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Presence of specific symbiotic bacteria in flies of the subfamily Tephritinae (Diptera Tephritidae) and their phylogenetic relationships: proposal of 'Candidatus Stammerula tephritidis'
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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/bf00410561openalex-snapshot
Die bakteriensymbiose der trypetiden (Diptera).
inferredcites →https://doi.org/10.1007/bf01570970openalex-snapshot
The eubacterial endosymbionts of whiteflies (homoptera: Aleyrodoidea) constitute a lineage distinct from the endosymbionts of aphids and mealybugs
inferredcites →https://doi.org/10.1007/bf02340157openalex-snapshot
Die Fliegen der palaearktischen Region
inferredcites →https://doi.org/10.1007/bf02498635openalex-snapshot
The Tryptophan Biosynthetic Pathway of Aphid Endosymbionts (Buchnera): Genetics and Evolution of Plasmid-Associated Anthranilate Synthase (trpEG) Within the Aphididae
inferredcites →https://doi.org/10.1007/pl00006362openalex-snapshot
Molecular Characterization of the Principal Symbiotic Bacteria of the Weevil Sitophilus oryzae: A Peculiar G + C Content of an Endocytobiotic DNA
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/10.1016/0965-1748(94)00107-sopenalex-snapshot
Phylogenetic position of yeast-like symbiotes of rice planthoppers based on partial 18S rDNA Sequences
inferredcites →https://doi.org/10.1016/1055-7903(92)90032-copenalex-snapshot
Phylogenetic relationships of the endosymbionts of mealybugs (Homoptera: Pseudococcidae) based on 165 rDNA sequences
inferredcites →https://doi.org/10.1016/s1016-8478(23)17394-8openalex-snapshot
Molecular Phylogeny of the Subfamily Tephritinae (Diptera: Tephritidae) Based on Mitochondrial 16S rDNA Sequences
inferredcites →https://doi.org/10.1023/a:1000239108771openalex-snapshot
Non-cultivable microorganisms from symbiotic associations of insects and other hosts
inferredcites →https://doi.org/10.1038/nrg931openalex-snapshot
Genome evolution in bacterial endosymbionts of insects
inferredcites →https://doi.org/10.1071/bi9860361openalex-snapshot
Bacteria Associated with some Dacus Species (Diptera: Tephritidae) and their Host Fruit in Queensland
inferredcites →https://doi.org/10.1073/pnas.82.6.1741openalex-snapshot
Evidence for higher rates of nucleotide substitution in rodents than in man.
inferredcites →https://doi.org/10.1073/pnas.93.7.2873openalex-snapshot
Accelerated evolution and Muller's rachet in endosymbiotic bacteria.
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150490522304openalex-snapshot
Model Selection and Model Averaging in Phylogenetics: Advantages of Akaike Information Criterion and Bayesian Approaches Over Likelihood Ratio Tests
inferredcites →https://doi.org/10.1093/aesa/87.3.400openalex-snapshot
Handbook of the Fruit Flies (Diptera: Tephritidae)of America North of Mexico
inferredcites →https://doi.org/10.1093/bib/5.2.150openalex-snapshot
MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment
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/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/genetics/132.1.269openalex-snapshot
Testing for equality of evolutionary rates.
inferredcites →https://doi.org/10.1093/molbev/msh063openalex-snapshot
Endosymbiont Phylogenesis in the Dryophthoridae Weevils: Evidence for Bacterial Replacement
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025958openalex-snapshot
Evolutionary rates for tuf genes in endosymbionts of aphids
inferredcites →https://doi.org/10.1098/rspb.1994.0092openalex-snapshot
Flavobacteria as intracellular symbionts in cockroaches
inferredcites →https://doi.org/10.1099/00207713-50-3-1187openalex-snapshot
Sequence analysis of domains III and IV of the 23S rRNA gene of verticillate streptomycetes.
inferredcites →https://doi.org/10.1099/ijs.0.63653-0openalex-snapshot
‘Candidatus Erwinia dacicola’, a coevolved symbiotic bacterium of the olive fly Bactrocera oleae (Gmelin)
inferredcites →https://doi.org/10.1111/j.1365-2583.1995.tb00004.xopenalex-snapshot
Molecular analysis of the endosymbionts of tsetse flies: 16S rDNA locus and over‐expression of a chaperonin
inferredcites →https://doi.org/10.1111/j.1365-2958.1996.tb02557.xopenalex-snapshot
Intracellular endosymbiotic bacteria of Camponotus species (carpenter ants): systematics, evolution and ultrastructural characterization
inferredcites →https://doi.org/10.1128/aem.61.1.1-7.1995openalex-snapshot
Mutualistic associations of aphids and prokaryotes: biology of the genus buchnera
inferredcites →https://doi.org/10.1128/aem.68.7.3198-3205.2002openalex-snapshot
The Genetic Properties of the Primary Endosymbionts of Mealybugs Differ from Those of Other Endosymbionts of Plant Sap-Sucking Insects
inferredcites →https://doi.org/10.1128/aem.71.6.3302-3310.2005openalex-snapshot
Evolutionary Relationships of Three New Species of Enterobacteriaceae Living as Symbionts of Aphids and Other Insects
inferredcites →https://doi.org/10.1128/jb.173.2.697-703.1991openalex-snapshot
16S ribosomal DNA amplification for phylogenetic study
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.217openalex-snapshot
THE BIOLOGY OF NONFRUGIVOROUS TEPHRITID FRUIT FLIES
inferredcites →https://doi.org/10.2307/3757184openalex-snapshot
Endosymbiosis of Animals with Plant Microorganisms
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.5196.3.3zenodo-depositor-declared
Host plants of fruit flies (Diptera: Tephritidae) in Morocco
inferred← citeshttps://doi.org/10.1007/978-3-319-43226-7_1openalex-snapshot
Taxonomy and Systematics of African Fruit Flies (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1007/978-3-642-21680-0_2openalex-snapshot
Insect “Symbiology” Is Coming of Age, Bridging Between Bench and Field
inferred← citeshttps://doi.org/10.1007/978-90-481-9449-0_13openalex-snapshot
Evolution and Consequences of Nutrition-Based Symbioses in Insects: More than Food Stress
inferred← citeshttps://doi.org/10.1007/s00248-015-0571-1openalex-snapshot
The Microbiome of Field-Caught and Laboratory-Adapted Australian Tephritid Fruit Fly Species with Different Host Plant Use and Specialisation
inferred← citeshttps://doi.org/10.1007/s00248-025-02686-yopenalex-snapshot
Detection of a Conserved Bacterial Symbiosis in non-frugivorous Australian Fruit Flies (Diptera, Tephritidae, Tephritinae) Supports its Widespread Association
inferred← citeshttps://doi.org/10.1007/s00284-012-0223-3openalex-snapshot
Survey of Heritable Endosymbionts in Southern Mexico Populations of the Fruit Fly Species Anastrepha striata and A. ludens
inferred← citeshttps://doi.org/10.1007/s00284-020-01939-yopenalex-snapshot
Variations in the Bacterial Communities in Anastrepha obliqua (Diptera: Tephritidae) According to the Insect Life Stage and Host Plant
inferred← citeshttps://doi.org/10.1007/s12892-011-0091-6openalex-snapshot
Threats to fruit and vegetable crops: Fruit flies (Tephritidae) - ecology, behaviour, and management
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.02.016openalex-snapshot
Phylogenetic relationships between flies of the Tephritinae subfamily (Diptera, Tephritidae) and their symbiotic bacteria
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.04.025openalex-snapshot
Pattern of association between endemic Hawaiian fruit flies (Diptera, Tephritidae) and their symbiotic bacteria: Evidence of cospeciation events and proposal of “Candidatus Stammerula trupaneae”
inferred← citeshttps://doi.org/10.1017/s0007485316000390openalex-snapshot
Bacterial communities associated with invasive populations of Bactrocera dorsalis (Diptera: Tephritidae) in China
inferred← citeshttps://doi.org/10.1017/s0007485318000834openalex-snapshot
The influence of antibiotics on gut bacteria diversity associated with laboratory-reared Bactrocera dorsalis
inferred← citeshttps://doi.org/10.1017/s0007485319000853openalex-snapshot
Tephritidae fruit fly gut microbiome diversity, function and potential for applications
inferred← citeshttps://doi.org/10.1038/s41598-023-38992-zopenalex-snapshot
Comparison of bacterial diversity in Bactrocera cucurbitae (Coquillett) ovaries and eggs based on 16S rRNA sequencing
inferred← citeshttps://doi.org/10.1038/s41598-024-73055-xopenalex-snapshot
The biogeographic patterns of the olive fly and its primary symbiont Candidatus Erwinia dacicola across the distribution area of the olive tree
inferred← citeshttps://doi.org/10.1098/rsos.150170openalex-snapshot
Symbiotic bacteria enable olive fly larvae to overcome host defences
inferred← citeshttps://doi.org/10.1098/rspb.2009.2102openalex-snapshot
Give us the tools and we will do the job: symbiotic bacteria affect olive fly fitness in a diet-dependent fashion
inferred← citeshttps://doi.org/10.1099/ijs.0.030668-0openalex-snapshot
Evidence of two lineages of the symbiont ‘Candidatus Erwinia dacicola’ in Italian populations of Bactrocera oleae (Rossi) based on 16S rRNA gene sequences
inferred← citeshttps://doi.org/10.1099/ijsem.0.003789openalex-snapshot
Lists of names of prokaryotic Candidatus taxa
inferred← citeshttps://doi.org/10.1111/1744-7917.12458openalex-snapshot
Metagenomic analysis reveals changes of the Drosophila suzukii microbiota in the newly colonized regions
inferred← citeshttps://doi.org/10.1111/1744-7917.12768openalex-snapshot
Diversity of bacteria in different life stages and their impact on the development and reproduction of Zeugodacus tau (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1111/1744-7917.70126openalex-snapshot
Characterization of the olive fly ( Bactrocera oleae ) microbiome across diverse geographic regions of Morocco
inferred← citeshttps://doi.org/10.1111/eea.12609openalex-snapshot
Review of the role of gut microbiota in mass rearing of the olive fruit fly, B actrocera oleae, and its parasitoids
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2012.01378.xopenalex-snapshot
Ultrastructural and molecular characterization of a bacterial symbiosis in the ecologically important scale insect family Coelostomidiidae
inferred← citeshttps://doi.org/10.1111/j.1751-7915.2011.00249.xopenalex-snapshot
Riding the Trojan horse: combating pest insects with their own symbionts
inferred← citeshttps://doi.org/10.1111/jen.12656openalex-snapshot
Microbiota of Telenomus tridentatus (Platygastroidea: Scelionidae): An unwanted parasitoid
inferred← citeshttps://doi.org/10.1126/science.adg5725openalex-snapshot
Ecology-relevant bacteria drive the evolution of host antimicrobial peptides in Drosophila
inferred← citeshttps://doi.org/10.1128/aem.01336-10openalex-snapshot
Acetic Acid Bacteria, Newly Emerging Symbionts of Insects
inferred← citeshttps://doi.org/10.1128/aem.02933-08openalex-snapshot
Acetobacter tropicalisIs a Major Symbiont of the Olive Fruit Fly (Bactrocera oleae)
inferred← citeshttps://doi.org/10.1128/aem.02983-10openalex-snapshot
Characterization of an Obligate Intracellular Bacterium in the Midgut Epithelium of the Bulrush Bug Chilacis typhae (Heteroptera, Lygaeidae, Artheneinae)
inferred← citeshttps://doi.org/10.1128/mbio.02608-24openalex-snapshot
Honey wasps differ from other wasps in possessing large gut communities dominated by host-restricted bacteria
inferred← citeshttps://doi.org/10.1139/w11-057openalex-snapshot
Green fluorescent protein (GFP)-labeling of enterobacteria associated with fruit flies (Diptera: Tephritidae) and persistence in their natural hostRhagoletis completaCresson.
inferred← citeshttps://doi.org/10.11606/d.11.2013.tde-17122013-084339openalex-snapshot
Microbiota intestinal de larvas e adultos de Anastrepha fraterculus (Wiedemann, 1830) (Diptera: Tephritidae): diversidade e efeito do alimento
inferred← citeshttps://doi.org/10.1186/1471-2156-15-s2-s9openalex-snapshot
Australian endemic pest tephritids: genetic, molecular and microbial tools for improved Sterile Insect Technique
inferred← citeshttps://doi.org/10.1186/1471-2180-13-129openalex-snapshot
A unique midgut-associated bacterial community hosted by the cave beetle Cansiliella servadeii(Coleoptera: Leptodirini) reveals parallel phylogenetic divergences from universal gut-specific ancestors
inferred← citeshttps://doi.org/10.1186/1741-7007-9-87openalex-snapshot
Multiple origins of endosymbiosis within the Enterobacteriaceae (γ-Proteobacteria): convergence of complex phylogenetic approaches
inferred← citeshttps://doi.org/10.1601/ex.19788openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19789openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19790openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19791openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19792openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19793openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19794openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19795openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19796openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19797openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19798openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19799openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19800openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/ex.19801openalex-snapshot
Exemplar Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008 and Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/nm.17774openalex-snapshot
Nomenclature Abstract for Stammerula tephritidis (sic) Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/nm.30779openalex-snapshot
Nomenclature Abstract for Stammerula (sic) Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/nm.35232openalex-snapshot
Nomenclature Abstract for Stammerella corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.1601/nm.35233openalex-snapshot
Nomenclature Abstract for Stammerella tephritidis corrig. Mazzon et al. 2008.
inferred← citeshttps://doi.org/10.21608/ajas.2023.189060.1225openalex-snapshot
Implement of Some Biocontrol Tactics as an Innovative Management Against Cucurbit Fly, Dacus ciliatus and Western Flower Thrips, Frankliniella occidentalis on Squash Crop
inferred← citeshttps://doi.org/10.31610/zsr/2022.31.1.118openalex-snapshot
Tephritid flies (Diptera: Tephritidae) of the Caucasus and Transcaucasia: new records and new host plants
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00928openalex-snapshot
Colonization of the Intestinal Tract of the Polyphagous Pest Spodoptera littoralis with the GFP-Tagged Indigenous Gut Bacterium Enterococcus mundtii
inferred← citeshttps://doi.org/10.3390/agronomy13030868openalex-snapshot
The Role of Symbiont-Targeted Strategies in the Management of Pentatomidae and Tephritidae Pests under an Integrated Vision
inferred← citeshttps://doi.org/10.3897/bdj.9.e69351openalex-snapshot
New and confirmed records of fruit flies (Diptera, Tephritidae) from Italy
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