1. Зиновьева С.В., Чижов В.Н., Приданников М.В., Субботин С.А., Рысс А.Ю., Хусаинов Р.В. Фитопаразитические нематоды России. Изд-во: Товарищество научных изданий КМК, 2012;374.
2. Кочетов А.В., Сырник О.А., Рогозин И.Б., Глазко Г.В., Комарова М.Л., Шумный В.К. Контекстная организация 5’-нетранслируемых районов генов высших растений. Молекулярная биология. 2002;36(4):649-656.
3. Кочетов А.В., Титов С.Е., Колодяжная Я.С., Комарова М.Л., Коваль В.С., Макарова Н.Н., Илинский Ю.Ю., Трифонова Е.А., Шумный В.К. Повышение содержания пролина и осмотического давления клеточного сока у трансформантов табака, несущих антисмысловой супрессор гена пролиндегидрогеназы. Генетика. 2004;40(2):282-285.
4. Справочник по карантинному фитосанитарному состоянию территорий государств - участников СНГ на 01.01.2017 г. М.: ФГБУ «ВНИИКР», 2017;106.
5. Amin R.B., Karegar A., Afsharifar A., Niazi A., Karimi M. Disruption of the pathogenicity and sex ratio of the beet cyst nematode Heterodera schachtii by host-delivered RNA interference. Mol. Plant. Microbe Interact. 2018;31(12):1337-1346. https://doi.org/10.1094/MPMI-0518-0141-R.
6. Bakker E., Achenbach U., Bakker J., van Vliet J., Peleman J., Segers B., van der Heijden S., van der Linde P., Graveland R., Hutten R., van Eck H., Coppoolse E., An der Vossen E., Bakker J., Goverse A. A high-resolution map of the H1 locus harboring resistance to the potato cyst nematode Globodera rostochiensis. Theor. Appl. Genet. 2004;109:146-152. https://doi.org/10.1007/s00122-004-1606-z.
7. Bali S., Vining K., Gleason C., Majtahedi H., Brown C.R., Sathuvalli V. Transcriptome profiling of resistance response to Meloidogyne chitwoodi introgressed from wild species Solanum bulbocastanum into cultivated potato. BMC Genomics. 2019;20(1):907. https://doi.org/10.1186/s12864-019-6257-1.
8. Ballvora A., Hesselbach J., Niewöhner J., Leiste D., Salamini F., Gebhardt C. Marker enrichment and high-resolution map of the segment of potato chromosome VII harbouring the nematode resistance gene Gro1. Mol. Gen. Genet. 1995;249:82-90.
9. Banerjee S., Gill S.S., Gawade B.H., Jain P.K., Subramaniam K., Sirohi A. Host Delivered RNAi of Two Cuticle Collagen Genes, Mi-col-1 and Lemmi-5 Hampers Structure and Fecundity in Meloidogyne incognita. Front. Plant Sci. 2018;8:2266. https://doi.org/10.3389/fpls.2017.02266.
10. Barone A., Ritter E., Schachtschabel U., Debener T., Salamini F., Gebhardt C. Localization by restriction fragment length polymorphism mapping in potato of a major dominant gene conferring resistance to the potato cyst nematode Globodera rostochiensis. Mol. Gen. Genet. 1990;224:177-182.
11. Bayless A.M., Zapotocny R.W., Grunwald D.J., Amundson K.K., Diers B.W., Bent A.F. An atypical N-ethylmaleimide sensitive factor enables the viability of nematode-resistant Rhg1 soybeans. Proc. Natl. Acad. Sci USA. 2018;115(19):E4512-E4521.
12. Bournaud C., Gillet F.-X., Murad A.M., Bresso E., Albuquerque E.V.S., Grossi-de-Sá M.F. Meloidogyne incognita PASSE-MURAILLE (MiPM ) gene encodes a cell-penetrating protein that interacts with the CSN5 subunit of the COP9 signalosome. Front. Plant Sci. 2018; 9:904. https://doi.org/10.3389/fpls.2018.00904.
13. Butler K.J., Chen S., Smith J.M., Wang X., Bent A.F. Soybean Resistance Locus Rhg1 Confers Resistance to Multiple Cyst Nematodes in Diverse Plant Species. Phytopathology. 2019;109(12):2107-2115. https://doi.org/10.1094/PHYTO-07-19-0225-R.
14. Chaudhary S., Dutta T.K., Tyagi N., Shivakumara T.N., Papolu P.K., Chobhe K.A., Rao U. Host-induced silencing of Mi-msp-1 confers resistance to root-knot nematode Meloidogyne incognita in eggplant. Transgenic. Res. 2019;28(3-4):327-340. https://doi.org/10.1007/s11248-01900126-5.
15. Dalamu B.V., Umamaheshwari R., Shrama R., Kaushik S.K., Joseph T.A., Singh B.P., Gebhardt C. Potato cyst nematode (PCN) resistance: genes, genotypes and markers - an update. SABRAO J. Breed. Genet. 2012;44:202-228.
16. Dandurand L.M., Zasada I.A., LaMondia J.A. Effect of the trap crop, Solanum sisymbriifolium, on Globodera pallida, Globodera tabacum, and Globodera ellingtonae. J. Nematol. 2019;51:1-11. https://doi.org/10.21307/jofnem-2019-030.
17. Dutta T.K., Papolu P.K., Banakar P., Choudhary D., Sirohi A., Rao U. Tomato transgenic plants expressing hairpin construct of a nematode protease gene conferred enhanced resistance to root-knot nematodes. Front. Microbiol. 2015;6:260. https://doi.org/10.3389/fmicb.2015.00260.
18. Evans K., Trudgill D.L. Pest aspects of potato production. Part 1. The nematode pests of potatoes. In: Harris P. (Ed.). The potato crop. London: Chapman & Hall, 1992.
19. Friedman W. Pests not known to occur in the United States or of limited distribution, No. 68: Golden Nematode. United States Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine, 1985;10.
20. Gheysen G., Mitchum M.G. Phytoparasitic nematode control of plant hormone pathways. Plant Physiol. 2019;179:1212-1226. https://doi.org/10.1104/pp.18.01067.
21. Hewezi T., Juvale P.S., Piya S., Maier T.R., Rambani A., Rice J.H., Mitchum M.G., Davis E.L., Hussey R.S., Baum T.J. The cyst nematode effector protein 10A07 targets and recruits host posttranslational machinery to mediate its nuclear trafficking and to promote parasitism in Arabidopsis. Plant Cell. 2015;27:891-907. https://doi.org/10.1105/tpc.114.135327.
22. Hu Y., You J., Li C., Pan F., Wang C. The Heterodera glycines effector Hg16B09 is required for nematode parasitism and suppresses plant defense response. Plant Sci. 2019;289:110271. https://doi.org/10.1016/j.plantsci.2019.110271.
23. Iqbal S., Fosu-Nyarko J., Jones M.G.K. Attempt to silence genes of the RNAi pathways of the root-knot nematode, Meloidogyne incognita results in diverse responses including increase and no change in expression of some genes. Front. Plant Sci. 2020;11:328. https://doi.org/10.3389/fpls.2020.00328.
24. Jones L.M., Koehler A.K., Trnka M., Balek J., Challinor A.J., Atkinson H.J., Urwin P.E. Climate change is predicted to alter the current pest status of Globodera pallida and G. rostochiensis in the United Kingdom. Glob. Chang Biol. 2017;23(11):4497-4507. https://doi.org/10.1111/gcb.13676.
25. Joshi I., Kumar A., Singh A.K., Kohli D., Raman K.V., Sirohi A., Chaudhury A., Jain P.K. Development of nematode resistance in Arabidopsis by HD-RNAi-mediated silencing of the effector gene Mi-msp2. Sci. Rep. 2019;9(1):17404. https://doi.org/10.1038/s41598-01953485-8.
26. Kaloshian I., Desmond O.J., Atamian H.S. Disease resistance-genes and defense responses during incompatible interactions. In: Jones J., Gheysen G., Fenoll C. (Eds.). Genomics and molecular genetics of plant-nematode interactions. New York: Springer, 2011;309-324.
27. Kearn J., Lilley C., Urwin P., O’Connor V., Holden-Dye L. Progressive metabolic impairment underlies the novel nematicidal action of fluensulfone on the potato cyst nematode Globodera pallida. Pestic. Biochem. Physiol. 2017;142:83-90. https://doi.org/10.1016/j.pestbp.2017.01.009.
28. Kochetov A.V., Egorova A.A., Glagoleva A.Y., Strygina K.V., Khlestkina E.K., Gerasimova S.V., Shatskaya N.V., Vasilyev G.V., Afonnikov D.A., Shmakov N.A., Antonova O.Y., Alpatyeva N.V., Khiutti A., Afanasenko O.S., Gavrilenko T.A. The mechanism of potato resistance to Globodera rostochiensis: comparison of root transcriptomes of resistant and susceptible Solanum phureja genotypes. BMC Plant Biol. 2020;20(Suppl 1):350. https://doi.org/10.1186/s12870-02002334-2.
29. Kochetov A.V., Glagoleva A.Y., Strygina K.V., Khlestkina E.K., Gerasimova S.V., Ibragimova S.M., Shatskaya N.V., Vasilyev G.V., Afonnikov D.A., Shmakov N.A., Antonova O.Y., Gavrilenko T.A., Alpatyeva N.V., Khiutti A., Afanasenko O.S. Differential expression of NBS-LRR-encoding genes in the root transcriptomes of two Solanum phureja genotypes with contrasting resistance to Globodera rostochiensis. BMC Plant Biol. 2017;17(Suppl 2):251. https://doi.org/10.1186/s12870-017-1193-1.
30. Kochetov A.V., Sarai A. Translational polymorphism as a potential source of plant proteins variety in Arabidopsis thaliana. Bioinformatics. 2004;20:445-447.
31. Kooliyottil R., Dandurand L.-M., Kuhl J.C., Caplan A., Xiao F., Mimee B., Lafond-Lapalme J. Transcriptome analysis of Globodera pallida from the susceptible host Solanum tuberosum or the resistant plant Solanum sisymbriifolium. Sci. Rep. 2019;9(1):13256. https://doi.org/10.1038/s41598-019-49725-6.
32. Kud J., Wang W., Gross R., Fan Y., Huang L., Yuan Y., Gray A., Duarte A., Kuhl J.C., Caplan A., Goverse A., Liu Y., Dandurand L.M., Xiao F. The potato cyst nematode effector RHA1B is a ubiquitin ligase and uses two distinct mechanisms to suppress plant immune signaling. PLoS Pathog. 2019;15(4):e1007720. https://doi.org/10.1371/journal.ppat.1007720.
33. Li X., Xing X., Tian P., Zhang M., Huo Z., Zhao K., Liu C., Duan D., He W., Yang T. Comparative transcriptome profiling reveals defenserelated genes against Meloidogyne incognita invasion in tobacco. Molecules. 2018;23(8):2081. https://doi.org/10.3390/molecules23082081.
34. Limantseva L., Mironenko N., Shuvalov O., Antonova O., Khiutti A., Novikova L., Afanasenko O., Spooner D., Gavrilenko T. Characterization of resistance to Globodera rostochiensis pathotype Ro1 in cultivated and wild potato species accessions from the Vavilov Institute of Plant Industry. Plant Breed. 2014;133:660-665.
35. Lin B., Zhuo K., Hu L., Sun L., Liao J., Zhang L.H., Chen S., Wang X. A novel nematode effector suppresses plant immunity by activating host reactive oxygen species scavenging system. New Phytol. 2016; 209:1159-1173. https://doi.org/10.1111/nph.13701.
36. Mei Y., Wright K.M., Haegeman A., Bauters L., Diaz-Granados A., Goverse A., Gheysen G., T Jones J., Mantelin S. The Globodera pallida SPRYSEC effector GpSPRY-414-2 that suppresses plant defenses targets a regulatory component of the dynamic microtubule network. Front. Plant Sci. 2018;9:1019. https://doi.org/10.3389/fpls.2018.01019.
37. Mejias J., Truong N.M., Abad P., Favery B., Quentin M. Plant proteins and processes targeted by parasitic nematode effectors. Front. Plant Sci. 2019;10:970. https://doi.org/10.3389/fpls.2019.00970.
38. Palomares-Rius J.E., Escobar C., Cabrera J., Vovlas A., Castillo P. Anatomical alterations in plant tissues induced by plant-parasitic nematodes. Front. Plant Sci. 2017;8:1987. https://doi.org/10.3389/fpls.2017.01987.
39. Qiu X., Yang L., Ye J., Wang W., Zhao T., Hu H., Zhou G. Silencing of cyp-33C9 gene affects the reproduction and pathogenicity of the pine wood nematode, Bursaphelenchus xylophilus. Int. J. Mol. Sci. 2019;20(18):4520. https://doi.org/10.3390/ijms20184520.
40. Rodiuc N., Vieira P., Banora M.Y., de Almeida Engler J. On the track of transfer cell formation by specialized plant-parasitic nematodes. Front. Plant Sci. 2014;5:160. https://doi.org/10.3389/fpls.2014.00160.
41. Sabeh M., Lord E., Grenier É., St-Arnaud M., Mimee B. What determines host specificity in hyperspecialized plant parasitic nematodes? BMC Genomics. 2019;20(1):457. https://doi.org/10.1186/s12864-0195853-4.
42. Schaff J.E., Nielsen D.M., Smith C.P., Scholl E.H., Bird D.M. Comprehensive transcriptome profiling in tomato reveals a role for glycosyltransferase in Mi-mediated nematode resistance. Plant Physiol. 2007;144(2):1079-1092. https://doi.org/10.1104/pp.106.090241.
43. Shivakumara T.N., Chaudhary S., Kamaraju D., Dutta T.K., Papolu P.K., Banakar P., Sreevathsa R., Singh B., Manjaiah K.M., Rao U. Host-induced silencing of two pharyngeal gland genes conferred transcriptional alteration of cell wall-modifying enzymes of Meloidogyne incognita vis-à-vis perturbed nematode infectivity in eggplant. Front. Plant Sci. 2017;8:473. https://doi.org/10.3389/fpls.2017.00473.
44. Shivakumara T.N., Somvanshi V.S., Phani V., Chaudhary S., Hada A., Budhwar R., Shukla R.N., Rao U. Meloidogyne incognita (Nematoda: Meloidogynidae) sterol-binding protein Mi-SBP-1 as a target for its management. Int. J. Parasitol. 2019;49(13-14):1061-1073. https://doi.org/10.1016/j.ijpara.2019.09.002.
45. Strachan S.M., Armstrong M.R., Kaur A., Wright K.M., Lim T.Y., Baker K., Jones J., Bryan G., Blok V., Hein I. Mapping the H2 resistance effective against Globodera pallida pathotype Pa1 in tetraploid potato. Theor. Appl. Genet. 2019;132(4):1283-1294. https://doi.org/10.1007/s00122-019-03278-4.
46. Sugawara T., Trifonova E.A., Kochetov A.V., Kanayama Y. Expression of extracellular ribonuclease gene increases resistance to cucumber mosaic virus in tobacco. BMC Plant Biol. 2016;16(Suppl 3):246. https://doi.org/10.1186/s12870-016-0928-8.
47. Trifonova E.A., Sapotsky M.V., Komarova M.L., Scherban A.B., Shumny V.K., Polyakova A.M., Lapshina L.A., Kochetov A.V., Malinovsky V.I. Protection of transgenic tobacco plants expressing bovine pancreatic ribonuclease against tobacco mosaic virus. Plant Cell Rep. 2007;26:1121-1126. https://doi.org/10.1007/s00299-0060298-z.
48. Trudgill D.L., Blok V.C. Apomictic, polyphagous root-knot nematodes: exceptionally successful and damaging biotrophic rootpathogens. Annu. Rev. Phytopathol. 2001;39:53-77. https://doi.org/10.1146/annurev.phyto.39.1.53.
49. Trudgill D.L., Elliot M.J., Evans K., Phillips M.S. The white potato cyst nematode (Globodera pallida) - a critical analysis of the threat in Britain. Ann. Appl. Biol. 2003;143:73-80.
50. Ventoso I., Kochetov A., Montaner D., Dopazo J., Santoyo J. Extensive translatome remodeling during ER stress response in mammalian cells. PLoS One. 2012;7(5):e35915. https://doi.org/10.1371/journal.pone.0035915.
51. Wang X.R., Moreno Y.A., Wu H.R., Ma C., Li Y.F., Zhang J.A., Yang C., Sun S., Ma W.-J., Geary T.G. Proteomic profiles of soluble proteins from the esophageal gland in female Meloidogyne incognita. Int. J. Parasitol. 2012;42:1177-1183. https://doi.org/10.1016/j.ijpara.2012.10.008.
52. Whitworth J.L., Novy R.G., Zasada I.A., Wang X., Dandurand L.M., Kuhl J.C. Resistance of potato breeding clones and cultivars to three species of potato cyst nematode. Plant Dis. 2018;102(11):21202128. https://doi.org/10.1094/PDIS-12-17-1978-RE.
53. Winslow R.D., Willis R.J. Nematode diseases of potatoes. II. Potato cyst nematode, Heterodera rostochiensis. In: Webster J. (Ed.). Economic Nematology. New York: Acad. Press, 1972;18-34.