Identification of
Candidatus Liberibacter asiaticus from Foshou (Citrus medica) in
China
X. Deng1, J. Chen2*, Z.
Shan1, G. Zhou1, H. Li1, and E. L. Civerolo2
1
Laboratory
of Citrus Huanglongbing Research, Department of Plant Pathology, South China
Agricultural University, Guangzhou, Guangdong 510642, P. R. China
2
Crop
Diseases, Pests, and Genetics Research Unit, San Joaquin Valley Agricultural
Sciences Center, United States Department of Agriculture-Agricultural Research
Service, Parlier, CA 93648, U.S.A.
*jichen@fresno.ars.usda.gov Accepted for
publication 26/07/07 In China, Foshou or Buddha’s hand (Citrus
medica var. sarcodactylus), is commonly cultured and valued for its
fragrance and used medicinally as a stomach stimulant, expectorant and tonic. We
have observed Huanglongbing (HLB) symptoms on Foshou since 1999 (Fig. 1). Yet,
the etiological agent, Candidatus Liberibacter sp., a nonculturable,
phloem-limited α-proteobacterium, had never been confirmed. Among the three
known candidatus species (Ca. L. asiaticus, Ca. L. africanus, and
Ca. L. americanus), only Ca. L. asiaticus has been reported in
China (Deng and Tang, 1996) but not from Foshou. In January 2006, we found nine
Foshou trees showing typical HLB symptoms (leaf mottling and yellowing in young
shoots) in Guangning City, Guangdong Province, People’s Republic of China.

Figure 1: Symptoms of Citrus medica
Huanglongbing (yellow shoot disease) in Guangdong, P. R. China To
identify the pathogen, DNA was extracted from symptomatic leaves with the cetyl
trimethylammonium bromide (CTAB) method. Samples were tested for presence of
Ca. L. asiaticus by PCR with primer sets OI1/OI2c targeting the 16S rDNA
locus (do Carmo Teixeira et al., 2005) and A2/J5 targeting the locus of
beta-operon of ribosomal proteins (Hocquellet et al., 1999). DNA samples
from all symptomatic leaves were positive with both primer sets. OI1/OI2c
generated an amplicon of approximately 1,160 bp. Further digestion of
the amplicon by XbaI yielded two DNA fragments of approximately 640 bp
and 520 bp and PCR with A2/J5 primer set generated an approximate 703 bp
amplicon, excluding Ca. L. africanus as the causal agent . The positive
control using a sweet orange (C. sinensis) tree known to have HLB showed
the same result. No DNA was amplified from the asymptomatic healthy Foshou tree.
Sequences of OI1/OI2c and A2/J5 amplicons were determined and showed 99.6-100%
similarity to those of Ca. L. asiaticus in the GenBank database. No DNA
was amplified by PCR with primer set GB1/GB2 specific to Ca. L.
americanus. These results show that the Foshou HLB etiological agent is Ca.
L. asiaticus. This is the first report of molecular identification of Ca.
L. asiaticus associated with C. medica HLB in Guangdong (southern) China.
Acknowledgements Part of this research was supported by Guangdong
Provincial Foundation of Natural Sciences (032262) and a Guangdong Provincial
Research Grant for Science and Technology (2004B20901010).
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