Tian Yan-Ping, Hepojoki Jussi, Ranki Harri, Lankinen Hilkka, Valkonen Jari P T
Department of Agricultural Sciences, Plant Pathology Laboratory, University of Helsinki, Helsinki, Finland.
Department of Virology, Peptide and Protein Laboratory, Infection Biology Research Program, Haartman Institute, University of Helsinki, Helsinki, Finland.
PLoS One. 2014 Dec 26;9(12):e115766. doi: 10.1371/journal.pone.0115766. eCollection 2014.
Potato virus Y (PVY, genus Potyvirus) causes substantial economic losses in solanaceous plants. Routine screening for PVY is an essential part of seed potato certification, and serological assays are often used. The commercial, commonly used monoclonal antibodies, MAb1128, MAb1129, and MAb1130, recognize the viral coat protein (CP) of PVY and distinguish PVYN strains from PVYO and PVYC strains, or detect all PVY strains, respectively. However, the minimal epitopes recognized by these antibodies have not been identified.
METHODOLOGY/PRINCIPAL FINDINGS: SPOT peptide array was used to map the epitopes in CP recognized by MAb1128, MAb1129, and MAb1130. Then alanine replacement as well as N- and C-terminal deletion analysis of the identified peptide epitopes was done to determine critical amino acids for antibody recognition and the respective minimal epitopes. The epitopes of all antibodies were located within the 30 N-terminal-most residues. The minimal epitope of MAb1128 was 25NLNKEK30. Replacement of 25N or 27N with alanine weakened the recognition by MAb1128, and replacement of 26L, 29E, or 30K nearly precluded recognition. The minimal epitope for MAb1129 was 16RPEQGSIQSNP26 and the most critical residues for recognition were 22I and 23Q. The epitope of MAb1130 was defined by residues 5IDAGGS10. Mutation of residue 6D abrogated and mutation of 9G strongly reduced recognition of the peptide by MAb1130. Amino acid sequence alignment demonstrated that these epitopes are relatively conserved among PVY strains. Finally, recombinant CPs were produced to demonstrate that mutations in the variable positions of the epitope regions can affect detection with the MAbs.
CONCLUSIONS/SIGNIFICANCE: The epitope data acquired can be compared with data on PVY CP-encoding sequences produced by laboratories worldwide and utilized to monitor how widely the new variants of PVY can be detected with current seed potato certification schemes or during the inspection of imported seed potatoes as conducted with these MAbs.
马铃薯Y病毒(PVY,马铃薯Y病毒属)在茄科植物中造成重大经济损失。PVY的常规检测是种薯认证的重要组成部分,血清学检测经常被使用。商业上常用的单克隆抗体MAb1128、MAb1129和MAb1130,分别识别PVY的病毒外壳蛋白(CP),区分PVYN株系与PVYO和PVYC株系,或检测所有PVY株系。然而,这些抗体识别的最小表位尚未确定。
方法/主要发现:使用斑点肽阵列来绘制MAb1128、MAb1129和MAb1130识别的CP中的表位。然后对鉴定出的肽表位进行丙氨酸替换以及N端和C端缺失分析,以确定抗体识别的关键氨基酸和各自的最小表位。所有抗体的表位都位于最靠近N端的30个残基内。MAb1128的最小表位是25NLNKEK30。用丙氨酸替换25N或27N会削弱MAb1128的识别,而替换26L、29E或30K几乎会消除识别。MAb1129的最小表位是16RPEQGSIQSNP26,识别的最关键残基是22I和23Q。MAb1130的表位由5IDAGGS10残基定义。6D残基的突变消除了MAb1130对该肽的识别,9G残基的突变则强烈降低了这种识别。氨基酸序列比对表明,这些表位在PVY株系中相对保守。最后,制备了重组CP,以证明表位区域可变位置的突变会影响MAb的检测。
结论/意义:获得的表位数据可与全球各实验室产生的PVY CP编码序列数据进行比较,并用于监测用当前种薯认证方案或使用这些MAb对进口种薯进行检测时,能在多大程度上检测到PVY的新变体。