شناسایی و بررسی مولکولی ویروس موزاییک معمولی لوبیا (BCMV) و موزاییک نکروتیک معمولی لوبیا (BCMNV) در استان مازندران

نوع مقاله : مقالات پژوهشی

نویسندگان

1 دانشگاه فردوسی مشهد

2 دانشگاه مازندران

چکیده

طی سال های 1392 و 1393، تعداد 50 نمونه برگ لوبیا دارای علائم از مزارع استان مازندران جمع آوری و RNA کل آنها استخراج شد. طی آزمون RT-PCR با استفاده از یک جفت آغازگر دژنره منطبق بر ژن کدکننده پروتئین Cylindrical inclusion (CI) قطعه ای به طول bp680 در 13 نمونه تکثیر گردید. تکثیر اختصاصی نمونه های آلوده با آغازگرهای CIF/R، نشان از آلودگی به یک پوتی ویروس داشت. محصول PCR مربوط به دو جدایه پس از همسانه سازی در حاملpTG19-T ، توالی یابی شد. آنالیز بلاست توالی ها نشان داد که قطعات تکثیر شده در واکنش PCR متعلق به ویروس موزاییک نکروتیک معمولی لوبیا (Bean common mosaic necrosis virus, BCMNV) (از لوبیا سفید) و ویروس موزاییک معمولی لوبیا (Bean common mosaic virus, BCMV) (از لوبیا چشم بلبلی) است. آنالیز فیلوژنتیکی جدایه های تعیین ترادف شده در ناحیه ژنی CI نشان داد که جدایه ی تعیین توالی شده BCMV-MAZ (از ساری) در سطح نوکلئوتیدی و اسید آمینه ای به ترتیب دارای بیشترین شباهت (8/96% و 7/98%) با جدایه آمریکا (RU1M) و کمترین شباهت (5/79% و 6/91 %) با جدایه کره جنوبی (Habin1) می باشد. همچنین جدایه BCMNV-MAZ (از جویبار) بیشترین شباهت (8/97%) را با جدایه های آمریکایی NL-3 K،NL5 و کمترین شباهت (9/96%) را با NL8 در سطح نوکلئوتیدی دارد. در سطح اسید آمینه ای نیز 7/97 % شباهت با سایر جدایه های مورد بررسی دارد. این اولین گزارش از وجود ویروس های مذکور در استان مازندران به روش مولکولی است.

کلیدواژه‌ها


عنوان مقاله [English]

Identification and Molecular Analysis of Bean common mosaic virus (BCMV) and Bean common mosaic necrosis virus (BCMNV) in Mazandaran Province

نویسندگان [English]

  • Z. Moradi 1
  • M. Mehrvar 1
  • E. Nazifi 2
1 Ferdowsi University of Mashhad
2 University of Mazandaran
چکیده [English]

Introduction: Among legume crops, common bean (Phaseolus vulgaris L.) is one of the most important worldwide crops, because of its cultivation area and nutritional value. The closely related potyviruses Bean common mosaic virus (BCMV) and Bean common mosaic necrosis virus (BCMNV) are the most common and most destructive viruses that infect common beans throughout the world. The viruses induced similar symptoms in numerous bean genotypes, including mosaic, leaf distortion, stunting, and lethal necrosis. Like all potyviruses, BCMV and BCMNV have non-enveloped flexuous filamentous virions of 750 nm long and 11–13 nm wide, which encapsidate a single-stranded, positive-sense RNA molecule of approximately 10,000 nt long. Both are naturally transmitted by aphids in a non-persistent manner and by seed, which explains their worldwide distribution. These viruses are major constraints on bean production and can cause serious crop losses. Mazanadaran province in north of Iran is one of the major producing areas of legumes, so identification of these viruses is a concern. However, so far, no studies have been done with these viruses in this province. The aim of this research was to study the existence of BCMV and BCMNV in research areas and determining of their phylogenetic relationship. Polymerase chain reaction (PCR) with degenerate primers for conserved sequences of the viral genomes has facilitated the rapid detection of many potyviruses and enabled partial genomic sequencing. In the absence of complete genomic sequences of potyviruses, CI-coding region is more suitable for diagnostic and taxonomy purposes, rather than the coat protein (CP) usually used. The CI gene most accurately reflects the taxonomic status according to the complete ORF.
Materials and Methods: From July to September 2013 and 2014, a total of 50 leaf samples of beans showing virus symptoms were collected from different bean fields in Mazandaran province. Total RNA was extracted from all samples. The RT-PCR assay was performed using potyvirus degenerate primers corresponding to the virus CI gene. Expected PCR products of 680 bp were purified from 1% agarose gels using the Gel Recovery kit, then cloned into the pTG19-T vector and sequenced. Sequences were compared to data available in GenBank. Phylogenetic tree for grouping based on nucleotide sequences was constructed by MEGA 5.1 software program using neighbor-joining method. Multiple alignments of the nucleotide and amino acid sequences were carried out using the Clustal W and DNAMAN7 software.
Results and Discussion: Using potyvirus degenerate primers CI F/R, an amplicon of the expected size (680 bp) was generated from 13 plant samples. Specific amplification using the potyvirus degenerate primers in infected samples, but not from healthy samples, confirmed the presence of a potyvirus. The most typical symptoms in positive samples were mosaic, mottling, rugosity, leaf distortion and necrosis. Two selected PCR positive samples were cloned into the pTG19-T vector, sequenced and submitted to BLASTn to identify the best matching sequences recorded in GenBank. BLASTn analysis of the sequenced data revealed that the PCR-amplified fragments belonged to Bean common mosaic virus (Cowpea) and Bean common mosaic necrosis virus (White bean). Phylogenetic tree based on multiple sequence alignment of 680 nt of CI gene divided all BCNMV isolates into two groups: I and II. Members of each group were divided into two subgroups: A, B. Isolates in subgroup IA included three isolates from China and two isolate from Indonesia. Iranian isolate (BCMV-MAZ) was classified in the group IB with RU1M isolate (USA). Group II included a wide range of Chinese isolates and also one isolate from USA, Germany, India and South Korea. Phylogenetic analysis by comparing the 680 bp of CI gene sequences showed that all BCMNV sequences can be placed into two groups: Only TN1 isolate (USA) was classified in group I. Group II included 2 subgroups A, B. Iranian isolate (BCMNV-MAZ) with NL8 isolate (USA) were classified in the subgroup IIA. Isolates in group IIB included a number of USA isolates and one isolate from the UK. Isolate of BCMV-MAZ (from Sari) showed the highest (96.8% - 98.7%) and the lowest (79.5%-91.6%) nucleotide and amino acid sequence identity with RU1M isolate (USA) and Habin1 (Korea), respectively. Also BCMNV-MAZ (from Jouybar) displayed the highest (97.8%) and the lowest (96.9%) nucleotide sequence identity with NL-3 K, NL5 and NL8, respectively. This isolate was 97.7 % identical with other isolates of the BCMNV at the amino acid identity level.
Conclusions: BCMV and BCMNV are widespread in almost all bean growing areas of Iran and often present in the mixture. In this study, for the first time we reported the occurrence of BCMV and BCMNV in common beans in Mazandaran province based on the RT-PCR, and CI gene analyses, and determining their phylogenetic relationship with other isolates of these viruses available in the GenBank. Primary detection was performed by using CI F/R degenerate primer based on the potyvirus CI gene motifs I and V. Since the sequence identity of CI gene is higher when compared to that of the CP gene and is involved in helicase activity during replication, the use of CI is more accurate in defining orders in potyvirus taxonomy and in evolutionary relationships. Due to ease in the spread of these viruses by seed and vectors, detection of such viruses has a crucial role in the control of these diseases. The data obtained in this study will be beneficial to improve control strategies for these viruses in Iran. Study on the distribution of BCMV and BCMNV will be useful for breeders to incorporate virus resistance into bean cultivars, where any or both of the two viral species occur.

کلیدواژه‌ها [English]

  • BCMV
  • BCMNV
  • Phylogenetic analysis
  • RT-PCR
1- Adams M.J., Antoniw J.F., and Fauquet C.M. 2005. Molecular criteria for genus and species discrimination within the family Potyviridae. Archives of Virology, 150:459–479.
2- Baradaran G.R., and Jafarpour B. 1998. Study on occurrence of bean common mosaic virus and Cucumber mosaic virus in Bean fields of Mashhad and Chenaran area. p. 157-163. Proceedings of the 13th Iranian plant protection congress, 23-27 Aug. 1998. Karaj, Iran. (In Persian)
3- Carrington J.C., Jensen P.E., and Schaad M.C. 1998. Genetic evidence for an essential role for potyvirus CI protein in cell-to-cell movement. Plant Journal, 14(4):393-400.
4- Chen J., and Adams M.J. 2001. A universal PCR primer to detect members of the Potyviridae and its use to examine the taxonomic status of several members of the family. Archives of Virology, 146:757-766.
5- Dorri H., lak M., bani-jamali S.M., Dadivar M., Ghanbari A., Khodshenas M., and Asadi B. 2003. Beans (from planting to harvest). Journal of Extension Education, 305, 77 p.(In Persian)
6- Drijfhout E. 1991. Bean common mosaic. Compendium of Bean Diseases. APS Press, pp 37-39.
7- Flores-Estevez N., Acosta-Gallegos J.A., Silva-Rosales L. 2003. Bean common mosaic virus and Bean common mosaic necrosis virus in Mexico. Plant Disease, 87:21-25.
8- Gibbs A.J., Mackenzie A.M., and Gibbs M.J. 2003. The 'potyvirid primers' will probably provide phylogenetically informative DNA fragments from all species of Potyviridae. Journal of Virological Methods, 112:41-44.
9- Ha C., Coombs S., Revill P.A., Harding R.M., Vu M., and Dale J.L. 2008. Design and application of two novel degenerate primer pairs for the detection and complete genomic characterization of potyviruses. Archives of Virology, 153(1):25-36.
10- Hsu Y.C., Yeh T.J., and Chang Y.C. 2005. A new combination of RT-PCR and reverse dot blot hybridization for rapid detection and identification of potyviruses. Journal of Virological Methods, 128:54-60.
11- Hull R. 2014. Plant virology (5th ed.). New York: Academic Press.1098 p.
12- Kelly J.D. 1997. A review of varietal response to bean common mosaic potyvirus in Phaseolus vulgaris. Plant Varieties and Seed, 10:1-6.
13- Khan J.A., LohuisD., Goldbach R., and Dijkstra J. 1993. Sequence data to settle the taxonomic position of Bean common mosaic virus and Blackeye cowpea mosaic virus isolates. Journal of General Virology, 74: 2243-2249.
14- Klein P.G., Klein R.R., Rodriguez-Cerezo E., Hunt A.G., and Shaw J.G. 1994. Mutational analysis of the Tobacco vein mottling virus genome. Virology, 204:759-769.
15- Lopez-Moya J.J., Valli A., and Garcıa J.A. 2009. Potyviridae. Encyclopedia of Life Sciences. Annual Review of Phytopathology, 34:227–247.
16- Lee K.C., Wong S.M., Mahtani P.H., and Chng C.G. 1997. Sequence and phylogenetic analysis of the cytoplasmic inclusion protein gene of Zucchini yellow mosaic potyvirus: its role in classification of the Potyviridae. Virus Genes, 14:41–53.
17- Mavric I. and Sustar-Vozlic J. 2004. Virus diseases and resistance to Bean commonmosaic and Bean common mosaic necrosis potyvirus in common bean (Phaseolusvulgaris L.). Acta agriculturae slovenica, 83:181-190.
18- McKern N.M., Mink G.I., BarnettO.W., MishraA., WhittakerL.A., SilbernagelM.J., Ward C.W. and Shukla D.D. 1992a. Isolates of Bean common mosaic virus comprising two distinct potyviruses. Phytopathology, 82:923-929.
19- McKern, N. M., Ward C.W., and Shukla D.D. 1992b. Strains of Bean common mosaic virus consist of at least two distinct potyviruses. Archives of Virology, [Suppl.5]:407-414.
20- Mink G.I., and Silbernagel M.J. 1992. Serological and biological relationship among viruses in the Bean common mosaic virus subgroup. In: Barnett OW (ed) Potyvirus taxonomy. Springer, Wien New York. Archives of Virology, pp 397-406.
21- Naderpour M.,Mosahebi G., and Kohi Habibi M. 2000. III, Vta & Vib Pathotypes and NL-5, NL-8 & NL-3 necrotic strains of BCMV, a new record for Iran. P. 280-283. Proceedings of the 14th Iranian plant protection congress, 5-8 Sep. 2000. Isfahan, Iran. (In Persian)
22- Naderpour M., Mosahebi G., and Kohi Habibi M. 2000. Detection of BCMV serotypes by using of physicochemical methods. p. 284-287. Proceedings of the 14th Iranian plant protection congress, 5-8 Sep. 2000. Isfahan, Iran. (In Persian)
23- Peyambari, M., Kohi habibi M., Mosahebi G., and Izatpanah K. 2011. Consideration of BCMV in some provinces of Iran and three genotypes response to BCMV. Journal of Plant Protection, 25(3):250-257.
24- Pudashini B.J., Shahid M.S., and Natsuaki K.T. 2013. First report of Bean common mosaic necrosis virus (BCMNV) infecting sweet bean in Nepal. Plant Disease, Vol. 97 No. 2 pp. 290.
25- Revers F., Le Gall O., Candresse T., and Maule A.J. 1999. New advances in understanding the molecular biology of plant: potyvirus interactions. Molecular Plant-Microbe Interactions, 12:367-376.
26- Saiz M., de Blas C., Carazo G., Fresno J., Romero J., and Castro S. 1995. Incidence and characterization of Bean common mosaic virus isolates in Spanish bean fields. Plant disease, 79:79-81.
27- Salari N., Seyed Musavi M., Shahraeen N., Ghobani S., and Maleki M. 2013. Identification and diagnosis of isolates of Bean common mosaic virus and bean common mosaic necrosis virus by immunocapture RT-PCR. New Cellular and Molecular Biotechnology Journal, 3 (11):21-28. (In Persian)
28- Shahraein N., Hasani mehraban H., Poordavaei H., Beyzaei A., Mostaed M., and Bananj k. 2001. Determination of genetically sources of resistance to three importance common bean viruses, CMV, BYMV and BCMV. Research final report, Khomain and bojnoord station (In Persian).
29- Shahraein N., Hasani mehraban H., Mostaed M., and Ghotbi T. 2002. Report on Bean common mosaic necrosis virus infecting French bean in Arak and Lorestan provinces.p. 282-287. Proceedings of the 15th Iranian plant protection congress, 7-11 Sep. 2002. Kermanshah, Iran. (In Persian)
30- Shukla D.D., Ward C.W., and Brunt A.A. 1994. The Potyviridae. CAB International, Walling ford, UK. p. 74-112.
31- Silbernagel M.J., Mink G.I., Zhao R.L., and Zheng G.Y. 2001. Phenotypic recombination between Bean common mosaic and Bean common mosaic necrosis potyviruses in vivo. Archive of Virology, 146:1007-1020.
32- Strausbaugh C.A., Miklas P.N., Singh S.P., Myers J.R., and Forster R.L. 2003. Genetic characterization of differential reaction among host group 3 common bean cultivars to NL-3 k strain of Bean common mosaic necrosis virus. Phytopathology, 93:683-690.
33- Tamura K., Peterson D., Peterson N., Stecher G., Nei M., and Kumar S. 2011. MEGA5: Molecular Evolutionary Genetics Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Molecular Biology and Evolution, 28:2731-2739.
34- Vallejos C.E., Gustavo A.M., Valerie J., Tommy R.P., Ney S.S, and Sally A.M. 2006. Genetic and molecular characterization of the I locus of Phaseolus vulgaris. Genetics, 172:1229-1242.
35- Vetten H.J., Lesemann D.E., and Maiss E. 1992. Serotype A and B Strain of Bean common mosaic virus are two distinct Potyvirus. Archive of Virology, Suppl 5:415-431.
36- Yazdi Samadi B., and Abdemeyshaei S. 1996. Agronomical plant breeding. Iran University press. PP 283 (In Persian)
37- Zheng H., Chen J., Chen J., Adams M.J., and Hou M. 2002. Bean common mosaic virus isolates causing different symptoms in asparagus bean in China differ greatly in the 5' parts of their genomes. Archives of Virology, 147:1257–1262.
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