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Virulence of recurrent infestations with Borrelia-infected ticks in a Borrelia-amplifying bird

https://doi.org/10.1038/srep16150
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What this work says

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

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Canary finches (Serinus canaria) as an avian infection model for Lyme borreliosis
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Models for Discrete Longitudinal Data
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Linear Mixed Models for Longitudinal Data
inferredcites →https://doi.org/10.1007/bf01200449openalex-snapshot
Role of saliva in tick/host interactions
inferredcites →https://doi.org/10.1007/s00265-009-0710-0openalex-snapshot
Nitric oxide production: an easily measurable condition index for vertebrates
inferredcites →https://doi.org/10.1007/s00436-013-3343-1openalex-snapshot
Do ticks and Borrelia burgdorferi s.l. constitute a burden to birds?
inferredcites →https://doi.org/10.1007/s004360050415openalex-snapshot
Susceptibility of BALB/c mice to nymphs and larvae of Ixodes ricinus after modulation of IgE production with anti-interleukin-4 or anti-interferon-γ monoclonal antibodies
inferredcites →https://doi.org/10.1016/0165-2478(94)90185-6openalex-snapshot
Killing of Borrelia burgdorferi by macrophages is dependent on oxygen radicals and nitric oxide and can be enhanced by antibodies to outer surface proteins of the spirochete
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Ectoparasites: Direct impact on host fitness
inferredcites →https://doi.org/10.1016/j.exppara.2012.09.008openalex-snapshot
Experimental inhibition of nitric oxide increases Plasmodium relictum (lineage SGS1) parasitaemia
inferredcites →https://doi.org/10.1016/j.idc.2007.12.013openalex-snapshot
Biology of Infection with Borrelia burgdorferi
inferredcites →https://doi.org/10.1016/j.ijpara.2009.07.011openalex-snapshot
Lack of resistance against the tick Ixodes ricinus in two related passerine bird species
inferredcites →https://doi.org/10.1016/j.ijpara.2012.05.010openalex-snapshot
Which forest bird species are the main hosts of the tick, Ixodes ricinus, the vector of Borrelia burgdorferi sensu lato, during the breeding season?
inferredcites →https://doi.org/10.1016/j.ijpara.2012.12.010openalex-snapshot
Ixodes ricinus ticks infected with the causative agent of Lyme disease, Borrelia burgdorferi sensu lato, have higher energy reserves
inferredcites →https://doi.org/10.1016/j.ijpara.2013.02.007openalex-snapshot
Ecological factors that determine Ixodes ricinus tick burdens in the great tit (Parus major), an avian reservoir of Borrelia burgdorferi s.l.
inferredcites →https://doi.org/10.1016/j.ttbdis.2010.03.001openalex-snapshot
Are birds reservoir hosts for Borrelia afzelii?
inferredcites →https://doi.org/10.1016/s0165-2427(98)00135-4openalex-snapshot
Saliva of Rhipicephalus sanguineus tick impairs T cell proliferation and IFN-γ-induced macrophage microbicidal activity
inferredcites →https://doi.org/10.1016/s0165-2427(98)00231-1openalex-snapshot
Up-regulation of inducible nitric oxide synthase mRNA in dogs experimentally infected with Borrelia burgdorferi
inferredcites →https://doi.org/10.1016/s0169-4758(96)10072-7openalex-snapshot
Co-feeding ticks: Epidemiological significance for tick-borne pathogen transmission
inferredcites →https://doi.org/10.1016/s0952-7915(99)00052-7openalex-snapshot
Reactive oxygen and reactive nitrogen intermediates in innate and specific immunity
inferredcites →https://doi.org/10.1016/s1438-4221(02)80015-7openalex-snapshot
Birds and Borrelia
inferredcites →https://doi.org/10.1017/s0031182011000618openalex-snapshot
Differential virulence in two congeneric ticks infesting songbird nestlings
inferredcites →https://doi.org/10.1034/j.1600-0706.2000.880110.xopenalex-snapshot
Trade‐offs in evolutionary immunology: just what is the cost of immunity?
inferredcites →https://doi.org/10.1038/35001663openalex-snapshot
Reactivation of Borrelia infection in birds
inferredcites →https://doi.org/10.1038/362500a0openalex-snapshot
The evolution of virulence
inferredcites →https://doi.org/10.1038/nature12231openalex-snapshot
Vector transmission regulates immune control of Plasmodium virulence
inferredcites →https://doi.org/10.1046/j.1198-743x.2001.00282.xopenalex-snapshot
Routine diagnosis of Borrelia burgdorferi (sensu lato) infections using a real-time PCR assay
inferredcites →https://doi.org/10.1046/j.1365-2656.1998.00215.xopenalex-snapshot
Patterns of natal and breeding dispersal in birds
inferredcites →https://doi.org/10.1086/415837openalex-snapshot
The Population Biology of Parasite-Induced Changes in Host Behavior
inferredcites →https://doi.org/10.1086/592865openalex-snapshot
Seasonal Redistribution of Immune Function in a Migrant Shorebird: Annual‐Cycle Effects Override Adjustments to Thermal Regime
inferredcites →https://doi.org/10.1089/vbz.2009.0215openalex-snapshot
Borrelia burgdorferi Has Minimal Impact on the Lyme Disease Reservoir Host Peromyscus leucopus
inferredcites →https://doi.org/10.1093/oso/9780198548935.003.0004openalex-snapshot
Behavioural defence
inferredcites →https://doi.org/10.1097/00007611-199803000-00001openalex-snapshot
The Erythrocyte Sedimentation Rate: Old and New Clinical Applications
inferredcites →https://doi.org/10.1098/rspb.1998.0358openalex-snapshot
The malaria parasite, Plasmodium falciparum, increases the frequency of multiple feeding of its mosquito vector, Anopheles gambiae
inferredcites →https://doi.org/10.1098/rspb.2001.1592openalex-snapshot
Global warming and body mass decline in Israeli passerine birds
inferredcites →https://doi.org/10.1098/rstb.2008.0184openalex-snapshot
Decomposing health: tolerance and resistance to parasites in animals
inferredcites →https://doi.org/10.1111/1462-2920.12059openalex-snapshot
Transmission dynamics of B orrelia burgdorferi s.l. in a bird tick community
inferredcites →https://doi.org/10.1111/1462-2920.12304openalex-snapshot
Songbirds as general transmitters but selective amplifiers of B orrelia burgdorferi sensu lato genotypes in I xodes rinicus ticks
inferredcites →https://doi.org/10.1111/j.1365-2435.2008.01463.xopenalex-snapshot
Effect of tick parasitism on the health status of a passerine bird
inferredcites →https://doi.org/10.1111/j.1365-2656.2012.01979.xopenalex-snapshot
Exposure of black‐legged kittiwakes to Lyme disease spirochetes: dynamics of the immune status of adult hosts and effects on their survival
inferredcites →https://doi.org/10.1111/j.1469-0691.2006.01509.xopenalex-snapshot
Evaluation of an internally controlled real-time PCR targeting the ospA gene for detection of Borrelia burgdorferi sensu lato DNA in cerebrospinal fluid
inferredcites →https://doi.org/10.1126/science.276.5320.1857openalex-snapshot
Macrophages as a Source of HIV During Opportunistic Infections
inferredcites →https://doi.org/10.1126/science.8503006openalex-snapshot
The Biological and Social Phenomenon of Lyme Disease
inferredcites →https://doi.org/10.1128/aem.01674-08openalex-snapshot
Differential Role of Passerine Birds in Distribution of Borrelia Spirochetes, Based on Data from Ticks Collected from Birds during the Postbreeding Migration Period in Central Europe
inferredcites →https://doi.org/10.1128/aem.02278-10openalex-snapshot
Synanthropic Birds Influence the Distribution of Borrelia Species: Analysis of Ixodes ricinus Ticks Feeding on Passerine Birds
inferredcites →https://doi.org/10.1128/aem.61.8.3082-3087.1995openalex-snapshot
Prevalence of Borrelia burgdorferi sensu lato-infected ticks on migrating birds
inferredcites →https://doi.org/10.1128/iai.62.8.3580-3582.1994openalex-snapshot
Experimental Borrelia garinii infection of Japanese quail
inferredcites →https://doi.org/10.1128/iai.63.10.3886-3895.1995openalex-snapshot
Nitric oxide production during murine Lyme disease: lack of involvement in host resistance or pathology
inferredcites →https://doi.org/10.1128/jcm.37.7.2215-2222.1999openalex-snapshot
Detection and Identification ofEhrlichia,Borrelia burgdorferiSensu Lato, andBartonellaSpecies in DutchIxodes ricinusTicks
inferredcites →https://doi.org/10.1146/annurev.en.41.010196.000245openalex-snapshot
Host Immunity to Ticks
inferredcites →https://doi.org/10.1179/136485905x51319openalex-snapshot
Murine extramedullary erythropoiesis induced by tick infestation
inferredcites →https://doi.org/10.1182/blood.v27.5.654.654openalex-snapshot
Factors Controlling Erythropoiesis in Birds
inferredcites →https://doi.org/10.14411/fp.2006.020openalex-snapshot
Effect of salivary gland extract from Ixodes ricinus ticks on the proliferation of Borrelia burgdorferi sensu stricto in vivo
inferredcites →https://doi.org/10.1647/1082-6742(2006)20[285:cam]2.0.co;2openalex-snapshot
Clinical Avian Medicine GJ Harrison, TL Lightfoot . Clinical Avian Medicine. Spix Publishing, Inc. Palm Beach, FL, USA. 2006. 1008 Price $249. ISBN: 00‐9754994‐0‐8.
inferredcites →https://doi.org/10.1890/02-0643openalex-snapshot
MICE IN SPACE: SPACE USE PREDICTS THE INTERACTION BETWEEN MICE AND SONGBIRDS
inferredcites →https://doi.org/10.2307/3677016openalex-snapshot
Dependence of Postjuvenile Moult on Hatching Date, Condition and Sex in the Great Tit
inferredcites →https://doi.org/10.2307/5390openalex-snapshot
Effect of an Ectoparasite on Reproduction in Great Tits
inferredcites →https://doi.org/10.2307/6007openalex-snapshot
Host-Parasite Evolution: General Principles and Avian Models
inferredcites →https://doi.org/10.3201/eid0602.000205openalex-snapshot
Competence of American Robins as Reservoir Hosts for Lyme Disease Spirochetes
inferredcites →https://doi.org/10.3201/eid1207.060127openalex-snapshot
Migratory Passerine Birds as Reservoirs of Lyme Borreliosis in Europe
inferredcites →https://doi.org/10.4269/ajtmh.1996.54.294openalex-snapshot
Ability of Experimentally Infected Chickens to Infect Ticks with the Lyme Disease Spirochete, Borrelia burgdorferi
inferredcites →https://doi.org/10.5253/078.098.0113openalex-snapshot
Variation in Haematological Indices and Immune Function During the Annual Cycle in the Great TitParus major
inferredcites →https://doi.org/10.5281/zenodo.16438078openalex-snapshot
A Test of the Condition-Bias Hypothesis Yields Different Results for Two Species of Sparrowhawks (Accipiter)
inferredcites →https://doi.org/10.7589/0090-3558-36.2.197openalex-snapshot
PATHOGENICITY OF AVIAN MALARIA IN EXPERIMENTALLY-INFECTED HAWAII AMAKIHI

What points at this work

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

inferred← citeshttps://doi.org/10.12688/openreseurope.13204.1zenodo-depositor-declared
Ineffective humoral anti-tick IgY-response in birds: reaction against pathogen constituents?
inferred← citeshttps://doi.org/10.12688/openreseurope.13204.2zenodo-depositor-declared
Ineffective humoral anti-tick IgY-response in birds: reaction against pathogen constituents?
inferred← citeshttps://doi.org/10.1007/s00436-020-06895-xopenalex-snapshot
Nest-type associated microclimatic conditions as potential drivers of ectoparasite infestations in African penguin nests
inferred← citeshttps://doi.org/10.1016/j.ijpara.2015.11.002openalex-snapshot
The more the merrier – experimental evidence for density-dependent feeding facilitation in the bird-specialised tick Ixodes arboricola
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2018.02.009openalex-snapshot
Experimental infection by microparasites affects the oxidative balance in their avian reservoir host the blackbird Turdus merula
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2026.102613openalex-snapshot
Microbial network stability, not diversity, drives colonization resistance against Borrelia afzelii in Ixodes ricinus ticks
inferred← citeshttps://doi.org/10.1186/s13071-025-06742-xopenalex-snapshot
Determinants of vector-borne avian pathogen occurrence in a mosaic of habitat fragmentation in California
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009801openalex-snapshot
Host tropism determination by convergent evolution of immunological evasion in the Lyme disease system
inferred← citeshttps://doi.org/10.3390/microorganisms11010060openalex-snapshot
The Infection Rate of Bird-Feeding Ixodes ricinus Ticks with Borrelia garinii and B. valaisiana Varies with Host Haemosporidian Infection Status
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