In collaboration with Iranian Phytopathological Society

Document Type : Plant Pathology

Authors

Plant Protection Division, Mazandaran Agricultural and Natural Resources Research and Education Center, AREEO, Sari, Iran.

Abstract

Cachexia (Citrus cachexia viroid, CCaVd) and exocortis (Citrus exocortis viroid, CEVd) are the most important citrus viroid diseases in the world. Detection of the viroids through the common serological methods is not feasible and the current methods are time consuming and costly with some limitation. Purification and accurate detection of the viroids was studied by column chromatography with CF-11 cellulose powder in presence of ethanol (common method for viruses’ dsRNA detection) in comparison to the conventional methods. During 2010-2012, sampling was done from twigs of 22 Mandarin and 15 orange trees have symptoms of cachexia and exocortis, respectively, in East Mazandaran. Leaf samples were ground and mixed with extraction buffer. Purification carried out in CF-11 column and viroid molecules extracted with ethanol and precipitated by adding sodium acetate. The nucleic acid extracts were analyzed by 1% agarose gel electrophoresis and specific bands of the two viroids with molecular sizes of 7000-7800bp (circular form) and 300-400bp (linear form) were detected in warm and all months, respectively. The dsRNA nature of the bands was confirmed by nuclease treatment (DNaseI and RNaseA) and 2M LiCl extraction methods.Viroid entity of the each nucleic acid sample was recognized by RT-PCR method using specific primers of cachexia and exocortis viroids. 500 orange and 300 mandarin seedlings were tested in healthy citrus seedling production program.As regards of advantages of this method (repeatability, reliability, saving time and price) and confirmation by RT-PCR, the method is recommended for viroid detection in healthy citrus seedling production programs.

Keywords

Main Subjects

AlAVI, S. V., P. TEIMOURI and H. R. ZAMANIZADE, 2010. First report of the new causal agent of concave gum disease on Thomson navel orange in northern Iran. 13th Congress of Mediterranian Phytopathological Union. p. 243-244.
AlAVI, V., B. KHATABI and G. HOSSEINI SALEKDEH, 2005. Comparison of biologically distinct isolates of Citrus tristeza virus from Iran using major coat protein sequences. Australasian Plant Pathology, No. 34: 577- 582.
ALMAYDA-LEON, I. H., M. A. ROCH-PENA, M. M. IRACHETACARDENAS, F. ORONA-STERO and C. J. KHALKE, 2007. A simple method for the multiple detection of citrus viroids. Agrociencia, No. 41: 87-93.
ALVARADO-GOMEZ, O. G., M. A. ROCH-PENA, S. SILVA-VARA, J. P. MARTINEZ-SORIANO, R. F. LEE, R. RIVERA-BUSTAMANTE and P. RUIZ-BELTRAN, 2000. Citrus exocortis and citrus cachexia viroids in commercial groves of Tahiti lime in Mexico. 15th Conf. IOCV: 289-293.
BEAUDRRY, D. and J. P. PERREAULT, 1995. An efficient strategy for the synthesis of circular RNA molecules. Nucleic Acids Research, No. 23: 3064-3066.
BEN–SHAUL, A., Y. GUANG, N. MOGILNER, R. HADAS, M. MAWASSI, R. GAFNY and M. BAR-JOSEPH, 1995. Genomic diversity among populations of two citrus viroids from different graft-transmissible dwarfing complexes in Israel. Phytopathology, No. 85: 359–64.
BITTER, W. P., N. DURAN-VILA and J. S. SEMANCIK, 1987. Effect of citrus exocortis viroid on flower and fruit structure and development citron. Plant Disease. No. 71: 397-399.
DE LATORRE, S. M. E., C. LOPEZ, O. GRAU and M. L. GARCIA, 2002. RNA2 of Citrus psorosis virus is of negative polarity and has a single open reading frame in its complementary strand, Journal.of General Virology, No. 83: 1777-1781.
DODDS, J. A. and M. BAR-JOSEPH, 1983. Double Stranded RNA from plants infected with closteroviruses. Phytopathology, No. 73: 419-423.
FALAKI, F., S. V. ALAVI and F. RAKHSHANDEHROO, 2013. Citrus psorosis virus, causal agent of ring pattern disorder in Thomson Navel trees in east of Mazandaran. Iranian Journal of Applied Entomology and Phytopathology, No. 80(2): 161-172. (In Persian with English summary).
FLORES, R., C. HERNANDES, A. MARTINEZDE-ALBA, A. DAROS and F. DISERIO, 2005. Viroid and viroid-host interaction. Annual Review.of Phytopathology, No. 43: 117-139.
FRANCIS, M. I., J. A. SZYCHOWSKI and J. S. SEMANSIK, 1995. Structural sites specific to citrus viroid groups. Journal of General.Virology, No. 76: 1081-1089.
FRISON, E. A. and M. M. TAHER, 1991. FAO/IBPGR technical guidelines for the safe movement of citrus germplasm. Food and Agricultural Organization of the United Nations, Rom, Italy. 50pp.
GARNSEY, S. M., D. L. ZIES, M. IREY, P. J. SIEBURTH, J. S. SEMANCIK, L. LEVY and M. E. HILF, 2002. Practical field detection of citrus viroids in Florida by RT-PCR.15th Conference, IOCV: 219–229.
HULL, R. 2002. “Mathews Plant Virology” (4th edition). Academic Press, SanDiego. 1001pp.
KEES, P. and R. H. SYMONS, 1985. Domain in Viroids: Evidence intermolecular RNA re arrangements and their contribution to viroid evolution. Proceeding of the.Nathional.Academic.Scinces of the United State. No. 82: 4582-4586.
LEVY, L. and A. HADIDI, 1993. Direct nucleotide sequencing of PCR amplified DNAs of the closely related viroids IIa and IIb (cachexia). 12 th Conference, IOCV: 180-186.
MORRIS, T. J. and J. A. DODDS, 1979. Isolation and analysis of double stranded RNA from virus-infected plant and fungal tissue .Phytopathology, No. 69: 854-858.
REZAIAN, M. A. 1999. Synthesis of infectious viroids and other circular RNAs. Molecular.Biology, No. 1: 13-20
REZAIAN, M. A., L. R. KRAK and Q. CUNYING, 1990. Detection of virus-associated dsRNA from leaf-roll infected Grapevines.Journal of Virology Methods, No. 31: 325-334.
RIVERA-BUSTAMANTE, R. F., R. GIN and J. S. SEMANCIK, 1986. Enhanced resolution of circular and linear forms of viroid and viroid like RNA by electrophoresis in a discontinuous  pH system. Analytical Biochemistry, No. 156: 91-95.
ROISTACHER. C. N. 1991. Graft - Transmissible Diseases of Citrus . FAO: Rom .286pp.
SEMANCIK, J. S. and C. N. ROISTACHER, 1988. A new viroid is the causal agent of the citrus Cachexia disease. Virology, No. 10: 125-135. 
SEMANCIK, J. S., A. K. VDAVER and J. L. VANETTEN, 1973. Characterization of segmented double-helical RNA from bacteriophage phi6. Journal Molecular Biology, No. 78: 617–625.
TIETZ, D. 1998. Nucleic Acid Electrophoresis. Springer, Berlin, Germany. 328 pp.
WAGNER, R. W. and L. SUN, 1998. Double- stranded RNA poses puzzle. Nature. No. 19: 391(6669): 744-745.
YANG, X. A., A. HADIDI and S. M. GARNSEY, 1992. Enzymatic amplification of citrus exocortis and cachexia from infected citrus hosts. Phytopathology, No. 82: 279-285.