Presence of necrotic strains of Potato virus Y in Mexican potatoes

Correction to Ramírez-Rodríguez VR, Frías-Treviño G, Aviña-Padilla K, Silva-Rosales L, Martínez-Soria JP: Presence of necrotic strains of Potato virus Y in Mexican potatoes. Virology Journal 2009, 6:48


Background
Potato virus Y (PVY), the type member of the family Potyviridae, can infect potato, tobacco, tomato and pepper as well as wild species, especially those in the Solanaceae family [1]. The conventional classification of PVY isolates is based on primary hosts, symptoms induced in differential plants and serological reaction to monoclonal antibodies. The isolates reported so far, have been classified in three main strains: PVY N , PVY O and PVY C [2]. Isolates belonging to the PVY N strain induce severe vein necrosis on Nicotiana tabacum leaves. This strain has been divided into two groups: the first one causing mild mosaic in most potato cultivars, while the second one provokes "potato tuber necrotic ring disease" (PTNRD) and severe chlorotic mosaic in the leaves [3]. It also produces veinal necrosis in tobaco leaves and is referred as PVY NTN [NTN = isolates belonging to the necrotic group (N) of PVY and inducing tuber necrosis (TN)], according to a decision of the European Association of Potato Research Virology Section [4,5]. The PVY O strain isolates induce non-necrotic mosaics on tobacco leaves but more severe symptoms on potato, such as crinkling, leaf dropping or severe necrotic mosaic. The PVY C strain causes stipple streak on potato cultivars carrying the Nc resistance gene and non-necrotic symptoms, similar to those of PVY O , on N. tabacum leaves [6]. The symptoms of mosaic are masked in temperatures out of the normal rank from 10°C to 25°C.
The serological classification of PVY isolates is a matter of discussion. Coat protein-directed polyclonal antibodies do not discriminate between PVY strains so monoclonal antibodies specific to O and N strains have been used to characterize selected PVY isolates [7,8]. Moreover, some isolates were determined as PVY O using monoclonal antibodies, nevertheless induced tobacco vein necrosis, which are but infectious and induce less severe symptoms in potato than the other PVY N isolates and it has been called PVY N -Wilga isolate [9,10]. Which shows that the serological and pathogenic traits of a determined PVY isolate seem not to have an absolute relationship and, on other hand, some serological detections have not showed the specificity expected [2,5,8,11].
Conventional methods of PVY classification do not result in a universal criterion for grouping virus isolates within species. Complete genomic nucleotide sequence analysis of isolates which showed that the degree of similarity differs across the genome, being the 5' terminal untranslatable segment the most variable region of the PVY genome [12]. This has led to a re-evaluation of the subgroup based on gene sequences analysis, which has led to an alignment with the phenotype-based classification with exceptions concerning the ability to induce tobacco veinal necrosis. The sequence-based clustering of all isolates reported so far. A comparative analysis of available sequences of necrotic and non necrotic isolates led to the hypothesis that the tobacco vein necrosis determinant is localized in the 3' terminal region covering the CP gene and 3' NTR [13]. Other studies using the CP and P1 genes and the 5' and 3' NTRs have concluded that those regions are not involved in the induction of vein necrosis in tobacco [14]. From de clustering and necrotizing properties, it has been suggested that the ability to cause vein necrosis in tobacco could be located in the 5' rather than in the 3' half of the viral RNA, in the HC-Pro protein specifically [15].
It has been suggested that the strain NTN of PVY resulted of the natural combination between PVY O , or PVY C , and PVY N [16]. Isolates of PVY, which might be intermediate forms of the PVY O and PVY N groups, have been reported, sharing similar symptoms as well as serological and genomic properties with both groups [17]. Moreover, it has been indicated upon comparisons of the 5'NTR and P1 sequences of PVY N and PVY NTN from American and European origin, that they formed separate geographic groups whit a 98% or higher similarities between them [18]. This suggests that the NTN strain detected in some geographic region may have arisen from an N strain of the same region. This may explain the difference among NTN isolates of different geographic regions in the world. A similar finding is reported from amino acid sequence analyses of the capsid protein gene of American and Japanese isolates [11].
To strengthen the PVY group classification and to determine the relationships between Mexican isolates and PVY isolates from other parts of the world, we determined the nucleotide sequence of the 5'NTR and P1 coding region for ten Mexican isolates and their biological characterization with six plants species. This is the first report of PVY W and PVY N presence in Mexico.

ELISA and biological tests
Two Mexican isolates showed positive reaction with PVY O antibodies, Pic3 and Vic20 isolates ( Table 1). The isolates were inoculated to six plants species (Capsicum annuum var. Serrano; Chenopodium quinoa; Solanum lycopersicum; Nicotiana tabacum cv. Burley; Physalis floridana and S. tuberosum cv. Alpha) (data no shown). In three species (N. tabacum, Ph. floridana and S. tuberosum) symptoms were more severe than in the other species tested. Three isolates belonging to the N strain, Pic1, Vic6 and Vic15 (Table 1), inoculated in plants of N. tabacum induced typical necrotic symptoms; i.e. vein necrosis 7-10 days after inoculation. The Pic3 and Vic20 isolates, both PVY O (Table 1), induced severe chlorotic mosaics on tobacco leaves as initial symptoms (7-10 days after inoculation) and moderate vein necrosis plus severe distortion of leaves three weeks post-inoculation. The aggressiveness of PVY Pic3, Vic6, Vic15 and Vic20 isolates on N. tabacum as well as the severity of symptoms showed by Ph. floridana plants infected with PVY Pic3, Vic6, Vic15 and Vic20 isolates was remarkable.

Sequence analysis 5'-NTR
Twentynine nucleotide sequences of PVY 5'NTR were analyzed: (five O, sixteen N and eight NTN strains respectively). Of these sequences five were from Mexico (this report, GenBank accession numbers AY700016-AY700020) and twentyfour from other parts of the world. The Mexican isolates of PVY O , namely Pic3 and Vic20 grouped in a cluster with those others identified as O and N strains (O-N cluster) while the PVY N isolates (Vic6, Vic15 and Pic1) grouped in a different cluster with other

P1 gene
Thirty four sequences of the whole P1 gene (five from Mexico) were analyzed, where they are included to O strain (eight isolates), N strain (eighteen isolates) and NTN strain (eight isolates), yielding a percentage of similarity ranking between 63-100%. The general clustering shows two main groups: "O-N" and "N-NTN" (data not shown). In the group "N-NTN" there is a subcluster composed by three isolates: two Mexican PVY O isolates (Pic3 and Vic20) with the PVY N -Wi-P Poland isolate (Accession Number AF248500), having the highest similarity among all the isolates analyzed: 96.5% (Vic20 and Wi-P) and 98.9% (Pic3 and Wi-P). In turn, the three Mexican isolates of the N strain showed a clustering with seven European isolates in the group "N-NTN" but separated from the cluster of nine North American isolates. The P1 gene amino acid sequences from the same isolates were analyzed; having a range in similarity of 55-100% and similar clustering to analysis of nucleotide sequences (data not shown).
The thirtyfour nucleotide sequences of the P1 gene were analyzed with the recombination program RDP. In this analysis, different windows sizes and different maximum acceptable probability values were used. In general, two potentially recombinant regions were detected in PVY N -N 5yt and two PVY O Mexican isolates, detecting potential crossover sites in the nucleotides in position 297, 301, 321 and 825 ( Figure 1).
Based on the results obtained from the recombination analysis of P1 gene, the thirtyfour nucleotides sequences were analyzed in two regions. For this analysis the CLUS-TALX, DNAStar, Mega3 and PAUP programs were used. One region that included the 519 nucleotides of the 3' end (with a similarity range of 62-100%), grouping the five Mexican isolates next to PVY N-NTN isolates (data not shown). The other putative region for recombination included the 306 nucleotides near the 5' end (with a range of 64-100%), produced a dendrogram that showed two clusters: "O-N", where are included the Pic3, Vic20 and PVY N -Wi-P (Accession Number AF248500) isolates, and the "N-NTN" group which included Pic1, Vic6 and Vic15 Mexican isolates ( Figure 2). The similarity between PVY O isolates (Pic3 and Vic20) and PVY N Wi-P was 98.7-99.3%, the two Mexican PVY O isolates have 66-67% similarity with three PVY necrotic isolates: Pic1, Vic6 and Vic15.

Discussion
Nucleotide sequence analysis of two hundred sequences of different regions of PVY genome (data not shown) and thirteen isolates with complete genomic sequence reported, showed that the degree of similarity differs across the genome, and that the 5' terminal segment is the most variable region of the PVY genome as previously reported [12]. In the nucleotide sequence analyses we found more variability in the 5'NTR than in the P1 gene (58 to 100% and 63 to 100%, respectively).
According to the antigenic and pathogenic properties showed by five PVY Mexican isolates (Pic1, Pic3, Vic6, Vic15 and Vic20) the serotype and the pathotype of three necrotic isolates, Pic1, Vic6 and Vic15, they agreed. Different results were obtained with Pic3 and Vic20 isolates wich might belong to pathotype "N" and serotype "O" (Table 1). Isolates with similar traits to Pic3 and Vic20 isolates have been reported in Poland, Canada, Spain and France [3,15,17,19,20]. For instance, the PVY N W (Wilga) isolate discovered in Poland in 1984, was first described as differing in virulence and aggressiveness in potato from the earlier PVY N isolates and was later shown to be serologically related to PVY O isolates [14]. Additionally, the nucleotide sequence comparisons from CP gene of Pic3 and Vic20 isolates (pathotype "N" and serotype "O" both isolates) with seventy isolates from outside Mexico, showed a 99% similarity with PVY O isolates and clustered with other fifteen PVY O isolates analyzed (data not shown). showed a similarity of 96%. This specific and apparently discordant clustering of two PVY O Mexican isolates with isolates from different geographic regions is similar to the one observed in other works [15,21]. Two Canadian isolates (I-136 and I-L56) were found to be closely related to the PVY N N242 (European) isolate in the 5'NTR region with 99% nucleotide similarity [15].
The dendrogram obtained using thirtyfour P1 gene whole sequences (data not shown) shows two main groups, the O-N and the N-NTN groups. The three Mexican isolates of the N strain cluster with seven European isolates in "N-NTN" group but in different subgroup of nine North American isolates. Interesting is the cluster "O-N" grouping three isolates: two from Mexico and one from Poland, which have the highest similarity values among the thirtyfour sequences analyzed: 96.5% (between Vic20 and Wi-P) and 98.9% (between Pic3 and Wi-P). This subgroup of new isolates is located in an independent branch different from the "N-NTN" and "O-N"groups (data not shown).
There is growing evidence that RNA recombination is a major evolutionary factor in plant RNA viruses. In our study, from the four crossover areas detected between PVY O -like and PVY N -like sequences, one putative recombination site was found in the P1 gene of several PVY N W isolates. Moreover, in the P1 N-terminal region (at position 499-500) of the PVY N Wi-P isolate there seems to be a switching from PVY O -to PVY N -like sequence [15,16].
In this work with thirty four P1 gene sequences were analyzed and potential crossover recombination sites were detected in the nucleotides 297, 301, 321 and 825 ( Figure  1

Conclusion
This is the first report of PVY necrotic strains in Mexico with two PVY isolates belonging to O strain (by serologic detection) that could be described as PVY N -like isolates (Wilga strains). Based in our analysis and observations, we suggest that the virus determinants of tobacco necrosis may be localized at the 3' end of the PVY P1 gene. The PVY isolates were inoculated in six host species maintained at greenhouse conditions on natural daylight periods (about 12 hours) and temperatures ranging between 15° to 26°C. Chenopodium quinoa, Capsicum annuum (var. Serrano),Solanum lycopersicum, Nicotiana tabacum (cv. Burley), Physalis floridana and Solanum tuberosum (cv. Alpha) were the host species used, and ten plants from each specie were inoculated with each one of the Mexican isolates.

RT-PCR and sequencing
RNA was extracted from the same plants used for ELISA test using the TRIZOL ® method (Gibco BRL). DNA amplification of the 5'NTR and P1 regions was done in two steps: the first one to perform the reverse transcription (RT) reaction and later the PCR. RT step was done using the enzyme M-MLV RT (Promega Corporation. Madison, WI, USA), using the reverse primer 3P1R (5'-AGGA-TATCTCATTCGTGCCC-3') in order to reverse transcribe the 5'NTR-P1 genomic region. The same primer used in RT and the forward primer G-121 (5'-AATTAAAACAACT-CAATACAACATAAGAAA-3') were used in the PCRs. The amplified products were cloned in the pGEM-T Easy vector (Promega Corporation, Madison, WI, USA). Nucleotide sequencing of cloned PCR products was carried out on plasmid minipreps (High Pure Plasmid Isolation Kit, Hoffman-La Roche, LTD, Basel, Switzerland)) using an