525openalex-snapshot
Genetic Revolutions in Relation to Speciation Phenomena: The Founding of New Populations
inferredcites →https://doi.org/10.11646/zootaxa.2805.1.1openalex-snapshot
Review of the native Hawaiian leafhopper genus Nesophrosyne (Hemiptera: Cicadellidae: Deltocephalinae) with description of eight new species associated with Broussaisia arguta (Hydrangeaceae)
inferredcites →https://doi.org/10.1186/1471-2148-5-35openalex-snapshot
Evolutionary history of Wolbachia infections in the fire ant Solenopsis invicta
inferredcites →https://doi.org/10.1534/genetics.106.058818openalex-snapshot
Heritable Endosymbionts of Drosophila
inferredcites →https://doi.org/10.1603/0022-2585-38.2.237openalex-snapshot
WolbachiaInfections of Phlebotomine Sand Flies (Diptera: Psychodidae)
inferredcites →https://doi.org/10.5860/choice.30-3258openalex-snapshot
Hawaiian insects and their kin
inferredcites →https://doi.org/10.5860/choice.39-2183openalex-snapshot
MacClade 4.0: analysis of phylogeny and character evolution
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.10612openalex-snapshot
Exploring and validating observations of non‐local species in eDNA samples
inferred← citeshttps://doi.org/10.1007/s00248-022-01982-1openalex-snapshot
Low Endosymbiont Incidence in Drosophila Species Across Peninsula Thailand
inferred← citeshttps://doi.org/10.1093/g3journal/jkab197openalex-snapshot
Molecular population genetics of Sex-lethal ( Sxl ) in the Drosophila melanogaster species group: a locus that genetically interacts with Wolbachia pipientis in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/gbe/evad031openalex-snapshot
Genomic Comparisons Reveal Selection Pressure and Functional Variation Between Nutritional Endosymbionts of Cave-Adapted and Epigean Hawaiian Planthoppers
inferred← citeshttps://doi.org/10.1111/evo.12330openalex-snapshot
ON THE COYNE AND ORR-IGIN OF SPECIES: EFFECTS OF INTRINSIC POSTZYGOTIC ISOLATION, ECOLOGICAL DIFFERENTIATION, X CHROMOSOME SIZE, AND SYMPATRY ONDROSOPHILASPECIATION
inferred← citeshttps://doi.org/10.1111/evo.12981openalex-snapshot
TropicalDrosophila pandoracarryWolbachiainfections causing cytoplasmic incompatibility or male killing
inferred← citeshttps://doi.org/10.1111/mec.12901openalex-snapshot
Wolbachiado not live by reproductive manipulation alone: infection polymorphism inDrosophila suzukiiandD. subpulchrella
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/10.1186/s12983-015-0107-zopenalex-snapshot
Wolbachia in butterflies and moths: geographic structure in infection frequency
inferred← citeshttps://doi.org/10.1371/journal.pone.0051597openalex-snapshot
Characterization of Transcription Factors That Regulate the Type IV Secretion System and Riboflavin Biosynthesis in Wolbachia of Brugia malayi
inferred← citeshttps://doi.org/10.1371/journal.ppat.1003607openalex-snapshot
Rapid Sequential Spread of Two Wolbachia Variants in Drosophila simulans
inferred← citeshttps://doi.org/10.3390/genes14081545openalex-snapshot
The Transmission Patterns of the Endosymbiont Wolbachia within the Hawaiian Drosophilidae Adaptive Radiation
inferred← citeshttps://doi.org/10.3390/insects12100853openalex-snapshot
The Incidence of Wolbachia Bacterial Endosymbiont in Bisexual and Parthenogenetic Populations of the Psyllid Genus Cacopsylla (Hemiptera, Psylloidea)
inferred← citeshttps://doi.org/10.3390/insects8040130openalex-snapshot
The Native Hawaiian Insect Microbiome Initiative: A Critical Perspective for Hawaiian Insect Evolution
inferred← citeshttps://doi.org/10.4103/0972-9062.313967openalex-snapshot
Prevalence and transmission potential of Wolbachia in Aedes albopictus population circulating in endemic coastal districts of Odisha, India
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