Multiple reciprocal adaptations and rapid genetic change upon experimental coevolution of an animal host and its microbial parasite - Test2 - elhamkhani - TriplyDB

Multiple reciprocal adaptations and rapid genetic change upon experimental coevolution of an animal host and its microbial parasite

Multiple reciprocal adaptations and rapid genetic change upon experimental coevolution of an animal host and its microbial parasite

http://www.wikidata.org/entity/Q24623000

about

Host-Pathogen Coevolution: The Selective Advantage of Bacillus thuringiensis Virulence and Its Cry Toxin Genes Ongoing phenotypic and genomic changes in experimental coevolution of RNA bacteriophage Qβ and Escherichia coli Running with the Red Queen: host-parasite coevolution selects for biparental sex Bacillus cereus Biofilms-Same, Only Different Host behaviour-parasite feedback: an essential link between animal behaviour and disease ecology Understanding the ecology and evolution of host-parasite interactions across scales The native microbiome of the nematode Caenorhabditis elegans: gateway to a new host-microbiome model Natural and experimental infection of Caenorhabditis nematodes by novel viruses related to nodaviruses Running with the Red Queen: the role of biotic conflicts in evolution Rapid and adaptive evolution of MHC genes under parasite selection in experimental vertebrate populations.Bacillus thuringiensis DB27 produces two novel protoxins, Cry21Fa1 and Cry21Ha1, which act synergistically against nematodes.The Natural Biotic Environment of Caenorhabditis elegans.Antagonistic coevolution limits population persistence of a virus in a thermally deteriorating environment.Experimental Evolution with Caenorhabditis Nematodes.Candidate innate immune system gene expression in the ecological model Daphnia.Experimental evolution of defense against a competitive mold confers reduced sensitivity to fungal toxins but no increased resistance in Drosophila larvae.Increased responsiveness in feeding behaviour of Caenorhabditis elegans after experimental coevolution with its microparasite Bacillus thuringiensis Protist-type lysozymes of the nematode Caenorhabditis elegans contribute to resistance against pathogenic Bacillus thuringiensis Complex adaptive responses during antagonistic coevolution between Tribolium castaneum and its natural parasite Nosema whitei revealed by multiple fitness components Antagonistic experimental coevolution with a parasite increases host recombination frequency.Macroevolutionary Immunology: A Role for Immunity in the Diversification of Animal life.Adaptive selection on bracovirus genomes drives the specialization of Cotesia parasitoid wasps Comparison of potato and asian citrus psyllid adult and nymph transcriptomes identified vector transcripts with potential involvement in circulative, propagative liberibacter transmission Host-parasite coevolution favours parasite genetic diversity and horizontal gene transfer.Lotka-Volterra dynamics kills the Red Queen: population size fluctuations and associated stochasticity dramatically change host-parasite coevolution.Rapid evolution of virulence leading to host extinction under host-parasite coevolution.Parting ways: parasite release in nature leads to sex-specific evolution of defence.Contrasting invertebrate immune defense behaviors caused by a single gene, the Caenorhabditis elegans neuropeptide receptor gene npr-1 The Integral Role of Genetic Variation in the Evolution of Outcrossing in the Caenorhabditis elegans-Serratia marcescens Host-Parasite System Ten years of life in compost: temporal and spatial variation of North German Caenorhabditis elegans populations.Evolutionary Transition from Pathogenicity to Commensalism: Global Regulator Mutations Mediate Fitness Gains through Virulence Attenuation.Integrating chytrid fungal parasites into plankton ecology: research gaps and needs.Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host-parasite coevolution.Temporal dynamics of outcrossing and host mortality rates in host-pathogen experimental coevolution.Host resistance influences patterns of experimental viral adaptation and virulence evolution.New role for DCR-1/dicer in Caenorhabditis elegans innate immunity against the highly virulent bacterium Bacillus thuringiensis DB27.Rapid evolution of microbe-mediated protection against pathogens in a worm host A phylogenetic test of the Red Queen Hypothesis: outcrossing and parasitism in the Nematode phylum.Using artificial systems to explore the ecology and evolution of symbioses.Bacterial genome evolution within a clonal population: from in vitro investigations to in vivo observations.

P2860

Q21145699-6B142279-6FDD-477F-849A-2CD54F489332 Q21563384-551C9C85-C09E-4BEE-9AD2-9E6B0D81273F Q24630269-6A5ADF0B-6DD0-4AEB-88EB-B69EE92EAF61 Q26741574-75BD6EC4-E376-42EC-A733-7B46D93916C1 Q26751047-5F89587B-4AF4-4719-ADF6-B067F61A8BA4 Q26752923-9434709C-4818-48D8-BBDC-DA1BF85BDB3F Q27304981-D6B7A7E2-2F73-4393-8067-91F8BD2958F7 Q27322475-FEDF2DF9-E544-425D-B31B-EE77AE833E11 Q28651598-D537A01F-616E-4701-B1AC-6A27C20CC458 Q33352821-5DC4ACFA-7332-465C-8A4A-DB6504AD7254 Q33602027-348AB91D-587F-4ED9-8D35-A7A95850F343 Q33642808-55E6AADA-9BDC-4BB9-BC9E-14277956682A Q33803343-4C2FE5D6-8CD5-48E9-8F2E-7FC3F2CD848C Q33877473-25FC7D01-1F61-48CE-9262-02159CA7BDD5 Q33891979-EC47CA35-12E8-46B5-844B-79FAF548A750 Q33960728-3C1A2229-6495-421C-8536-6A2820C8F8EB Q34006703-409533D5-D24E-432F-9C4F-2CC998B2889A Q34023766-C1E55F01-80A6-4A19-A6AB-734B13637C35 Q34142124-CD968431-DC1A-4C66-93D3-182C4C1B902B Q34157895-40E5A9D3-FFC2-44CC-B488-1F175E412D0F Q34261452-79F69928-4669-4F20-92F8-3E775DD25909 Q34749578-F97C0E66-5DB0-47D2-A3EE-15D58B507AD2 Q34809699-A7CAD3AA-87CC-4CB9-A0A4-F93A37954E18 Q34833346-D088F19E-4837-4D41-BFD2-3EA3EB0CF5B8 Q35046833-6D36C1AA-D3A1-483F-8A16-26A6F5E8587C Q35662538-7BD171C3-2DC6-429C-BD29-A9F08DC35E5E Q35769305-2DA628A9-D819-4E14-8A4E-06B6D8DF2829 Q35986214-4C617F99-A73D-4245-A4F1-0C8DB87175A1 Q36000559-F385714E-6282-4E46-9453-C52D02FFBAF1 Q36057856-75B32454-EDEA-4DCF-8D75-D736E67FC8EA Q36295376-686EEE34-5CB9-45C7-8C11-C2EA5DECE1B6 Q36406490-C0E641BA-1A1A-47F1-8A1F-AF75070C5047 Q36848646-B1CFE09C-7A57-438A-AF6E-61D53CF2A3A6 Q36990499-818DBE37-C244-4979-8833-EC81BEB8146F Q37021498-77DB34A1-2FB6-42BF-A247-41AF0FCFC11D Q37264602-A98A98C0-BB85-4122-A522-0CA3CDF82BA1 Q37268119-3D8DECBF-DD04-4344-B7E6-6EA2E2315E83 Q37662450-E4D74B52-9A5A-4891-BC6E-A0DE9842F097 Q37855695-5432604A-C028-4588-84CE-60E99C6CBB93 Q38103942-A572ECB8-66F9-4D0A-AD21-2400421B2A0B

P2860

Multiple reciprocal adaptations and rapid genetic change upon experimental coevolution of an animal host and its microbial parasite

http://www.wikidata.org/entity/Q24623000

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Multiple reciprocal adaptation ...... ost and its microbial parasite

@ast

Multiple reciprocal adaptation ...... ost and its microbial parasite

@en

Multiple reciprocal adaptation ...... ost and its microbial parasite

@nl

type

label

Multiple reciprocal adaptation ...... ost and its microbial parasite

@ast

Multiple reciprocal adaptation ...... ost and its microbial parasite

@en

Multiple reciprocal adaptation ...... ost and its microbial parasite

@nl

prefLabel

Multiple reciprocal adaptation ...... ost and its microbial parasite

@ast

Multiple reciprocal adaptation ...... ost and its microbial parasite

@en

Multiple reciprocal adaptation ...... ost and its microbial parasite

@nl

P1433

Q24623000-C56CFC2D-D621-4A8E-AFE9-A06E2D638C39

P1476

Q24623000-799F84F4-C924-46AA-83C2-24BB50CE9FD6

P2093

Q24623000-11E30AA7-C52D-45D5-89DA-787A2B79CFCE

Q24623000-454F4EE3-6DE3-473B-B1AF-546ED526DEFC

Q24623000-4BB73737-E8AC-4A5B-B154-34F06C28B436

Q24623000-596B9BA2-56A0-489B-8088-BA7C3E9A9102

Q24623000-F4882042-13C9-4BAB-8AF9-D579342CDAD4

P2860

Q24623000-017E5E35-716E-4CA0-9C0D-0E2BD0BBF905

Q24623000-09A7FC60-D53F-4ED1-84D4-B77103153DCE

Q24623000-0E058D6C-80A6-4072-8BA1-6397310A7556

Q24623000-10C754E4-E552-493E-8AC8-0774E729CEF5

Q24623000-1B396335-1589-4215-A103-F72114D0DEF4

Q24623000-1CA2E251-35D7-4463-AFE6-AD0771575241

Q24623000-1CC20ED8-6D1B-4F2C-855D-FC3F8A958B17

Q24623000-1F8C560A-2DB6-4892-8D03-EA8951D839A4

Q24623000-25A1E00F-EDDF-45DF-8193-D968450B4C85

Q24623000-2B81C1EE-FB86-421C-9738-B9AE39631625

P304

Q24623000-2262A7EE-A92E-4D8F-9994-7B58448FEAC7

P31

Q24623000-10672D32-BAFB-490F-92DB-1596CDA2CB80

P3181

Q24623000-4DA3F440-A2F5-4118-9FA9-FAB62BB13050

P356

Q24623000-60F11E8F-7D4E-48D1-B318-ECB8E6AE3832

P407

Q24623000-B0FD86DA-09FF-41CA-9028-8AA74047486E

P433

Q24623000-61FC936E-C468-4E10-8217-09D649439DC8

P478

Q24623000-920876F5-88DA-4651-8DF4-774409AC76D0

P577

Q24623000-6C34EEB7-4043-41B9-84B0-EAA2A799009F

P5875

Q24623000-85E485B6-CD74-4383-9405-DE88172361F9

P698

Q24623000-69DF3887-D295-4CCA-B622-2155E4482D49

P921

Q24623000-C49CDD7D-16F2-4A14-9EAD-0CD47BAC5F18

P932

Q24623000-9E8B49C4-9EF7-47B5-B8A8-94779CB1F71C

P3181

P356

PNAS.1003113107

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Multiple reciprocal adaptation ...... ost and its microbial parasite

@en

P2093

Barbara Hasert

http://www.w3.org/2001/XMLSchema#string

Carsten Makus

http://www.w3.org/2001/XMLSchema#string

Hinrich Schulenburg

http://www.w3.org/2001/XMLSchema#string

Nico K Michiels

http://www.w3.org/2001/XMLSchema#string

Rebecca D Schulte

http://www.w3.org/2001/XMLSchema#string

P2860

Antagonistic coevolution between a bacterium and a bacteriophage

Is host-schistosome coevolution going anywhere?

The Maintenance of Sex, Clonal Dynamics, and Host‐Parasite Coevolution in a Mixed Population of Sexual and Asexual Snails

Host-parasite 'Red Queen' dynamics archived in pond sediment.

Role of coevolution in generating biological diversity: spatially divergent selection trajectories.

Hypoxia and the hypoxic response pathway protect against pore-forming toxins in C. elegans.

Natural variation and copulatory plug formation in Caenorhabditis elegans.

Biological and biomedical implications of the co-evolution of pathogens and their hosts.

The role of parasites in sympatric and allopatric host diversification.

Mutation load and rapid adaptation favour outcrossing over self-fertilization.

P304

7359-64

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

1779702

http://www.w3.org/2001/XMLSchema#string

P356

10.1073/PNAS.1003113107

http://www.w3.org/2001/XMLSchema#string

P407

P433

16

http://www.w3.org/2001/XMLSchema#string

P478

107

http://www.w3.org/2001/XMLSchema#string

P577

2010-04-20T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

43023416

http://www.w3.org/2001/XMLSchema#string

P698

20368449

http://www.w3.org/2001/XMLSchema#string

P921

P932

2867683

http://www.w3.org/2001/XMLSchema#string