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Veluswamy karthikeyan

university of Turin, italy
karthickeyanv@yahoo.com
Dr.V.Karthikeyan, working for more then seven years on rice pathology research, and working as Postdoctoral fellow in University of Turin, Italy.

Journal articles

2010
V Karthikeyana*, P P Karthikeyanb, D Saravanakumara, S Patharajana, P Saravanakumarc, Patrizia Titonea, Davide Spadaroa, M Lodovica gullinoa gullinoa Garibaldia (2010)  Phylogenecity and sequence alignment of Fusarium mycotoxin gene (Fum5) with other mycotoxin producing fungi   Archives of Phytopathology and Plant Protection  
Abstract: The phylogenecity of the four Fusarium mycotoxin gene (Fum 5) that has already been deposited in NCBI 2 gene bank was studied with a comparative sequence alignment with other fungi like Aspergillus sps. Cochiliobolus sps. These results clearly indicated that the Fum 5 genes of Fusarium species were originated from Aspergillues fumigates and Cochliobolus heterostrophus. Fum5 gene closer identity was also observed clearly with other fungal Fusarium species of Aspergillus and Gibberella species.
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S 1 * Patharajan, V 2 Karthikeyan (2010)  Integration of Indian traditional medicines with modern technologies   Pharmacologyonline 1: 964-968 June  
Abstract: The booming of traditional medicine industries in India results an increasing demand on medicinal plants. Being chemically diverse they are able to modulate several targets simultaneously in a complex system. Analysis of gene expression by using modern technologies like genomics and proteomics becomes necessary for the better understanding of molecular mechanisms. Conventional strategies for gene expression have been optimized for single gene expression. Besides, DNA microarray and 2D gel electrophoresis serves as suitable high throughput tools for simultaneous analysis of multiple genes. This review highlights the applications of modern technologies for the development of traditional medicines research in India.
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P 1 Saravanakumar, V * 1 Karthikeyan, S 2 Patharajan, T 3 Kannan, K 4and Kalaichelvan P T1 Sathya (2010)  EFFECT OF 1,3-β-D GLUCA! OF GAODERMA LUCIDUM O! FIBRO SARCOMA INDUCED MICE   Pharmacologyonline 1: 958-970  
Abstract: The maximal mycelial growth recorded in glucose amended cuture, and in the Production and isolation of extra cellular carbohydrates and proteins the maximum amount of protein 231 mg/L was record in sucrose amended medium besides Ganoderma lucidium produced maximum amount of carbohydrate (975 mg/L) and protein (55.4 mg/L) in synthetic medium. The absorption peaks of polysaccharide isolated from the fruit body of G. lucidium coincide with the 1,3-β-D glucan (Sigma). Effect of polysaccharide on fibrosarcoma 180 induced mice. The body weight of sarcomainduced mice was increased by 11% than the normal mice. In polysaccharide treated mice the body weight significantly decreased and was similar to that of the normal mice, and remarkable increase in the weight of the spleen (336%) and kidney (10.6%) in sarcoma induced mice than normal mice whereas the weight of liver decreased to much as 29.3% in induced mice. In polysaccharide treated mice a remarkable percent of decrease in weigh of the liver (116%), spleen (53.1%) and kidney (35.46%) were observed. The concentration of DNA and RNA were elevated in induced mice.
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2009
Veluswamy Karthikeyan, Davide Spadaro, M Lodovica Gullino, Angelo Garibaldi (2009)  Bakanae disease of rice in North-Western Italy and PCR based detection of Fusarium species   journal of swamy botonical club 23: 69 jan  
Abstract: ABSTRACT – Bakanae disease of rice caused by Fusarium verticillioides (Gibberella moniliformis) occurs on rice world-wide. In order to have a specific species level identification two set of PCR primers VERT1/2 (based on ITS region and specific for F. verticillioides) and PRO1/2 (based on calmodulin gene and specific for F. proliferatum) were used on 92 strains of Fusarium isolated from rice collected from different locations of rice growing areas in North-Western Italy. Among the 92 strains, 38 confirmed to be Fusarium verticillioides amplificating a PCR product size of 578bp, and the amplification of 585bp product size was observed in 23 strains, confirming the species Fusarium proliferatum. The primer specificity was confirmed with the strains ITEM-231, ITEM-1746 and ITEM 504 of F. verticillioides and ITEM-1720, of F. proliferatum coming from the ITEM collection of ISPA (Bari, Italy).
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V Karthikeyan*, S S Gnanamanickam (2009)  Induction of systemic resistance in rice to bacterial blight by 1,2,3- benzothiadiazole 7-carbothioic acid-S-methyl ester (BTH) treatments   Archives of Phytopathology and Plant Protection  
Abstract: Use of BTH to evaluate the disease severity and induction of systemic resistance in rice to bacterial blight caused by Xanthomonas oryzae pv. Oryzae is investigated. A new batch of 25 isolates of Xanthomonas oryzae pv. oryzae was obtained from infected rice lead tissues collected from Pattambi, Kerala, south India. Their identification was confirmed by the plant inoculation test on to IR24 rice plants which produced characteristic bacterial blight lesions. Among the 25 of X.o. pv. oryzae, four of the isolates were also virulent to IRBB21 rice plants (a near isogenic line of IR24) which carry the Xa-21 gene for BB resistance. The results confirm that there are pathogen strains in India which can overcome Xa- 21. Development of BB lesions developed in IR24 (BB susceptible) plants after they were treated with BTH applications either as seed treatment or as foliar spray at 0.1, 0.5, 0.1 and 2.0 mM concentrations showed that even at 2.0 mM concentrations, IR24 plants were still susceptible to the pathogen. There was very little or marginal effect of BTH on the induction of resistance to BB in IR24 rice plants. When the same concentrations of BTH were applied to IRBB21 (Xa-21) rice plants, they showed pronounced triggering of systemic resistance to BB pathogen even at 0.1 mM concentration of BTH applied either as seed treatment or as foliar spry. Disease severity index was reduced to 5 (against a score of 9 in untreated) and there was 85–86% reduction in BB incidence in plants that received 0.1 mMBTH. These results provide evidence that BTH-induced systemic resistance complements the R-gene resistance in IRBB21 plants but not in IR24 rice plants.
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2008
V Karthikeyan, S S Gnanamanickam (2008)  Biological control of Setaria blast (Magnaporthe grisea) with bacterial strains.   Crop protection 27: 2. 263-267  
Abstract: Efficient strains of bacterial antagonists for Magnaporthe grisea were identified through laboratory dual-plate assays. Two bacterial strains of Pseudomonas fluorescens and two strains of Bacillus were tested against 30 isolates of M. grisea that cause Setaria blast for their inhibition of the fungus. On plates spread with the fungus mycelium, 12 of the isolates had a zone of inhibition caused by the bacteria that ranged between 2.5 and 3.0 cm in diameter. In the field trails, the bacterial strains Pf-52 and KRU-22 suppressed disease by 86.64% and 87.87% respectively, in Setaria italica line 1, and 86.64% and 83.21% in line 2. The mixture of all four strains afforded 88.87% (line 1) and 88.80% (line 2) blast suppression and this was the highest level of biological blast control observed. In addition to disease suppression, the bacterial strains significantly increased root and shoot length when compared with untreated plants. Of the four strains, Pf-52, KRU-22 and the mixture of all four strains showed significant increases of root length of 10.02, 7.44 and 13.29 cm (line 1), and 9.2, 5.7 and 13.11 cm (line 2) in the root growth stage. As in the case of root length, Pf-52, KRU-22 and the mixture of all four strains showed significant increases of shoot length of 11.38, 10.42 and 11.99 cm (line 1), and 9.87, 11.44 and 12.11 cm (line 2) in the shoot growth stage.
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V Karthikeyan, D Spadaro, A Garibaldi, M L Gullino (2008)  Gibberella fujikuroi strain 2-27 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817881   NCBI  
Abstract: 1: EU817881. Reports Gibberella fujiku...[gi:195542145] Links * Features * Sequence LOCUS EU817881 369 bp DNA linear PLN 09-AUG-2008 DEFINITION Gibberella fujikuroi strain 2-27 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817881 VERSION EU817881.1 GI:195542145 KEYWORDS . SOURCE Gibberella fujikuroi (anamorph: Fusarium fujikuroi) ORGANISM Gibberella fujikuroi Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Sordariomycetes; Hypocreomycetidae; Hypocreales; Nectriaceae; Gibberella; Gibberella fujikuroi complex. REFERENCE 1 (bases 1 to 369) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE To detect the fumonisin responsible genes present in Fusarium isolates of rice JOURNAL Unpublished REFERENCE 2 (bases 1 to 369) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE Direct Submission JOURNAL Submitted (11-JUN-2008) AGROINNOVA, University of Torino, Via L. Da Vinci 44, Grugliasco, TO 10095, Italy FEATURES Location/Qualifiers source 1..369 /organism="Gibberella fujikuroi" /mol_type="genomic DNA" /strain="2-27" /specific_host="rice" /db_xref="taxon:5127" gene <1..>369 /gene="Fum5" mRNA <1..>369 /gene="Fum5" /product="fumonisin synthase" CDS <1..>369 /gene="Fum5" /codon_start=1 /product="fumonisin synthase" /protein_id="ACF98282.1" /db_xref="GI:195542146" /translation="LTHSLLAVDGIFYRAEKLCVPTAIGRLYLADGKLWEVEGARAEA LAATNSGGSISGAAIVVSQHDSVLLSLEDGKFSPLEMDLGGEGNADLVGAARLEWKPN LDFADMHSLVRPSHGSMNDSH" ORIGIN 1 ctcactcatt ctctgctagc tgtagacgga atcttttacc gagccgagaa actatgcgtt 61 ccaacagcaa tcggacgctt gtatcttgcg gatgggaagc tgtgggaggt agagggtgcc 121 cgagctgaag cattggccgc gacaaactcc gggggctcga tttctggggc cgctatcgtg 181 gtgtcccaac atgactctgt cctgctctct ctggaggatg gaaaattctc cccactggaa 241 atggatcttg gaggggaagg aaacgcagat ttggttggtg cggcacgtct cgaatggaaa 301 ccaaacttgg actttgccga tatgcatagc cttgttcgcc caagtcatgg atctatgaac 361 gacagtcac
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V Karthikeyan, D Spadaro, A Garibaldi, M L Gullino (2008)  Fusarium proliferatum strain 2-36 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817878   NCBI  
Abstract: 1: EU817878. Reports Fusarium prolifer...[gi:195542139] Links * Features * Sequence LOCUS EU817878 371 bp DNA linear PLN 09-AUG-2008 DEFINITION Fusarium proliferatum strain 2-36 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817878 VERSION EU817878.1 GI:195542139 KEYWORDS . SOURCE Fusarium proliferatum ORGANISM Fusarium proliferatum Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Sordariomycetes; Hypocreomycetidae; Hypocreales; Nectriaceae; Gibberella; Gibberella fujikuroi complex. REFERENCE 1 (bases 1 to 371) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE To detect the fumonisin responsible genes present in Fusarium isolates of rice JOURNAL Unpublished REFERENCE 2 (bases 1 to 371) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE Direct Submission JOURNAL Submitted (11-JUN-2008) AGROINNOVA, University of Torino, Via L. Da Vinci 44, Grugliasco, TO 10095, Italy FEATURES Location/Qualifiers source 1..371 /organism="Fusarium proliferatum" /mol_type="genomic DNA" /strain="2-36" /specific_host="rice" /db_xref="taxon:42674" /PCR_primers="fwd_name: Fum5F, fwd_seq: gtcctacgcgatacatcccaccacaat, rev_name: Fum6R, rev_seq: gatcaagctcggggccgtcgttcatag" gene <1..>371 /gene="Fum5" mRNA <1..>371 /gene="Fum5" /product="fumonisin synthase" CDS <1..>371 /gene="Fum5" /codon_start=1 /product="fumonisin synthase" /protein_id="ACF98279.1" /db_xref="GI:195542140" /translation="LAVDGIFYRAEKLCVPTAIGRLYLADGKLWEVEGARAEALAATN SGGSISGAAIVVSQHDSVLLSLEDGKFSPLEMDLGGEGNADLVGAARLEWKPNLDFAD MHSLVRPSHGSMNDSPRQEQGR" ORIGIN 1 ctagctgtag acggaatctt ttaccgagcc gagaaactat gcgttccaac agcaatcgga 61 cgcttgtatc ttgcggatgg gaagctgtgg gaggtagagg gtgcccgagc tgaagcattg 121 gccgcgacaa actccggggg ctcgatttct ggggccgcta tcgtggtgtc ccaacatgac 181 tctgtcctgc tctctctgga ggatggaaaa ttctccccac tggaaatgga tcttggaggg 241 gaaggaaacg cagatttggt tggtgcggca cgtctcgaat ggaaaccaaa cttggacttt 301 gccgatatgc atagccttgt tcgcccaagt catggatcta tgaacgacag cccccggcaa 361 gaacaaggtc g //
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V Karthikeyan, D Spadaro, A Garibaldi, M L Gullino (2008)  Fusarium equiseti strain 11-3 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817879   NCBI  
Abstract: 1: EU817879. Reports Fusarium equiseti...[gi:195542141] Links * Features * Sequence LOCUS EU817879 365 bp DNA linear PLN 09-AUG-2008 DEFINITION Fusarium equiseti strain 11-3 fumonisin synthase (Fum5) gene, partial cds. ACCESSION EU817879 VERSION EU817879.1 GI:195542141 KEYWORDS . SOURCE Fusarium equiseti ORGANISM Fusarium equiseti Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Sordariomycetes; Hypocreomycetidae; Hypocreales; mitosporic Hypocreales; Fusarium; Fusarium incarnatum-equiseti species complex. REFERENCE 1 (bases 1 to 365) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE To detect the fumonisin responsible genes present in Fusarium isolates of rice JOURNAL Unpublished REFERENCE 2 (bases 1 to 365) AUTHORS Karthikeyan,V., Spadaro,D., Garibaldi,A. and Gullino,M.L. TITLE Direct Submission JOURNAL Submitted (11-JUN-2008) AGROINNOVA, University of Torino, Via L. Da Vinci 44, Grugliasco, TO 10095, Italy FEATURES Location/Qualifiers source 1..365 /organism="Fusarium equiseti" /mol_type="genomic DNA" /strain="11-3" /specific_host="rice" /db_xref="taxon:61235" /PCR_primers="fwd_name: Fum5F, fwd_seq: gtcctacgcgatacatcccaccacaat, rev_name: Fum6R, rev_seq: gatcaagctcggggccgtcgttcatag" gene <1..>365 /gene="Fum5" mRNA <1..>365 /gene="Fum5" /product="fumonisin synthase" CDS <1..>365 /gene="Fum5" /codon_start=1 /product="fumonisin synthase" /protein_id="ACF98280.1" /db_xref="GI:195542142" /translation="HAVDGIFYRAEKLCVPTAIGRLYLADGKLWEVEGARTEALAATY SGGSISGAAILVSQHDSGLLSLGDGKFSPLEMDLGGEGKLHLVGAARLEWKPNLDFAD MHSLIRPSHGSMNDGPELD" ORIGIN 1 catgctgtag acggaatctt ttaccgagcc gagaaactat gcgttccaac agcaatcgga 61 cgcttgtatc ttgcggatgg gaagctgtgg gaggtagagg gtgcccgaac tgaagctttg 121 gccgcgacat actccggggg ctccatttct ggggccgcta tcttggtgtc ccaacatgac 181 tctggcctgc tctctctggg ggatggaaaa ttctcccccc tggaaatgga tcttggaggg 241 gagggaaagc tgcatttggt tggtgcggcg cgtctcgaat ggaaaccaaa cttggacttt 301 gccgatatgc atagccttat tcgcccaagt catggatcta tgaacgacgg ccccgagctt 361 gatca
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P Saravanakumara, V Karthikeyanb*, B Kannabiran  Antifungal activity of Plumbago species against anthracnose fungus Colletotrichum gloeosporidodes (Penz) of chilli    
Abstract: The efficacy of aqueous leaf extracts of three Plumbago (Plumbago indica, P. capensis, P. zeylanica) species on anthracnose fungus Colletotrichum gloeosporioides were assessed. Out of the extract of three plants screened, that of Plumbago indica showed the best result both in inhibition of conidial germination up to (98.9%), and radial mycelial growth (98.75%) of the pathogen over the control and in the pectinolytic enzyme studies also P. indica showed a minimum activity of Polymethyl esterase (1.91U), Polymethyl galacturonase (endo PMG-2.77%; exo PMG-0.028U) and Pectin trans eliminate; the least amount of sugar (endo PTE-17.14%; exo PTE-11.11U) was released in P. indica. In cellulolytic enzyme studies, the amount of viscosity loss due to the activity of 1,4-b endoglucanase was remarkably reduced (3.57%) in P. indica compared to the other two species. P. capensis showed moderate results; P. zeylanica showed minimum inhibition of the enzyme activity of the pathogen. Results show that among all three plumbago species tested, Plumbago indica was reported to be an effective plant extract against anthracnose fungus.
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