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Current state of knowledge on Wolbachia infection among Coleoptera: a systematic review
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118945568.ch11openalex-snapshot
Biodiversity of Coleoptera
inferredcites →https://doi.org/10.1002/9781444308211.ch11openalex-snapshot
Biodiversity of Coleoptera
inferredcites →https://doi.org/10.1002/ece3.1641openalex-snapshot
W olbachiadistribution in selected beetle taxa characterized by PCR screens and MLST data
inferredcites →https://doi.org/10.1006/jipa.1996.0032openalex-snapshot
WolbachiaInfections in the Flour BeetleTribolium confusum:Evidence for a Common Incompatibility Type across Strains
inferredcites →https://doi.org/10.1007/978-3-642-33989-9_8openalex-snapshot
Endosymbiont Infections in Spiders
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/10.1007/s00248-007-9230-5openalex-snapshot
Presence of Wolbachia in Insect Eggs Containing Antimicrobially Active Anthraquinones
inferredcites →https://doi.org/10.1007/s00248-014-0561-8openalex-snapshot
Endosymbiotic Candidates for Parasitoid Defense in Exotic and Native New Zealand Weevils
inferredcites →https://doi.org/10.1007/s00284-002-3969-1openalex-snapshot
Wolbachia Infections of the Whitefly Bemisia tabaci
inferredcites →https://doi.org/10.1007/s00284-007-0055-8openalex-snapshot
Revisiting Wolbachia Supergroup Typing Based on WSP: Spurious Lineages and Discordance with MLST
inferredcites →https://doi.org/10.1016/0965-1748(92)90136-3openalex-snapshot
Phylogeny of symbiotic bacteria of four weevil species (coleoptera: curculionidae) based on analysis of 16S ribosomal DNA
inferredcites →https://doi.org/10.1016/j.anbehav.2016.07.004openalex-snapshot
Costs and benefits of symbiosis between a bean beetle and Wolbachia
inferredcites →https://doi.org/10.1016/j.aspen.2008.11.001openalex-snapshot
Wolbachia infection in the Korean endemic firefly, Luciola unmunsana (Coleoptera: Lampyridae)
inferredcites →https://doi.org/10.1016/j.biocontrol.2005.12.004openalex-snapshot
Mitochondrial DNA diversity and Wolbachia infection in the flea beetle Aphthona nigriscutis (Coleoptera: Chrysomelidae): An introduced biocontrol agent for leafy spurge
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.10.002openalex-snapshot
Transcriptome analysis of the salivary glands of potato leafhopper, Empoasca fabae
inferredcites →https://doi.org/10.1016/j.jspr.2009.07.003openalex-snapshot
Detection and identification of Wolbachia endosymbionts from laboratory stocks of stored-product insect pests and their parasitoids
inferredcites →https://doi.org/10.1016/j.jspr.2009.08.001openalex-snapshot
Genome size and base composition in Oryzaephilus surinamensis (Coleoptera: Sylvanidae) and differences between native (feral) and silo pest populations in Israel
inferredcites →https://doi.org/10.1016/j.jspr.2013.03.002openalex-snapshot
Local genetic population divergence in a saw-toothed grain beetle, Oryzaephilus surinamensis (L.) (Coleoptera, Cucujidae)
inferredcites →https://doi.org/10.1016/j.jspr.2014.05.004openalex-snapshot
Evidence of horizontal transmission of primary and secondary endosymbionts between maize and rice weevils (Sitophilus zeamais and Sitophilus oryzae) and the parasitoid Theocolax elegans
inferredcites →https://doi.org/10.1016/j.jspr.2015.04.009openalex-snapshot
Prevalence and diversity of Wolbachia bacteria infecting insect pests of stored products
inferredcites →https://doi.org/10.1016/j.mib.2007.05.002openalex-snapshot
Wolbachia–host interactions: connecting phenotype to genotype
inferredcites →https://doi.org/10.1016/j.syapm.2015.05.005openalex-snapshot
Species in Wolbachia? Proposal for the designation of ‘Candidatus Wolbachia bourtzisii’, ‘Candidatus Wolbachia onchocercicola’, ‘Candidatus Wolbachia blaxteri’, ‘Candidatus Wolbachia brugii’, ‘Candidatus Wolbachia taylori’, ‘Candidatus Wolbachia collembolicola’ and ‘Candidatus Wolbachia…
inferredcites →https://doi.org/10.1016/j.syapm.2016.03.001openalex-snapshot
Wolbachia pipientis should not be split into multiple species: A response to Ramírez-Puebla et al., “Species in Wolbachia? Proposal for the designation of ‘Candidatus Wolbachia bourtzisii’, ‘Candidatus Wolbachia onchocercicola’, ‘Candidatus Wolbachia blaxteri’, ‘Candidatus Wolbachia brugii’,…
inferredcites →https://doi.org/10.1016/j.tig.2011.05.002openalex-snapshot
The impact of endosymbionts on the evolution of host sex-determination mechanisms
inferredcites →https://doi.org/10.1016/j.ympev.2017.12.022openalex-snapshot
Species delimitation within the Bothryorrhynchapion weevils: Multiple evidence from genetics, morphology and ecological associations
inferredcites →https://doi.org/10.1016/s0006-3207(01)00048-9openalex-snapshot
The species status of Cathormiocerus britannicus, an endemic, endangered British Weevil
inferredcites →https://doi.org/10.1016/s0169-4758(99)01533-1openalex-snapshot
Wolbachia Bacteria of Filarial Nematodes
inferredcites →https://doi.org/10.1016/s0169-5347(02)02480-1openalex-snapshot
Wolbachia dynamics and host effects: what has (and has not) been demonstrated?
inferredcites →https://doi.org/10.1016/s1433-1128(04)80013-5openalex-snapshot
Pathogens and symbionts in ticks: prevalence of Anaplasma phagocytophilum (Ehrlichia sp.), Wolbachia sp., Rickettsia sp., and Babesia sp. in Southern Germany
inferredcites →https://doi.org/10.1017/s000748530999023xopenalex-snapshot
Superinfection of fiveWolbachiain the alnus ambrosia beetle,Xylosandrus germanus(Blandford) (Coleoptera: Curuculionidae)
inferredcites →https://doi.org/10.1017/s0031182000007149openalex-snapshot
A phylogenetic analysis of filarial nematodes: comparison with the phylogeny of Wolbachia endosymbionts
inferredcites →https://doi.org/10.1017/s0031182005009789openalex-snapshot
A new male-killing parasitism:Spiroplasmabacteria infect the ladybird beetleAnisosticta novemdecimpunctata(Coleoptera: Coccinellidae)
inferredcites →https://doi.org/10.1017/s0031182015000530openalex-snapshot
Symbiosis in an overlooked microcosm: a systematic review of the bacterial flora of mites
inferredcites →https://doi.org/10.1017/s0031182098003655openalex-snapshot
Adonia variegata (Coleoptera: Coccinellidae) bears maternally inherited Flavobacteria that kill males only
inferredcites →https://doi.org/10.1038/hdy.2008.71openalex-snapshot
Wolbachia modification of sperm does not always require residence within developing sperm
inferredcites →https://doi.org/10.1038/ismej.2013.27openalex-snapshot
Diversification of endosymbiosis: replacements, co-speciation and promiscuity of bacteriocyte symbionts in weevils
inferredcites →https://doi.org/10.1038/ismej.2016.164openalex-snapshot
Plant–mediated horizontal transmission of Wolbachia between whiteflies
inferredcites →https://doi.org/10.1038/sj.hdy.6884380openalex-snapshot
Extreme variation in the prevalence of inherited male-killing microorganisms between three populations of Harmonia axyridis (Coleoptera: Coccinellidae)
inferredcites →https://doi.org/10.1038/srep27364openalex-snapshot
The ghost sex-life of the paedogenetic beetle Micromalthus debilis
inferredcites →https://doi.org/10.1046/j.0962-1083.2001.01432.xopenalex-snapshot
Prevailing triple infection withWolbachiainCallosobruchus chinensis(Coleoptera: Bruchidae)
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00710.xopenalex-snapshot
Multiple causes of male-killing in a single sample of the two-spot ladybird, Adalia bipunctata (Coleoptera: Coccinellidae) from Moscow
inferredcites →https://doi.org/10.1046/j.1365-2540.2001.00848.xopenalex-snapshot
Rickettsia associated with male-killing in a buprestid beetle
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.1365-294x.2000.00836.xopenalex-snapshot
Molecular evidence for multiple infections of a new subgroup ofWolbachiain the European raspberry beetleByturus tomentosus
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01793.xopenalex-snapshot
Wolbachia infection complexity among insects in the tropical rice‐field community
inferredcites →https://doi.org/10.1046/j.1462-2920.2003.00537.xopenalex-snapshot
Detection and phylogenetic analysis of Wolbachia in Collembola
inferredcites →https://doi.org/10.1073/pnas.1618094114openalex-snapshot
Unique clade of alphaproteobacterial endosymbionts induces complete cytoplasmic incompatibility in the coconut beetle
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.94.21.11439openalex-snapshot
The role of Wolbachia bacteria in reproductive incompatibilities and hybrid zones of Diabrotica beetles and Gryllus crickets
inferredcites →https://doi.org/10.1073/pnas.96.12.6814openalex-snapshot
Four intracellular genomes direct weevil biology: Nuclear, mitochondrial, principal endosymbiont, and Wolbachia
inferredcites →https://doi.org/10.1080/10635150600755453openalex-snapshot
Approximate Likelihood-Ratio Test for Branches: A Fast, Accurate, and Powerful Alternative
inferredcites →https://doi.org/10.1093/jee/tov053openalex-snapshot
Wolbachia Infection Dynamics in Tribolium confusum (Coleoptera: Tenebrionidae) and Their Effects on Host Mating Behavior and Reproduction
inferredcites →https://doi.org/10.1093/jee/tow067openalex-snapshot
Effects of Tetracycline and Rifampicin Treatments on the Fecundity of theWolbachia-Infected Host,Tribolium confusum(Coleoptera: Tenebrionidae)
inferredcites →https://doi.org/10.1093/molbev/msp275openalex-snapshot
Lateral Phage Transfer in Obligate Intracellular Bacteria (Wolbachia): Verification from Natural Populations
inferredcites →https://doi.org/10.1093/molbev/mst024openalex-snapshot
Ultrafast Approximation for Phylogenetic Bootstrap
inferredcites →https://doi.org/10.1093/nar/gkw256openalex-snapshot
W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis
inferredcites →https://doi.org/10.1093/oso/9780198577867.003.0001openalex-snapshot
The evolution of heritable symbionts
inferredcites →https://doi.org/10.1093/sysbio/syq010openalex-snapshot
New Algorithms and Methods to Estimate Maximum-Likelihood Phylogenies: Assessing the Performance of PhyML 3.0
inferredcites →https://doi.org/10.1098/rsbl.2005.0340openalex-snapshot
Infection density ofWolbachiaendosymbiont affected by co-infection and host genotype
inferredcites →https://doi.org/10.1098/rsbl.2007.0373openalex-snapshot
Are we underestimating the diversity and incidence of insect bacterial symbionts? A case study in ladybird beetles
inferredcites →https://doi.org/10.1098/rspb.1995.0196openalex-snapshot
Distribution ofWolbachiaamong neotropical arthropods
inferredcites →https://doi.org/10.1098/rspb.1997.0147openalex-snapshot
Molecular evidence for singleWolbachiainfections among geographic strains of the flour beetleTribolium confusum
inferredcites →https://doi.org/10.1098/rspb.1999.0698openalex-snapshot
Male–killingWolbachiain two species of insect
inferredcites →https://doi.org/10.1098/rspb.2000.1166openalex-snapshot
Male-killingWolbachiain a flour beetle
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.2003.2640openalex-snapshot
Natural interspecific and intraspecific horizontal transfer of parthenogenesis–inducingWolbachiainTrichogrammawasps
inferredcites →https://doi.org/10.1098/rspb.2005.3056openalex-snapshot
Problems with mitochondrial DNA as a marker in population, phylogeographic and phylogenetic studies: the effects of inherited symbionts
inferredcites →https://doi.org/10.1098/rspb.2009.1022openalex-snapshot
Longicorn beetle that vectors pinewood nematode carries manyWolbachiagenes on an autosome
inferredcites →https://doi.org/10.1098/rspb.2011.2095openalex-snapshot
Horizontal transmission of the insect symbiont Rickettsia is plant-mediated
inferredcites →https://doi.org/10.1098/rspb.2015.0249openalex-snapshot
The incidence of bacterial endosymbionts in terrestrial arthropods
inferredcites →https://doi.org/10.1101/gr.7144908openalex-snapshot
Wolbachia genome integrated in an insect chromosome: Evolution and fate of laterally transferred endosymbiont genes
inferredcites →https://doi.org/10.1111/1744-7917.12096openalex-snapshot
A screen for bacterial endosymbionts in the model organisms Tribolium castaneum, T. confusum, Callosobruchus maculatus, and related species
inferredcites →https://doi.org/10.1111/1755-0998.12205openalex-snapshot
Characterizing DNA preservation in degraded specimens of A mara alpina( C arabidae: C oleoptera)
inferredcites →https://doi.org/10.1111/1758-2229.12425openalex-snapshot
Wolbachia endosymbionts in haplodiploid and diploid scolytine beetles (Coleoptera: Curculionidae: Scolytinae)
inferredcites →https://doi.org/10.1111/eea.12588openalex-snapshot
Melanic mutation causes a fitness decline in bean beetles infected by W olbachia
inferredcites →https://doi.org/10.1111/imb.12255openalex-snapshot
Selective sweep of Wolbachia and parthenogenetic host genomes – the example of the weevil Eusomus ovulum
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.1365-2583.2010.01018.xopenalex-snapshot
Wolbachia infection in the tribe Naupactini (Coleoptera, Curculionidae): association between thelytokous parthenogenesis and infection status
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02203.xopenalex-snapshot
Distribution of the bacterial symbiont Cardinium in arthropods
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02213.xopenalex-snapshot
Reproductive effects and geographical distributions of twoWolbachiastrains infecting the Neotropical beetle,Chelymorpha alternansBoh. (Chrysomelidae, Cassidinae)
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02802.xopenalex-snapshot
Wolbachia and other endosymbiont infections in spiders
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04572.xopenalex-snapshot
The mushroom habitat as an ecological arena for global exchange ofWolbachia
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04980.xopenalex-snapshot
Diversity and infection prevalence of endosymbionts in natural populations of the chestnut weevil: relevance of local climate and host plants
inferredcites →https://doi.org/10.1111/j.1365-3032.2006.00504.xopenalex-snapshot
Oogenesis in the date stone beetle, Coccotrypes dactyliperda , depends on symbiotic bacteria
inferredcites →https://doi.org/10.1111/j.1461-9555.2004.00231.xopenalex-snapshot
Distribution, mechanisms and evolutionary significance of clonality and polyploidy in weevils
inferredcites →https://doi.org/10.1111/j.1461-9563.2008.00369.xopenalex-snapshot
Effects and implications of antibiotic treatment on Wolbachia ‐infected vine weevil (Coleoptera: Curculionidae)
inferredcites →https://doi.org/10.1111/j.1462-2920.2009.01914.xopenalex-snapshot
Evidence for low‐titre infections in insect symbiosis: Wolbachia in the bark beetle Pityogenes chalcographus (Coleoptera, Scolytinae)
inferredcites →https://doi.org/10.1111/j.1570-7458.2010.00974.xopenalex-snapshot
Occurrence ofWolbachiain central European weevils: correlations with host systematics, ecology, and biology
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/j.1744-7410.2012.00276.xopenalex-snapshot
Conservation genetics of highly isolated populations of the xerothermic beetle C rioceris quatuordecimpunctata ( C hrysomelidae)
inferredcites →https://doi.org/10.1111/j.1744-7917.2011.01448.xopenalex-snapshot
Genetic distinctness of parthenogenetic forms of European Polydrusus weevils of the subgenus Scythodrusus
inferredcites →https://doi.org/10.1111/jeb.12186openalex-snapshot
The direct effects of male killer infection on fitness of ladybird hosts ( C oleoptera: C occinellidae)
inferredcites →https://doi.org/10.1111/mec.12362openalex-snapshot
Evidence for a recent horizontal transmission and spatial spread of W olbachiafrom endemic R hagoletis cerasi( D iptera: T ephritidae) to invasive R hagoletis cingulatain E urope
inferredcites →https://doi.org/10.1111/mec.12389openalex-snapshot
Evidence for selective sweeps by W olbachia infections: phylogeny of A ltica leaf beetles and their reproductive parasites
inferredcites →https://doi.org/10.1111/mec.13702openalex-snapshot
The gut microbiota of the pine weevil is similar across Europe and resembles that of other conifer‐feeding beetles
inferredcites →https://doi.org/10.1111/mec.14186openalex-snapshot
Gut microbiota of the pine weevil degrades conifer diterpenes and increases insect fitness
inferredcites →https://doi.org/10.1111/syen.12109openalex-snapshot
Host‐associated genetic divergence and taxonomy in the Rhinusa pilosa G yllenhal species complex: an integrative approach
inferredcites →https://doi.org/10.1126/science.1142490openalex-snapshot
Widespread Lateral Gene Transfer from Intracellular Bacteria to Multicellular Eukaryotes
inferredcites →https://doi.org/10.1126/science.281.5376.555openalex-snapshot
"Inordinate Fondness" Explained: Why Are There So Many Beetles?
inferredcites →https://doi.org/10.1128/aem.00416-06openalex-snapshot
Asymmetrical Interactions betweenWolbachiaandSpiroplasmaEndosymbionts Coexisting in the Same Insect Host
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.69.10.6082-6090.2003openalex-snapshot
Diversity ofWolbachiaEndosymbionts in Heteropteran Bugs
inferredcites →https://doi.org/10.1128/jb.176.2.388-394.1994openalex-snapshot
Rickettsial relative associated with male killing in the ladybird beetle (Adalia bipunctata)
inferredcites →https://doi.org/10.1134/s1022795415080037openalex-snapshot
Genotypic diversity of Wolbachia pipientis in native and invasive Harmonia axyridis Pall., 1773 (Coleoptera, Coccinellidae) populations
inferredcites →https://doi.org/10.1136/bmj.b2535openalex-snapshot
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement
inferredcites →https://doi.org/10.1146/annurev.micro.53.1.71openalex-snapshot
Wolbachia Pipientis: Microbial Manipulator of Arthropod Reproduction
inferredcites →https://doi.org/10.1186/1471-2148-10-340openalex-snapshot
Mito-nuclear genetic comparison in a Wolbachia infected weevil: insights on reproductive mode, infection age and evolutionary forces shaping genetic variation
inferredcites →https://doi.org/10.1186/1741-7007-6-27openalex-snapshot
The diversity of reproductive parasites among arthropods: Wolbachiado not walk alone
inferredcites →https://doi.org/10.1371/journal.pgen.1004397openalex-snapshot
Palaeosymbiosis Revealed by Genomic Fossils of Wolbachia in a Strongyloidean Nematode
inferredcites →https://doi.org/10.1371/journal.pone.0011339openalex-snapshot
Microbial Symbionts in Insects Influence Down-Regulation of Defense Genes in Maize
inferredcites →https://doi.org/10.1371/journal.pone.0027834openalex-snapshot
Recent Speciation in Three Closely Related Sympatric Specialists: Inferences Using Multi-Locus Sequence, Post-Mating Isolation and Endosymbiont Data
inferredcites →https://doi.org/10.1371/journal.pone.0036514openalex-snapshot
Wolbachia and DNA Barcoding Insects: Patterns, Potential, and Problems
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.pone.0082402openalex-snapshot
Uncovering Wolbachia Diversity upon Artificial Host Transfer
inferredcites →https://doi.org/10.1371/journal.pone.0155392openalex-snapshot
Bacterial Community Diversity Harboured by Interacting Species
inferredcites →https://doi.org/10.1371/journal.ppat.1004672openalex-snapshot
The Intracellular Bacterium Wolbachia Uses Parasitoid Wasps as Phoretic Vectors for Efficient Horizontal Transmission
inferredcites →https://doi.org/10.14411/eje.2017.038openalex-snapshot
Metagenomic survey of bacteria associated with the invasive ladybird Harmonia axyridis (Coleoptera: Coccinellidae)
inferredcites →https://doi.org/10.14411/eje.2017.057openalex-snapshot
Preliminary evidence of the horizontal transmission of Wolbachia between Crioceris leaf beetles (Coleoptera: Chrysomelidae) and their Asparagus host plants
inferredcites →https://doi.org/10.1603/0013-8746(2001)094[0877:oowisd]2.0.co;2openalex-snapshot
Occurrence of Wolbachia in Selected Diabroticite (Coleoptera: Chrysomelidae) Beetles
inferredcites →https://doi.org/10.1603/0013-8746(2002)095[0374:wiitcb]2.0.co;2openalex-snapshot
Wolbachia Infection in the Coffee Berry Borer (Coleoptera: Scolytidae)
inferredcites →https://doi.org/10.1603/0013-8746(2007)100[522:wbiltm]2.0.co;2openalex-snapshot
Wolbachia Bacterial Infections Linked to Mitochondrial DNA Reproductive Isolation Among Populations of Northern Corn Rootworm (Coleoptera: Chrysomelidae)
inferredcites →https://doi.org/10.1603/an13145openalex-snapshot
Culture-Independent Analysis of Bacterial Communities in the Gut of Rice Water Weevil (Coleoptera: Curculionidae)
inferredcites →https://doi.org/10.1603/en09276openalex-snapshot
Analysis ofWolbachiaStrains Associated WithConotrachelus nenuphar(Coleoptera: Curculionidae) in the Eastern United States
inferredcites →https://doi.org/10.1603/en10315openalex-snapshot
A Test Using Wolbachia Bacteria to Identify Eurasian Source Populations of Cabbage Seedpod Weevil,Ceutorhynchus obstrictus(Marsham), in North America
inferredcites →https://doi.org/10.1603/en11195openalex-snapshot
Identification and Biological Role of the EndosymbiontsWolbachiain Rice Water Weevil (Coleoptera: Curculionidae)
inferredcites →https://doi.org/10.1603/en13228openalex-snapshot
A New Strain ofWolbachiain an Alpine Population of the ViviparousOreina cacaliae(Coleoptera: Chrysomelidae)
inferredcites →https://doi.org/10.2108/zsj.16.955openalex-snapshot
High Prevalence of Wolbachia in the Azuki Bean Beetle Callosobruchus chinensis (Coleoptera, Bruchidae)
inferredcites →https://doi.org/10.2108/zsj.28.501openalex-snapshot
WolbachiaInfections in World Populations of Bean Beetles (Coleoptera: Chrysomelidae: Bruchinae) Infesting Cultivated and Wild Legumes
inferredcites →https://doi.org/10.22099/ijvr.2009.1695openalex-snapshot
PCR SCREENING OF THE WOLBACHIA IN SOME ARTHROPODS AND NEMATODES IN KHUZESTAN PROVINCE
inferredcites →https://doi.org/10.3390/insects8010008openalex-snapshot
Wolbachia Affects Reproduction and Population Dynamics of the Coffee Berry Borer (Hypothenemus hampei): Implications for Biological Control
inferredcites →https://doi.org/10.3897/zookeys.14.188openalex-snapshot
Economically Beneficial Ground Beetles. The specialized predators Pheropsophus aequinoctialis (L.) and Stenaptinus jessoensis (Morawitz): Their laboratory behavior and descriptions of immature stages (Coleoptera: Carabidae: Brachininae)
inferredcites →https://doi.org/10.5860/choice.36-1561openalex-snapshot
Influential passengers: inherited microorganisms and arthropod reproduction
inferredcites →https://doi.org/10.7326/0003-4819-151-4-200908180-00135openalex-snapshot
Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement
inferredcites →https://doi.org/10.7717/peerj.1479openalex-snapshot
Wolbachia co-infection in a hybrid zone: discovery of horizontal gene transfers from two Wolbachia supergroups into an animal genome
inferredcites →https://doi.org/10.7717/peerj.2514openalex-snapshot
The origin of widespread species in a poor dispersing lineage (diving beetle genus Deronectes )
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.3389/fevo.2019.00157openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2022.866930openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/d17030186openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/insects16020114openalex-snapshot
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inferred← citeshttps://doi.org/10.6026/97320630019336openalex-snapshot
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inferred← citeshttps://doi.org/10.6084/m9.figshare.13357266openalex-snapshot
Additional file 1 of Wolbachia infection in wild mosquitoes (Diptera: Culicidae): implications for transmission modes and host-endosymbiont associations in Singapore
inferred← citeshttps://doi.org/10.6084/m9.figshare.13357269openalex-snapshot
Additional file 2 of Wolbachia infection in wild mosquitoes (Diptera: Culicidae): implications for transmission modes and host-endosymbiont associations in Singapore
inferred← citeshttps://doi.org/10.7554/elife.100079openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.100079.1openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.61989openalex-snapshot
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