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Evidence for natural hybridisation and novel Wolbachia strain superinfections in the Anopheles gambiae complex from Guinea

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/expr.1995.1119openalex-snapshot

Wolbachia pipientis: Bacterial Density and Unidirectional Cytoplasmic Incompatibility between Infected Populations of Aedes albopictus

inferredcites →https://doi.org/10.1007/s40475-016-0066-2openalex-snapshot

Wolbachia Biocontrol Strategies for Arboviral Diseases and the Potential Influence of Resident Wolbachia Strains in Mosquitoes

inferredcites →https://doi.org/10.1016/j.cell.2009.11.042openalex-snapshot

A Wolbachia Symbiont in Aedes aegypti Limits Infection with Dengue, Chikungunya, and Plasmodium

inferredcites →https://doi.org/10.1016/j.cub.2019.11.007openalex-snapshot

Establishment of Wolbachia Strain wAlbB in Malaysian Populations of Aedes aegypti for Dengue Control

inferredcites →https://doi.org/10.1038/163109a0openalex-snapshot

D.D.T. and ‘Gammexane' as Residual Insecticides Against Anopheles gambiÆ in African Houses

inferredcites →https://doi.org/10.1038/embor.2011.84openalex-snapshot

Wolbachia and the biological control of mosquito‐borne disease

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/nature21391openalex-snapshot

Prophage WO genes recapitulate and enhance Wolbachia-induced cytoplasmic incompatibility

inferredcites →https://doi.org/10.1038/ncomms11772openalex-snapshot

Wolbachia infections in natural Anopheles populations affect egg laying and negatively correlate with Plasmodium development

inferredcites →https://doi.org/10.1038/ncomms4985openalex-snapshot

Evidence of natural Wolbachia infections in field populations of Anopheles gambiae

inferredcites →https://doi.org/10.1038/s41598-018-31117-xopenalex-snapshot

Unexpectedly high Plasmodium sporozoite rate associated with low human blood index in Anopheles coluzzii from a LLIN-protected village in Burkina Faso

inferredcites →https://doi.org/10.1038/s41598-018-35658-zopenalex-snapshot

Diverse novel resident Wolbachia strains in Culicine mosquitoes from Madagascar

inferredcites →https://doi.org/10.1038/srep03932openalex-snapshot

Temperature alters Plasmodium blocking by Wolbachia

inferredcites →https://doi.org/10.1038/srep17952openalex-snapshot

Unexpected diversity of Anopheles species in Eastern Zambia: implications for evaluating vector behavior and interventions using molecular tools

inferredcites →https://doi.org/10.1038/srep46451openalex-snapshot

Massive introgression drives species radiation at the range limit of Anopheles gambiae

inferredcites →https://doi.org/10.1073/pnas.0610451104openalex-snapshot

Bacteria of the genus Asaia stably associate with Anopheles stephensi , an Asian malarial mosquito vector

inferredcites →https://doi.org/10.1073/pnas.1112021108openalex-snapshot

Wolbachia strain w Mel induces cytoplasmic incompatibility and blocks dengue transmission in Aedes albopictus

inferredcites →https://doi.org/10.1073/pnas.1408888111openalex-snapshot

Native microbiome impedes vertical transmission of Wolbachia in Anopheles mosquitoes

inferredcites →https://doi.org/10.1073/pnas.1716181114openalex-snapshot

Effect of naturally occurring Wolbachia in Anopheles gambiae s.l. mosquitoes from Mali on Plasmodium falciparum malaria transmission

inferredcites →https://doi.org/10.1080/00034983.1997.11813227openalex-snapshot

Detection of hybrids in natural populations of theAnopheles gambiaecomplex by the rDNA-based, PCR method

inferredcites →https://doi.org/10.1080/00034989760383openalex-snapshot

Detection of hybrids in natural populations of the Anopheles gambiae complex by the rDNA based, PCR method

inferredcites →https://doi.org/10.1093/jmedent/41.5.01openalex-snapshot

DNA Barcodes Can Distinguish Species of Indian Mosquitoes (Diptera: Culicidae)

inferredcites →https://doi.org/10.1093/molbev/msy096openalex-snapshot

MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040023openalex-snapshot

Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.

inferredcites →https://doi.org/10.1093/trstmh/try069openalex-snapshot

Identification of Anopheles species in Sud Kivu, Democratic Republic of Congo, using molecular tools

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/10.1099/00207713-50-2-823openalex-snapshot

Asaia bogorensis gen. nov., sp. nov., an unusual acetic acid bacterium in the alpha-Proteobacteria.

inferredcites →https://doi.org/10.1111/j.1365-2583.1996.tb00034.xopenalex-snapshot

A review of the use of ribosomal DNA (rDNA) to differentiate among cryptic Anopheles species

inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05724.xopenalex-snapshot

Genetic isolation within the malaria mosquito A nopheles melas

inferredcites →https://doi.org/10.1126/science.1165326openalex-snapshot

Stable Introduction of a Life-Shortening Wolbachia Infection into the Mosquito Aedes aegypti

inferredcites →https://doi.org/10.1126/science.1236192openalex-snapshot

Wolbachia Invades Anopheles stephensi Populations and Induces Refractoriness to Plasmodium Infection

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.01038-08openalex-snapshot

Host Adaptation of aWolbachiaStrain after Long-Term Serial Passage in Mosquito Cell Lines

inferredcites →https://doi.org/10.1128/aem.06751-11openalex-snapshot

Wolbachia Strain wAlbB Enhances Infection by the Rodent Malaria Parasite Plasmodium berghei in Anopheles gambiae Mosquitoes

inferredcites →https://doi.org/10.1128/mbio.00784-19openalex-snapshot

Is Anopheles gambiae a Natural Host of Wolbachia ?

inferredcites →https://doi.org/10.1186/1471-2105-5-86openalex-snapshot

mlstdbNet – distributed multi-locus sequence typing (MLST) databases

inferredcites →https://doi.org/10.1186/1475-2875-7-163openalex-snapshot

Insertion polymorphisms of SINE200 retrotransposons within speciation islands of Anopheles gambiae molecular forms

inferredcites →https://doi.org/10.1186/1475-2875-7-182openalex-snapshot

Anopheles gambiae complex along The Gambia river, with particular reference to the molecular forms of An. gambiae s.s

inferredcites →https://doi.org/10.1186/1475-2875-9-161openalex-snapshot

Population genetic structure of the malaria vector Anopheles nili in sub-Saharan Africa

inferredcites →https://doi.org/10.1186/1756-3305-5-253openalex-snapshot

Malaria transmission after five years of vector control on Bioko Island, Equatorial Guinea

inferredcites →https://doi.org/10.1186/s12936-018-2189-5openalex-snapshot

The importance of morphological identification of African anopheline mosquitoes (Diptera: Culicidae) for malaria control programmes

inferredcites →https://doi.org/10.1186/s12936-018-2559-zopenalex-snapshot

First report of natural Wolbachia infection in wild Anopheles funestus population in Senegal

inferredcites →https://doi.org/10.1186/s12936-019-2875-yopenalex-snapshot

Characterizing the molecular and metabolic mechanisms of insecticide resistance in Anopheles gambiae in Faranah, Guinea

inferredcites →https://doi.org/10.1186/s13071-015-0888-0openalex-snapshot

Mutual exclusion of Asaia and Wolbachia in the reproductive organs of mosquito vectors

inferredcites →https://doi.org/10.1186/s13071-018-2870-0openalex-snapshot

A Wolbachia triple-strain infection generates self-incompatibility in Aedes albopictus and transmission instability in Aedes aegypti

inferredcites →https://doi.org/10.1186/s13071-018-3249-yopenalex-snapshot

First report of natural Wolbachia infection in the malaria mosquito Anopheles arabiensis in Tanzania

inferredcites →https://doi.org/10.1186/s13071-020-04023-3openalex-snapshot

An assessment of adult mosquito collection techniques for studying species abundance and diversity in Maferinyah, Guinea

inferredcites →https://doi.org/10.12688/gatesopenres.12844.3openalex-snapshot

Scaled deployment of Wolbachia to protect the community from dengue and other Aedes transmitted arboviruses

inferredcites →https://doi.org/10.12688/gatesopenres.13061.1openalex-snapshot

Establishment of wMel Wolbachia in Aedes aegypti mosquitoes and reduction of local dengue transmission in Cairns and surrounding locations in northern Queensland, Australia

inferredcites →https://doi.org/10.12688/gatesopenres.13061.2openalex-snapshot

Establishment of wMel Wolbachia in Aedes aegypti mosquitoes and reduction of local dengue transmission in Cairns and surrounding locations in northern Queensland, Australia

inferredcites →https://doi.org/10.12688/wellcomeopenres.14765.2openalex-snapshot

Novel Wolbachia strains in Anopheles malaria vectors from Sub-Saharan Africa

inferredcites →https://doi.org/10.1371/journal.pntd.0001989openalex-snapshot

The Native Wolbachia Symbionts Limit Transmission of Dengue Virus in Aedes albopictus

inferredcites →https://doi.org/10.1371/journal.pntd.0002688openalex-snapshot

Limited Dengue Virus Replication in Field-Collected Aedes aegypti Mosquitoes Infected with Wolbachia

inferredcites →https://doi.org/10.1371/journal.pone.0011977openalex-snapshot

The Native Wolbachia Endosymbionts of Drosophila melanogaster and Culex quinquefasciatus Increase Host Resistance to West Nile Virus Infection

inferredcites →https://doi.org/10.1371/journal.pone.0013102openalex-snapshot

Use of ITS2 Region as the Universal DNA Barcode for Plants and Animals

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.0181678openalex-snapshot

Wolbachia and dengue virus infection in the mosquito Aedes fluviatilis (Diptera: Culicidae)

inferredcites →https://doi.org/10.1371/journal.ppat.1000833openalex-snapshot

The Endosymbiotic Bacterium Wolbachia Induces Resistance to Dengue Virus in Aedes aegypti

inferredcites →https://doi.org/10.1371/journal.ppat.1002043openalex-snapshot

Wolbachia Infections Are Virulent and Inhibit the Human Malaria Parasite Plasmodium Falciparum in Anopheles Gambiae

inferredcites →https://doi.org/10.1371/journal.ppat.1004182openalex-snapshot

Wolbachia Can Enhance Plasmodium Infection in Mosquitoes: Implications for Malaria Control?

inferredcites →https://doi.org/10.1371/journal.ppat.1005434openalex-snapshot

Establishment of a Wolbachia Superinfection in Aedes aegypti Mosquitoes as a Potential Approach for Future Resistance Management

inferredcites →https://doi.org/10.1371/journal.ppat.1006751openalex-snapshot

Novel Wolbachia-transinfected Aedes aegypti mosquitoes possess diverse fitness and vector competence phenotypes

inferredcites →https://doi.org/10.1371/journal.ppat.1006815openalex-snapshot

The Wolbachia strain wAu provides highly efficient virus transmission blocking in Aedes aegypti

inferredcites →https://doi.org/10.1534/g3.116.031906openalex-snapshot

Genome-Wide Divergence in the West-African Malaria Vector Anopheles melas

inferredcites →https://doi.org/10.1590/s0074-02762011000900026openalex-snapshot

Can Wolbachia be used to control malaria?

inferredcites →https://doi.org/10.1603/0022-2585(2007)44[1:dbcdso]2.0.co;2openalex-snapshot

DNA Barcodes Can Distinguish Species of Indian Mosquitoes (Diptera: Culicidae)

inferredcites →https://doi.org/10.4269/ajtmh.15-0562openalex-snapshot

Molecular Characterization Reveals Diverse and Unknown Malaria Vectors in the Western Kenyan Highlands

inferredcites →https://doi.org/10.4269/ajtmh.1962.11.702openalex-snapshot

Preliminary Experiments on the Hybridization of Anopheles Gambiae Giles and Anopheles Melas Theobald

inferredcites →https://doi.org/10.4269/ajtmh.1993.49.520openalex-snapshot

Identification of Single Specimens of the Anopheles Gambiae Complex by the Polymerase Chain Reaction

inferredcites →https://doi.org/10.4269/ajtmh.1995.53.478openalex-snapshot

Discrimination of all Members of the Anopheles punctulatus Complex by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis

inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot

Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.cub.2021.03.056openalex-snapshot

Stable high-density and maternally inherited Wolbachia infections in Anopheles moucheti and Anopheles demeilloni mosquitoes

inferred← citeshttps://doi.org/10.1101/2020.11.22.393652openalex-snapshot

Low prevalence of natural Wolbachia in major malarial vectors Anopheles culicifacies s.l., and Anopheles stephensi: a first report

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