Unraveling the Etiology of North American Grapevine Yellows (NAGY): Novel NAGY Phytoplasma Sequevars Related to ‘Candidatus Phytoplasma pruni’

Author:

Davis Robert E.1,Dally Ellen L.1,Zhao Yan1,Lee Ing-Ming1,Wei Wei1,Wolf Tony K.2,Beanland LeAnn2,LeDoux Douglas G.3,Johnson David A.3,Fiola Joseph A.4,Walter-Peterson Hans5,Dami Imed6,Chien Mark7

Affiliation:

1. Molecular Plant Pathology Laboratory, United States Department of Agriculture–Agricultural Research Service, Beltsville, MD 20705

2. Alson H. Smith, Jr. Agricultural Research and Extension Center, Virginia Tech, Winchester 22602

3. Missouri Department of Agriculture, Jefferson City 65109

4. University of Maryland Extension, Western MD Research & Education Center, Keedysville 21756

5. Cornell Cooperative Extension, Cornell University College of Agriculture and Life Sciences, Penn Yan, NY 14527

6. Ohio Agricultural Research and Development Center, The Ohio State University, Wooster 44691

7. Penn State Cooperative Extension, College of Agricultural Sciences, Lancaster, PA 17601

Abstract

North American grapevine yellows (NAGY) disease has sometimes been attributed to infection of Vitis vinifera L. by Prunus X-disease phytoplasma (‘Candidatus Phytoplasma pruni’) but this attribution may not be fully adequate. In this study, phytoplasma strains related to ‘Ca. Phytoplasma pruni’ were found in NAGY-diseased grapevines in Maryland, Pennsylvania, Virginia, Ohio, Missouri, and New York State. Based on restriction fragment length polymorphism analysis of 16S ribosomal RNA gene (16S rDNA) sequences, the strains (termed NAGYIII strains) were classified in group 16SrIII (X-disease group) but they contained a recognition site for the restriction endonuclease MseI that is not present in the 16S rDNA of ‘Ca. Phytoplasma pruni’. The 16S rDNA of the strains differed by three or four nucleotides from that of ‘Ca. Phytoplasma pruni’, indicating that they belonged to two novel 16S rDNA sequevars, designated NAGYIIIα and NAGYIIIβ. Both sequevars differed from ‘Ca. Phytoplasma pruni’ by a single base in each of three regions corresponding to species-unique (signature) sequences described for ‘Ca. Phytoplasma pruni’. Phylogenetic analyses of 16S rRNA genes and SecY proteins, and single-nucleotide polymorphism analyses of secY and ribosomal protein genes, further distinguished the two grapevine sequevar lineages from one another and from ‘Ca. Phytoplasma pruni’. The NAGYIIIα and NAGYIIIβ sequevars also differed from ‘Ca. Phytoplasma pruni’ in regions of the folded SecY protein that are predicted to be near or exposed at the outer surface of the phytoplasma membrane. No evidence indicated that diseased grapevines contained any phytoplasma strain conforming to ‘Ca. Phytoplasma pruni’ sensu stricto. Because the NAGYIII sequevars have not been reported in X-disease, a question is raised as to whether NAGYIII and Prunus X-disease are caused by different phytoplasma genotypes.

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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