Thumbnail Image

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.

Browse

2001 - 20047
Reset filters
Subject: Microbiology × Author: KAU × Start date: 2001 × Thesis Type: M.V.Sc. ×
Reset filters

Search Results

Now showing 1 - 7 of 7
  • Thumbnail Image
    ThesisItemOpen Access
    Microbial agents associated with eye infection in chicken
    (Department of microbiology, College of veterinary and animal sciences, Mannuthy, 2003) Jaison, George; KAU; Jayaprakasan, V
    A study was undertaken to find out the microbial agents associated with the recently reported eye infection of chickens in many parts of Kerala. Samples were collected from 83 birds from different parts of Kerala. The bio-materials employed for the study were the conjunctival swabs and air sac materials. Organisms isolated from different stages of infection include 45 isolates of E. coli, 28 isolates of S. aureus, 11 isolates of B. coagulans, , eight isolates of Pseudomonas aeruginosa, two isolates of S. epidermidis, ten isolates of Alloscheria sp., five isolates of Penicillin sp. and three isolates of Scopulariopsis sp. and three isolates of M gallisepticum. On an average, the rate of isolation of microbial agents per sample at the beginning, mid and advanced stage of infection were 0.5, 1.3 and 2.8 respectively, showing that the number and type of organism isolated increased as the disease advanced except in the case of MG which was isolated only from the beginning stage of infection. No viral agents or e . chlamydia could be isolated through embryonated egg inoculation. The findings of the present study suggest that MG could be the primary agent leading to conjunctivitis while other eubacterial and fungal isolates could be secondary invaders complicating the condition. The antibiogram of the eubacterial isolates suggest that proper treatment with antibiotics like ciproflaxacin/gentamycin at the beginning stage of infection could prevent secondary invaders from complicating the condition.
  • Thumbnail Image
    ThesisItemOpen Access
    Detection of Pasteurella multocida in domestic ruminants by isolation and polymerase chain reaction
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2004) Sunitha Karunakaran; KAU; Krishnannair, G
    A study was undertaken to examine the occurrence of P. multocida organisms causing HS in apparently healthy and clinically ill domestic ruminants in a specified area of Thrissur district viz., Ollukkara block, covering one per cent of total ruminant population in the area. Besides the samples collected from Ollukkara block area, those brought to the Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy from suspected cases of HS, were also included in the study. A total of 309 samples comprising of nasal swabs, pharyngeal swabs, lung samples and blood samples were processed for isolation of P. multocida and detection by PCR. Detection of P. multocida by PCR was carried out using species-specific (PM-PCR), type-B specific (HS-B PCR) and nested primers. Pasteurella multocida could not be isolated from any of the clinical samples cultured for isolation from Ollukkara block area. Five isolates could be obtained from the blood samples from Palakkad district. Isolates obtained were characterized as P. multocida using standard bacteriological procedures. A reference strain P52 obtained from IVRI was used for comparison. All the isolates were found to be pathogenic for mice. Based on the fermentation patterns of dulcitol, sorbitol, trehalose and xylose all isolates as well as P52 could be biotyped as P. multocida subsp. multocida. All isolates were uniformly sensitive to ten out of twelve antibiotics tested and uniformly resistant to metronidazole. All isolates were confirmed as type-B P. multocida using species-specific primer pairs, KMT1SP6 and KMT1T7 and HS-B specific primer pairs, KTSP61 and KTT72. Multiplex PCR was used to characterize all the serotype B isolates, which generated two bands of size 460 bp and 590 bp. Only 14 clinical samples including the isolates were positive for P. multocida by PM-PCR. The entire samples tested positive by PM-PCR were confirmed as type-B P. multocida by HS-B specific PCR. The 14 samples found positive by PM-PCR when subjected to nested PCR, gave an amplified product of size 214 bp. Since nested PCR could detect Pasteurella multocida DNA in a high proportion of clinical samples found previously negative by PM-PCR, a definite conclusion could not be arrived about the feasibility of using this PCR assay for enhanced detection of P. multocida as only a random number of negative clinical samples could be screened. All the isolates showed a single REP-PCR profile, indicating a high level of homogeneity among them. Among the five isolates examined, only two (BP2 and BuP1) harboured plasmids. The sequence similarity searches of HS-B PCR amplified product with BLAST network showed that the sequence had 99 per cent identity with Pasteurella multocida unknown protein 1 and protein 2 gene (Accession No AF016260).
  • Thumbnail Image
    ThesisItemOpen Access
    Prevalence of leptospirosis in animals in and around Thrissur
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2004) Manju Soman; KAU; Jayaprakasan, V
    A study was undertaken to assess the prevalence of leptospirosis in animals and man, in and around Thrissur. A total of 501 sera samples, collected from dogs, cattle, pigs, rodents (bandicoots and rats) and human beings were subjected to serologic testing, for detection of Leptospira specific antibodies, by MAT, PHA and indirect IgG ELISA. Isolation of Leptospira was tried from blood of clinically suspected cases of human and canine leptospirosis and from kidney tissues of rodents. The study revealed the presence of antibodies against Leptospira in human beings and all the four species of animals examined by the three tests employed. The prevalence rates detected by MAT in canines, bovines, porcines, murines and human beings were 36.36 per cent, 47 per cent, 23.8 per cent, 21.42 per cent and 54.54 per cent respectively. Out of 30 human blood samples subjected to isolation trials in Fletcher'slEMJH semisolid media with enrichment, Leptospira could be isolated from a single human patient, in Fletcher's semisolid medium with 10 per cent rabbit serum. Of the 35 rodent kidney tissues tried for isolation in Fletcher's semi solid media, leptospires were isolated from three bandicoots and two rats. Indirect ELISA was found to be most sensitive, of the three tests,for rapid screening of the population for leptospirosis, while PHA was found to be a fairly good test for diagnosis of acute leptospirosis. The MAT proved to be the most specific test which could also identify the serogroup identity of the infecting Leptospira. Leptospira pomona and L. australis were detected by MAT as the common serogroups prevalent in man, animals and rodents in this area. The prevalence of common leptospiral serovars in animals and man, indicated that human beings which were the end hosts for Leptospira could have acquired the infection mostly from animals like dogs, cattle and pigs, while the isolation ofleptospires from rodents revealed the carrier status of these animals.
  • Thumbnail Image
    ThesisItemOpen Access
    Seroprevalence of BlueTongue in Sheep and Goats in Kerala
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2003) Chintu Ravishankar; KAU; Krishnan Nair, G
    A study was conducted to assess the seroprevalence of BT in sheep and goats in Kerala, employing AGID, T-ELISA and dot-ELTSA tests. A total of 1010 samples collected from all the 14 districts of the State were screened for the presence of group specific antibodies to BTV. Seropositive samples were obtained from 12 out of the 14 districts. Both sheep and goats were found to harbour antibodies to BTY. Based on the results of the 1- ELISA test, the highest prevalence was observed in Thrissur district (21.10 per cent) and the lowest in Ernakulam district (1.25 per cent). Higher prevalence rates were observed in organized farms. The overall prevalence of the disease in the state was found to be 7.82 per cent. Of the tests employed, AGID test was found to be the least sensitive: The maximum number of positive samples were detected by I-ELISA. To check the validity of the I-ELISA results C-I~:LISA was done and there was good correlation between the results of the two tests as only four samples were detected as false positive in the C-ELISA. Dot-ELISA was found to be a simple, quick and specific test with detection levels comparable to T-ELlSA and could be used in the field conditions. Screening of the cattle population also should be done to get a better picture of the disease in the State as they comprise the largest reservoir of BTV in nature.
  • Thumbnail Image
    ThesisItemOpen Access
    Characterization of genomic and plasmid DNA of Chlamydia psittaci isolates
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2001) Sreeja, R Nair; KAU; Mini, M
    Four isolates of Chlamydia psittaci (M-28, M-430, M-121, P-156) obtained from ruminant abortion were subjected to restriction enzyme analysis and plasmid profiling to assess molecular level differences/homogenity among the isolates. The changes produced in developing chick embryo and the cytopathic effect in Me Coy cell line by the isolates were also investigated in this study. The C. psittaci isolates preserved in the Department of Microbiology were revived by passaging in embryonated chicken eggs through yolk sac route. Six to seven day-old developing chick embryo were used for propagation of the isolates. The isolates, M-28 and M-430 were found to produce death of the embryos within 10 days. The isolates M-121 and P-156 were not able to cause death within 10 days. The embryos appeared stunted with patchy haemorrhages all over the body and hyperemic legs. The yolk sac was thin walled, with deeply injected blood vessels and the yolk was thin and watery. M-28 and M-430 produced more severe lesions of the inoculated embryos compared with the other isolates. The isolates were grown in Me Coy cell line. All isolates revealed marked CPE, characteristic of C. psittaci, with rounding and clumping of cells to form syncytia at 48 h PI and formation of intra cytoplasmic inclusion bodies by 96 h PI. The isolates M-121 and P-156 took more time for the production of CPE compared with that of M-28 and M-430. The isolates were confirmed as C. psittaci by fluorescence antibody technique which revealed, apple green fluorescing chlamydial inclusions in the infected cell line by 96 h PI. The CE as well as cell line propagated isolates were used as a source of elementary bodies for DNA extraction. The purified EBs were prepared by urografin density gradient centrifugation. After obtaining sufficient amount of EBs, it was subjected to DNA extraction. The isolates M-28, M-430, M-121 and P-156 had DNA concentrations of 1710 ug/ml, 1130 Jlgl Iml, 1545 ug/ml and 1475 ug/ml respectively. Restriction enzyme digestion of all the isolates were done separately with Eeo RI, Hae III and Barn HI. Eeo RI cleaved DNA of the isolates M-430 and P-156 into rune fragments, M-28 into eight and M-121 into ten fragments respectively. The molecular size of bands for all isolates had variation in heavier fragments. Common bands were observed at five regions for all isolates. Hae III cleaved the caprine isolates into eight fragments and the bovine isolate M-121 into seven and P-156 into nine fragments. Variation could be observed on the molecular size of the fragments. Bam HI digested all isolates except M-121 into eight fragments. For M-121, seven fragments were obtained. Common bands were noticed at 0.2 and 0.7 kbp region. All enzymes were found to be useful in the differentiation of C. psittaci isolates as these REs produced variation as well as similarity in the restriction fragment sizes. Plasmid profiling revealed the absence of plasmids ill all the four isolates screened. Thus, a combination of phenotypic and genotypic methods could be used as epidemiological tools in the differentiation of C. psittaci strains of mammalian origin.
  • Thumbnail Image
    ThesisItemOpen Access
    Nucleic acid and protein profile of Pasteurella multocida of avian origin
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2001) Rajalakshmi Radabai, S; KAU; Krishnan Nair, G
    Four avian field isolates (one from quail and three from ducks) suggestive of Pasteurella sp. were compared with the avian Pasteurella multocida reference strain (LKO) for their biochemical properties, drug resistance patterns, whole cell and outer membrane protein profiles and restriction enzyme digestion pattern of chromosomal DNA. Biochemical characterisation revealed two biotypes among the four field isolates; namely P. multocida subsp. septica (quail isolate) and P. multocida subsp. multocida (duck isolates). The study of antibiogram using 14 chemotherapeutic agents revealed the presence of multiple drug resistance in all the four field isolates and reference strain. Whole cell protein profiles of the four field isolates and reference strain revealed 7 to 11 bands of molecular weights ranging from 197.4 kDa to 2.5 kDa. Polypeptide bands in the molecular weight range of 36 to 38 kDa (which were attributable to the protein-H), 29 to 32 kDa and 10 to 11 kDa were common to all the isolates of P. multocida. The major outer membrane proteins (OMPs) in the molecular weight range of 32 to 33 kDa and 27 kDa region were common to all the four field isolates and reference strain. II Unique protein bands in each of the isolate were indicative of variant forms of the same organism. Restriction enzyme analysis of chromosomal DNA yielded different restriction fragments in each of the isolates which were not easily distinguishable. Hence, of the tests used, phenotypic characters, biotype, antibiogram and protein profile were found to be more effective in differentiating the isolates rather than restriction enzyme digestion patterns of genomic DNA.
  • Thumbnail Image
    ThesisItemOpen Access
    Isolation and characterization of Chlamydia psittaci with emphasis on protein profile
    (Department of Microbiology, College of Veterinary and Animal Sciences, Mannuthy, 2001) Binu, K Mani; KAU; Mini, M
    For isolation of Chlamydia psittaci 46 clinical cases associated with abortions in livestock from livestock farms and Veterinary hospitals in and around Thrissur were screened. Impression smear staining of the clinical materials USin9 Giemsa, Modified Ziehl Neelsen and Gimenez revealed two positive cases. Both were from aborted foetuses, one from bovine (M-121) and the other from caprine (M-430). Chick embryo inoculation by YS route was used for isolation of the organism. The organisms could be isolated only from the two cases positive by preliminary screening, as confirmed by staining of YS impression smears. The mortality rate in CE was more in case of M-430 compared to the other two isolates (M-121 and reference isolate, P-156). All the three isolates produced patchy haemorrhagic lesions in YS and skin of embryoS. An overall isolation percentage of 4.3 was obtained in this study. All the three isolates were resistant to sodium sulphadiazine. Pathogenicity studies indicated that, all the three isolates were of moderate virulence for mice and guinea pigs. Based on AGPT, the local isolates were confirmed as Chlamydia psittaci. All the three isolates caused rounding and swelling of fibroblast cells and syncytia formation at 24h PI in Mc Coy cell line. By 48 to 72 h PI, these effects became more prominent with detachment of cells from adjacent cells and from the glass surface. Purified EBs were prepared from infected Mc Coy cell line by Urografin gradient centrifugation. After confirming the presence of sufficient amount of protein by Biuret method, they were used for SDS-PAGE. A total of 12 polypeptide bands were obtained for both the bovine isolates while the caprine isolate gave 10 bands. Molecular weights of 148 kDa and 135 kDa were present only in P-156 and 152 kDa and 137 kDa were unique for M-121. Bands at 152 kDa, 148 kDa, 137 kDa, 135 kDa, 32 kDa, 18 kDa, 15 kDa and 7 kDa were lacking in M-430. This isolate was having unique bands of 155 kDa, 19 kDa, 12.2 kDa and 6.4 kDa.