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Kerala Agricultural University, Thrissur

The history of agricultural education in Kerala can be traced back to the year 1896 when a scheme was evolved in the erstwhile Travancore State to train a few young men in scientific agriculture at the Demonstration Farm, Karamana, Thiruvananthapuram, presently, the Cropping Systems Research Centre under Kerala Agricultural University. Agriculture was introduced as an optional subject in the middle school classes in the State in 1922 when an Agricultural Middle School was started at Aluva, Ernakulam District. The popularity and usefulness of this school led to the starting of similar institutions at Kottarakkara and Konni in 1928 and 1931 respectively. Agriculture was later introduced as an optional subject for Intermediate Course in 1953. In 1955, the erstwhile Government of Travancore-Cochin started the Agricultural College and Research Institute at Vellayani, Thiruvananthapuram and the College of Veterinary and Animal Sciences at Mannuthy, Thrissur for imparting higher education in agricultural and veterinary sciences, respectively. These institutions were brought under the direct administrative control of the Department of Agriculture and the Department of Animal Husbandry, respectively. With the formation of Kerala State in 1956, these two colleges were affiliated to the University of Kerala. The post-graduate programmes leading to M.Sc. (Ag), M.V.Sc. and Ph.D. degrees were started in 1961, 1962 and 1965 respectively. On the recommendation of the Second National Education Commission (1964-66) headed by Dr. D.S. Kothari, the then Chairman of the University Grants Commission, one Agricultural University in each State was established. The State Agricultural Universities (SAUs) were established in India as an integral part of the National Agricultural Research System to give the much needed impetus to Agriculture Education and Research in the Country. As a result the Kerala Agricultural University (KAU) was established on 24th February 1971 by virtue of the Act 33 of 1971 and started functioning on 1st February 1972. The Kerala Agricultural University is the 15th in the series of the SAUs. In accordance with the provisions of KAU Act of 1971, the Agricultural College and Research Institute at Vellayani, and the College of Veterinary and Animal Sciences, Mannuthy, were brought under the Kerala Agricultural University. In addition, twenty one agricultural and animal husbandry research stations were also transferred to the KAU for taking up research and extension programmes on various crops, animals, birds, etc. During 2011, Kerala Agricultural University was trifurcated into Kerala Veterinary and Animal Sciences University (KVASU), Kerala University of Fisheries and Ocean Studies (KUFOS) and Kerala Agricultural University (KAU). Now the University has seven colleges (four Agriculture, one Agricultural Engineering, one Forestry, one Co-operation Banking & Management), six RARSs, seven KVKs, 15 Research Stations and 16 Research and Extension Units under the faculties of Agriculture, Agricultural Engineering and Forestry. In addition, one Academy on Climate Change Adaptation and one Institute of Agricultural Technology offering M.Sc. (Integrated) Climate Change Adaptation and Diploma in Agricultural Sciences respectively are also functioning in Kerala Agricultural University.

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Author: KAU × Author: Sreeja, S × Start date: 1978 ×
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    ThesisItemOpen Access
    Clinico-therapeutic studies on bacterial mastitis in goats
    (Department of Veterinery Epidmiology and Preventive Medicine, College of Veterinary and Animal Science,Mannuthy, 2005) Sreeja, S; KAU; Vijayakumar, K
    The lactating does in the University goat and sheep farm were screened for subclinical mastitis once in three months using the California mastitis test. The occurrence of subclinical mastitis was found to be 30.2 per cent. Statistical analysis showed no significant association between occurrence of subclinical mastitis and teat length whereas there was significant association between distance from teat tip to floor. Among 642 samples screened 194 samples were found to be positive by CMT. The arithmetic mean cell counts for each CMT score ranged between 0.736 ± 0.033 x106 and 20.417 ± 0.851 x106 cells/ml. Among CMT positive samples MWST and MAMP detected 62.89 per cent and 43.29 per cent as positive for subclinical mastitis. Comparison of screening tests revealed that significant positive correlation existed among the four tests namely CMT, MWST, MAMP and SCC. Comparison with culture results showed that score ‘3’ of CMT score ‘3+’ of MWST and grade 3 of MAMP reaction detected the maximum positive cases. CMT scores and SCC in bacteriologicaly positive samples showed significant association. Among the TIST positive milk samples 20 (44.44 per cent) were culture positive. Staphylococcus aureus was the most predominant isolate in both clinical and subclinical caprine mastitis. In vitro antibiotic sensitivity pattern revealed that chloramphenicol was the most sensitive antibiotic followed by ceftriaxone and ciprofloxacin. The isolated pathogens showed maximum resistance to sulpha. Comparison of treatment trials in 24 clinical goat mastitis cases using ceftriaxone and ciprofloxacin with 12 animals in each group revealed that clinical and bacteriological cure was better in the case of ciprofloxacin. Clinical and bacteriological cure was comparatively less in gangrenous mastitis cases. Eighteen Staphylococcus isolates from clinical mastitis cases and 23 Staphylococcus isolates from subclinical cases were typed by RAPD fingerprinting. Twelve different genotypes were obtained among which genotype c predominated in clinical mastitis whereas in subclinical cases b and i were the common Staphylococcal genotypes. Clinical and bacteriological cure rates were 100 per cent for RAPD type l in the ceftriaxone treated group and genotypes c and i in the ciprofloxacin treated group of animals. A possible relationship regarding the genetic make up of the different Staphylococcal isolates was elucidated from the phylogenetic tree generated from the RAPD fingerprints.
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    ThesisItemOpen Access
    Metabolite Profiling and gene expression analysis for gingerol production in selected somaclones of ginger (zingiber officinale rosc.)
    (Centre for Plant Biotechnology and Molecular Biology, College of Horticulture, Vellanikkara, 2017) Sreeja, S; KAU; Shylaja, M R
    Ginger (Zingiber officinale Rosc.) is one of the oldest known spices and is much valued for its medicinal properties. Ginger rhizome is a source of active biological compounds which are responsible for its medicinal properties. Gingerol is the major pungent polyphenol in ginger which has got a wide array of pharmacological properties. Research on somaclonal variation done at Kerala Agricultural University could locate ginger somaclones with high gingerol content and in the course of investigations high somaclonal variation was observed for quality components. Ginger has a very big genome of 23,618 Mbp which is little exploited and reports on the genomic base of gingerol biosynthesis are scanty. The present investigations hence aim at profiling the metabolites in selected ginger somaclones using high throughput analytical platforms and to analyze the gene expression with respect to gingerol production. One released ginger variety from KAU (Athira), two selected ginger somaclones (B3 and 132M) and parent cultivar (Maran) formed the experimental materials for the study. Studies were carried out at Centre for Plant Biotechnology and Molecular Biology, Distributed Information Centre of College of Horticulture and Arjuna Natural Extracts Pvt. Ltd., Aluva during August 2013 to July 2017. The profiling of aroma principles using Gas Chromatography-Mass Spectrometry (GC-MS) and pungency principles using High Performance Liquid Chromatography (HPLC) at various growth stages viz. five months after planting (5MAP), six months after planting (6MAP) and seven months after planting (7MAP), revealed that aroma and pungency principles accumulated in ginger rhizomes at the rhizome formation stage (5MAP). Clone to clone variation was observed in the number and quantity of aroma and pungency principles accumulated in the rhizome. Total gingerol content in somaclone B3 (19.07%) was high when compared to the control cultivar Maran (17.49%) irrespective of the growth stages. Gene expression for Chalcone synthase in selected somaclones done using real time PCR assay showed highest gene expression in somaclone B3 when the control cultivar Maran was set as calibrator. Somaclone B3 recorded 54 per cent increase in Chalcone synthase gene expression over the control cultivar Maran. Suppression subtractive hybridization done to identify differentially expressed genes in somaclone B3 and control cultivar Maran could prepare Expressed Sequence Tag (EST) libraries both for rhizome and leaf. Analysis of EST sequences (25 rhizome ESTs and 19 leaf ESTs) using various bioinformatic tools revealed that there were no differentially expressed genes for gingerol production in rhizome ESTs. But eleven differentially expressed proteins involved in signaling response, protein trafficking, photosynthesis, ATP formation and transposon mediated mutation were observed in rhizome ESTs. The analysis of leaf ESTs showed differential gene expression in somaclone B3 for 3-ketoacyl CoA thiolase (ACAA1) gene which is involved in gingerol biosynthetic pathway. Hence the higher expression of 3-ketoacyl CoA thiolase gene is responsible for the high gingerol content in somaclone B3 as compared to control cultivar Maran. Eighteen other differentially expressed proteins involved in biological processes like transportation of plant secondary metabolites and their intermediates, mobilization of sucrose into pathways involved in metabolism, lipid biosynthesis, transportation of cellular material to microtubules, biogenesis of metabolic pathways in Calvin cycle were observed in leaf ESTs. The differentially expressed gene (ACAA1) can be further validated using northern blotting and quantitative real time PCR by designing specific primers from the ESTs. Expressed sequence tags and corresponding differentially expressed proteins can be used as molecular markers. Post translational modification in differentially expressed proteins can be used to study the mechanism of gingerol production. Forty four sequences deposited at NCBI form the base sequences for further research.
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    ArticleItemOpen Access
    Cobweb theory approach: An application to rice production in Kerala
    (Kerala Agricultural University, 1995) Sreeja, S; Chandrabhanu, P; KAU
    Ail attempt is made to examine how rice fanners respond to output with movements in prices, over the last fifteen years, using Cobweb model. It is found that the slope of the demand curve to be greater than the slope of the supply curve of paddy and the price structure of paddy in Kerala is following a convergent Cobweb starting above the equilibrium. The projected values based on the model show that the instability of the supply behaviour to adjust to changes in price should be changed to reduce the time lag in achieving the equilibrium price and output.