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Molecular mechanisms of thermal resistance of the insect trypanosomatid Crithidia thermophila

Bibliographic reference Ishemgulova, Aygul ; Butenko, Anzhelika ; Kortišová, Lucie ; Boucinha, Carolina ; Grybchuk-Ieremenko, Anastasiia ; et. al. Molecular mechanisms of thermal resistance of the insect trypanosomatid Crithidia thermophila. In: PLoS One, Vol. 12, no.3, p. e0174165 (2017)
Permanent URL http://hdl.handle.net/2078.1/186302
  1. K Vickerman, 35 (1976)
  2. RB McGhee, Microbiol Rev, 44, 140 (1980)
  3. Yurchenko V. Yu., Kolesnikov A. A., 10.1023/a:1004813414607
  4. Vickerman Keith, The evolutionary expansion of the trypanosomatid flagellates, 10.1016/0020-7519(94)90198-8
  5. Rodrigues Juliany Cola Fernandes, Godinho Joseane Lima Prado, de Souza Wanderley, Biology of Human Pathogenic Trypanosomatids: Epidemiology, Lifecycle and Ultrastructure, Subcellular Biochemistry (2014) ISBN:9789400773042 p.1-42, 10.1007/978-94-007-7305-9_1
  6. Ready Paul, Epidemiology of visceral leishmaniasis, 10.2147/clep.s44267
  7. Podlipaev Sergei, The more insect trypanosomatids under study-the more diverse Trypanosomatidae appears, 10.1016/s0020-7519(01)00139-4
  8. Maslov Dmitri A., Votýpka Jan, Yurchenko Vyacheslav, Lukeš Julius, Diversity and phylogeny of insect trypanosomatids: all that is hidden shall be revealed, 10.1016/j.pt.2012.11.001
  9. Lukeš Julius, Skalický Tomáš, Týč Jiří, Votýpka Jan, Yurchenko Vyacheslav, Evolution of parasitism in kinetoplastid flagellates, 10.1016/j.molbiopara.2014.05.007
  10. Hamilton Phineas T., Votýpka Jan, Dostálová Anna, Yurchenko Vyacheslav, Bird Nathan H., Lukeš Julius, Lemaitre Bruno, Perlman Steve J., Infection Dynamics and Immune Response in a Newly DescribedDrosophila-Trypanosomatid Association, 10.1128/mbio.01356-15
  11. Kozminsky Eugene, Kraeva Natalya, Ishemgulova Aygul, Dobáková Eva, Lukeš Julius, Kment Petr, Yurchenko Vyacheslav, Votýpka Jan, Maslov Dmitri A., Host-specificity of Monoxenous Trypanosomatids: Statistical Analysis of the Distribution and Transmission Patterns of the Parasites from Neotropical Heteroptera, 10.1016/j.protis.2015.08.004
  12. Votýpka Jan, Klepetková Helena, Yurchenko Vyacheslav Y., Horák Aleš, Lukeš Julius, Maslov Dmitri A., Cosmopolitan Distribution of a Trypanosomatid Leptomonas pyrrhocoris, 10.1016/j.protis.2011.12.004
  13. Kraeva Natalya, Butenko Anzhelika, Hlaváčová Jana, Kostygov Alexei, Myškova Jitka, Grybchuk Danyil, Leštinová Tereza, Votýpka Jan, Volf Petr, Opperdoes Fred, Flegontov Pavel, Lukeš Julius, Yurchenko Vyacheslav, Leptomonas seymouri: Adaptations to the Dixenous Life Cycle Analyzed by Genome Sequencing, Transcriptome Profiling and Co-infection with Leishmania donovani, 10.1371/journal.ppat.1005127
  14. Pacheco Raquel S, Marzochi Mauro CA, Pires Marize Q, Brito Célia MM, Madeira Maria de Fátima, Barbosa-Santos Elizabeth GO, Parasite Genotypically Related to a Monoxenous Trypanosomatid of Dog's Flea Causing Opportunistic Infection in an HIV Positive Patient, 10.1590/s0074-02761998000400021
  15. Chicharro C., Alvar J., Lower trypanosomatids in HIV/AIDS patients, 10.1179/000349803225002552
  16. Wallace Franklin G., The trypanosomatid parasites of insects and arachnids, 10.1016/0014-4894(66)90015-4
  17. Votýpka Jan, d’Avila-Levy Claudia M., Grellier Philippe, Maslov Dmitri A., Lukeš Julius, Yurchenko Vyacheslav, New Approaches to Systematics of Trypanosomatidae: Criteria for Taxonomic (Re)description, 10.1016/j.pt.2015.06.015
  18. Yurchenko V. Y., Lukes J., Jirku M., Maslov D. A., Selective recovery of the cultivation-prone components from mixed trypanosomatid infections: a case of several novel species isolated from Neotropical Heteroptera, 10.1099/ijs.0.001149-0
  19. Teixeira Marta M.G., Borghesan Tarcilla C., Ferreira Robson C., Santos Marcia A., Takata Carmen S.A., Campaner Marta, Nunes Vania L.B., Milder Regina V., de Souza Wanderley, Camargo Erney P., Phylogenetic Validation of the Genera Angomonas and Strigomonas of Trypanosomatids Harboring Bacterial Endosymbionts with the Description of New Species of Trypanosomatids and of Proteobacterial Symbionts, 10.1016/j.protis.2011.01.001
  20. Jirků Milan, Yurchenko Vyacheslav Y., Lukeš Julius, Maslov Dmitri A., New Species of Insect Trypanosomatids from Costa Rica and the Proposal for a New Subfamily within the Trypanosomatidae, 10.1111/j.1550-7408.2012.00636.x
  21. Frolov Alexander O., Malysheva Marina N., Yurchenko Vyacheslav, Kostygov Alexei Yu., Back to monoxeny: Phytomonas nordicus descended from dixenous plant parasites, 10.1016/j.ejop.2015.08.002
  22. d’Avila-Levy Claudia Masini, Boucinha Carolina, Kostygov Alexei, Santos Helena Lúcia Carneiro, Morelli Karina Alessandra, Grybchuk-Ieremenko Anastasiia, Duval Linda, Votýpka Jan, Yurchenko Vyacheslav, Grellier Philippe, Lukeš Julius, Exploring the environmental diversity of kinetoplastid flagellates in the high-throughput DNA sequencing era, 10.1590/0074-02760150253
  23. Votýpka Jan, Kostygov Alexei Yu, Kraeva Natalya, Grybchuk-Ieremenko Anastasiia, Tesařová Martina, Grybchuk Danyil, Lukeš Julius, Yurchenko Vyacheslav, Kentomonas gen. n., a New Genus of Endosymbiont-containing Trypanosomatids of Strigomonadinae subfam. n., 10.1016/j.protis.2014.09.002
  24. Du Y., Maslov D. A., Chang K. P., Monophyletic origin of beta-division proteobacterial endosymbionts and their coevolution with insect trypanosomatid protozoa Blastocrithidia culicis and Crithidia spp., 10.1073/pnas.91.18.8437
  25. de Souza W, Endosymbiosis in protozoa of the Trypanosomatidae family, 10.1016/s0378-1097(99)00005-1
  26. FREYMULLER EDNA, CAMARGO E. PLESSMANN, Ultrastructural Differences Between Species of Trypanosomatids With and Without Endosymbionts1, 10.1111/j.1550-7408.1981.tb02829.x
  27. Hollar Laura, Lukeš Julius, Maslov Dmitri A., Monophyly of Endosymbiont Containing Trypanosomatids: Phylogeny versus Taxonomy, 10.1111/j.1550-7408.1998.tb04539.x
  28. Kostygov Alexei Yu., Grybchuk-Ieremenko Anastasiia, Malysheva Marina N., Frolov Alexander O., Yurchenko Vyacheslav, Molecular revision of the genus Wallaceina, 10.1016/j.protis.2014.07.001
  29. Gerasimov Evgeny S., Kostygov Alexei Yu., Yan Shi, Kolesnikov Alexander A., From cryptogene to gene? ND8 editing domain reduction in insect trypanosomatids, 10.1016/j.ejop.2011.09.002
  30. V Yurchenko, Folia Parasitol, 61, 97 (2014)
  31. L Léger, Comp R Séances Soc Biol Ses Fil, 54, 354 (1902)
  32. Laird Marshall, BLASTOCRITHIDIA N.G. (MASTIGOPHORA: PROTOMONADINA) FOR CRITHIDIA (IN PART), WITH A SUBARCTIC RECORD FOR B. GERRIDIS (PATTON), 10.1139/z59-075
  33. Yurchenko Vyacheslav Y., Lukeš Julius, Tesařová Martina, Jirků Milan, Maslov Dmitri A., Morphological Discordance of the New Trypanosomatid Species Phylogenetically Associated with the Genus Crithidia, 10.1016/j.protis.2007.07.003
  34. MERZLYAK EKATERINA, YURCHENKO VYACHESLAV, KOLESNIKOV ALEXANDER A., ALEXANDROV KIRILL, PODLIPAEV SERGEI A., MASLOV DMITRI A., Diversity and Phylogeny of Insect Trypanosomatids Based on Small Subunit rRNA Genes: Polyphyly of Leptomonas and Blastocrithidia, 10.1111/j.1550-7408.2001.tb00298.x
  35. DE SÁ MARIA F. G., DE SÁ CEZAR M., VERONESE MARCO A., FILHO SPARTACO ASTOLFI, GANDER EUGEN S., Morphologic and Biochemical Characterization ofCrithidia BrasiliensisSp. N.* : Crithidia brasiliensis SP.N., 10.1111/j.1550-7408.1980.tb04248.x
  36. McGhee R. B., The Infection of Avian Embryos with Crithidia Species and Leishmania Tarentola, 10.1093/infdis/105.1.18
  37. ROITMAN CELINA, ROITMAN ISAAC, de AZEVEDO HELIO PEIXOTO, Growth of an Insect Trypanosomatid at 37 C in a Defined Medium*, 10.1111/j.1550-7408.1972.tb03473.x
  38. ROITMAN ISAAC, MUNDIM MARIA HERMELINDA, AZEVEDO HELIO PEIXOTO DE, KITAJIMA ELLIOT W., Growth ofCrithidiaat High Temperature:Crithidia hutnerisp. n. andCrithidia luciliae thermophilas. sp. n.*, 10.1111/j.1550-7408.1977.tb01013.x
  39. FG Wallace, J Eukaryot Microbiol, 30, 308 (1983)
  40. d’Avila-Levy Claudia M., Yurchenko Vyacheslav, Votýpka Jan, Grellier Philippe, Protist Collections: Essential for Future Research, 10.1016/j.pt.2016.08.001
  41. Yurchenko Vyacheslav, Kostygov Alexei, Havlová Jolana, Grybchuk-Ieremenko Anastasiia, Ševčíková Tereza, Lukeš Julius, Ševčík Jan, Votýpka Jan, Diversity of Trypanosomatids in Cockroaches and the Description ofHerpetomonas tarakanasp. n., 10.1111/jeu.12268
  42. YURCHENKO VYACHESLAV, LUKES JULIUS, XU XING, MASLOV DMITRI A., An Integrated Morphological and Molecular Approach to a New Species Description in the Trypanosomatidae: the Case of Leptomonas podlipaevi n. sp., a Parasite of Boisea rubrolineata (Hemiptera: Rhopalidae), 10.1111/j.1550-7408.2005.00078.x
  43. Maslov Dmitri A., Lukeš Julius, Jirku Milan, Simpson Larry, Phylogeny of trypanosomes as inferred from the small and large subunit rRNAs: implications for the evolution of parasitism in the trypanosomatid protozoa, 10.1016/0166-6851(95)02526-x
  44. WESTENBERGER S. J., STURM N. R., YANEGA D., PODLIPAEV S. A., ZELEDÓN R., CAMPBELL D. A., MASLOV D. A., Trypanosomatid biodiversity in Costa Rica: genotyping of parasites from Heteroptera using the spliced leader RNA gene, 10.1017/s003118200400592x
  45. Hamilton Patrick B., Stevens Jamie R., Gaunt Michael W., Gidley Jennifer, Gibson Wendy C., Trypanosomes are monophyletic: evidence from genes for glyceraldehyde phosphate dehydrogenase and small subunit ribosomal RNA, 10.1016/j.ijpara.2004.08.011
  46. TA Hall, Nucl Acids Symp Ser, 41, 95 (1999)
  47. Jobb G (2011) TREEFINDER. March 2011 ed. Munich, Germany.
  48. Ronquist Fredrik, Teslenko Maxim, van der Mark Paul, Ayres Daniel L., Darling Aaron, Höhna Sebastian, Larget Bret, Liu Liang, Suchard Marc A., Huelsenbeck John P., MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space, 10.1093/sysbio/sys029
  49. Bolger Anthony M., Lohse Marc, Usadel Bjoern, Trimmomatic: a flexible trimmer for Illumina sequence data, 10.1093/bioinformatics/btu170
  50. Grabherr Manfred G, Haas Brian J, Yassour Moran, Levin Joshua Z, Thompson Dawn A, Amit Ido, Adiconis Xian, Fan Lin, Raychowdhury Raktima, Zeng Qiandong, Chen Zehua, Mauceli Evan, Hacohen Nir, Gnirke Andreas, Rhind Nicholas, di Palma Federica, Birren Bruce W, Nusbaum Chad, Lindblad-Toh Kerstin, Friedman Nir, Regev Aviv, Full-length transcriptome assembly from RNA-Seq data without a reference genome, 10.1038/nbt.1883
  51. Robinson M. D., Smyth G. K., Small-sample estimation of negative binomial dispersion, with applications to SAGE data, 10.1093/biostatistics/kxm030
  52. Emms David M., Kelly Steven, OrthoFinder: solving fundamental biases in whole genome comparisons dramatically improves orthogroup inference accuracy, 10.1186/s13059-015-0721-2
  53. Aslett Martin, Aurrecoechea Cristina, Berriman Matthew, Brestelli John, Brunk Brian P., Carrington Mark, Depledge Daniel P., Fischer Steve, Gajria Bindu, Gao Xin, Gardner Malcolm J., Gingle Alan, Grant Greg, Harb Omar S., Heiges Mark, Hertz-Fowler Christiane, Houston Robin, Innamorato Frank, Iodice John, Kissinger Jessica C., Kraemer Eileen, Li Wei, Logan Flora J., Miller John A., Mitra Siddhartha, Myler Peter J., Nayak Vishal, Pennington Cary, Phan Isabelle, Pinney Deborah F., Ramasamy Gowthaman, Rogers Matthew B., Roos David S., Ross Chris, Sivam Dhileep, Smith Deborah F., Srinivasamoorthy Ganesh, Stoeckert Christian J., Subramanian Sandhya, Thibodeau Ryan, Tivey Adrian, Treatman Charles, Velarde Giles, Wang Haiming, TriTrypDB: a functional genomic resource for the Trypanosomatidae, 10.1093/nar/gkp851
  54. CLARK C. GRAHAM, Riboprinting: A Tool for the Study of Genetic Diversity in Microorganisms, 10.1111/j.1550-7408.1997.tb05667.x
  55. WALLACE F. G., CLARK TRUMAN B., Flagellate Parasites of the Fly,Phaenicia sericata(Meigen)*, 10.1111/j.1550-7408.1959.tb03927.x
  56. Strickland C., Description of a Herpetomonas parasitic in the alimentary tract of the common green-bottle fly, Lucilia sp, 10.1017/s0031182000002705
  57. Lahav T., Sivam D., Volpin H., Ronen M., Tsigankov P., Green A., Holland N., Kuzyk M., Borchers C., Zilberstein D., Myler P. J., Multiple levels of gene regulation mediate differentiation of the intracellular pathogen Leishmania, 10.1096/fj.10-157529
  58. Balogh Gábor, Péter Mária, Glatz Attila, Gombos Imre, Török Zsolt, Horváth Ibolya, Harwood John L., Vígh László, Key role of lipids in heat stress management, 10.1016/j.febslet.2013.05.016
  59. Opperdoes Fred R., Butenko Anzhelika, Flegontov Pavel, Yurchenko Vyacheslav, Lukeš Julius, Comparative Metabolism of Free-livingBodo saltansand Parasitic Trypanosomatids, 10.1111/jeu.12315
  60. Verner Zdeněk, Čermáková Petra, Škodová Ingrid, Kováčová Bianka, Lukeš Julius, Horváth Anton, Comparative analysis of respiratory chain and oxidative phosphorylation in Leishmania tarentolae, Crithidia fasciculata, Phytomonas serpens and procyclic stage of Trypanosoma brucei, 10.1016/j.molbiopara.2014.02.003
  61. Škodová-Sveráková Ingrid, Verner Zdeněk, Skalický Tomáš, Votýpka Jan, Horváth Anton, Lukeš Julius, Lineage-specific activities of a multipotent mitochondrion of trypanosomatid flagellates : Multipotent mitochondrion of trypanosomatid flagellates, 10.1111/mmi.12920
  62. Lacomble Sylvain, Portman Neil, Gull Keith, A Protein-Protein Interaction Map of the Trypanosoma brucei Paraflagellar Rod, 10.1371/journal.pone.0007685
  63. Hughes Louise C., Ralston Katherine S., Hill Kent L., Zhou Z. Hong, Three-Dimensional Structure of the Trypanosome Flagellum Suggests that the Paraflagellar Rod Functions as a Biomechanical Spring, 10.1371/journal.pone.0025700
  64. Portman Neil, Gull Keith, The paraflagellar rod of kinetoplastid parasites: From structure to components and function, 10.1016/j.ijpara.2009.10.005
  65. Docampo Roberto, Moreno Silvia N.J., Plattner Helmut, Intracellular calcium channels in protozoa, 10.1016/j.ejphar.2013.11.015
  66. Voos Wolfgang, Röttgers Karin, Molecular chaperones as essential mediators of mitochondrial biogenesis, 10.1016/s0167-4889(02)00264-1
  67. Dutkiewicz Rafal, Schilke Brenda, Knieszner Helena, Walter William, Craig Elizabeth A., Marszalek Jaroslaw, Ssq1, a Mitochondrial Hsp70 Involved in Iron-Sulfur (Fe/S) Center Biogenesis : SIMILARITIES TO AND DIFFERENCES FROM ITS BACTERIAL COUNTERPART, 10.1074/jbc.m303527200
  68. Liu Q., Regulated Cycling of Mitochondrial Hsp70 at the Protein Import Channel, 10.1126/science.1083379
  69. Tschopp Florence, Charrière Fabien, Schneider André, In vivo study in Trypanosoma brucei links mitochondrial transfer RNA import to mitochondrial protein import, 10.1038/embor.2011.111
  70. J Týč, MBio, 6 (2015)
  71. Krauth-Siegel R. Luise, Comini Marcelo A., Redox control in trypanosomatids, parasitic protozoa with trypanothione-based thiol metabolism, 10.1016/j.bbagen.2008.03.006
  72. Vickers Tim J., Fairlamb Alan H., TrypanothioneS-Transferase Activity in a Trypanosomatid Ribosomal Elongation Factor 1B, 10.1074/jbc.m311039200
  73. Fairlamb A., Blackburn P, Ulrich P, Chait B., Cerami A, Trypanothione: a novel bis(glutathionyl)spermidine cofactor for glutathione reductase in trypanosomatids, 10.1126/science.3883489
  74. Tomás Ana M., Castro Helena, Redox Metabolism in Mitochondria of Trypanosomatids, 10.1089/ars.2012.4948
  75. N Kraeva, Infect Genet Evol (2017)