The two members of the watermelon mosaic virus subgroup, WMV-1 and WMV-2, were considered to be different viruses on the basis of host range and serology. Immune electron microscopy with serological differentiation indices of 2 to 3 confirmed this serological difference. Molecular

hybridization analysis using complementary DNA prepared by reverse transcription of randomly primed WMV-I RNA showed no homology between WMV-I and WMV-2 and the complementary

DNA from a range of legume infecting poty viruses and potato virus Y (PVY). Molecular hybridization

analysis further confirmed that WMV-I and WMV-2 are distinct viruses

Abu-Samah, Norani

Universiti Putra Malaysia Institutional Repository

Pertanika 8(2). 281 - 287 (1985)Relationship Between Watermelon Mosaic Virus (WMV-I) andWatermelon Mosaic Virus 2 (WMV-2) on the basis ofNucleotide Sequence HomologyNORANI ABU-SAMAHDepartment of Biochemistry and Microbiology,Faculty of Science and Environmental Studies,Universiti Pertanian Malaysia,Serdang, Selangor, Malaysia.Key words: Potyvirus; immune electron microscopy; molecular hybridization analysis.ABSTRAKKedua ahli subkumpulan 'watermelon mosaic virus', WMV-I dan WMV-2 dianggap sebagaivirus-virus yang berlainan berdasarkan kepada bidang hos dan serologi. lmmun mikroskop elektrondengan penunjuk pembezaan indeks 2 ke 3 mengsahkan perbezaan serologi ini. Analisis hibridisasimolikul dengan menggunakan DNA berkomplimen yang disediakan oleh transkrzpsi berbalz"k RNAWMV-I berprima rawak, menunjukkan tiada homologi di antara WMV-I dan WMV-2 dan DNAberkomplimen juga menunjukkan tiada homologi dengan RNA dari beberapa 'potyvirus' yangmenjangkiti kekacang dan 'potato virus Y' (PVY). Analisa hibridisasi molikul selanjutnya meng-sahkan yang WMV-I dan WMV-2 adalah virus-virus yang nyata berbeza.ABSTRACTThe two members of the watermelon mosaic virus subgroup, WMV-I and WMV-2, wereconsidered to be different viruses on the basis ofhost range and serology. Immune electron microscopywith serological differentiation indices of 2 to 3 confirmed this serological difference. Molecularhybridization analysis using complementary DNA prepared by reverse transcrzption of randomlyprimed WMV-I RNA showed no homology between WMV-I and WMV-2 and the complementaryDNA from a range of legume infecting potyviruses and'potato virus Y (PVY). Molecular hybridizationanalysisfurther confirmed that WMV-I and WMV-2 are distinct viruses.INTRODUCTIONWatermelon mosaic virus - 1 (WMV-l)and watermelon mosaic virus - 2 (WMV-2)have been differentiated on their biological andserological properties. Using agar double-diffu-sion tests. Milne and Grogan (1969) found aclose serological relationship between variousisolates of WMV-l and WMV-2 and concluded,that they were strains of WMV even though theirhost ranges differed.Purcifull and Hiebert (1979) indicated thatby SDS-immunodiffusion tests the Floridaisolates of WMV-l and WMV-2 were serolo-gically distinct as no cross-reactions were detect-ed.The Queensland isolates of WMV-1 andWMV-2 were found to have some distinct host. range differences. WMV-2 Q has a much widerhost range as compared to WMV-l Q (Greber,1978). They were serologically distinct from oneanother but closely related to Florida isolates ofthe respective types using the SDS-immunodiffu-sion tests with crude sap (Greber, 1978). Physicalproperties of these WMV isolates and electronmicroscopic examination of the virus particlesNORANI ABU-SAMAHand inclusions were found to be similar to theother isolates reported elsewhere.Makkouk and Lesemann (1980) found thattheir WMV-1 reacted with the Florida isolate ofWMV-l but not with WMV-2 Florida isolateantiserum when tested in SDS-immunodiffusiontests and with the decoration technique ofimmune electron microscopy.Inconsistencies in the reported relationshipsbetween WMV·I and WMV-2 probably resultedfrom the use of different strains and techniques.In this paper, the relationship betweenWMV-l and WMV-2 was reexamined bymolecular hybridization analysis (MHA) whichdiscriminates isolates and strains of the potyvirus,bean yellow mosaic virus (BYMV) (Abu-Samah,1982; Abu-Samah & Randles, 1981; Abu-Samah& Randles, 1983). Molecular hybridizationanalysis (MHA) allows more sensitive discrimina-tion and provides a semi-quantitative estimatebetween closely related isolates. But MHA is toospecific to show relationships between distantlyrelated strains or different viruses. Therefore inthis study serological relationships were alsoexamined by immune electron microscopy(IEM).MATERIALS AND METHODSSources of VirusIsolates of WMV-l and WMV-2 weresupplied by a government department* in Indo-oroopilly, Queensland and maintained in theglassholtse on Cucumis sativus cv. Polaris. In thispaper, these isolates are referred to as WMV:!Qand WMV-2 Q.Purification of WMV-l Qand WMV-2 andTheirRNAsPurification of WMV-l Q and WMV-2 Qwas from systemically infected leaves of C.sativus cv. Polaris harvested 2 - 3 weeks afterinoculation. Both viruses were purified bymethods based on those of Purcifull and Hiebert(1979) with modifications of the steps after thepolyethylene glycol (PEG 6000) concentrationstep.For WMV-1 Q, the PEG pellets were resus-pended in 0.05 M potassium phosphate buffer,pH 7.5 The virus was centrifuged through 1 mlof a 30% buffered sucrose cushion in a Spinco 65rotor at 78,000 g for 105 min. The pellet wasresuspended in water.For WMV-2 Q, after the precipitation stepwith PEG and sedimentation by high speedcentrifugation as above, the virus pellet wasresuspended in 0.05 M potassium phosphatebuffer, pH 7.5. The resuspended material wassubjected to centrifugation in a CsCI gradient( p = 1.28 g/ml) using the SW 50 rotor at40,000 rpm for 18 hrs. The virus containing zonewas removed, diluted with buffer and wasfurther subjected to high speed centrifugation at78,000 g in the Spinco 65 rotor for 120 min. Thepellet was resuspended in water.The RNAs were extracted from the virussuspension by the pronase procedure as describ-ed for BYMV-RNA (Abu-Samah & Randles,1981). Only WMV-l was purified furtherthrough two cycles of sucrose density gradients(Abu-Samah & Randles, 1981).Comparison by Immune Electron Microscopy(IEM)The antisera of the Florida isolate ofWMV-l (WMV-l Fl) and WMV-2 (WMV-2 Fl)used in this study were kindly provided by Dr.D.E. Purcifull, University of Florida, Gaines-ville. The Florida antisera were used in antibodydecoration and dilution end-point clumpingIEM tests to compare WMV-l Qand WMV-2 Q(Milne and Luisoni, 1977).Molecular Hybridization Analysis (MHA)The random primer method of Taylor etal., (1976) as used for BYMV-RNA (Abu-Samah.Supplied by Mr. R.S. Greber of the Department of Primary Industries.282 PERTANlKA VOL. 8 NO.2. 1985COMPARISON OF WMV-RNA& Randles, 1981) was used to synthesize comple-mentary DNA (cDNA) to WMV-l. Thehybridization solution contained 0.01 M Tris-HCI, pH 7.0, 0.18 M NaCI, 1 mM EDTA and0.05% SDS (Gould & Symons, 1977; Abu-Samah & Randles, 1981).Hybridization was carried out in siliconizedglass test tubes, approx. 7 X 50 mm with reactionmixtures overlaid with paraffin oil. To 40 ,ul ofthe appropriately diluted RNA solution wasadded 2 ,ul of [ 3H] cDNA (c. 2000 cpm). Thereaction mixtures were immersed in boilingwater for 2 - 3 mins and then incubated at 65 -66°C. Hybridizations were terminated by chill-ing the tubes, removing 30 ,ul aliquots, andadding them to 300,u1 of a low salt S I assay buffer(0.03 M sodium acetate, 0.05 M NaCI, 1 mMZnSO 4' 5% glycerol, pH 4.6) containing 40,ug/ml of denaturated calf thymus DNA. Twosamples, each 150 ,lIt were taken and to one wasadded 2 units of S 1nuclease; the other was left asa control. After incubation of both samples at45°C for 30 mins, nuclease resistence was deter-mined by comparing the duplicates incubatedeither with or without enzymes, as described byGould & Symons (1977).The T m of DNA-RNA hybrid was set up in atotal vol. of 100 ,ul and incubated at 65° to aRtvalue exceeding 1.0 mol sec liter -1. The mixtu;ewas chilled and placed in a waterbath in whichthe temperature was raised by approx. 1°C permin. At the appropriate temperatures, 5 ,ulportions were transferred to 150 ,u I of cold S 1buffer and the percentage hybrids remaining ateach temperature was determined by S 1nucleaseresistence.RESULTSComparison by IEMIn the decoration IEM test at an antiserumdilution of 1/10, both WMV-l Qand WMV-2 Qparticles were heavily decorated with the anti-body of WMV-l FI and WMV-2 FI respectively.Therefore the Queensland isolates of WMV-land WMV-2 were closely related to their Floridacounterparts using IEM (Figs. 1 and 2). Theseresults were consistent with those of Greber(1978) who showed a serological relationship ofthe Q isolates with the Florida type isolates bySDS-immunodiffusion tests.Fig. 1. Serological relationship between WMV-1 Qand WMV-2 Q by decoration lEM.WMV-1 Q against antisera to (A) WMV-1 Fland (B) WMV-2 Fl at a 1/10 dilution.Bar represents 500 nm.Fig. 2. Serological relationshIp between WMV-2 Qand WMV-I Q by decoration lEM.WMV-2 against antisera to (A) WMV-2 Fland (B) WMV-I Fl at a 1/10 dilution.Bar represents 500 nm.PERTANIKA VOL. 8 NO.2, 1985 283NORANI ABU-SAMAHAt the antiserum dilution used, cross-re-actions were detected In reciprocal tests,although with much less decoration for theheterologous tests. The dilution end-points ofboth antisera with both WMV-1 Qand WMV-2 Qby the clumping IEM test are presented in Table1. The serological differentiation index betweenWMV-l FI antiserum and WMV-2 Q was 2 andbetween WMV-2 FI antiserum and WMV-l Qwas 3. These antisera failed to decorate the beanisolate of tobacco mosaic virus (B-TMV) andantiserum to UI isolate of tobacco mosaic virus(UI-TMV) failed to decorate WMV-l Q orWMV-2Q.TABLE 1Titres of WMV-l Fl and WMV-2 Fl antisera toWMV -1 Q and WMV-2 Q as determined byclumping IEMAntigensAntiserumWMV-l Q WMV-2 Q B-TMVComparison by Molecular HybridizationAnalysis (MHA)Reverse transcription of WMV-1 RNA gavecDNA with 2 X 10 6 count/min (13.4 ng) for aninput of 2 Jlg of RNA. The specificity of thecDNA is illustraded in Table 2; hybridization Qfthe cDNA with other viral RNAs or with nucleicacid extracted from healthy cucumber was notobserved.Homologous and heterologous hybridiza-tion kinetics between WMV-l Q cDNA andWMV-l Q and WMV-2 Q RNAs are presentedin Fig. 3. The WMV-l Q cDNA showed amaximum percentage hybridization of appro-ximately 90% with homologous RNA. Thesingle phase curve up to the maximum Rottested indicates that the RNA used was uncon-taminated (Gould and Symons, 1977) with otherRNAs and probably had few reiteratedsequences.Figures in the Table are reciprocal titres of antisera.Antisera kindly supplied by Dr. D.E. Purcifull(') , and Dr.R.I.B. Franck/b).WMV-l Fl'WMV-2 FI'U - TMv b12048512o5124096ooooThe R t~ value for the homologous hybridi-zation was 1.2 X 10 -zmol sec liter -1 similar tothat obtained by the BYMV-RNAs (Abu-Samah& Randles, 1981). Thermal denaturation of thehomologous hybrid showed a sharp transitionand a high T m of 84°C undenhe conditions used(Fig. 4). This indicated that hybrid formationwas specific with no evidence of mismatching.TABLE 2Percentage sequence homologies of WMV -1 Q and WMV-2 Q RNAs with WMV-1 Q complimentary DNARNANo RNAHealthy cucumber totalnucleic acidTMV-RNAYeast RNAWMV-l RNAWMV-l RNARNA concentraion(ug/ml)96.875.2400.04.04.0Rto104.581.2432.04.34.3Percent hybridization5.72.0 a2.1 'Ob89.1' ± 5.6 bo"Hybridization percentages were corrected for self-hybridization of eDNA.bStandard errors of the mean of three replicates.284 PERTANlKA VOL. 8 NO.2, 1985COMPARISON OF WMV-RNATABLE 3Percentage sequence homologies betweenWMV -1 Q cDNA and RNAs of a range oflegume infecting potyviruses and PVYTest ofRelationshzp Between WMV-l andaRange ofPotyviruses .The relationship of WMV -1 Q to a range ofpotyviruses from South Australia was examinedby MHA using cDNA synthesize to WMV -1 QRNA. Potyvirus RNAs from partially purifiedpreparations concentrated by polyethylene 6000(PEG), were phenol extracted and ethanolprecipitated (Abu-Samah & Randles, 1981).The results in Table 3 show that WMV -1 Q hadno detectable homology with any of the legume-infecting potyviruses tested or with PVY.•/~ ./:/:-I·iO+-_-oo-..,~=O;=O~OQ-O-"'""1'-5 -4 -3 -2 -1 0Log Rot (mol sec lilre-11602040100l8°1OL--S,O---s"r0---7rO----,SO,---g'O-----,100TEMPERATURE (oclFig. 3. Kinetics of hybridization of WMV-l cDNAwith WMV-I RNA (e) and WMV-2 RNA(0). TheR /~ value is indicated by an arrow.100so604020••• •RNA b Percentage homologyawith WMV-1 cDNAPVY 0 ± 0.77LMV 0 ± 0.45PMV 0 ± 0.68SoMV 0 ± 0.08SPMV 0 ± 0.53CAMV 0 ± 0.31BCMV 0 ± 0.81BYMV-G 0 ± 1.1BYMV-Q 0 ± 1.6BYMV-S 0 ± 1.9Homologous 91.6 ± 5.4aHybridizations were done to aRt of 10.8 mol sec litre-}oStandard errors of the mean of three replicates are given foreach hybridization reaction.bpVY = potato virus Y; LMV = lettuce mosaic virus; PMV= pea mosaic virus; SoMV = soybean mosaic virus; SPMV= sweet pea mosaic virus; CAMV = cowpea aphid-bornemosaic virus; BCMV = bean common mosaic virus; BYMV-G = G isolate of bean yellow mosaic virus; BYMV-Q = Qisolate of bean yellow mosaic virus; BYMV-s = S isolate ofbean yellow mosaic virus.DISCUSSIONFig. 4.. Thermal stability of the hybrid ofWMV-l Q cDNA with homologous RNA.The T m value (84°C) is indicated by anarrow.Host reactions can differentiate WMV-1 Qand WMV-2 Q (Greber, 1978). WMV-2 Qinfected cucurbits, legumes and chenopodiaceaePERTANIKA VOL. 8 NO.2. 1985 285NORANI ABU-SAMAHbut WMV -1 Q infected only cucurbits. Therewas an apparent similarity of the wide-host-range type of WMV-2 and the limited-host-range type of WMV-l worldwide. This was inagreement with Milne and Grogan (1969);Purcifull and Hiebert (1979) and Makkouk andLesemann (1980).Serological data for the two viruses by IEMindicate that they were distantly related. This,however, is not surprising considering thatdistant serological relationships are widespreadamong members of the potyvirus group (Hollingsand Brunts, 1981a, b). Cross-contaminationbetween WMV-1 Q seemed unlikely since theSDI values were different and would have beendetected in hybridization analysis experiments.The inability to detect cross-reactions betweenWMV-1 and WMV -2 in SDS-immunodiffusiontests (Greber, 1978; Purcifull & Hiebert, 1979;Makkouk & Lesemann, 1980) could be due tothe insensitivity of the method as a result of thealteration of the antigenic specificity betweenSDS-treated virus and the untreated virus whichhad been used in preparing antiserum (Shalla &Shepard, 1970; Shepard & Shalla, 1970;Shepard & Secor, 1972).From previous work (Abu-Samah &Randles, 1981, 1983) significant homology wasdemonstrable only between potyviruses that wereclosely related. For example, the G, Q and Sisolates of bean yellow mosaic virus (BYMV),which are closely related serologically andbiologically, were distinguished quantitativelyby their percentage homology. The present studyshows that WMV-l Qand WMV-2 Q, which arebiologically and serologically distantly related toeach other (Greber, 1978; Purcifull & Hiebert,1979; Makkouk & Lesemann, 1980), had nodetectable base sequence homology in common.These data confirm that WMV-l Qand WMV-2Q cannot be considered as strains and are dis-tinct under the conditions used for analysis.Therefore these data imply that distantlyrelated strains do not show homology, but withTMV (Palukaitis & Symons, 1980; Palukaitis etat., 1981) further relationships were demonstrat-ed under less stringent conditions. Randles etat., (1981) showed that under conditions of lowstringency for MHA, low homology was detectedin several TMV isolates which showed nohomology under stringent conditions. SinceMHA between WMV-l Q and WMV-2 Q wascarried out under conditions of high stringency(Abu-~amah & Randles, 1981), conditions oflower stringency might detect some relationshipsbetween ~he viruses.As all attempts to synthesize eDNA toWMV-2 were unsuccessful, the relationshipbetween WMV-l and WMV-2 was determinedby u~ing the cDNA synthesized to WMV -1 only.It has been shown previously that the percentagehomology was the same in reciprocal testsbetween three isolates of BYMV (Abu-Samah &Randles 1981)_ Heterologous hybridizationsbetween WMV-2 QRNA and WMV-l QcDNAshowed no detectable homology (Fig. 3) understringent conditions which allowed reactionsamong strains of BYMV (Abu Samah &Randles, 1981).ACKNOWLEDGEMENTSThe author wishes to thank Dr. J.W.Randles for comments and suggestions in themanuscripts; Mr. A. Ghani for illustrations; andthe Department of Plant Pathology, Waite Agri-cultural Research Institute, University. ofAdelaide for research facilities. Support fromUniversiti Pertanian Malaysia is also gratefullyacknowledged. This work was partially fundedby the Australian Research Grant Scheme.REFERENCESABU-SAMAH, N. (1982): Nucleotide sequence homo-logy within two subgroups of the potyviruses.Ph.D. Thesis. University of Adelaide, SouthAustralia.ABU-SAMAH, N. & RANDLES, J.W. (1981): A compa-rison of the nucleotide sequence homologies ofthree isolates of bean yellow mosaic virus andtheir relationship to other potyviruses. Virology.110: 436 - 444.ABU-SAMAH, N. & RANDLES, J.W. (1983): A compa-rison of Australia bean yellow mosaic virusisolates using molecular hybridization analysis.Ann. appl. BioI. 103: 97 -107.286 PERTANIKA VOL. 8 NO.2, 1985COMPARISON OF WMV-RNAGOULD, A.R. & SYMONS, R.H. (1977): Detenninationof the sequence homology between the four RNAspecies of cucumber mosaic virus by hybridizationanalysis with complementary DNA. NucleicAcids Research. 4: 3787 - 3802.GREBER, R.S. (1978): Watennelon mosaic virus 1 and2 in Queensland cucurbit crops. Aust. J. Agric.Res. 29: 1235 - 1245.HOLLINGS, M. & BRUNT, A.A. (1981a): Potyvirusgroup. CMIIAAB Descnption of Plant Viruses.No. 245, 7pp.HOLLINGS. M. & BRUNT, A.A. (198Ib): In Handbookof Plant Virus Infections: Comparative Diagnosis.pp. 731-807. Ed. E. Kurstak, Amsterdam:Elsevier/North Holland. Biomedical Press.MAKKOUK, K.M. & LESEMANN, D.E. (1980): A severemosaic of cucumbers in Lebanon caused bywatennelon mosaic virus I. Plant Dis. 64: 799-801.MILNE. K.S. & GROGAN, R.G. (1969): Characteriza-tion of watennelon mosaic virus strains byserology and other properties. Phytopathology.59: 809 - 818.MILNE, R.G. & LUISONI, E. (1977): Rapid, immuneelectron microscopy of virus preparations. InMethods in Virology. (eds. K. Maramorosch andH. Koprowski). Vol. 6, 265 - 281.PALUKAITIS, P. & SYMONS, R.H. (1980): Nucleotidesequence homology of thirteen tobamovirusRNAs as detennined by hybridization analysiswith complementary DNA. Virology. 107: 354-361.PALUKAITIS, P., RANDLES, J.W., TIAN, Y.T., KANG,I.Y. & TIEN, P. (1981): Taxonomy of severaltobamoviruses from China as detennined bymolecular hybridization analysis with comple·mentary DNA. InteTV1.Tology. 16: 136 -141.PURCIFULL, D,E, & HIEBERT, E. (1979): Serologicaldistinction of watennelon mosaic virus isolates.Phytopathology. 69: 112 -116.RANDLES, J.W., PALUKAITIS, P. & DAVIES, C. (1981):Natural distribution, spread and variation, in thetobacco mosaic virus infecting Nicotiana glaucain Australia. Ann. appl. Biol. 98: 109 - 119,SHALLA, T.A. & SHEPARD, J.F. (1970): An antigenicanalysis of potato virus X and of its degradedprotein. II. Evidence for a conformationalchange associated with the depolyffierization ofstructural protein. Virology. 42: 835 - 847,SHEPARD, J.F. & SHALLA, T.A. (1970): An antigenicanalysis of potato virus X and of its degradedprotein. I. Evidence for and degree of antigenicdisparity, Virology. 4: 825 - 834.SHEPARD, J.F. & SECOR, G. (1972): The effects ofenzymatic digestion on the molecular weight andantigenic specificity of potato virus X protein.Phytopathology. 62: 1154 -1160,TAYLOR, J.M., ILLMENSEE, R" and SUMMERS, J.(1976): Efficient transcription of RNA into DNAby avian sarcoma virus polymerase. Biochim.Biophys. Acta. 442: 324 - 330.(Received 31 December, 1984)PERTANIKA VOL. 8 NO.2, 1985 287

Relationship between watermelon mosaic virus (WMV-I) and

watermelon mosaic virus 2 (WMV-2) on the basis of

nucleotide sequence homology

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Relationship between watermelon mosaic virus (WMV-I) and watermelon mosaic virus 2 (WMV-2) on the basis of nucleotide sequence homology

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