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Wolbachia: intracellular manipulators of mite reproduction
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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/mrd.1080400404openalex-snapshot
Induction of paternal genome loss by the paternal‐sex‐ratio chromosome and cytoplasmic incompatibility bacteria (Wolbachia): A comparative study of early embryonic events
inferredcites →https://doi.org/10.1007/bf00271154openalex-snapshot
Post-fertilization effect of incompatibility factors in Mormoniella
inferredcites →https://doi.org/10.1007/bf00277059openalex-snapshot
Cloning and characterization of an ftsZ homologue from a bacterial symbiont of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00309428openalex-snapshot
Vererbung durch Kerngene und das Problem der ausserkaryotischen Vererbung bei Culex pipiens
inferredcites →https://doi.org/10.1007/bf00576992openalex-snapshot
Untersuchungen zur Inkompatibilitt imCulex pipiens-Komplex
inferredcites →https://doi.org/10.1007/bf01194091openalex-snapshot
Developmental success and reproductive incompatibility among populations of the European red mite,Panonychus ulmi (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1007/bf01854097openalex-snapshot
An analysis of non-reciprocal cross incompatibility in Mormoniella vitripennis (Walker)
inferredcites →https://doi.org/10.1016/0022-2011(71)90124-8openalex-snapshot
Microorganisms associated with the two-spotted spider mite Tetranychus urticae
inferredcites →https://doi.org/10.1016/0022-2011(73)90141-9openalex-snapshot
The etiological agent of cytoplasmic incompatibility in Culex pipiens
inferredcites →https://doi.org/10.1016/0022-2011(82)90041-6openalex-snapshot
Microorganisms associated with the spider mite predator Metaseiulus (= Typhlodromus) occidentalis: Electron microscope observations
inferredcites →https://doi.org/10.1016/0022-2011(87)90080-2openalex-snapshot
The effect of tetracycline on nonreciprocal cross incompatibility in Mormoniella [= Nasonia] vitripennis
inferredcites →https://doi.org/10.1017/s0031182000022666openalex-snapshot
The Rickettsia,Wolbachia pipientis(gen. et sp.n.) and Associated Inclusions of the Mosquito,Culex pipiens
inferredcites →https://doi.org/10.1038/346558a0openalex-snapshot
Microorganisms associated with chromosome destruction and reproductive isolation between two insect species
inferredcites →https://doi.org/10.1038/348178a0openalex-snapshot
Bidirectional incompatibility between conspecific populations of Drosophila simulans
inferredcites →https://doi.org/10.1038/353440a0openalex-snapshot
Rapid spread of an inherited incompatibility factor in California Drosophila
inferredcites →https://doi.org/10.1038/361066a0openalex-snapshot
Molecular identification of microorganisms associated with parthenogenesis
inferredcites →https://doi.org/10.1038/373072a0openalex-snapshot
Increased male fertility in Tribolium confusum beetles after infection with the intracellular parasite Wolbachia
inferredcites →https://doi.org/10.1038/hdy.1995.140openalex-snapshot
Wolbachia and cytoplasmic incompatibility in mycophagous Drosophila and their relatives
inferredcites →https://doi.org/10.1038/hdy.1995.58openalex-snapshot
Nucleus–cytoplasm interactions causing reproductive incompatibility between two populations of Tetranychus quercivorus Ehara et Gotoh (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1046/j.1420-9101.1991.4010069.xopenalex-snapshot
Cytoplasmic incompatibilities in the mosquito Culex pipiens: How to explain a cytotype polymorphism?*
inferredcites →https://doi.org/10.1073/pnas.87.7.2424openalex-snapshot
Antibiotics cause parthenogenetic Trichogramma (Hymenoptera/Trichogrammatidae) to revert to sex.
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/10.1080/11250008609355500openalex-snapshot
Rôle des bactéries symbiotiques dans l'intersexualité, la monogénie et la spéciation chez des crustacés oniscoïdes
inferredcites →https://doi.org/10.1086/285432openalex-snapshot
Multispecies Interactions Affect Cytoplasmic Incompatibility in Tribolium Flour Beetles
inferredcites →https://doi.org/10.1093/aesa/51.5.441openalex-snapshot
Reproductive Isolation among Certain Spider Mites of the Tetranychus Telarius Complex, with Preliminary Systematic Notes
inferredcites →https://doi.org/10.1093/aesa/63.6.1558openalex-snapshot
Comparative Studies on Four Strains of Typhlodromus occidentalis (Acarina: Phytoseiidae). I. Hybridization and Reproductive Isolation Studies
inferredcites →https://doi.org/10.1093/aesa/89.3.435openalex-snapshot
Wolbachia in a Predator–Prey System: 16S Ribosomal Dna Analysis of Two Phytoseiids (Acari: Phytoseiidae) and Their Prey (Acari: Tetranychidae)
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/135.2.565openalex-snapshot
Cytoplasmic incompatibility and bacterial density in Nasonia vitripennis.
inferredcites →https://doi.org/10.1093/genetics/136.3.993openalex-snapshot
Cytoplasmic incompatibility in Australian populations of Drosophila melanogaster.
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/jmedent/14.1.89openalex-snapshot
Sex Ratios in Rickettsia Tsutsugamushi-Infected and Noninfected Colonies of Leptotrombidium (Acari: Trombiculidae)12
inferredcites →https://doi.org/10.1093/jmedent/24.5.542openalex-snapshot
Evaluation of Leptotrombidium (Leptotrombidium) fletcheri (Acari: Trombiculidae) as a Potential Vector of Ehrlichia sennetsu
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a110382openalex-snapshot
Separation of factors containing R-locus genes in Mormoniella stocks derived from aberrant segregation following incompatible crosses
inferredcites →https://doi.org/10.1098/rspb.1992.0135openalex-snapshot
Wolbachiaendosymbionts responsible for various alterations of sexuality in arthropods
inferredcites →https://doi.org/10.1098/rspb.1995.0117openalex-snapshot
Evolution and phylogeny of Wolbachia : reproductive parasites of arthropods
inferredcites →https://doi.org/10.1111/j.1365-2583.1993.tb00074.xopenalex-snapshot
Phylogeny of cytoplasmic incompatibility microorganisms in the parasitoid wasp genus Nasonia (Hymenoptera: Pteromalidae) based on 16S ribosomal DNA sequences
inferredcites →https://doi.org/10.1111/j.1365-2583.1996.tb00057.xopenalex-snapshot
Molecular identification of a Wolbachia endosymbiont in a Tetranychus urticae strain (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1111/j.1558-5646.1959.tb03045.xopenalex-snapshot
ON THE EVOLUTIONARY IMPORTANCE OF CYTOPLASMIC STERILITY IN MOSQUITOES
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.tb02192.xopenalex-snapshot
EVOLUTION OF INCOMPATIBILITY‐INDUCING MICROBES AND THEIR HOSTS
inferredcites →https://doi.org/10.1111/j.1570-7458.1965.tb00866.xopenalex-snapshot
GENETIC AFFINITIES BETWEEN ADJACENT POPULATIONS OF SPIDER MITES (TETRANYCHUS URTICAE KOCH)
inferredcites →https://doi.org/10.1111/j.1570-7458.1973.tb00255.xopenalex-snapshot
A COMPARATIVE STUDY OF SEVERAL STRAINS OF THE TETRANYCHUS NEOCALEDONICUS COMPLEX AND STERILIZATION TESTS OF MALES BY X‐RAYS
inferredcites →https://doi.org/10.1111/j.1570-7458.1983.tb03305.xopenalex-snapshot
A case of hybrid inviability in the two‐spotted spider mite, Tetranychus urticae
inferredcites →https://doi.org/10.1111/j.1570-7458.1985.tb03550.xopenalex-snapshot
Geographic variations and combining abilities in the two‐spotted spider mite, Tetranychus urticae
inferredcites →https://doi.org/10.1111/j.1570-7458.1993.tb01667.xopenalex-snapshot
Influence of microbe‐associated parthenogenesis on the fecundity of Trichogramma deion and T. pretiosum
inferredcites →https://doi.org/10.1111/j.1570-7458.1993.tb01700.xopenalex-snapshot
Host race formation in Tetranychus urticae: genetic differentiation, host plant preference, and mate choice in a tomato and a cucumber strain
inferredcites →https://doi.org/10.1126/science.3966160openalex-snapshot
Microorganism Mediated Reproductive Isolation in Flour Beetles (Genus Tribolium )
inferredcites →https://doi.org/10.1128/jb.173.2.697-703.1991openalex-snapshot
16S ribosomal DNA amplification for phylogenetic study
inferredcites →https://doi.org/10.1242/jcs.107.3.673openalex-snapshot
The distribution of cytoplasmic bacteria in the early Drosophila embryo is mediated by astral microtubules
inferredcites →https://doi.org/10.1303/aez.28.189openalex-snapshot
Divergence of the Northern and Southwestern Populations of Panonychus mori YOKOYAMA(Acari:Tetranychidae)in Japan in Host Range and Reproductive Compatibility
inferredcites →https://doi.org/10.1303/aez.30.361openalex-snapshot
Genetic Incompatibility in Local Populations of the Spider Mite, Tetranychus quercivorus EHARA et GOTOH (Acari: Tetranychidae)
inferredcites →https://doi.org/10.2144/000114018openalex-snapshot
Chelex 100 as a Medium for Simple Extraction of DNA for PCR-Based Typing from Forensic Material
inferredcites →https://doi.org/10.3733/hilg.v56n05p016openalex-snapshot
Reuse of Drainage Water for Irrigation: Results of Imperial Valley Study: I. Hypothesis, Experimental Procedures, and Cropping Results
inferredcites →https://doi.org/10.3733/hilg.v56n06p020openalex-snapshot
Premating and Postmating Isolation among Populations ofMetaseiulus occidentalis(Nesbitt) (Acarina: Phytoseiidae)
inferredcites →https://doi.org/10.5281/zenodo.10754859openalex-snapshot
Microorganismes symbiotiques et speciation.
inferredcites →https://doi.org/10.7326/0003-4819-102-1-151_3openalex-snapshot
Bergey's Manual of Systematic Bacteriology.
inferredcites →https://doi.org/10.7326/0003-4819-112-5-391_3openalex-snapshot
Bergey's Manual of Systematic Bacteriology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5852/ejt.2022.836.1921zenodo-depositor-declared
Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
inferred← citeshttps://doi.org/10.1002/9781118735893.ch5openalex-snapshot
Ecological Genomics ofTrichoderma
inferred← citeshttps://doi.org/10.1002/evl3.282openalex-snapshot
Interacting host modifier systems control Wolbachia -induced cytoplasmic incompatibility in a haplodiploid mite
inferred← citeshttps://doi.org/10.1002/njz2.70044openalex-snapshot
Investigating the Possibility of Wolbachia ‐ and Cardinium ‐Induced Parthenogenesis in Two Mite Species
inferred← citeshttps://doi.org/10.1006/jipa.1997.4739openalex-snapshot
Screening Mollusks forWolbachiaInfection
inferred← citeshttps://doi.org/10.1007/3-540-28185-1_6openalex-snapshot
Collembola as a Habitat for Microorganisms
inferred← citeshttps://doi.org/10.1007/978-0-387-78225-6_9openalex-snapshot
Wolbachia- Based Technologies for Insect Pest Population Control
inferred← citeshttps://doi.org/10.1007/978-1-4020-9695-2_25openalex-snapshot
Verified and potential pathogens of predatory mites (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1007/978-3-319-15042-0_12openalex-snapshot
Mite Pathogens and Their Use in Biological Control
inferred← citeshttps://doi.org/10.1007/978-90-481-8606-8_11openalex-snapshot
IPM Potentials of Microbial Pathogens and Diseases of Mites
inferred← citeshttps://doi.org/10.1007/978-90-481-9837-5_1openalex-snapshot
From sequence to phoresy – molecular biology in acarology
inferred← citeshttps://doi.org/10.1007/978-981-10-1594-6_20openalex-snapshot
Biological Control of Phytophagous Mites
inferred← citeshttps://doi.org/10.1007/pl00011978openalex-snapshot
The transmission and effects of Wolbachia bacteria in parasitoids
inferred← citeshttps://doi.org/10.1007/s00248-012-0042-xopenalex-snapshot
Distribution Patterns of Wolbachia Endosymbionts in the Closely Related Flower Bugs of the Genus Orius: Implications for Coevolution and Horizontal Transfer
inferred← citeshttps://doi.org/10.1007/s00248-013-0198-zopenalex-snapshot
Diversity of Wolbachia in Natural Populations of Spider Mites (genus Tetranychus): Evidence for Complex Infection History and Disequilibrium Distribution
inferred← citeshttps://doi.org/10.1007/s00284-004-4346-zopenalex-snapshot
Wolbachia pipientis in Australian Spiders
inferred← citeshttps://doi.org/10.1007/s00284-009-9433-8openalex-snapshot
Wolbachia in Anastrepha Fruit Flies (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1007/s00403-009-0984-0openalex-snapshot
PCR analysis for Wolbachia in human and canine Demodex mites
inferred← citeshttps://doi.org/10.1007/s10493-005-6075-9openalex-snapshot
Negative Evidence of Wolbachia in the Predaceous Mite Phytoseiulus persimilis
inferred← citeshttps://doi.org/10.1007/s10493-006-0014-2openalex-snapshot
Biological Cycle of Lorryia formosa (Acari, Tydeidae) on Rubber Tree Leaves: A Case of Thelytoky
inferred← citeshttps://doi.org/10.1007/s10493-006-0020-4openalex-snapshot
A Novel Disease Affecting the Predatory Mite Phytoseiulus persimilis (Acari, Phytoseiidae): 2. Disease Transmission by Adult Females
inferred← citeshttps://doi.org/10.1007/s10493-007-9080-3openalex-snapshot
Incidence of the endosymbionts Wolbachia, Cardinium and Spiroplasma in phytoseiid mites and associated prey
inferred← citeshttps://doi.org/10.1007/s10493-007-9092-zopenalex-snapshot
Spider mite (Acari: Tetranychidae) mitochondrial COI phylogeny reviewed: host plant relationships, phylogeography, reproductive parasites and barcoding
inferred← citeshttps://doi.org/10.1007/s10493-008-9188-0openalex-snapshot
Verified and potential pathogens of predatory mites (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1007/s10493-009-9303-xopenalex-snapshot
Life cycle and behaviour of the predaceous mite Cunaxatricha tarsospinosa (Acari: Prostigmata: Cunaxidae)
inferred← citeshttps://doi.org/10.1007/s10493-011-9453-5openalex-snapshot
A critical review on some closely related species of Tetranychus sensu stricto (Acari: Tetranychidae) in the public DNA sequences databases
inferred← citeshttps://doi.org/10.1007/s13199-010-0065-3openalex-snapshot
Bacterial symbionts in insects: balancing life and death
inferred← citeshttps://doi.org/10.1007/s13199-017-0503-6openalex-snapshot
The nature of the immune response in novel Wolbachia-host associations
inferred← citeshttps://doi.org/10.1007/s13355-012-0152-4openalex-snapshot
No seasonal trend in infection of the pale grass blue butterfly, Zizeeria maha (Lepidoptera: Lycaenidae), by Wolbachia
inferred← citeshttps://doi.org/10.1016/b978-012257305-7/50054-0openalex-snapshot
Culture and Colonization
inferred← citeshttps://doi.org/10.1016/j.asd.2021.101047openalex-snapshot
Female reproductive system and oogenesis in the mite Bakericheyla chanayi
inferred← citeshttps://doi.org/10.1016/j.aspen.2011.04.008openalex-snapshot
Wolbachia in field populations of Forcipomyia taiwana (Diptera: Ceratopogonidae) in Taiwan
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2016.02.017openalex-snapshot
Phytoseiid mites under environmental stress
inferred← citeshttps://doi.org/10.1016/j.cub.2007.09.022openalex-snapshot
Evolutionary Genomics: Transdomain Gene Transfers
inferred← citeshttps://doi.org/10.1016/j.ijpara.2004.11.007openalex-snapshot
Analysis of Sarcoptes scabiei finds no evidence of infection with Wolbachia
inferred← citeshttps://doi.org/10.1016/j.jembe.2018.09.002openalex-snapshot
Female-biased sex ratios unrelated to Wolbachia infection in European species of the Jaera albifrons complex (marine isopods)
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2026.105061openalex-snapshot
Microbial diversity and cytoplasmic incompatibility in Tetranychus urticae Spanish populations
inferred← citeshttps://doi.org/10.1016/j.jip.2008.03.006openalex-snapshot
Novel bacterial pathogen Acaricomes phytoseiuli causes severe disease symptoms and histopathological changes in the predatory mite Phytoseiulus persimilis (Acari, Phytoseiidae)
inferred← citeshttps://doi.org/10.1016/j.jip.2011.09.005openalex-snapshot
Extended starvation reduced and eliminated Wolbachia, but not Cardinium, from Metaseiulus occidentalis females (Acari: Phytoseiidae): A need to reassess Wolbachia’s status in this predatory mite?
inferred← citeshttps://doi.org/10.1016/j.jip.2018.02.010openalex-snapshot
Successful reproduction of unmated Tropilaelaps mercedesae and its implication on mite population growth in Apis mellifera colonies
inferred← citeshttps://doi.org/10.1016/j.mib.2007.05.002openalex-snapshot
Wolbachia–host interactions: connecting phenotype to genotype
inferred← citeshttps://doi.org/10.1016/j.micron.2015.12.003openalex-snapshot
Morphostructural investigation of the female reproductive system and molecular evidence for Wolbachia in Balclutha brevis Lindberg 1954 (Hemiptera, Cicadellidae)
inferred← citeshttps://doi.org/10.1016/j.tim.2009.11.004openalex-snapshot
Functional diversity of ankyrin repeats in microbial proteins
inferred← citeshttps://doi.org/10.1016/j.tpb.2007.08.004openalex-snapshot
Coexistence of cytoplasmic incompatibility and male-killing-inducing endosymbionts, and their impact on host gene flow
inferred← citeshttps://doi.org/10.1016/j.vetpar.2020.109297openalex-snapshot
Wolbachia: A tool for livestock ectoparasite control
inferred← citeshttps://doi.org/10.1016/s0014-4894(03)00058-4openalex-snapshot
Tunga penetrans: molecular identification of Wolbachia endobacteria and their recognition by antibodies against proteins of endobacteria from filarial parasites
inferred← citeshttps://doi.org/10.1016/s0169-5347(99)01599-2openalex-snapshot
Further Wolbachia endosymbiont diversity: a tree hiding in the forest?
inferred← citeshttps://doi.org/10.1016/s0925-4773(01)00594-9openalex-snapshot
The distribution and proliferation of the intracellular bacteria Wolbachia during spermatogenesis in Drosophila
inferred← citeshttps://doi.org/10.1016/s0966-842x(99)01531-0openalex-snapshot
Evolution of Wolbachia pipientis transmission dynamics in insects
inferred← citeshttps://doi.org/10.1016/s1286-4579(03)00192-8openalex-snapshot
Identification of Wolbachia–host interacting factors through cytological analysis
inferred← citeshttps://doi.org/10.1017/cbo9780511542053.012openalex-snapshot
Sex ratio control in arrhenotokous and pseudo-arrhenotokous mites
inferred← citeshttps://doi.org/10.1017/s0007485316000444openalex-snapshot
Geography has a greater effect thanWolbachiainfection on population genetic structure in the spider mite,Tetranychus pueraricola
inferred← citeshttps://doi.org/10.1017/s0031182015000530openalex-snapshot
Symbiosis in an overlooked microcosm: a systematic review of the bacterial flora of mites
inferred← citeshttps://doi.org/10.1017/s1431927600035807openalex-snapshot
A Rickettsia in the Ovary of the Twospotted Spider Mite, Tetranychus Urticae KOCH (Acarina: Tetranychedae)
inferred← citeshttps://doi.org/10.1017/s174275840000847xopenalex-snapshot
Polymorphism for Wolbachia infections in eastern and southern African Cotesia sesamiae (Cameron) (Hymenoptera: Braconidae) populations
inferred← citeshttps://doi.org/10.1023/a:1006363604916openalex-snapshot
High Temperatures Eliminate Wolbachia, a Cytoplasmic Incompatibility Inducing Endosymbiont, From the Two-spotted Spider Mite
inferred← citeshttps://doi.org/10.1023/a:1006497906793openalex-snapshot
The Application of Molecular Markers in the Study of Diversity in Acarology: a Review
inferred← citeshttps://doi.org/10.1023/a:1017934218898openalex-snapshot
Genetic diversity and phylogeny of the Kanzawa spider mite, Tetranychus kanzawai, in Japan
inferred← citeshttps://doi.org/10.1023/a:1018441325762openalex-snapshot
Mating, cross-mating and related behaviours of Neoseiulus californicus and Neoseiulus fallacis (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1023/a:1024279831966openalex-snapshot
No variation for Wolbachia-induced hybrid breakdown in two populations of a spider mite
inferred← citeshttps://doi.org/10.1038/hdy.1997.121openalex-snapshot
Wolbachia and cytoplasmic incompatibility in the spider mites Tetranychus urticae and T. turkestani
inferred← citeshttps://doi.org/10.1038/hdy.2008.71openalex-snapshot
Wolbachia modification of sperm does not always require residence within developing sperm
inferred← citeshttps://doi.org/10.1038/hdy.2009.4openalex-snapshot
The effects of, and interactions between, Cardinium and Wolbachia in the doubly infected spider mite Bryobia sarothamni
inferred← citeshttps://doi.org/10.1038/s41598-019-49662-4openalex-snapshot
Feeding by Tropilaelaps mercedesae on pre- and post-capped brood increases damage to Apis mellifera colonies
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800329openalex-snapshot
Wolbachia distribution and cytoplasmic incompatibility based on a survey of 42 spider mite species (Acari: Tetranychidae) in Japan
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800596openalex-snapshot
Multiple infections and diversity of cytoplasmic incompatibility in a haplodiploid species
inferred← citeshttps://doi.org/10.1046/j.0962-1083.2001.01432.xopenalex-snapshot
Prevailing triple infection withWolbachiainCallosobruchus chinensis(Coleoptera: Bruchidae)
inferred← citeshttps://doi.org/10.1046/j.1365-2583.2000.00233.xopenalex-snapshot
Wolbachia infections in native and introduced populations of fire ants ( Solenopsis spp.)
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2002.01556.xopenalex-snapshot
The incidence and diversity ofWolbachiain gallwasps (Hymenoptera; Cynipidae) on oak
inferred← citeshttps://doi.org/10.1046/j.1420-9101.2003.00679.xopenalex-snapshot
Wolbachia affects oviposition and mating behaviour of its spider mite host
inferred← citeshttps://doi.org/10.1080/01647950608684489openalex-snapshot
Effect of infection rate ofWolbachiaon the reproduction inTetranychus kanzawaiKishida (Acari: Tetranychidae) in China
inferred← citeshttps://doi.org/10.1080/01647954.2014.953999openalex-snapshot
Life cycle of Tydeus californicus (Acari: Tydeidae) on leaves of Inga marginata with and without pollen of Typha angustifolia under laboratory conditions
inferred← citeshttps://doi.org/10.1080/01647954.2025.2591303openalex-snapshot
Biosystematics and morphological assessment of Euseius concordis (Chant) populations (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1080/03079457.2019.1635679openalex-snapshot
Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssus gallinae (De Geer, 1778)
inferred← citeshttps://doi.org/10.1080/07924259.2015.1050560openalex-snapshot
A very rare case of intersexuality in water mites of the genusArrenurusDugès, 1834 (Acari, Hydrachnidia)
inferred← citeshttps://doi.org/10.1080/09583150701718255openalex-snapshot
A novel disease affecting the predatory mite Phytoseiulus persimilis (Acari, Phytoseiidae): evidence for the involvement of bacteria
inferred← citeshttps://doi.org/10.1086/345856openalex-snapshot
Genetic Conflicts over Sex Ratio: Mite‐Endosymbiont Interactions
inferred← citeshttps://doi.org/10.1093/evolut/qpae149openalex-snapshot
Wolbachia strengthens the match between premating and early postmating isolation in spider mites
inferred← citeshttps://doi.org/10.1093/jee/tow032openalex-snapshot
Differences in the Bacterial Community of Laboratory and Wild Populations of the Predatory MiteCheyletus eruditus(Acarina: Cheyletidae) and Bacteria Transmission From Its PreyAcarus siro(Acari: Acaridae)
inferred← citeshttps://doi.org/10.1093/jmedent/42.2.120openalex-snapshot
Using In Situ Hybridization to Detect Endosymbiont Wolbachia in Dissected Tissues of Mosquito Host
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/oxfordjournals.molbev.a026084openalex-snapshot
Phylogenetic evidence for horizontal transmission of Wolbachia in host- parasitoid associations
inferred← citeshttps://doi.org/10.1098/rspb.1998.0455openalex-snapshot
Successful horizontal transfer of Wolbachia symbionts between Trichogramma wasps
inferred← citeshttps://doi.org/10.1098/rspb.1998.0456openalex-snapshot
Widespread occurrence of the microorganism Wolbachia in ants
inferred← citeshttps://doi.org/10.1098/rspb.2000.1232openalex-snapshot
Wolbachia–induced ‘hybrid breakdown’ in the two–fspotted spider miteTetranychus urticaeKoch
inferred← citeshttps://doi.org/10.1098/rspb.2005.3383openalex-snapshot
Wolbachiainfection suppresses both host defence and parasitoid counter-defence
inferred← citeshttps://doi.org/10.1101/2020.06.29.178699openalex-snapshot
Wolbachia and host intrinsic reproductive barriers contribute additively to post-mating isolation in spider mites
inferred← citeshttps://doi.org/10.1107/s1744309108000055openalex-snapshot
Crystallization and preliminary diffraction analysis of a DsbA homologue fromWolbachia pipientis
inferred← citeshttps://doi.org/10.1111/1462-2920.12573openalex-snapshot
A host as an ecosystem: W olbachia coping with environmental constraints
inferred← citeshttps://doi.org/10.1111/brv.12663openalex-snapshot
Wolbachiahost shifts: routes, mechanisms, constraints and evolutionary consequences
inferred← citeshttps://doi.org/10.1111/een.13271openalex-snapshot
Substantial fitness costs in terms of parasitization rates, offspring production and sex ratio of Wolbachia infection in Nasonia vitripennis without modified host preference
inferred← citeshttps://doi.org/10.1111/ens.12113openalex-snapshot
Mating rates and the prevalence of male‐killing S piroplasma in H armonia axyridis ( C oleoptera: C occinellidae)
inferred← citeshttps://doi.org/10.1111/evo.12402openalex-snapshot
EVOLUTION OF ASEXUALITY VIA DIFFERENT MECHANISMS IN GRASS THRIPS (THYSANOPTERA:Aptinothrips)
inferred← citeshttps://doi.org/10.1111/evo.14286openalex-snapshot
Wolbachia and host intrinsic reproductive barriers contribute additively to postmating isolation in spider mites
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2000.tb00019.xopenalex-snapshot
EVIDENCE FOR FEMALE MORTALITY IN WOLBACHIA-MEDIATED CYTOPLASMIC INCOMPATIBILITY IN HAPLODIPLOID INSECTS: EPIDEMIOLOGIC AND EVOLUTIONARY CONSEQUENCES
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2002.tb01447.xopenalex-snapshot
WITHIN- AND BETWEEN-POPULATION VARIATION FOR WOLBACHIA-INDUCED REPRODUCTIVE INCOMPATIBILITY IN A HAPLODIPLOID MITE
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01516.xopenalex-snapshot
Two synonymy cases within the genus Neoseiulella (Acari: Phytoseiidae): is the molecular evidence so evident?
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2010.00996.xopenalex-snapshot
THE MAINTENANCE OF GENETIC VARIATION FOR OVIPOSITION RATE IN TWO-SPOTTED SPIDER MITES: INFERENCES FROM ARTIFICIAL SELECTION
inferred← citeshttps://doi.org/10.1111/j.1570-7458.2010.00974.xopenalex-snapshot
Occurrence ofWolbachiain central European weevils: correlations with host systematics, ecology, and biology
inferred← citeshttps://doi.org/10.1111/j.1574-6968.2008.01110.xopenalex-snapshot
How many species are infected with Wolbachia? – a statistical analysis of current data
inferred← citeshttps://doi.org/10.1111/jeb.12357openalex-snapshot
Genetic causes of transitions from sexual reproduction to asexuality in plants and animals
inferred← citeshttps://doi.org/10.11158/saa.10.1.2openalex-snapshot
Laboratory population life table of Amphitetranychus viennensis (Zacher) (Acari: Tetranychidae) at different temperatures
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1128/aem.63.10.3926-3932.1997openalex-snapshot
Endosymbionts of ticks and their relationship to Wolbachia spp. and tick-borne pathogens of humans and animals
inferred← citeshttps://doi.org/10.1128/aem.68.8.4074-4080.2002openalex-snapshot
Internal Spatiotemporal Population Dynamics of Infection with ThreeWolbachiaStrains in the Adzuki Bean Beetle,Callosobruchus chinensis(Coleoptera: Bruchidae)
inferred← citeshttps://doi.org/10.1128/jb.187.15.5136-5145.2005openalex-snapshot
Distribution, Expression, and Motif Variability of Ankyrin Domain Genes in Wolbachia pipientis
inferred← citeshttps://doi.org/10.1134/s1062359024701255openalex-snapshot
Metagenomic Analysis of the Microbiota of a Laboratory Mite Population of Neoseiulus californicus (Mesostigmata, Phytoseiidae) and Optimization of the Microbiota Composition to Improve the Efficiency of Mite Breeding
inferred← citeshttps://doi.org/10.1134/s2079086422070027openalex-snapshot
Bacterial Symbionts and Pathogens in Populations of Phytoseiidae Mites (Phytoseiidae, Mesostigmata)
inferred← citeshttps://doi.org/10.1146/annurev.genet.41.110306.130354openalex-snapshot
The Genetics and Cell Biology of Wolbachia-Host Interactions
inferred← citeshttps://doi.org/10.1146/annurev.micro.53.1.71openalex-snapshot
Wolbachia Pipientis: Microbial Manipulator of Arthropod Reproduction
inferred← citeshttps://doi.org/10.1155/2014/731291openalex-snapshot
Evidence against the Presence ofWolbachiain a Population of the Crayfish SpeciesProcambarus clarkii
inferred← citeshttps://doi.org/10.11606/d.11.2011.tde-18102011-163626openalex-snapshot
A interação Wolbachia - Trichogramma galloi Zucchi, 1988 (Hymenoptera: Trichogrammatidae)
inferred← citeshttps://doi.org/10.11606/d.41.2007.tde-30082007-143156openalex-snapshot
Endossimbionte Wolbachia em moscas-das-frutas do gênero Anastrepha (Tephritidae) e em vespas parasitóides (Braconidae) associadas
inferred← citeshttps://doi.org/10.11606/t.11.2002.tde-15072002-173031openalex-snapshot
Caracterização morfológica e molecular de ácaros predadores do gênero Euseius (Acari, Phytoseiidae).
inferred← citeshttps://doi.org/10.1186/1756-3305-4-228openalex-snapshot
Parasites of vectors - Ixodiphagus hookeri and its Wolbachia symbionts in ticks in the Netherlands
inferred← citeshttps://doi.org/10.1201/9780203009918-22openalex-snapshot
Symbiosis and the Origin of Species
inferred← citeshttps://doi.org/10.1201/9780203009918.ch17openalex-snapshot
Symbiosis And The Origin Of Species
inferred← citeshttps://doi.org/10.1201/9781420042030-14openalex-snapshot
The spread of genetic constructs in natural insect populations
inferred← citeshttps://doi.org/10.1201/9781420042030.ch10openalex-snapshot
The spread of genetic constructs in natural insect populations
inferred← citeshttps://doi.org/10.12681/eh.11597openalex-snapshot
Wolbachia-induced reproductive parasitism and applications
inferred← citeshttps://doi.org/10.1303/aez.2002.379openalex-snapshot
Sensitivity comparison of PCR primers for detecting Wolbachia in spider mites.
inferred← citeshttps://doi.org/10.1303/aez.32.485openalex-snapshot
Wolbachia Having No Effect on Reproductive Incompatibility in Tetranychus kanzawai KISHIDA (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1303/aez.34.551openalex-snapshot
Incompatibility and host plant differences among populations of Tetranychus kanzawai Kishida (Acari : Tetranychidae)
inferred← citeshttps://doi.org/10.13057/biodiv/d211216openalex-snapshot
Wolbachia infection prevalence as common insects’ endosymbiont in the rural area of Yogyakarta, Indonesia
inferred← citeshttps://doi.org/10.1371/journal.pone.0054964openalex-snapshot
Multiple Infections with Cardinium and Two Strains of Wolbachia in The Spider Mite Tetranychus phaselus Ehara: Revealing New Forces Driving the Spread of Wolbachia
inferred← citeshttps://doi.org/10.1371/journal.pone.0128660openalex-snapshot
Feminization of the Isopod Cylisticus convexus after Transinfection of the wVulC Wolbachia Strain of Armadillidium vulgare
inferred← citeshttps://doi.org/10.1371/journal.pone.0144552openalex-snapshot
The Rickettsia Endosymbiont of Ixodes pacificus Contains All the Genes of De Novo Folate Biosynthesis
inferred← citeshttps://doi.org/10.1371/journal.ppat.0010014openalex-snapshot
Wolbachia Utilizes Host Microtubules and Dynein for Anterior Localization in the Drosophila Oocyte
inferred← citeshttps://doi.org/10.1371/journal.ppat.0020043openalex-snapshot
The Tripartite Associations between Bacteriophage, Wolbachia, and Arthropods
inferred← citeshttps://doi.org/10.1534/g3.112.005140openalex-snapshot
Functional Analyses ofTrichoderma reeseiLAE1 Reveal Conserved and Contrasting Roles of This Regulator
inferred← citeshttps://doi.org/10.15666/aeer/1602_18191833openalex-snapshot
ABSENCE OF WOLBACHIA IN RED PALM WEEVIL, RYNCHOPHORUS FERRUGINEUS OLIVIER (COLEOPTERA: CURCULIONIDAE): A PCR-BASED APPROACH
inferred← citeshttps://doi.org/10.1590/s0074-02762010000800002openalex-snapshot
Assessing key safety concerns of a Wolbachia-based strategy to control dengue transmission by Aedes mosquitoes
inferred← citeshttps://doi.org/10.1590/s1519-566x2002000400004openalex-snapshot
Compatibilidade Reprodutiva Entre Populações de Euseius citrifolius Denmark & Muma (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1603/0022-2585-41.4.677openalex-snapshot
Molecular (Sub)Grouping of EndosymbiontWolbachiaInfection Among Mosquitoes of Taiwan
inferred← citeshttps://doi.org/10.1603/022.038.0503openalex-snapshot
Influence of Continuous High Temperature Conditions onWolbachiaInfection Frequency and the Fitness ofLiposcelis tricolor(Psocoptera: Liposcelididae)
inferred← citeshttps://doi.org/10.1603/en13085openalex-snapshot
Wolbachia Play an Important Role in Affecting mtDNA Variation of Tetranychus truncatus (Trombidiformes: Tetranychidae)
inferred← citeshttps://doi.org/10.1653/024.097.0421openalex-snapshot
Geographical Range and Laboratory Studies onApanteles opuntiarum(Hymenoptera: Braconidae) in Argentina, a Candidate for Biological Control ofCactoblastis cactorum(Lepidoptera: Pyralidae) in North America
inferred← citeshttps://doi.org/10.22099/ijvr.2009.1695openalex-snapshot
PCR SCREENING OF THE WOLBACHIA IN SOME ARTHROPODS AND NEMATODES IN KHUZESTAN PROVINCE
inferred← citeshttps://doi.org/10.2300/acari.7.83openalex-snapshot
Intracellular symbiotes in mites and ticks.
inferred← citeshttps://doi.org/10.24349/acarologia/20174178openalex-snapshot
Complementary description of Neoseiulus tunus (De Leon) (Acari: Mesostigmata: Phytoseiidae) and observation on its reproductive strategy
inferred← citeshttps://doi.org/10.29133/yyutbd.1805326openalex-snapshot
Identification of Wolbachia Strains in Two Sibling Species of Neoseiulus Predatory Mites and Their Prey
inferred← citeshttps://doi.org/10.31857/s0044513424030011openalex-snapshot
Metagenomic analysis of the microbiota of a laboratory mite population of Neoseiulus californicus (mesostigmata, phytoseiidae) and the optimisation of microbiota composition to improve mite breeding efficiency
inferred← citeshttps://doi.org/10.3329/ujzru.v26i0.691openalex-snapshot
Wolbachia-mediated reproductive alterations in invertebrate hosts and biocontrol implications of the bacteria: an update
inferred← citeshttps://doi.org/10.3389/fevo.2021.748212openalex-snapshot
Building on 150 Years of Knowledge: The Freshwater Isopod Asellus aquaticus as an Integrative Eco-Evolutionary Model System
inferred← citeshttps://doi.org/10.3389/fmicb.2016.01046openalex-snapshot
Populations of Stored Product Mite Tyrophagus putrescentiae Differ in Their Bacterial Communities
inferred← citeshttps://doi.org/10.3389/fmicb.2022.703183openalex-snapshot
Microbiome Heritability and Its Role in Adaptation of Hosts to Novel Resources
inferred← citeshttps://doi.org/10.3390/ijms18010182openalex-snapshot
Independent Effects of a Herbivore’s Bacterial Symbionts on Its Performance and Induced Plant Defences
inferred← citeshttps://doi.org/10.3390/insects14060558openalex-snapshot
Interaction of High Temperature Stress and Wolbachia Infection on the Biological Characteristic of Drosophila melanogaster
inferred← citeshttps://doi.org/10.3390/plants8080272openalex-snapshot
Botanicals Against Tetranychus urticae Koch Under Laboratory Conditions: A Survey of Alternatives for Controlling Pest Mites
inferred← citeshttps://doi.org/10.35662/unine-thesis-2297openalex-snapshot
Mites and endosymbionts- towards improved biological control
inferred← citeshttps://doi.org/10.36790/epistemus.v19i38.436openalex-snapshot
Manipuladores microscópicos: Cómo Wolbachia controla el destino de los ácaros
inferred← citeshttps://doi.org/10.3897/alpento.7.111214openalex-snapshot
Micro-endemism pattern and Wolbachia infection of Quedius obliqueseriatus (Coleoptera, Staphylinidae), a montane rove beetle endemic of the North-Western Caucasus
inferred← citeshttps://doi.org/10.3897/zookeys.176.2284openalex-snapshot
Widespread Wolbachia infection in terrestrial isopods and other crustaceans
inferred← citeshttps://doi.org/10.3920/978-90-8686-744-8_8openalex-snapshot
Wolbachia in Aedes mosquitoes: towards biological control of vector-borne diseases
inferred← citeshttps://doi.org/10.4039/ent129691-4openalex-snapshot
OBLIGATE THELYTOKY IN ORIBATID MITES: NO EVIDENCE FORWOLBACHIAINDUCEMENT
inferred← citeshttps://doi.org/10.5454/mi.3.3.5openalex-snapshot
Horizontal Transfer of the “Popcorn-Effect” Strain of Wolbachia from Drosophila melanogaster to Stomoxys calcitrans
inferred← citeshttps://doi.org/10.5661/bger-25-203openalex-snapshot
The Diversity of Insect-bacteria Interactions and its Applications for Disease Control
inferred← citeshttps://doi.org/10.59720/22-042openalex-snapshot
The presence of Wolbachia in Brood X cicadas
inferred← citeshttps://doi.org/10.6035/14104.2019.183893openalex-snapshot
Àcars en cítrics: defensa de les plantes i interacció del microbioma
inferred← citeshttps://doi.org/10.70675/041df502zaae0z40baz8305z6611223b456eopenalex-snapshot
Bases génétiques et mécanismes cytologiques à l'origine de la diversité de l'incompatibilité cytoplasmique induite par Wolbachia chez le moustique Culex pipiens
inferred← citeshttps://doi.org/10.70675/291a3043z7085z4fc6z8537ze59e410a08fbopenalex-snapshot
Isolement reproductif et architecture génomique de la différenciation chez deux espèces du complexe Jaera albifrons (isopodes marins) - Etude de populations mixtes présentant des niveaux d'isolement interspécifique contrastés
inferred← citeshttps://doi.org/10.70675/46128b62zb459z4ffaz86afz17a70a83c37dopenalex-snapshot
Etudes taxonomiques de deux genres d'acariens prédateurs de la famille des Phytoseiidae (Acari Mesostigmata) : Phytoseiulus Evans et Neoseiulella Muma
inferred← citeshttps://doi.org/10.70675/620daafazacdbz4501za553z4ba6cd421d6bopenalex-snapshot
Interactions multipartites entre communautés symbiotiques, pathogènes et vecteurs : le système vectoriel bactéries, endosymbiotiques, virus chikungunya, moustiques aedes
inferred← citeshttps://doi.org/10.70675/74bb4eecz2e11z42e3zb361zc46a2ae4943copenalex-snapshot
Transferts horizontaux des Wolbachia chez les isopodes terrestres : conséquences immédiates et évolutives chez les hôtes et les symbiotes
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