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The emerging diversity of Rickettsia
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-0-387-21609-6openalex-snapshot
Bergey’s Manual® of Systematic Bacteriology
inferredcites →https://doi.org/10.1007/s00248-004-0140-5openalex-snapshot
Rickettsia Infection in Natural Leech Populations
inferredcites →https://doi.org/10.1007/s00284-005-0092-0openalex-snapshot
The First Finding of a Rickettsia Bacterium Associated with Parthenogenesis Induction Among Insects
inferredcites →https://doi.org/10.1007/s002849900086openalex-snapshot
A New Rickettsia from a Herbivorous Insect, the Pea Aphid Acyrthosiphon pisum (Harris)
inferredcites →https://doi.org/10.1007/s002849900172openalex-snapshot
Occurrence and Transmission of Facultative Endosymbionts in Aphids
inferredcites →https://doi.org/10.1007/s002849900283openalex-snapshot
Rickettsial Relative Associated with Papaya Bunchy Top Disease
inferredcites →https://doi.org/10.1016/0923-2508(96)80284-1openalex-snapshot
Phylogenetic analysis of the genus Rickettsia by 16S rDNA sequencing
inferredcites →https://doi.org/10.1016/j.biocontrol.2004.12.012openalex-snapshot
Microbial diversity in the predatory mite Metaseiulus occidentalis (Acari: Phytoseiidae) and its prey, Tetranychus urticae (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1016/j.femsec.2004.03.007openalex-snapshot
Diversity of bacteria associated with Collembola – a cultivation-independent survey based on PCR-amplified 16S rRNA genes
inferredcites →https://doi.org/10.1016/j.femsre.2004.09.002openalex-snapshot
Some lessons fromRickettsiagenomics
inferredcites →https://doi.org/10.1016/s0014-5793(01)02618-7openalex-snapshot
Evolutionary relationship of Rickettsiae and mitochondria
inferredcites →https://doi.org/10.1016/s0022-474x(02)00098-xopenalex-snapshot
Characterisation of Wolbachia-like bacteria isolated from the parthenogenetic stored-product pest psocid Liposcelis bostrychophila (Badonnel) (Psocoptera)
inferredcites →https://doi.org/10.1016/s0140-6736(05)61814-4openalex-snapshot
A new tick-transmitted disease due to Rickettsia slovaca
inferredcites →https://doi.org/10.1016/s0140-6736(05)65037-4openalex-snapshot
A new spotted-fever-group Rickettsiosis
inferredcites →https://doi.org/10.1016/s0169-5347(00)01902-9openalex-snapshot
Lifestyle evolution in symbiotic bacteria: insights from genomics
inferredcites →https://doi.org/10.1016/s0723-2020(11)80448-0openalex-snapshot
Evolutionary Analysis of the Spotted Fever and Thyphus Groups of Rickettsia Using 16S rRNA Gene Sequences
inferredcites →https://doi.org/10.1016/s1286-4579(01)01394-6openalex-snapshot
Microsporidian life cycles and diversity: the relationship between virulence and transmission
inferredcites →https://doi.org/10.1023/a:1007341721795openalex-snapshot
Occurrence of high ratio of males after introduction of minocycline in a colony of leptotrombidium fletcheri infected with orientia tsutsugamushi
inferredcites →https://doi.org/10.1038/24094openalex-snapshot
The genome sequence of Rickettsia prowazekii and the origin of mitochondria
inferredcites →https://doi.org/10.1046/j.1365-2311.2002.00393.xopenalex-snapshot
Facultative bacterial endosymbionts benefit pea aphids Acyrthosiphon pisum under heat stress
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.1365-2583.2002.00368.xopenalex-snapshot
Two novel strains of Wolbachia coexisting in both species of mulberry leafhoppers
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.02015.xopenalex-snapshot
Strain‐specific regulation of intracellularWolbachiadensity in multiply infected insects
inferredcites →https://doi.org/10.1046/j.1420-9101.2002.00446.xopenalex-snapshot
Contrasting effects of Wolbachia on cytoplasmic incompatibility and fecundity in the haplodiploid mite Tetranychus urticae
inferredcites →https://doi.org/10.1046/j.1570-7458.2000.00670.xopenalex-snapshot
Fitness effects of two facultative endosymbiotic bacteria on the pea aphid, Acyrthosiphon pisum, and the blue alfalfa aphid, A. kondoi
inferredcites →https://doi.org/10.1046/j.1570-7458.2001.00878.xopenalex-snapshot
Survival in Dalbulus leafhopper vectors improves after exposure to maize stunting pathogens
inferredcites →https://doi.org/10.1056/nejmp058138openalex-snapshot
Rocky Mountain Spotted Fever — Changing Ecology and Persisting Virulence
inferredcites →https://doi.org/10.1073/pnas.0335320100openalex-snapshot
Facultative bacterial symbionts in aphids confer resistance to parasitic wasps
inferredcites →https://doi.org/10.1073/pnas.0506131102openalex-snapshot
Variation in resistance to parasitism in aphids is due to symbionts not host genotype
inferredcites →https://doi.org/10.1084/jem.191.8.1429openalex-snapshot
Inflammatory Responses Induced by the Filarial Nematode Brugia malayi Are Mediated by Lipopolysaccharide-like Activity from Endosymbiotic Wolbachia Bacteria
inferredcites →https://doi.org/10.1086/381894openalex-snapshot
Rickettsia parkeri:A Newly Recognized Cause of Spotted Fever Rickettsiosis in the United States
inferredcites →https://doi.org/10.1093/infdis/121.4.367openalex-snapshot
Serologic Evidence of Rickettsia canada Infection of Man
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/42.6.945openalex-snapshot
First Report of the Male of Amblyomma rotundatum (Acari: Ixodidae) from a Field-Collected Host
inferredcites →https://doi.org/10.1093/molbev/msi199openalex-snapshot
Molecular Evolution of Rickettsia Surface Antigens: Evidence of Positive Selection
inferredcites →https://doi.org/10.1093/molbev/msj009openalex-snapshot
Genome Phylogenies Indicate a Meaningful α-Proteobacterial Phylogeny and Support a Grouping of the Mitochondria with the Rickettsiales
inferredcites →https://doi.org/10.1093/oso/9780198577867.001.0001openalex-snapshot
Influential Passengers
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004195openalex-snapshot
Host-Symbiont Conflicts: Positive Selection on an Outer Membrane Protein of Parasitic but not Mutualistic Rickettsiaceae
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026201openalex-snapshot
Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference
inferredcites →https://doi.org/10.1097/00000441-193506000-00035openalex-snapshot
RATS, LICE AND HISTORY
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/rspb.2000.1232openalex-snapshot
Wolbachia–induced ‘hybrid breakdown’ in the two–fspotted spider miteTetranychus urticaeKoch
inferredcites →https://doi.org/10.1098/rspb.2003.2475openalex-snapshot
A bacterial symbiont in theBacteroidetesinduces cytoplasmic incompatibility in the parasitoid waspEncarsia pergandiella
inferredcites →https://doi.org/10.1098/rspb.2003.2537openalex-snapshot
Changing partners in an obligate symbiosis: a facultative endosymbiont can compensate for loss of the essential endosymbiont Buchnera in an aphid
inferredcites →https://doi.org/10.1098/rspb.2005.3436openalex-snapshot
Costs and benefits of a superinfection of facultative symbionts in aphids
inferredcites →https://doi.org/10.1099/00207713-33-1-94openalex-snapshot
Rickettsia bellii sp. nov.: a Tick-Borne Rickettsia, Widely Distributed in the United States, That Is Distinct from the Spotted Fever and Typhus Biogroups
inferredcites →https://doi.org/10.1099/00207713-44-4-798openalex-snapshot
Ancestral Divergence of Rickettsia bellii from the Spotted Fever and Typhus Groups of Rickettsia and Antiquity of the Genus Rickettsia
inferredcites →https://doi.org/10.1099/00207713-45-3-589openalex-snapshot
Classification of Rickettsia tsutsugamushi in a New Genus, Orientia gen. nov., as Orientia tsutsugamushi comb. nov.
inferredcites →https://doi.org/10.1099/00207713-47-2-252openalex-snapshot
Citrate Synthase Gene Comparison, a New Tool for Phylogenetic Analysis, and Its Application for the Rickettsiae
inferredcites →https://doi.org/10.1099/00207713-50-4-1449openalex-snapshot
Phylogenetic analysis of members of the genus Rickettsia using the gene encoding the outer-membrane protein rOmpB (ompB).
inferredcites →https://doi.org/10.1099/ijs.0.02957-0openalex-snapshot
Characterization of a ‘Bacteroidetes’ symbiont in Encarsia wasps (Hymenoptera: Aphelinidae): proposal of ‘Candidatus Cardinium hertigii’
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00361.xopenalex-snapshot
HOST GROWTH CONDITIONS REGULATE THE PLASTICITY OF HORIZONTAL AND VERTICAL TRANSMISSION IN HOLOSPORA UNDULATA, A BACTERIAL PARASITE OF THE PROTOZOAN PARAMECIUM CAUDATUM
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.1365-2958.2005.04806.xopenalex-snapshot
A novel and naturally occurring transposon, ISRpe1 in the Rickettsia peacockii genome disrupting the rickA gene involved in actin‐based motility
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.1462-2920.2004.00683.xopenalex-snapshot
Neorickettsia risticii is vertically transmitted in the trematode Acanthatrium oregonense and horizontally transmitted to bats
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03560.xopenalex-snapshot
THE EVOLUTION OF VIRULENCE IN PATHOGENS WITH VERTICAL AND HORIZONTAL TRANSMISSION
inferredcites →https://doi.org/10.1111/j.1749-6632.2003.tb07358.xopenalex-snapshot
‘Candidatus Rickettsia tarasevichiae’ in Ixodes persulcatus Ticks Collected in Russia
inferredcites →https://doi.org/10.1111/j.1749-6632.2003.tb07409.xopenalex-snapshot
Wolbachia in the Inflammatory Pathogenesis of Human Filariasis
inferredcites →https://doi.org/10.1126/science.1060411openalex-snapshot
A Mite Species That Consists Entirely of Haploid Females
inferredcites →https://doi.org/10.1126/science.1061471openalex-snapshot
Mechanisms of Evolution in Rickettsia conorii and R. prowazekii
inferredcites →https://doi.org/10.1126/science.1094611openalex-snapshot
Host Plant Specialization Governed by Facultative Symbiont
inferredcites →https://doi.org/10.1126/science.1120180openalex-snapshot
Aphid Protected from Pathogen by Endosymbiont
inferredcites →https://doi.org/10.1128/aem.65.2.773-778.1999openalex-snapshot
Lethal Effect ofRickettsia rickettsiion Its Tick Vector (Dermacentor andersoni)
inferredcites →https://doi.org/10.1128/aem.66.7.2748-2758.2000openalex-snapshot
The Secondary Endosymbiotic Bacterium of the Pea AphidAcyrthosiphon pisum(Insecta: Homoptera)
inferredcites →https://doi.org/10.1128/aem.67.1.270-277.2001openalex-snapshot
Incidence of Male-KillingRickettsiaspp. (α-Proteobacteria) in the Ten-Spot Ladybird BeetleAdalia decempunctataL. (Coleoptera: Coccinellidae)
inferredcites →https://doi.org/10.1128/aem.67.3.1284-1291.2001openalex-snapshot
Spiroplasma Symbiont of the Pea Aphid, Acyrthosiphon pisum (Insecta: Homoptera)
inferredcites →https://doi.org/10.1128/aem.68.2.999-1004.2002openalex-snapshot
Novel Clade of Rickettsia spp. from Leeches
inferredcites →https://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)
inferredcites →https://doi.org/10.1128/aem.70.11.6628-6636.2004openalex-snapshot
Sequence and Expression Analysis of the ompA Gene of Rickettsia peacockii , an Endosymbiont of the Rocky Mountain Wood Tick, Dermacentor andersoni
inferredcites →https://doi.org/10.1128/aem.70.5.2596-2602.2004openalex-snapshot
A Novel Alpha-Proteobacterium Resides in the Mitochondria of Ovarian Cells of the Tick Ixodes ricinus
inferredcites →https://doi.org/10.1128/aem.70.5.2816-2822.2004openalex-snapshot
Transposon Mutagenesis of the Obligate Intracellular Pathogen Rickettsia prowazekii
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/aem.71.7.4069-4075.2005openalex-snapshot
Rickettsia Symbiont in the Pea Aphid Acyrthosiphon pisum : Novel Cellular Tropism, Effect on Host Fitness, and Interaction with the Essential Symbiont Buchnera
inferredcites →https://doi.org/10.1128/aem.72.5.3646-3652.2006openalex-snapshot
Identification and Localization of a Rickettsia sp. in Bemisia tabaci (Homoptera: Aleyrodidae)
inferredcites →https://doi.org/10.1128/cmr.10.4.694openalex-snapshot
Rickettsioses as paradigms of new or emerging infectious diseases
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/10.1128/jb.186.17.5842-5855.2004openalex-snapshot
Complete Genome Sequence ofRickettsia typhiand Comparison with Sequences of Other Rickettsiae
inferredcites →https://doi.org/10.1128/jcm.35.11.2715-2727.1997openalex-snapshot
Laboratory diagnosis of rickettsioses: current approaches to diagnosis of old and new rickettsial diseases
inferredcites →https://doi.org/10.1146/annurev.en.40.010195.001253openalex-snapshot
Cellular and Molecular Interrelationships Between Ticks and Prokaryotic Tick-Borne Pathogens
inferredcites →https://doi.org/10.1146/annurev.micro.53.1.71openalex-snapshot
Wolbachia Pipientis: Microbial Manipulator of Arthropod Reproduction
inferredcites →https://doi.org/10.1196/annals.1286.016openalex-snapshot
Steroid Hormones and Growth Factors Act in an Integrated Manner at the Levels of Hypothalamic Astrocytes
inferredcites →https://doi.org/10.1201/9780203009918.ch16openalex-snapshot
Insights Into Wolbachia Obligatory Symbiosis
inferredcites →https://doi.org/10.1303/aez.34.391openalex-snapshot
Molecular characterization of Rickettsia sp. in a bruchid beetle, Kytorhinus sharpianus (Coleoptera : Bruchidae)
inferredcites →https://doi.org/10.1371/journal.pbio.0030248openalex-snapshot
The Genome Sequence of Rickettsia felis Identifies the First Putative Conjugative Plasmid in an Obligate Intracellular Parasite
inferredcites →https://doi.org/10.14411/fp.2003.030openalex-snapshot
Nuclearia pattersoni sp. n. (Filosea), a new species of amphizoic amoeba isolated from gills of roach (Rutilus rutilus), and its rickettsial endosymbiont
inferredcites →https://doi.org/10.1534/genetics.104.026716openalex-snapshot
Virulence, Multiple Infections and Regulation of Symbiotic Population in the Wolbachia-Asobara tabida Symbiosis
inferredcites →https://doi.org/10.1603/0022-2585-39.6.809openalex-snapshot
Rickettsial Infection in Dermacentor variabilis (Acari: Ixodidae) Inhibits Transovarial Transmission of a Second Rickettsia
inferredcites →https://doi.org/10.1603/0022-2585-40.6.1000openalex-snapshot
Evaluation of Transovarial Transmission and Transmissibility of Ehrlichia chaffeensis (Rickettsiales: Anaplasmataceae) in Amblyomma americanum (Acari: Ixodidae)
inferredcites →https://doi.org/10.1603/0022-2585-41.3.340openalex-snapshot
Culture-Independent Analysis of Midgut Microbiota in the Arbovirus VectorCulicoides sonorensis(Diptera: Ceratopogonidae)
inferredcites →https://doi.org/10.1603/0022-2585-41.6.1073openalex-snapshot
Rickettsia bellii and Rickettsia amblyommii in Amblyomma Ticks from the State of Rondônia, Western Amazon, Brazil
inferredcites →https://doi.org/10.3201/eid0402.980205openalex-snapshot
Rickettsial Pathogens and Their Arthropod Vectors
inferredcites →https://doi.org/10.3201/eid0604.000402openalex-snapshot
Male-Killing Bacteria in Insects: Mechanisms, Incidence, and Implications
inferredcites →https://doi.org/10.3201/eid0604.000412openalex-snapshot
Evidence of Infection in Humans with Rickettsia helvetica in Eastern France
inferredcites →https://doi.org/10.4269/ajtmh.1982.31.4.tm0310040863aopenalex-snapshot
Rickettsiae and Rickettsial Diseases
inferredcites →https://doi.org/10.5860/choice.36-1561openalex-snapshot
Influential passengers: inherited microorganisms and arthropod reproduction
inferredcites →https://doi.org/10.7326/0003-4819-104-5-606openalex-snapshot
Acute Febrile Cerebrovasculitis: A Syndrome of Unknown, Perhaps Rickettsial, Cause
inferredcites →https://doi.org/10.7326/0003-4819-105-5-802openalex-snapshot
Acute Febrile Cerebrovasculitis
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/10.2139/ssrn.4650897openalex-extracted
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inferred← citeshttps://doi.org/10.1002/ece3.6993openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ece3.71535openalex-snapshot
Positive Molecular Detection of Rickettsia helvetica in Great Tits From Central Poland
inferred← citeshttps://doi.org/10.1002/mbo3.1431openalex-snapshot
Reassessment of the genetic basis of natural rifampin resistance in the genus Rickettsia
inferred← citeshttps://doi.org/10.1002/ps.70167openalex-snapshot
Rickettsia symbionts favor whitefly ovary development by promoting germ cell mitosis
inferred← citeshttps://doi.org/10.1002/vms3.70014openalex-snapshot
First molecular diagnosis of the human pathogen Rickettsia raoultii and other spotted fever group rickettsiae in Sudanese ixodid ticks from domestic ruminants
inferred← citeshttps://doi.org/10.1007/978-1-4020-9695-2_26openalex-snapshot
Symbionts, including pathogens, of the predatory mite Metaseiulus occidentalis: current and future analysis methods
inferred← citeshttps://doi.org/10.1007/978-1-4614-4000-0_23openalex-snapshot
Brazilian Spotted Fever: The Role of Capybaras
inferred← citeshttps://doi.org/10.1007/978-3-030-51849-3_16openalex-snapshot
The Wolbachia Symbiont: Here, There and Everywhere
inferred← citeshttps://doi.org/10.1007/978-3-030-51849-3_2openalex-snapshot
Gene Transfer Agents in Symbiotic Microbes
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Populations and Communities
inferred← citeshttps://doi.org/10.1007/978-3-319-46859-4_19openalex-snapshot
Human Rickettsioses: Host Response and Molecular Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-46859-4_3openalex-snapshot
Biodiversity of “Non-model” Rickettsiales and Their Association with Aquatic Organisms
inferred← citeshttps://doi.org/10.1007/978-3-642-21396-0_16openalex-snapshot
What Else Besides TBE and Borreliosis? Tick-Transmitted Pathogens in Germany and Beyond
inferred← citeshttps://doi.org/10.1007/978-90-481-2770-2_17openalex-snapshot
Thelytoky in Hymenoptera with Venturia canescens and Leptopilina clavipes as Case Studies
inferred← citeshttps://doi.org/10.1007/978-94-007-2114-2_13openalex-snapshot
How Does Biodiversity Influence the Ecology of Infectious Disease?
inferred← citeshttps://doi.org/10.1007/s00049-009-0036-4openalex-snapshot
Chemical communication and coevolution in an ant–plant mutualism
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Coxiella Symbionts in the Cayenne Tick Amblyomma cajennense
inferred← citeshttps://doi.org/10.1007/s00248-014-0561-8openalex-snapshot
Endosymbiotic Candidates for Parasitoid Defense in Exotic and Native New Zealand Weevils
inferred← citeshttps://doi.org/10.1007/s00248-015-0565-zopenalex-snapshot
Dynamics of the Endosymbiont Rickettsia in an Insect Pest
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The Hidden World of Rickettsiales Symbionts: “Candidatus Spectririckettsia obscura,” a Novel Bacterium Found in Brazilian and Indian Paramecium caudatum
inferred← citeshttps://doi.org/10.1007/s00248-019-01358-yopenalex-snapshot
How Hosts Taxonomy, Trophy, and Endosymbionts Shape Microbiome Diversity in Beetles
inferred← citeshttps://doi.org/10.1007/s00248-020-01568-9openalex-snapshot
Incidence and Diversity of Torix Rickettsia–Odonata Symbioses
inferred← citeshttps://doi.org/10.1007/s00248-020-01611-9openalex-snapshot
Changes in Bacterial Diversity, Composition and Interactions During the Development of the Seabird Tick Ornithodoros maritimus (Argasidae)
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Species Identity, Life History, and Geographic Distance Influence Gut Bacterial Communities in Lab-Reared and European Field-Collected Culicoides Biting midges
inferred← citeshttps://doi.org/10.1007/s00248-023-02290-yopenalex-snapshot
Microbiome of Zoophytophagous Biological Control Agent Nesidiocoris tenuis
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The Microbiome of an Invasive Spider: Reduced Bacterial Richness, but no Indication of Microbial-Mediated Dispersal Behaviour
inferred← citeshttps://doi.org/10.1007/s00284-011-9893-5openalex-snapshot
Origin and Examination of a Leafhopper Facultative Endosymbiont
inferred← citeshttps://doi.org/10.1007/s10340-016-0782-3openalex-snapshot
Use the insiders: could insect facultative symbionts control vector-borne plant diseases?
inferred← citeshttps://doi.org/10.1007/s10340-019-01113-9openalex-snapshot
Relative polyphagy of “Mediterranean” cryptic Bemisia tabaci whitefly species and global pest status implications
inferred← citeshttps://doi.org/10.1007/s10393-011-0726-6openalex-snapshot
Effect of Forest Fragmentation on Tick Infestations of Birds and Tick Infection Rates by Rickettsia in the Atlantic Forest of Brazil
inferred← citeshttps://doi.org/10.1007/s10493-006-9040-3openalex-snapshot
Rickettsial pathogens in the tropical rat mite Ornithonyssus bacoti (Acari: Macronyssidae) from Egyptian rats (Rattus spp.)
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Detection of a novel spotted fever group rickettsia in Amblyomma parvum ticks (Acari: Ixodidae) from Argentina
inferred← citeshttps://doi.org/10.1007/s10493-008-9185-3openalex-snapshot
Symbionts, including pathogens, of the predatory mite Metaseiulus occidentalis: current and future analysis methods
inferred← citeshttps://doi.org/10.1007/s10493-008-9228-9openalex-snapshot
Asymmetric reproductive interference between two closely related spider mites: Tetranychus urticae and T. turkestani (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1007/s10493-009-9260-4openalex-snapshot
Molecular detection of Rickettsia, Coxiella and Rickettsiella DNA in three native Australian tick species
inferred← citeshttps://doi.org/10.1007/s10493-014-9851-6openalex-snapshot
Ticks and rickettsial infection in the wildlife of two regions of the Brazilian Amazon
inferred← citeshttps://doi.org/10.1007/s10493-017-0132-zopenalex-snapshot
Rickettsia spp. in Dermacentor marginatus ticks: analysis of the host-vector-pathogen interactions in a northern Mediterranean area
inferred← citeshttps://doi.org/10.1007/s10493-020-00508-zopenalex-snapshot
Molecular characterization of Cardinium, Rickettsia, Spiroplasma and Wolbachia in mite species from citrus orchards
inferred← citeshttps://doi.org/10.1007/s10493-020-00522-1openalex-snapshot
Molecular detection of Rickettsia species and host associations of Laelaps mites (Acari: Laelapidae) in Taiwan
inferred← citeshttps://doi.org/10.1007/s10530-011-0140-6openalex-snapshot
Strong genetic structure among populations of the invasive avocado pest Pseudacysta perseae (Heidemann) (Hemiptera: Tingidae) reveals the source of introduced populations
inferred← citeshttps://doi.org/10.1007/s10646-024-02783-7openalex-snapshot
Effects of cadmium on the intestinal health of the snail Bradybaena ravida Benson
inferred← citeshttps://doi.org/10.1007/s10750-022-04862-4openalex-snapshot
Turning the tide on sex and the microbiota in aquatic animals
inferred← citeshttps://doi.org/10.1007/s10886-014-0466-5openalex-snapshot
Cytokinin-Induced Phenotypes in Plant-Insect Interactions: Learning from the Bacterial World
inferred← citeshttps://doi.org/10.1007/s11427-020-1801-7openalex-snapshot
New insights into the transovarial transmission of the symbiont Rickettsia in whiteflies
inferred← citeshttps://doi.org/10.1007/s11756-021-00813-xopenalex-snapshot
A case report of Rickettsia-like infection in a human patient from Slovakia
inferred← citeshttps://doi.org/10.1007/s11829-020-09800-6openalex-snapshot
Are bacterial symbionts associated with gall induction in insects?
inferred← citeshttps://doi.org/10.1007/s11908-026-00890-6openalex-snapshot
Asymptomatic Scrub Typhus Infection in Humans: Current Understanding and the Knowledge Gaps
inferred← citeshttps://doi.org/10.1007/s12223-013-0222-1openalex-snapshot
Hard ticks and their bacterial endosymbionts (or would be pathogens)
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/s42770-026-02030-7openalex-snapshot
Pangenomic and genomic plasticity analyses of the genus Rickettsia
inferred← citeshttps://doi.org/10.1016/b978-0-443-06839-3.00187-9openalex-snapshot
Rickettsia rickettsii and Other Spotted Fever Group Rickettsiae (Rocky Mountain Spotted Fever and Other Spotted Fevers)
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4801-3.00188-0openalex-snapshot
Rickettsia rickettsii and Other Spotted Fever Group Rickettsiae (Rocky Mountain Spotted Fever and Other Spotted Fevers)
inferred← citeshttps://doi.org/10.1016/bs.aiip.2018.07.001openalex-snapshot
The Potential Control Strategies Based on the Interaction Between Indoor Cockroaches and Their Symbionts in China
inferred← citeshttps://doi.org/10.1016/j.actatropica.2016.12.020openalex-snapshot
Multiple-host pathogens in domestic hunting dogs in Nicaragua’s Bosawás Biosphere Reserve
inferred← citeshttps://doi.org/10.1016/j.atmosenv.2017.10.048openalex-snapshot
Variations of bacteria and fungi in PM2.5 in Beijing, China
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2015.12.003openalex-snapshot
Algae–bacteria interactions: Evolution, ecology and emerging applications
inferred← citeshttps://doi.org/10.1016/j.cimid.2013.01.001openalex-snapshot
Connection of toxin–antitoxin modules to inoculation eschar and arthropod vertical transmission in Rickettsiales
inferred← citeshttps://doi.org/10.1016/j.cimid.2020.101541openalex-snapshot
Molecular investigation of zoonotic intracellular bacteria in Chilean bats
inferred← citeshttps://doi.org/10.1016/j.cimid.2022.101769openalex-snapshot
A serosurvey for spotted fever group Rickettsia and Coxiella burnetii antibodies in rural dogs and foxes, Chile
inferred← citeshttps://doi.org/10.1016/j.cimid.2022.101798openalex-snapshot
Molecular detection and identification of Rickettsia spp. in collected ticks from domestic animals in Southeastern of Iran
inferred← citeshttps://doi.org/10.1016/j.cll.2017.01.009openalex-snapshot
Rickettsiae as Emerging Infectious Agents
inferred← citeshttps://doi.org/10.1016/j.cois.2019.05.003openalex-snapshot
Importance of endosymbionts Wolbachia and Rickettsia in insect resistance development
inferred← citeshttps://doi.org/10.1016/j.cois.2022.101001openalex-snapshot
Competitive interactions in insect parasitoids: effects of microbial symbionts across tritrophic levels
inferred← citeshttps://doi.org/10.1016/j.crvi.2008.09.010openalex-snapshot
Infection by Wolbachia: from passengers to residents
inferred← citeshttps://doi.org/10.1016/j.cub.2018.02.008openalex-snapshot
Symbiosis: Wolbachia Host Shifts in the Fast Lane
inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.020openalex-snapshot
Selfish Mitonuclear Conflict
inferred← citeshttps://doi.org/10.1016/j.dci.2007.01.011openalex-snapshot
Rickettsia peacockii, an endosymbiont of Dermacentor andersoni, does not elicit or inhibit humoral immune responses from immunocompetent D. andersoni or Ixodes scapularis cell lines
inferred← citeshttps://doi.org/10.1016/j.dci.2024.105272openalex-snapshot
Identification and antibacterial activity of a novel phage-type lysozyme from the freshwater mussel Hyriopsis cumingii
inferred← citeshttps://doi.org/10.1016/j.ejop.2017.12.002openalex-snapshot
Host and symbiont intraspecific variability: The case of Paramecium calkinsi and “ Candidatus Trichorickettsia mobilis”
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109692openalex-snapshot
Temporal trends of antibiotic resistance in culturable bacteria reveal the role of potential pathogens as pioneering carriers and resistance accumulators
inferred← citeshttps://doi.org/10.1016/j.ibmb.2010.04.012openalex-snapshot
Disrupting the Amblyomma americanum (L.) CD147 receptor homolog prevents ticks from feeding to repletion and blocks spontaneous detachment of ticks from their host
inferred← citeshttps://doi.org/10.1016/j.idnow.2026.105370openalex-snapshot
Tick-borne diseases in French Guiana: A comprehensive review pinpointing differences from mainland France
inferred← citeshttps://doi.org/10.1016/j.ijidoh.2026.100128openalex-snapshot
Rickettsia beyond pathogenicity: endosymbiosis, evolution, and implications for One Health
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2009.12.001openalex-snapshot
Tritrophic interactions among Macrosiphum euphorbiae aphids, their host plants and endosymbionts: Investigation by a proteomic approach
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.04.002openalex-snapshot
The hemolymph microbiome of insects
inferred← citeshttps://doi.org/10.1016/j.jip.2010.05.017openalex-snapshot
A divergent Cardinium found in daddy long-legs (Arachnida: Opiliones)
inferred← citeshttps://doi.org/10.1016/j.meegid.2014.03.014openalex-snapshot
Genotyping, evolution and epidemiological findings of Rickettsia species
inferred← citeshttps://doi.org/10.1016/j.micinf.2015.08.010openalex-snapshot
Rickettsia bellii in Amblyomma rotundatum ticks parasitizing Rhinella jimi from northeastern Brazil
inferred← citeshttps://doi.org/10.1016/j.nmni.2019.100646openalex-snapshot
Molecular detection of Rickettsia infection in field-collected bed bugs
inferred← citeshttps://doi.org/10.1016/j.onehlt.2025.101022openalex-snapshot
Microbiome-based surveillance of zoonotic tick-borne pathogens from urban wild boars in Barcelona, 2022–2023
inferred← citeshttps://doi.org/10.1016/j.parint.2021.102286openalex-snapshot
Rickettsial agents detected in the genus Psathyromyia (Diptera:Phlebotominae) from a Biosphere Reserve of Veracruz, Mexico
inferred← citeshttps://doi.org/10.1016/j.pt.2024.06.006openalex-snapshot
Nutritional symbiosis in ticks: singularities of the genus Ixodes
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.07.097openalex-snapshot
Seasonal variation characteristic of inhalable microbial communities in PM2.5 in Beijing city, China
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.151088openalex-snapshot
Different characteristics of microbial diversity and special functional microbes in rainwater and topsoil before and after 2019 new coronavirus epidemic in Inner Mongolia Grassland
inferred← citeshttps://doi.org/10.1016/j.scp.2020.100339openalex-snapshot
Malaria vector control strategies. What is appropriate towards sustainable global eradication?
inferred← citeshttps://doi.org/10.1016/j.tig.2007.08.002openalex-snapshot
Intracellular pathogens go extreme: genome evolution in the Rickettsiales
inferred← citeshttps://doi.org/10.1016/j.tim.2021.05.004openalex-snapshot
Engineering insects from the endosymbiont out
inferred← citeshttps://doi.org/10.1016/j.tim.2021.06.008openalex-snapshot
Diversity and function of arthropod endosymbiont toxins
inferred← citeshttps://doi.org/10.1016/j.tree.2011.10.005openalex-snapshot
Population genetics of beneficial heritable symbionts
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2012.10.011openalex-snapshot
Vectors of rickettsiae in Africa
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2012.12.005openalex-snapshot
Prevalence and burden of two rickettsial phylotypes (G021 and G022) in Ixodes pacificus from California by real-time quantitative PCR
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2013.04.006openalex-snapshot
Host blood meal-dependent growth ensures transovarial transmission and transstadial passage of Rickettsia sp. phylotype G021 in the western black-legged tick (Ixodes pacificus)
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2013.10.008openalex-snapshot
Molecular detection of Rickettsia bellii and Rickettsia sp. strain Colombianensi in ticks from Cordoba, Colombia
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2014.05.011openalex-snapshot
Co-circulation of multiple species of Rickettsiales bacteria in one single species of hard ticks in Shenyang, China
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2015.02.001openalex-snapshot
High prevalence of “Candidatus Rickettsia andeanae” and apparent exclusion of Rickettsia parkeri in adult Amblyomma maculatum (Acari: Ixodidae) from Kansas and Oklahoma
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2015.04.011openalex-snapshot
Experimental vertical transmission of Rickettsia parkeri in the Gulf Coast tick, Amblyomma maculatum
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2015.10.002openalex-snapshot
Population dynamics of multiple symbionts in the hard tick, Dermacentor silvarum Olenev (Acari: Ixodidae)
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2016.02.004openalex-snapshot
‘Candidatus Rickettsia mendelii’, a novel basal group rickettsia detected in Ixodes ricinus ticks in the Czech Republic
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2017.04.012openalex-snapshot
Molecular analyses reveal an abundant diversity of ticks and rickettsial agents associated with wild birds in two regions of primary Brazilian Atlantic Rainforest
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2018.02.003openalex-snapshot
Rickettsial infection in ticks (Acari: Ixodidae) from reptiles in the Colombian Caribbean
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2019.04.003openalex-snapshot
Endosymbionts carried by ticks feeding on dogs in Spain
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2020.101376openalex-snapshot
Two novel Rickettsia species of soft ticks in North Africa: ‘Candidatus Rickettsia africaseptentrionalis’ and ‘Candidatus Rickettsia mauretanica’
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2020.101633openalex-snapshot
The genus Rickettsia in Mexico: Current knowledge and perspectives
inferred← citeshttps://doi.org/10.1016/j.vetpar.2023.109907openalex-snapshot
First molecular evidence of Wolbachia occurrence in Amblyomma sculptum (Acari: Ixodidae)
inferred← citeshttps://doi.org/10.1016/j.vprsr.2024.101041openalex-snapshot
Evaluating the circulation of Ehrlichia canis and Rickettsia spp. in domestic dogs from a semiarid region in Brazil
inferred← citeshttps://doi.org/10.1017/cbo9781139794749.012openalex-snapshot
The diversity and phylogeny ofRickettsia
inferred← citeshttps://doi.org/10.1017/s0007485307005159openalex-snapshot
Biotype-dependent secondary symbiont communities in sympatric populations of Bemisia tabaci
inferred← citeshttps://doi.org/10.1017/s0007485309990630openalex-snapshot
Evidence for pre-zygotic reproductive barrier between the B and Q biotypes ofBemisia tabaci(Hemiptera: Aleyrodidae)
inferred← citeshttps://doi.org/10.1021/acs.biochem.6b00870openalex-snapshot
Arthropod Innate Immune Systems and Vector-Borne Diseases
inferred← citeshttps://doi.org/10.1021/acs.jpcb.6b07884openalex-snapshot
A Distal Disulfide Bridge in OXA-1 β-Lactamase Stabilizes the Catalytic Center and Alters the Dynamics of the Specificity Determining Ω Loop
inferred← citeshttps://doi.org/10.1038/ismej.2016.201openalex-snapshot
Genomic changes associated with the evolutionary transition of an insect gut symbiont into a blood-borne pathogen
inferred← citeshttps://doi.org/10.1038/nrg2798openalex-snapshot
Evolutionary microbial genomics: insights into bacterial host adaptation
inferred← citeshttps://doi.org/10.1038/s41396-019-0433-9openalex-snapshot
Deianiraea , an extracellular bacterium associated with the ciliate Paramecium , suggests an alternative scenario for the evolution of Rickettsiales
inferred← citeshttps://doi.org/10.1038/s41396-021-00977-zopenalex-snapshot
Transitions in symbiosis: evidence for environmental acquisition and social transmission within a clade of heritable symbionts
inferred← citeshttps://doi.org/10.1038/s41467-022-30385-6openalex-snapshot
Genomic diversity across the Rickettsia and ‘Candidatus Megaira’ genera and proposal of genus status for the Torix group
inferred← citeshttps://doi.org/10.1038/s41598-018-37629-wopenalex-snapshot
Diversity and environmental distribution of the cosmopolitan endosymbiont “Candidatus Megaira”
inferred← citeshttps://doi.org/10.1038/s41598-020-59488-0openalex-snapshot
Novel Rickettsia genotypes in ticks in French Guiana, South America
inferred← citeshttps://doi.org/10.1038/s41598-020-73986-1openalex-snapshot
Widespread Torix Rickettsia in New Zealand amphipods and the use of blocking primers to rescue host COI sequences
inferred← citeshttps://doi.org/10.1038/s41598-022-07725-zopenalex-snapshot
Genomic evolution and adaptation of arthropod-associated Rickettsia
inferred← citeshttps://doi.org/10.1038/s41598-022-16955-0openalex-snapshot
Gut microbiota plasticity in insular lizards under reversed island syndrome
inferred← citeshttps://doi.org/10.1038/s41598-023-31894-0openalex-snapshot
Genetic sequencing of a 1944 Rocky Mountain spotted fever vaccine
inferred← citeshttps://doi.org/10.1051/vetres/2009017openalex-snapshot
The relationship between spotted fever groupRickettsiaeand Ixodid ticks
inferred← citeshttps://doi.org/10.1051/vetres:2008050openalex-snapshot
Louse- and flea-borne rickettsioses: biological and genomic analyses
inferred← citeshttps://doi.org/10.1073/pnas.1105467108openalex-snapshot
Cryptic sexual populations account for genetic diversity and ecological success in a widely distributed, asexual fungus-growing ant
inferred← citeshttps://doi.org/10.1073/pnas.1421391112openalex-snapshot
Maternal transmission, sex ratio distortion, and mitochondria
inferred← citeshttps://doi.org/10.1073/pnas.2406788121openalex-snapshot
Rickettsia symbionts spread via mixed mode transmission, increasing female fecundity and sex ratio shift by host hormone modulating
inferred← citeshttps://doi.org/10.1080/24750263.2020.1844322openalex-snapshot
The microbiota of the Lasius fuliginosus – Pella laticollis myrmecophilous interaction
inferred← citeshttps://doi.org/10.1086/720282openalex-snapshot
On the Spread of Microbes That Manipulate Reproduction in Marine Invertebrates
inferred← citeshttps://doi.org/10.1089/vbz.2007.0122openalex-snapshot
Prevalence of Antibodies to Rickettsiae in Different Regions of Serbia
inferred← citeshttps://doi.org/10.1089/vbz.2008.0006openalex-snapshot
Detection and Identification of Rickettsia Species in the Northeast of Italy
inferred← citeshttps://doi.org/10.1089/vbz.2008.0083openalex-snapshot
Molecular Detection of Rickettsia bellii , Rickettsia montanensis , and Rickettsia rickettsii in a Dermacentor variabilis Tick from Nature
inferred← citeshttps://doi.org/10.1089/vbz.2015.1786openalex-snapshot
Ectoparasite Infestations and Canine Infection by Rickettsiae and Ehrlichiae in a Semi-Arid Region of Northeastern Brazil
inferred← citeshttps://doi.org/10.1089/vbz.2018.2432openalex-snapshot
Patterns, Drivers, and Challenges of Vector-Borne Disease Emergence
inferred← citeshttps://doi.org/10.1093/aesa/saab025openalex-snapshot
Parthenogenesis and Sex-Ratio Distorting Bacteria inEmpoasca(Hemiptera: Cicadellidae) Leafhoppers
inferred← citeshttps://doi.org/10.1093/ee/nvad015openalex-snapshot
Bacterial Endosymbionts Identified From Leafhopper (Hemiptera: Cicadellidae) Vectors of Phytoplasmas
inferred← citeshttps://doi.org/10.1093/ee/nvy188openalex-snapshot
Bacterial Endosymbionts Are Common Among, but not Necessarily Within, Insect Species
inferred← citeshttps://doi.org/10.1093/femsec/fiv047openalex-snapshot
Extensive screen for bacterial endosymbionts reveals taxon-specific distribution patterns among bees (Hymenoptera, Anthophila)
inferred← citeshttps://doi.org/10.1093/femsec/fix087openalex-snapshot
Life inside a gall: closeness does not favour horizontal transmission of Rickettsia between a gall wasp and its parasitoid
inferred← citeshttps://doi.org/10.1093/femsec/fix138openalex-snapshot
Plant-mediated horizontal transmission of Rickettsia endosymbiont between different whitefly species
inferred← citeshttps://doi.org/10.1093/femsec/fiy235openalex-snapshot
Bacteriome-associatedWolbachiaof the parthenogenetic termiteCavitermes tuberosus
inferred← citeshttps://doi.org/10.1093/femsle/fnw147openalex-snapshot
Endosymbiotic bacteria in honey bees:Arsenophonusspp. are not transmitted transovarially
inferred← citeshttps://doi.org/10.1093/femspd/ftab019openalex-snapshot
The enigmatic biology of rickettsiae: recent advances, open questions and outlook
inferred← citeshttps://doi.org/10.1093/gbe/evaf142openalex-snapshot
From macro to micro: De novo genomes of Aedes mosquitoes enable comparative genomics among close and distant relatives
inferred← citeshttps://doi.org/10.1093/gbe/evu262openalex-snapshot
Genomic Diversification in Strains of Rickettsia felis Isolated from Different Arthropods
inferred← citeshttps://doi.org/10.1093/gbe/evy036openalex-snapshot
Culture-Facilitated Comparative Genomics of the Facultative Symbiont Hamiltonella defensa
inferred← citeshttps://doi.org/10.1093/gigascience/giab021openalex-snapshot
Torix Rickettsia are widespread in arthropods and reflect a neglected symbiosis
inferred← citeshttps://doi.org/10.1093/jhered/esr090openalex-snapshot
Genetic Signature of Reproductive Manipulation in the Phylogeography of the Bat Fly, Trichobius major
inferred← citeshttps://doi.org/10.1093/jme/tjaf155openalex-snapshot
Serological evidence of Rickettsia in horses and survey of tick-borne agents in ticks from horses and wildlife in the state of Pernambuco, Brazil
inferred← citeshttps://doi.org/10.1093/jme/tjag051openalex-snapshot
Microbial communities of the Southeast Asian black flies (Diptera: Simuliidae) based on multiple hypervariable regions of 16S rRNA
inferred← citeshttps://doi.org/10.1093/jme/tjag091openalex-snapshot
Diversity, spatiotemporal distribution, and host associations of flea species, with detection of co-infection with Rickettsia asembonensis and Wolbachia spp.
inferred← citeshttps://doi.org/10.1093/jmedent/45.2.289openalex-snapshot
Infection and Co-infection Rates of Anaplasma phagocytophilum Variants, Babesia spp., Borrelia burgdorferi, and the Rickettsial Endosymbiont in Ixodes scapularis (Acari: Ixodidae) from Sites in Indiana, Maine, Pennsylvania, and Wisconsin
inferred← citeshttps://doi.org/10.1093/molbev/msr239openalex-snapshot
The Rhizome of Life: The Sympatric Rickettsia felis Paradigm Demonstrates the Random Transfer of DNA Sequences
inferred← citeshttps://doi.org/10.1093/sysbio/syv084openalex-snapshot
The Phylogeny ofRickettsiaUsing Different Evolutionary Signatures: How Tree-Like is Bacterial Evolution?
inferred← citeshttps://doi.org/10.1096/fj.07-101162openalex-snapshot
Inherited intracellular ecosystem: symbiotic bacteria share bacteriocytes in whiteflies
inferred← citeshttps://doi.org/10.1096/fj.10-156992openalex-snapshot
Independent evolution of the core domain and its flanking sequences in small heat shock proteins
inferred← citeshttps://doi.org/10.1098/rsbl.2024.0310openalex-snapshot
Addictive manipulation: a perspective on the role of reproductive parasitism in the evolution of bacteria–eukaryote symbioses
inferred← citeshttps://doi.org/10.1098/rspb.2009.0875openalex-snapshot
Conjugation genes are common throughout the genus Rickettsia and are transmitted horizontally
inferred← citeshttps://doi.org/10.1098/rspb.2011.2095openalex-snapshot
Horizontal transmission of the insect symbiont Rickettsia is plant-mediated
inferred← citeshttps://doi.org/10.1098/rspb.2024.0238openalex-snapshot
Association between the gut microbiome and carotenoid plumage phenotype in an avian hybrid zone
inferred← citeshttps://doi.org/10.1098/rspb.2024.0680openalex-snapshot
Rickettsia induces strong cytoplasmic incompatibility in a predatory insect
inferred← citeshttps://doi.org/10.1098/rstb.2013.0364openalex-snapshot
Genetic conflict, kin and the origins of novel genetic systems
inferred← citeshttps://doi.org/10.1098/rstb.2016.0083openalex-snapshot
The evolution of transmission mode
inferred← citeshttps://doi.org/10.1099/ijsem.0.007294openalex-snapshot
Phylogenetic, genomic and morphological characterization of Rickettsia senegalensis sp. nov., a novel Rickettsia species detected worldwide
inferred← citeshttps://doi.org/10.1101/2021.10.04.462948openalex-snapshot
Structure of an ant-myrmecophile-microbe community
inferred← citeshttps://doi.org/10.1101/2021.10.04.463023openalex-snapshot
Ancient and modern geochemical signatures in the 13,500-year sedimentary record of Lake Cadagno
inferred← citeshttps://doi.org/10.1101/2021.10.06.463315openalex-snapshot
Large-scale comparative genomics unravels great genomic diversity across the Rickettsia and Ca . Megaira genera and identifies Torix group as an evolutionarily distinct clade
inferred← citeshttps://doi.org/10.1101/2023.02.26.530123openalex-snapshot
Metagenome diversity illuminates origins of pathogen effectors
inferred← citeshttps://doi.org/10.1101/2024.01.04.574207openalex-snapshot
Species-associated bacterial diversity increases along a gradient of habitat degradation
inferred← citeshttps://doi.org/10.1101/2024.06.24.600492openalex-snapshot
A conserved interaction between the effector Sca4 and host endocytic machinery suggests additional roles for Sca4 during rickettsial infection
inferred← citeshttps://doi.org/10.1101/2024.10.23.619971openalex-snapshot
The diversification of mealybugs was triggered by new symbiont acquisitions and followed by adaptive radiations on host plants
inferred← citeshttps://doi.org/10.1101/2025.05.06.25327046openalex-snapshot
Assessment of the pathogenicity of Candidatus Rickettsia colombiensis in a Syrian hamster ( Mesocricetus auratus ) model and serological cross-reactivity between spotted fever species
inferred← citeshttps://doi.org/10.1111/1462-2920.13887openalex-snapshot
Torix group Rickettsia are widespread in Culicoides biting midges (Diptera: Ceratopogonidae), reach high frequency and carry unique genomic features
inferred← citeshttps://doi.org/10.1111/1462-2920.14933openalex-snapshot
Analysis of interdomain taxonomic patterns in urban street mats
inferred← citeshttps://doi.org/10.1111/1462-2920.15396openalex-snapshot
‘ Candidatus Sarmatiella mevalonica’ endosymbiont of the ciliate Paramecium provides insights on evolutionary plasticity among Rickettsiales
inferred← citeshttps://doi.org/10.1111/1462-2920.16138openalex-snapshot
Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma
inferred← citeshttps://doi.org/10.1111/1574-6976.12084openalex-snapshot
Secretome of obligate intracellularRickettsia
inferred← citeshttps://doi.org/10.1111/1744-7917.12782openalex-snapshot
Similarities and spatial variations of bacterial and fungal communities in field rice planthopper (Hemiptera: Delphacidae) populations
inferred← citeshttps://doi.org/10.1111/1744-7917.12797openalex-snapshot
Impact of a novel Rickettsia symbiont on the life history and virus transmission capacity of its host whitefly (Bemisia tabaci)
inferred← citeshttps://doi.org/10.1111/1744-7917.13000openalex-snapshot
Characterization of the firstWolbachiafrom the genusScaptodrosophila, a male‐killer from the rainforest speciesS. claytoni
inferred← citeshttps://doi.org/10.1111/1744-7917.70256openalex-snapshot
Conversion of a thelytokous to a stable bisexual line by non‐target effect antibiotic elimination of Rickettsia in Anastatus gansuensis
inferred← citeshttps://doi.org/10.1111/1748-5967.70125openalex-snapshot
Investigating Secondary Endosymbiotic Bacterial Infections in Harvestman: Diversity and Evolutionary Dynamics
inferred← citeshttps://doi.org/10.1111/1755-0998.13629openalex-snapshot
Spider webs as eDNA samplers: Biodiversity assessment across the tree of life
inferred← citeshttps://doi.org/10.1111/aec.13259openalex-snapshot
Symbiotic bacteria in the relationship between Anaphes nitens (Hymenoptera: Mymaridae) and Gonipterus platensis (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2008.03914.xopenalex-snapshot
Microbial communities and interactions in the lone star tick, Amblyomma americanum
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04448.xopenalex-snapshot
Association between Wolbachia and Spiroplasma within Drosophila neotestacea: an emerging symbiotic mutualism?
inferred← citeshttps://doi.org/10.1111/j.1461-0248.2010.01564.xopenalex-snapshot
Defensive endosymbionts: a cryptic trophic level in community ecology
inferred← citeshttps://doi.org/10.1111/j.1469-0691.2008.02231.xopenalex-snapshot
Molecular detection and identification of Rickettsia endosymbiont in different biotypes of Bemisia tabaci
inferred← citeshttps://doi.org/10.1111/j.1469-185x.2010.00151.xopenalex-snapshot
Rickettsial evolution in the light of comparative genomics
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2009.00611.xopenalex-snapshot
ASYMMETRIC VIABILITY OF RECIPROCAL-CROSS HYBRIDS BETWEEN CRESTED AND MARBLED NEWTS ( TRITURUS CRISTATUS AND T. MARMORATUS )
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2009.00665.xopenalex-snapshot
Characterization and localization of Rickettsia sp. in water beetles of genus Deronectes (Coleoptera: Dytiscidae)
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2010.00890.xopenalex-snapshot
Molecular characterization and localization of the obligate endosymbiotic bacterium in the birch catkin bug Kleidocerys resedae (Heteroptera: Lygaeidae, Ischnorhynchinae)
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2009.04529.xopenalex-snapshot
The Science and Fiction of Emerging Rickettsioses
inferred← citeshttps://doi.org/10.1111/jpy.12385openalex-snapshot
Rickettsial endosymbiont in the “early‐diverging” streptophyte green alga Mesostigma viride
inferred← citeshttps://doi.org/10.1111/jzs.12141openalex-snapshot
Parthenogenesis in Hexapoda: Entognatha and non-holometabolous insects
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