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First Report of Natural Hybrids of Phytophthora nicotianae and P. cactorum on Loquat in Taiwan

January 2001 , Volume 85 , Number  1
Pages  98.2 - 98.2

W. A. Man in 't Veld , Plant Protection Service, P.O. Box 9102, 6700 HC Wageningen, The Netherlands

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Accepted for publication 7 November 2000.

In 1995 loquat trees (Eriobotrya japonica [Thunb.] Lindl.) in several orchards in central Taiwan suffered from a severe stemrot and rootrot (2). Two populations of Phytophthora spp. isolates were recovered from diseased trees by placing pieces of plant tissue in a petri dish containing selective medium (2). One group of isolates possessed papillate sporangia, appeared to be heterothallic with amphigynous antheridia, and had a maximum growth temperature of 36°C. Upon mating, isolates of this group produced oogonia and oospores measuring 26.1 and 21.4 μm in diameter, respectively. These isolates were identified as typical strains of P. parasitica (=P. nicotianae) (2). The second group of isolates showed papillate sporangia, was homothallic with predominantly amphigynous antheridia, and had a maximum growth temperature of 34.5°C. However, the sizes of oogonia and oospores were considerably larger (average 34.7 and 30.3 μm in diameter, respectively) than those of P. nicotianae. Amplification of genomic DNA of one isolate (95023) of the second group by polymerase chain reaction (PCR) using P. nicotianae species specific primers PAR1 and PAR2, produced a special 1,000 bp sequence, indicating that the atypical isolates of second group were closely related to P. nicotianae. Isozyme analysis of two isolates (95023 and 95034, provided by L. L. Chern, Taiwan) of the second group, using the dimeric enzymes malic enzyme (MDHP; EC and malate dehydrogenase (MDH; EC, was applied as described before (1,3). These two isolates generated the same three banded patterns using either enzyme (genotype: MDHP: 92/100; MDH-2: 93/100); the Mdhp92 allele and the Mdh-293 allele are diagnostic for P. cactorum, whereas the Mdhp100 allele and the Mdh-2100 allele are diagnostic for P. nicotianae. These well-defined heterozygous band patterns were exactly identical to those generated in atypical isolates which were identified earlier as hybrids of P. nicotianae and P. cactorum (1,3). Based on their atypical morphology and isozyme genotyping, it was concluded that these two isolates of the second group represent hybrids of P. nicotianae and P. cactorum. One of the parents, P. nicotianae, was also found closely associated with diseased loquat trees; the other parental species, P. cactorum, was not isolated from loquat in this study. It is the first time that natural hybrids of P. nicotianae and P. cactorum were found on loquat in Asia.

References: (1) P. J. M. Bonants et al. Phytopathology 90:867--874, 2000. (2) L. L. Chern et al. Plant Dis. 82:651--656, 1998. (3) W. A. Man in 't Veld et al. Phytopathology 88:922--929, 1998.

© 2001 The American Phytopathological Society