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Restricted distribution of potato leafroll virus antigen in resistant potato genotypes and its effect on transmission of the virus by aphids
Author(s) -
BARKER H.,
HARRISON B. D.
Publication year - 1986
Publication title -
annals of applied biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 80
eISSN - 1744-7348
pISSN - 0003-4746
DOI - 10.1111/j.1744-7348.1986.tb03216.x
Subject(s) - potato leafroll virus , biology , phloem , luteovirus , aphid , myzus persicae , virology , plant virus , macrosiphum euphorbiae , virus , homoptera , horticulture , botany , aphididae , pest analysis
SUMMARY Enzyme‐linked immunosorbent assay was used to measure the concentration of potato leafroll virus (PLRV) antigen in different parts of field‐grown secondarily infected plants of three potato genotypes known to differ in resistance to infection. The antigen concentration in leaves of cv. Maris Piper (susceptible) was 10–30 times greater than that in cv. Pentland Crown or G 7445(1), a breeder's line (both resistant). Differences between genotypes in antigen concentration were smaller in petioles and tubers (5–10‐fold) and in above‐ground stems (about 4‐fold), and were least in below‐ground stems, stolons and roots (about 2‐fold). PLRV antigen, detected by fluorescent antibody staining of tissue sections, was confined to phloem companion cells. In Pentland Crown, the decrease in PLRV antigen concentration in leaf mid‐veins and petioles, relative to that in Maris Piper, was proportional to the decrease in number of PLRV‐containing companion cells; this decrease was greater in the external phloem than in the internal phloem. The spread of PLRV infection within the phloem system seems to be impaired in the resistant genotypes. Green peach aphids ( Myzuspersicae) acquired < 2800 pg PLRV/aphid when fed for 4 days on infected field‐grown Maris Piper plants and < 58% of such aphids transmitted the virus to Physalis floridana test plants. In contrast, aphids fed on infected Pentland Crown plants acquired <120 pg PLRV/aphid and <3% transmitted the virus to P. floridana. The ease with which M. persicae acquired and transmitted PLRV from field‐grown Maris Piper plants decreased greatly after the end of June without a proportionate drop in PLRV concentration. Spread of PLRV in potato crops should be substantially decreased by growing cultivars in which the virus multiplies to only a limited extent.