Sh. Choi et al., DISTRIBUTION OF XANTHOMONAS-ORYZAE PV. ORYZAE DNA MODIFICATION SYSTEMS IN ASIA, Applied and environmental microbiology, 64(5), 1998, pp. 1663-1668
The presence or absence of two DNA modification systems, XorI and XorI
I, in 195 strains of Xanthomonas oryzae pv. oryzae collected from diff
erent major rice-growing countries of Asia was assessed. All four poss
ible phenotypes (XorI(+) XorII(+), XorI(+) XorII(-), XorI(-) XorII(+)
and XorI(-) XorII(-)) were detected in the population at a ratio of ap
proximately 1:2:2:2. The XorI(+) XorII(+) and XorI(-) XorII(+) phenoty
pes were observed predominantly in strains from southeast Asia (Philip
pines, Malaysia, and Indonesia), whereas strains with the phenotypes X
orI(-) XorII(-) and XorI(+) XorII(-) were distributed in south Asia (I
ndia and Nepal) and northeast Asia (China, Korea, and Japan), respecti
vely. Based on the prevalence and geographic distribution of the XorI
and XorII systems, we suggest that the XorI modification system origin
ated in northeast Asia and was later introduced to southeast Asia, whi
le the XorII system originated in southeast Asia and moved to northeas
t Asia and south Asia. Genomic DNA from all tested strains of X. oryza
e pv, oryzae that were resistant to digestion by endonuclease XorII or
its isoschizomer PvuI also hybridized with a 7.0-kb clone that contai
ned the XorII modification system, whereas strains that were digested
by XorII or PvuI lacked DNA that hybridized with the clone. Size polym
orphisms were observed in fragments that hybridized with the 7.0-kb cl
one. However, a single hybridization pattern generally was found in Xo
rII(+) strains within a country, indicating clonal maintenance of the
XorII methyltransferase gene locus, The locus was monomorphic for X. o
ryzae pv. oryzae strains from the Philippines and all strains from Ind
onesia and Korea.