Characterization of Citrus tristeza virus isolates from grapefruit (Citrus paradisi Macf.) accessions of Citrus Active Germplasm Bank

Caracterização de isolados do vírus da tristeza dos citros de acessos de pomelos (Citrus paradisi Macf.) do Banco Ativo de Germoplasma de Citros

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ARTIGOS

Characterization of Citrus tristeza virus isolates from grapefruit (Citrus paradisi Macf.) accessions of Citrus Active Germplasm Bank

Caracterização de isolados do vírus da tristeza dos citros de acessos de pomelos (Citrus paradisi Macf.) do Banco Ativo de Germoplasma de Citros

Maria Júlia Corazza-Nunes^{I, V}; Marcos Antonio Machado^II; Dagmar Ruth Stach-Machado^III; William Mário Carvalho Nunes^{IV, V}; Sérgio Alves de Carvalho^II; Gerd Walter Müller^V

^IDepto. de Biologia, Universidade Estadual de Maringá. 87020-900 Maringá, PR, Brazil. e-mail: [e-mail]

^IIC.C.S.M.-IAC. Cordeirópolis, SP, Brazil

^IIIDepto. de Imunologia, Unicamp, Campinas, SP, Brazil

^IVDepto. de Agronomia, UEM. Maringá, PR, Brazil

VNúcleo de Pesquisa em Biotecnologia Aplicada - Universidade Estadual de Maringá – NBA/UEM

ABSTRACT

Citrus tristeza virus (CTV) isolates from 35 grapefruit accessions belonging to Citrus Active Germplasm Bank of the "Instituto Agronômico de Campinas" located at the "Centro APTA Citros Sylvio Moreira", Cordeirópolis, São Paulo state, Brazil, were characterized and evaluated through symptoms in the trees, biological indexing, immunological diagnosis with different monoclonal antibodies and SSCP analysis (single-strand conformation polymorphism) of the coat protein gene. Symptomatology indicated that, in general, the group of plants with smaller canopy volume and severe stem pitting differed significantly from the group that presented greater vegetative development and mild to moderate stem pitting. However, the isolates from most of the accessions induced mild reaction on Mexican lime. The serological evaluation through the DAS-ELISA using monoclonal antibodies did not reveal any association between virus titer in the plant tissue and symptoms. The reaction with different monoclonal antibodies and the distinct electrophoresis patterns obtained through SSCP showed that there is a high degree of diversity among the isolates that infect these grapefruit accessions. High complexity within the same isolate was also observed in the SSCP profiles. This finding indicates that the CTV isolates from these plants are a complex mixture of CTV haplotypes. Similar SSCP banding patterns were observed among some plants with strong stem pitting symptoms, and among some plants with weak or moderate stem pitting symptoms.

Additional keywords: ELISA, monoclonal antibodies, single-strand conformation polymorphism

RESUMO

Isolados do vírus da tristeza dos citros (CTV) de 35 acessos de pomelos que fazem parte do Banco Ativo de Germoplasma de Citros, localizado no Centro APTA Citros Sylvio Moreira, Cordeirópolis, São Paulo, Brasil, pertencente ao Instituto Agronômico de Campinas (IAC), foram caracterizados através dos sintomas observados nas árvores, indexação biológica, diagnóstico imunológico e análise SSCP (polimorfismo de conformação de fita simples) do gene da proteína do capsídeo. O grupo de plantas que, em geral, apresentou menor volume de copa e severo sintoma de canelura diferenciou-se significativamente do grupo com maior desenvolvimento vegetativo e fraco a moderado sintoma de canelura. No entanto, a maioria dos isolados de CTV das plantas de ambos os grupos induziu fraca reação em limão galego e nenhuma relação entre títulos do vírus nos tecidos e sintomatologia foi observada na avaliação sorológica conduzida por DAS-ELISA. A reação com diferentes anticorpos monoclonais e os distintos padrões eletroforéticos obtidos por SSCP demonstraram que há uma grande diversidade entre os isolados de CTV que infectam os acessos de pomelos. Alta complexidade de bandas dentro de um mesmo isolado foi também observada nos perfis SSCP, demonstrando que cada isolado é constituído por uma mistura de diferentes haplótipos de CTV. Padrões SSCP semelhantes foram observados entre algumas plantas com fortes sintomas de caneluras e entre algumas plantas com sintomas fracos ou moderados de caneluras.

Palavras-chave adicionais: ELISA, anticorpos monoclonais, SSCP.

The Citrus Active Germplasm Bank (Citrus-AGB) of "Instituto Agronômico de Campinas" (IAC), located at the "Centro APTA Citros Sylvio Moreira", Cordeirópolis, State of São Paulo, Brazil, was initiated in 1930 and is one of the most important citrus collections of the world (7).

The collections were increased and renewed along the years, serving as material source for research and production of new scion and rootstock varieties to the Brazilian citriculture (14, 22). Nowadays the IAC Citrus-AGB has 1.750 accessions being 59 out of them represented by different grapefruit varieties (Citrus paradisi Macf) grafted on Cleopatra mandarin (C reshni Hort. Ex Tan.) (5).

In Brazil the grapefruit production is small because this fruit is not popular besides being susceptible to the Citrus tristeza virus (CTV). They were probably the first citrus plants to show altered growth and development when infected by CTV even on tolerant rootstocks (16). The most evident tristeza symptoms for these cultivars are reduced growth and development, small fruits and thick rinds, and especially the presence of stem pitting in young branches and twigs. However, the possibility to exploit some commercial niches requires vigorous and productive groves. In this perspective, the characterization of CTV isolates of some grapefruit accesses of the Citrus-AGB to find out those naturally infected with mild isolates could contribute to the selection of mother trees with commercial potential.

The procedures more often used for these purposes involve biological indexing (3, 5); immunological methods via different monoclonal antibodies (12, 20, 24, 25); dsRNA (double-strand RNA) analysis (17); restriction fragment length polymorphism (RFLP) (9, 30), reverse transcription-polymerase chain reaction (RT-PCR) (10), and single-strand DNA conformation polymorphism (SSCP) (4, 6, 27).

In this study CTV isolates from 35 grapefruit accessions belonging to IAC Citrus-AGB were characterized and evaluated through tristeza symptoms in the tree, biological indexing, immunological diagnosis with different monoclonal antibodies, and SSCP analysis of the coat protein gene.

MATERIALS AND METHODS

Virus isolates and plant materials. The CTV isolates were obtained from 35 grapefruit accessions, which belong to the new and old clone collection from the IAC Citrus-AGB (Table 1). The plants had about 10 years when evaluated. The evaluation of tristeza symptomatology and serological analysis were carried out on three repetitions of each access. The biological indexing and molecular analyses were done with one clone of each access.

Evaluation of tristeza symptomatology. Stem pitting symptoms were evaluated by peeling of the bark from 15 cm long segments, cut from young twigs, which were sampled from the North, South, East and West quadrants in a total of four segments for plant. A rating scale (15), from 0 to 5, was used to quantify the presence of the stem pitting, where: 0 = no stem pitting, 1 = 1 to 15 stem pits, 2 = 16 to 30 stem pits, 3 = 31 to 50 stem pits, 4 = 51 to 80 stem pits and 5 = the total segment was covered with stem pits. The plant growth and development was calculated by evaluating the canopy volumes by the formula: V = 2/3 p R² H (23). Tukey's HSD test (P > 0.05) was used to verify the correlation between canopy volume and stem pitting intensity.

Biological indexing. The biological indexing was conducted under greenhouse conditions. The indicator plants were prepared by grafting two buds from every one of the 35 source trees and one bud from a healthy Mexican lime (C aurantifolia Swing.) onto a Rangpur lime (C limonia Osbeck) rootstock. Each test had five plants with positive and negative controls. CTV symptoms (presence and intensity of vein clearing) on the indicator plants were evaluated two to four months after grafting. They were characterized according to Carvalho et al. (5) as: mild (+) (very faint traces of vein clearing); severe (++) (vein clearing); and very severe (+++) (intensive vein clearing up to the point of vein suberization and leaf curling).

ELISA. The serological analyses and purification of virus dsRNA were processed from the bark of young branches, which were taken around the canopy and combined to make one sample. The DAS-ELISA (double antibody sandwich indirect enzyme-linked immunosorbent assay) was applied according to Garnsey & Cambra (8). The polyclonal antibodies PCA 1006/Br (1:10.000 dilution), monoclonal antibodies (MAbs) 30E-09, 37D-09 and 39-09 (1:10.000 dilution) were produced from recombinant proteins obtained from the coat protein of severe Brazilian isolates (31) and MCA-13 to the T-36 isolate of CTV from Florida (1:15.000 dilution) (21). The PCA 1006/Br was used to cover the plates, while the MAbs were used as a second antibody. Approximately 0.1g of fresh tissue was prepared by grinding and homogenizing in 2ml of phosphate buffer, pH 7.4, containing 0.5ml/l tween 20 (PBST) and 20g/l polyvinylpyrrolidone (PVP-40) at 1:20 (w/v) dilution. Extracts from healthy and infected plants were utilized as negative and positive controls, respectively. The assay had two repetitions per sample and was evaluated after 3h of incubation. The plates were read with a BioRad ELISA Plate Reader at a 405 nm wavelength. The samples were considered positive if the optical density was higher three times greater than the mean of healthy controls (21).

Purification of CTV dsRNA. The dsRNA was extracted from CTV infected lyophilized tissue according to Valverde et al. (33). Phenol, chloroform-isoamyl alcohol (24:1), SDS (sodium dodecyl sulfate) and 2X STE extraction buffer (1x STE = 0.05 mM Trisma base; 0.1 M NaCL; 1 mM EDTA pH: 6.8) were used. Afterwards, the dsRNA was purified through two cycles of chromatography with cellulose columns (Whatman CF 11).

cDNA synthesis and PCR amplication. The dsRNA was denatured at 94ºC for 5 min and used as templates for the synthesis of the first strand cDNA of the coat protein gene (CPG). This procedure was carried out according to Sambrook et al. (28) with modifications. The amplification of the CPG region was done with primers CN-119-CTV (5' AGATCTACCATGGACGACGAAACAAAG 3') and CN-120-CTV (5' GAATTCGCGGCCGCTCAACGTGTGTTAAATTTCC 3'), which were derived from the tristeza T-36 haplotypes from Florida, USA (32). The amplifications were performed in a MJ thermocycler, programmed for 35 cycles of 1 min at 94ºC (denaturation), followed by 1 min at 55ºC (annealing), and 2 min at 72ºC (DNA synthesis) followed by a final extension at 72ºC for 5 min. The final CPG product was purified in 0.8% low melting agarose.

SSCP analysis. For the SSCP analysis of the 35 CTV isolates, 1-5 µL of the amplified CPG purified fragments were mixed with an equal volume of denaturing solution (95% de formamide, 2 mM de EDTA and 0.05% bromophenol blue). The samples were heated for 10 min at 95ºC and placed immediately on ice. The denatured CPG fragments were resolved in a 8% non-denaturing polyacrylamide gel containing TBE buffer (45 mM Tris-Boric, 1 mM EDTA, pH 8,4). The electrophoresis was conducted at a constant voltage of 200 V for 7 h at 25ºC. Subsequently the gels were stained with silver nitrate based upon Beidler et al. (2).

RESULTS AND DISCUSSION

The results obtained from the immunological diagnosis, CTV severity, evaluated through of the stem pitting symptoms, canopy volume measurements and biological-indexing assays of CTV isolates from 35 grapefruit accessions are represented in Table 1. The stem pitting and canopy volume measurements represent the average of three repetitions.

CTV severity, vegetative development and biological indexing

Severe stem pitting symptoms (rating 4-5) were observed in approximately 46% of the grapefruit accessions of the old clone (OC) and of the new clone collections (NC) from AGB. The remaining plants showed mild (1,2) to moderate (3) stem pitting symptoms (Table 1).

Data from the canopy volume also indicated a great variation in vegetative development among the accesses of both collections, due to this, two groups were formed: group 1, where plants had canopy volume inferior to 11 m³ and in general severe stem pitting, and group 2, plants with canopy volume superior to 11 m³ and mild to moderate stem pitting (Table 1). These groups differed significantly according to Tukey's HSD test (P > 0.05).

Many of the accessions that were placed into group 1, especially the varieties 'Viçosa', 'Marsh Seedless', 'Marsh Seedy', 'Redblush' and 'Red Mexican', were badly affected in their growth and showed severe stem pitting, probably due to infection by severe CTV isolates. However, some plants from this group had poor growth and showed mild stem pitting. This fact to mean that the growth of these plants was so seriously affected that didn't allow not even the expression of stem pitting symptom. Further, some factors other than the presence of CTV could have affected the canopy development.

On the contrary of group 1, the plants of group 2 had much better growth and less stem pitting, standing this out in the cases of accessions 'Dalandan', 'Pamplemousse', 'Siamesa', 'Mac Carthy' and 'De Maurítius', all with mild stem pitting symptoms and values for the canopy volume higher than for most of the other plants. A few accessions such as 'Rubi', 'Thompson Pink', and 'Shamber' had high canopy volume values even though they had moderate stem pitting symptoms.

Biological indexing results showed that the isolates from most of the 35 accessions induced mild reaction on Mexican lime, although some of these accessions ranged from moderate to severe stem pitting symptoms. On the other hand, others, which incited mild or moderate stem pitting symptoms, developed severe reactions on Mexican lime (Table 1).

These results confirm the hypothesis about the specificity of isolates in a complex when interacting with the host. Different studies have demonstrated that the expression of CTV symptoms vary according to the isolate severity as well as with the species of the indicator plant (1, 13). The Mexican lime is a sensitive indicator for the expression of vein clearing, leaf curling, dwarfism and stem pitting. However, these symptoms do not necessarily always reflect the severity of the isolates in other species and varieties of Citrus (26).

ELISA

For the serological evaluation (Table 1), it was observed that plants from both groups had a positive reaction with all monoclonal antibodies tested. This indicates the presence of different CTV isolates, which infected the grapefruit accessions from the AGB. Titers above 1.00 were noted in all plants, from both groups, with the monoclonal antibody 30E-09, which imply its universal properties.

The detection of CTV haplotypes by the MCA-13, 37D-09 and 39-09 specific monoclonal antibodies revealed that plants from Group 1 (those with reduced canopy volumes and strong stem pitting symptoms) as well as from Group 2 (those with high canopy volumes and mild stem pitting symptoms) had titer between 0.1 and 1.5. Therefore, no correlation was observed between the CTV severity and the detection by the antibodies. It confirms previous observations that these traits are not necessarily correlated (12, 24). According to Nickel et al. (17), field plants are often infected by a mixture of CTV haplotypes and the predominating haplotypes in an infected tree determine the symptomatology in the plant. The explanation of the results from plants with severe symptoms, but with low antibody detection, could be due to the absence of epitopes for their detection. Additionally, Powell et al. (24) argument that positive plants goes isolated severe of CTV cannot express symptoms during various years. By contrast, plants with strong decline symptoms can have their growth and development affected by other factors besides the presence of CTV.

The MAbs 37D-09 and 39-09 showed high titers (above 0.5) for a large number of accessions when compared to MCA-13. The MCA-13 monoclonal antibody recognizes a linear epitope and selectively reacts with isolates that induce citrus decline in Florida (USA), however, it does not react with mild isolates (21). According to Pappu et al. (19), the reaction of MCA-13 depends upon the presence of phenylalanine amino acid in position 124 of the CTV coat protein gene. For Nikolaeva et al. (18), the MCA-13 is not able to distinguish isolates that cause decline from those that provoke stem pitting and it can fail to react with isolates that incite decline from regions outside of Florida. In Japan, Kano et al. (11) documented that this monoclonal antibody reacted with mild isolates. This Mab has also reacted with Brazilian mild isolates, and it is not able to recognize severe isolates (35).

In contrast, the MAbs 37D-09 and 39-09 obtained from recombinant coat protein extracted from the complex of severe isolates from 'Capão Bonito' (32) reacted with CTV isolates from various grapefruit accessions. This result suggests that these isolates and those from 'Capão Bonito' share the specific epitope of the coat protein recognized by MAbs 37D-09 and 39-09. Further, low titers with these antibodies were also observed in many plants with severe stem pitting symptoms.

SSCP analysis

The great diversity among CTV isolates, that infect grapefruit accessions from AGB, was also shown by the SSCP analysis (Figure 1). Through the number of bands and their positions, it was observed high heterogeneity in the SSCP profile pattern among isolates and high complexity within the same isolate. Considering that each band corresponds to one of the two DNA strands from the dsDNA obtained after RT-PCR, one to four haplotypes were observed in the CTV isolates infecting grapefruit accessions from IAC Citrus-AGB.

Similar electrophoresis patterns were documented among isolates from the following accession groups: between 'Rubi' (OC 315) and 'Red Mexican' (OC 317); among 'Redblush' (OC 316), 'Foster' (OC 328), 'Marsh da Florida'(NC 345), 'Redblush' (NC 667), 'Marsh Seedless S. Sebastião' (NC 668) and 'Marsh Seedless Limeira' (NC 669); among 'Marsh Seedless' (OC 321), 'Marsh Seedy' (OC 323), 'Cannores' (OC 326), 'Marsh Seedless' (NC 331), 'Coco Variação' (NC 341) and 'Arananyan' (NC 342). Almost all these accessions (except OC 315 and OC 326) belong to the group 1 and showed moderate to severe stem pitting symptoms (ranging 3-5). Only accession OC-328 showed mild stem pitting symptoms, but developed severe reactions on Mexican lime and presented high titer with specific monoclonal antibodies.

Similar SSCP banding patterns were also documented for the accessions 'Mac Carthy' (OC 324) and 'Retiro' (OC 329), and between 'De Maurítius' (NC 672) and 'Pamplemousse' (NC 673). These accessions belong to group 2 and showed mild stem pitting.

However, all the accesses reacted positively with all the specific monoclonais and not always it happens correlation among SSCP banding patterns and title of the virus.

The evidence obtained through the stem pitting symptoms, canopy volume analyses, immunological diagnosis with different monoclonal antibodies and SSCP analyses demonstrated that the different grapefruit accessions from the old and new clone collections from the IAC Citrus-AGB are infected with severe CTV isolates. The accesses of the group 2, that presented better performance in relation to the CTV, are not varieties of commercial importance. Therefore, considering that a commercial grapefruit variety from the IAC Citrus-AGB needs to be used as mother tree, it must be "cleaned" from CTV by micro shoot grafting and than undergo the pre-immunization procedure.

Pre-immunization studies with grapefruit plants were conducted in Australia (3), South Africa (34), Japan (29), Florida (25) and Brazil (16). Many of the pre-immunized plant materials showed superior vigor and production when compared to the non-pre-immunized plants.

Data de chegada: 19/07/2005. Aceito para publicação em: 23/01/2006.

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Publication Dates

• Publication in this collection
  11 Jan 2007
• Date of issue
  Sept 2006

History

• Accepted
  23 Jan 2006
• Received
  19 July 2005