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Anand Agricultural University, Anand

Anand Agricultural University (AAU) was established in 2004 at Anand with the support of the Government of Gujarat, Act No.(Guj 5 of 2004) dated April 29, 2004. Caved out of the erstwhile Gujarat Agricultural University (GAU), the dream institution of Sardar Vallabhbhai Patel and Dr. K. M. Munshi, the AAU was set up to provide support to the farming community in three facets namely education, research and extension activities in Agriculture, Horticulture Engineering, product Processing and Home Science. At present there seven Colleges, seventeen Research Centers and six Extension Education Institute working in nine districts of Gujarat namely Ahmedabad, Anand, Dahod, Kheda, Panchmahal, Vadodara, Mahisagar, Botad and Chhotaudepur AAU's activities have expanded to span newer commodity sectors such as soil health card, bio-diesel, medicinal plants apart from the mandatory ones like rice, maize, tobacco, vegetable crops, fruit crops, forage crops, animal breeding, nutrition and dairy products etc. the core of AAU's operating philosophy however, continues to create the partnership between the rural people and committed academic as the basic for sustainable rural development. In pursuing its various programmes AAU's overall mission is to promote sustainable growth and economic independence in rural society. AAU aims to do this through education, research and extension education. Thus, AAU works towards the empowerment of the farmers.

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  • ThesisItemOpen Access
    ISOLATION AND MOLECULAR CHARACTERIZATION OF EXTENDED SPECTRUM BETA LACTAMASE PRODUCING ESCHERICHIA COLI FROM MILK
    (Department of Veterinary Public Health & Epidemiology College of Veterinary Science and Animal Husbandry Anand Agricultural University Anand, 2019) PAGHDAR DHARABEN M.; Dr. J. B. NAYAK
    The present study was carried out in the post graduate laboratory, Department of Veterinary Public Heath and Epidemiology, College of Veterinary Science and Animal Husbandary, A.A.U., Anand in order to isolation and molecular characterization of Extended Beta Lactamase Producing Escherichia coli from milk to study their cultural characteristic and to judge the hygienic level of different local dairy cattle farms in and around Anand, Gujarat. A total of 150 samples were collected from different dairy cattle farms located in Navali (25), Sai dairy farm (50), Chikhodara (25), Bedva (25) and Mogar (25). All the samples were first inoculated on MacConkey Agar (MCA) and isolates showing pink colonies (lactose fermenting) were further transferred to Eosin Methylene Blue Agar (EMB) for confirmation and greenish metallic sheen producing isolates were confirmed as E. coli isolates.
  • ThesisItemOpen Access
    ISOLATION AND MOLECULAR CHARACTERIZATION OF EXTENDED SPECTRUM BETA LACTAMASE PRODUCING ESCHERICHIA COLI FROM CHICKEN
    (Department of Veterinary Public Health and Epidemiology College of Veterinary Science and Animal Husbandry Anand Agricultural University, Anand, 2019) Gida Harpalbhai; Dr. M. N. Brahmbhatt
    This study was undertaken in order to isolate and molecularly characterize extended spectrum beta lactamase producing Escherichia coli from chicken, to check their prevalence and to judge hygienic level of different local chicken butcher’s and retail market meat in and around anand. Total 150 chicken muscle samples were collected from chicken shops in and around Anand under aseptic precautions in sterile screw lid sample collector for further processing and microbiological analysis. Samples were collected aseptically in sterile test screw capped vials and immediately transferred to the laboratory for processing and bacteriological investigation.
  • ThesisItemOpen Access
    DETECTION OF TETRACYCLINE ANTIBIOTICS IN MILK OF ANAND DISTRICT
    (COLLEGE OF VETERINARY SCIENCE AND ANIMAL HUSBANDRY ANAND AGRICULTURAL UNIVERSITY ANAND, 2017) Mistry Urvish Pravinbhai; Dr. M. N. Brahmbhatt
    This study was undertaken with the objective of determining the overall presence of the Tetracycline antibiotic residues in raw and pasteurized milk samples collected from different localities of Anand district, Gujarat. Establishing sensitivity and specificity of immuno-photometric test and comparing the method with traditional chromatographic techniques for residue detection was the complementary objective. The research work was done at Department of Veterinary Public Health, College of Veterinary Science and Animal Husbandry, AAU, Anand and Food Quality Testing Laboratory, College of Food Processing Technology and Bio-Energy, AAU, Anand.
  • ThesisItemOpen Access
    SEROPREVALENCE OF BRUCELLOSIS IN SMALL RUMINANTS AND HUMANS OF ANAND DISTRICT
    (DEPARTMENTOF VETERINARY PUBLIC HEALTH AND EPIDEMIOLOGY COLLEGE OF VETERINARY SCIENCE AND ANIMAL HUSBANDRY ANAND AGRICULTURAL UNIVERSITY ANAND, 2017) RADHABEN R. PADHER; DR. J. B. NAYAK
    The present study was carried out at the post graduate laboratory, Department of Veterinary Public Health and Epidemiology, College of Veterinary Science and Animal Husbandry, A.A.U., Anand with the intention to determine the seroprevalence of brucellosis among small ruminants and human beings of Anand district, Gujarat employing RBPT, STAT and I-ELISA and compared the efficacy of these tests.
  • ThesisItemOpen Access
    ISOLATION, IDENTIFICATION AND DETECTION OF VIRULENCE FACTOR ASSOCIATED GENES OF CAMPYLOBACTER SPP. FROM BUFFALO MEAT
    (AAU, Anand, 2015) PATEL, SWATI N.; BRAHMBHATT, M. N.
    Campylobacter spp. has been recognized as one of the most frequent cause of gastrointestinal illness in humans throughout world. In recent years, the frequency of human enteritis caused by Campylobacter spp. has exceeded those caused by salmonella especially in developed countries. The association of zoonotic Campylobacters with chronic and life threatening complications such as Guillain- Barre syndrome, reactive arthritis, haemolytic uraemic syndrome, abortion, meningitis etc. which increases the public health concern of this pathogen worldwide. Campylobacter is normal inhabitant of intestinal tract of food animals and faulty handling, lack of sanitation at processing and improper storage has been considered as the major factor contaminating all types of animal foods. Inadequately cooked meat, unpasteurized milk and contaminated drinking water are the most common sources for epidemic and sporadic food borne cases. Therefore, the present study was undertaken with the objective to isolate identify and characterize the Campylobacter spp. from raw buffalo meat intended for the human consumption available in the retail meat market in Anand, Gujarat. A total 200 samples including 75 beef, 75 liver, 25 intestinal content and 25 water samples were collected aseptically and processed immediately after arrival. The samples were enriched into 25 ml of Blood free Campylobacter broth base containing CCDA selective supplement. Mixed properly and incubated at under microaerophilic condition (85% N2, 5% O2 and 10% CO2) at 42° C for 48 hours and further inoculation on blood free Campylobacter selective agar (mCCDA). The presumptive Campylobacter isolates were further confirmed at genus and species level by the series of biochemical tests and also confirmed by polymerase chain reaction assay. The confirmed isolates were subjected for the antibiotic susceptibility test using seven antibiotics, detection of virulence determinants by PCR. In the present study, 7 out of 200 (3.5%)) samples in which 2 out of 75 (2.67 %)) buffalo beef, 3 out of 75 (4 %) liver, 2 out of 25 (8 %>) intestinal content and no any water sample were found positive for the Campylobacter spp. In all the seven isolates the only identified species was Campylobacter jejuni. All the seven isolates of Campylobacter were further processed to study antibiotic resistance and sensitivity pattern against seven antibiotics by using agar disc diffusion technique. All Campylobacter isolates were resistant to Ciprofloxacin (100%)), where as 85.71% and 28.57% resistant to Nalidixic acid and Tetracycline, respectively. All the Campylobacter isolates were sensitive to Chloramphenicol, Erythromycin, Gentamicin and Strepyomycin sulphate (100%)) followed by Tetracycline (71.42%o) and Nalidixic acid (14.28%). All the isolates were also subjected for in vitro detection of five virulence gene encoding for viz., Flagellin gene (flaA), Campylobacter adherence gene (CadF), Invasion associated marker (iamA) gene. Flagellar synthesis and modification (flgR) and Cytolethal distending toxin Subunit B gene (cdtB) by polymerase chain reaction (PCR) using specific primers. The result indicated that all the seven isolates were found positive for CadF, CdtB and JlgR gene (100%) while six isolates were positive for flaA gene (85.71%) and three isolates were positive for iamA gene (42.85%). Therefore, the presence of Campylobacter in buffalo meat confirms that raw meat consumption could be a significant risk factor for human beings and there is need for routine study of this pathogen in buffalo meat to decrease the chances of infection with Campylobacter by consumption.
  • ThesisItemOpen Access
    ISOLATION, IDENTIFICATION AND MOLECULAR CHARACTERIZATION OF SALMONELLA ISOLATES OF FISH
    (AAU, Anand, 2010) TEKALE, ASHISH ANANTRAO; Savalia, C. V.
    The present study was carried out in the post graduate laboratory, Department of Veterinary Public Health, CVSc, AAU, Anand with intension to find out prevalence of Salmonella spp. in raw fish sold at retail fish shops in Anand city of Gujarat. The samples of raw fish consisted of different parts such as skin, gills, muscles and intestines (54 each) collected aseptically from local fish market and subjected first to pre-enrichment in lactose broth and then enrichment in tetrathionate (TTB) and Rappaport-Vassiliadis soybean meal (RVSM) broth, followed by plating on two selective media viz. xylose lysine deoxycholate (XLD) and bismuth sulphite agar (BSA). The colonies showing typical colony characteristics were further characterized on the basis of their morphological and biochemical characteristics. Cultures identified as Salmonella were further subjected to detection of different virulence associated genes and sensitivity to various antibiotics used in treatment. In the present study, 4.16 per cent (9/216) prevalence oi Salmonella spp. in raw fish samples was recorded. The organ wise the highest isolation rate was from gills' samples (7.40%) followed by intestines (5.55%), skin (1.85%)) and muscles (1.85%)). Serotyping of the isolates demonstrated that only Salmonella Weltevreden was main serotype recovered fi-om raw fish samples of Anand market (66.66%) o{Salmonella positive fish samples). The study of antibiogram of the isolates showed that all the Salmonella isolates were cent percent sensitive to chloramphenicol, gentamicin and norfloxacin; followed by the sensitivity pattern in descending order for cefepime and kanamycin (88.88% each), ciprofloxacin (66.66%), streptomycin (55.55%), carbenicilHn and cefotaxime (33.33%) each) and ampicillin (22.22%)). The cent per cent resistance towards erythromycin (100%) was observed followed by tetracycline (66.66%)), carbenicillin (44.44%)), ampicillin (33.33%)) and streptomycin (22.22%o). Looking to the sensitivity pattern of six S. Weltevreden isolates, all isolates were 100 per cent resistant to erythromycin followed by carbenicillin (66.66%)), ampicillin and tetracycline (50.00%) each) and streptomycin (33.33%)). All the Salmonella isolates were screened for the presence or absence of virulence genes viz. wvA, spvC, spVR. and stn using specific primers. All the isolates revealed presence of mvA gene suggesting their invasive ability and enteritoxin gene (stn) was present in all the isolates suggesting their potential to cause gastroenteritis among the consumers on account of consumption of such contaminated fish. None of the isolates showed presence of spvC gene or spvR. gene indicating their inability to cause systemic infections.
  • ThesisItemOpen Access
    ISOLATION, IDENTIFICATION AND MOLECULAR CHARACTERIZATION OF AEROMONAS FROM MARKET MILK
    (AAU, Anand, 2010) DHANDE, MANOJ S; Brahmbhatt, M. N.
    The aim of the present study was to isolate, identify and characterize Aeromonas species from raw milk in an around Anand market. A total of 160 samples were processed for estimating prevalence o^ Aeromonas spp. Out of those 160 samples tested, 29 Aeromonas isolates were recovered. On the basis of biochemical characterization 19 (13.6%) isolates of ^. sobria, 6 (4.3%) isolates of A. hydrophila and 4 (2.8%) isolates oiA. caviae were detected in raw milk. When different selective culture media were evaluated for isolation of Aeromonas spp. from raw milk it was found that percent recovery of Aeromonas isolates were more from Ampicillin Dextrin Agar (82.75%) as compared to Aeromonas Starch DNAse agar (62.06%)) All 29 Aeromonas isolates were tested for presence of aerolysin, haemolysin and enterotoxin gene. None of the isolate showed presence of aerolysin and enterotoxin, while overall prevalence of haemolysin gene was 78.78 per cent. In A. hydrophila, 54.54 per cent; A. caviae, 37.5 per cent and in A. sobria, 91.48 per cent isolates were found to possess haemolysin gene. All the isolates of Aeromonas were subjected to antimicrobial dmg sensitivity test against gentamicin, chloramphenicol, ciprofloxacin, kanamycin, bacitracin, rifampicin, tetracycline, ampicillin, penicillin G and erythromycin. Maximum sensitivity pattern was recorded with chloramphenicol (86.20 per cent), bacitracin (31.03 per cent) gentamicin and rifampicin (20.68 per cent) each, erythromycin (17.24 per cent), kanamycin (6.89 per cent). The resistance pattern of Aeromonas isolated from raw milk to various antibiotics was observed as cent per cent resistance towards tetracycline, ampicillin, penicillin G, ciprofloxacin (93.10 per cent), kanamycin (72.41 per cent), bacitracin (68.96 per cent) followed by gentamicin (65.51 per cent), rifampicin (62.06 per cent), erythromycin (58.62 per cent. Owing to the potential hazard of pathogenic Aeromonas spp., it was concluded that it is necessary to put more emphasis on food hygiene. Therefore, the surveillance of potential contaminant is crucial for sustenance of public health.
  • ThesisItemOpen Access
    “ISOLATION AND IDENTIFICATION OF STAPHYLOCOCCUS AUREUS FROM POULTRY AND POULTRY HOUSE ENVIRONMENT WITH SPECIAL REFERENCE TO MRSA
    (Anand Agricultural University, Anand, 2016) KIRIT BHEDI; DR. J.B. NAYAK
    Foodborne diseases and poisoning are the widely concern and have great public health concern worldwide . Foodborne diseases not only affect people’s health and well-being, but also have economic impacts on individuals and the countries. Staphylococcus aureus is one of the foods borne pathogen responsible for causing food borne illness worldwide after ingestion of food contaminated with staphylococcal toxins. Methicillin resistant Staphylococcus aureus (MRSA) is also a pathogen of human as well as animals of great concern responsible for causing severe morbidity and mortality worldwide. Additionally MRSA is widely spread in different animals of food origin
  • ThesisItemOpen Access
    ISOLATION, IDENTIFICATION AND CHARACTERIZATION OF LISTERIA SPECIES FROM MARKET MILK
    (Anand Agricultural University, Anand, 2010) SONAR SANDIP SUDHAKAR; Dr. M.N. Brahmbhatt
    The aim of the present study was to isolate, identify and characterize Listeria spp. from milk and milk products sold at and around Anand city, Gujarat State. A total of 237 samples comprising 147 raw milk (68 Cow milk and 79 buffalo milk), 38 pasteurized milk, and 52 milk products (12 Curd, 11 Ice cream, 12 Butter milk, 9 Lassi, 8 Cheese) samples were collected aseptically from various organized (branded) as well as unorganized (unbranded) sectors supplying milk and milk products to consumers at and around Anand city and subjected to two-step enrichment in University of Vermont broth and Frasers broth , followed by plating on three selective media viz. PALCAM, LPM agar and Oxford media. The presumptive isolates were identified at genus and species level by the battery of biochemical tests. These isolates were further subjected to in vitro pathogenicity (hemolysis on sheep blood agar, CAMP test and Phosphatidylinositol-specific phospholipase