New Disease Reports (2012) 25, 8. [http://dx.doi.org/10.5197/j.2044-0588.2012.025.008]
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First report of a 'Candidatus Phytoplasma aurantifolia' isolate associated with a yellowing disease of Barleria prionitis

S. Kumar*, V. Singh and S. Lakhanpaul

*sach_inom@yahoo.co.in

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Received: 09 Dec 2011; Published: 01 Mar 2012

Barleria prionitis (Acanthaceae), known as porcupine flower, is a medicinal plant species native to India and commonly found across Africa, Sri Lanka, and tropical Asia (Chavana et al., 2010). B. prionitis leaves are used as expectorant, pain relief and a remedy against ulcer and fever. Plants showing symptoms of yellowing, little leaf and early senescence (Fig. 1) were observed during June 2010 at the Botanical Garden of Delhi University, India. Five plants with symptoms indicating phytoplasma infection and two symptomless plants were collected for genomic DNA isolation from stem tissue. Purified DNA was subjected to nested-PCR using generic phytoplasma primers targeting the 16S ribosomal RNA gene P1/P7 (Deng & Hiruki, 1991), followed by fU5/rU3 (Lorenz et al., 1995). PCR amplification products from the first round (P1/P7) were diluted (1:30) and used in the second round (fU5/rU3). The symptom-bearing plant samples exhibited a PCR band of expected size (~880bp), while symptomless samples showed no PCR amplification. The PCR amplicons were gel eluted and purified using the QIAquick gel extraction kit (QIAGEN, USA), and directly sequenced bi-directionally. BLAST comparisons of the partial 16S rDNA sequence (GenBank Accession No. JF958127) corresponding to B. prionitis phytoplasma, strain Dhba1, revealed the highest sequence identity (99%) with those of members of the 16SrII group 'Candidatus phytoplasma aurantifolia'. A maximum parsimony dendrogram (MEGA version 4.01) based on the partial 16S rDNA sequences of the B. prionitis phytoplasma and 15 other reference phytoplasmas (http://www.ncbi.nlm.nih.gov) supported the sequencing results since the B. prionitis phytoplasma grouped within the 16SrII phytoplasma clade.

The current study reports B. prionitis as a new host for the 16SrII phytoplasma group in India and worldwide. Previous reported diseases from India including leaf yellowing, chlorosis and little leaf of lettuce, carrot and French bean have shown to be associated with phytoplasmas belonging to group 16SrII (Arocha et al., 2008). Therefore, these results have a significant phytosanitary impact for the epidemiology of 16SrII phytoplasma diseases in the country.

Figure1+
Figure 1: Plants of Barleria prionitis without symptoms (a) and affected by phytoplasma showing symptoms of yellowing disease (b).
Figure 1: Plants of Barleria prionitis without symptoms (a) and affected by phytoplasma showing symptoms of yellowing disease (b).
Figure2+
Figure 2: Phylogenetic tree constructed by MEGA 4.01, based on nearly full-length phytoplasma 16S rDNA sequences of the B. prionitis phytoplasma and 15 reference phytoplasmas. Bootstrap values are shown on branches. Acholeplasma palmae was used as the outgroup to root the tree. Ca. P.: ‘Candidatus Phytoplasma’.
Figure 2: Phylogenetic tree constructed by MEGA 4.01, based on nearly full-length phytoplasma 16S rDNA sequences of the B. prionitis phytoplasma and 15 reference phytoplasmas. Bootstrap values are shown on branches. Acholeplasma palmae was used as the outgroup to root the tree. Ca. P.: ‘Candidatus Phytoplasma’.

References

  1. Arocha Y, Singh A, Pandey M, Tripathi AN, Chandra B, Shukla SK, Singh Y, Kumar A, Srivastava RK, Zaidi NW, Arif M, Narwal S, Tewari AK, Gupta MK, Nath PD, Rabindran R, Khirbat SK, Byadgi AS, Singh G, Boa E, 2008. New plant hosts for group 16SrII, 'Candidatus Phytoplasma aurantifolia', in India. Plant Pathology 17,391. [http://dx.doi.org/10.1111/j.1365-3059.2008.01969.x]
  2. Chavan CB, Hogade MG, Bhinge S, Kumbhar M, Tamboli A, 2010. In vitro anthelmintic activity of fruit extract of Barleria prionitis Linn. against Pheretima posthuma. International Journal of Pharmacy and Pharmaceutical Sciences 2, 49-50.
  3. Deng S, Hiruki C, 1991. Amplification of 16 S rRNA genes from culturable and non-culturable mollicutes. Journal of Microbiological Methods 14, 53-61. [http://dx.doi.org/10.1016/0167-7012(91)90007-D]
  4. Lorenz KH, Schneider B, Ahrens U, Seemüller E, 1995. Detection of the apple proliferation and pear decline phytoplasmas by PCR amplification of ribosomal and nonribosomal DNA. Phytopathology 85, 771-776. [http://dx.doi.org/10.1094/Phyto-85-771]

To cite this report: Kumar S, Singh V, Lakhanpaul S, 2012. First report of a 'Candidatus Phytoplasma aurantifolia' isolate associated with a yellowing disease of Barleria prionitis. New Disease Reports 25, 8. [http://dx.doi.org/10.5197/j.2044-0588.2012.025.008]

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