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1.
Vet World ; 9(1): 1-5, 2016 Jan.
Article in English | MEDLINE | ID: mdl-27051176

ABSTRACT

AIM: With the aim of revealing the epidemiological intricacies of bluetongue (BT) in the southern part of West Bengal state, the present study was undertaken to assess seroprevalence of BT along with identification of the vector of the disease, i.e., Culicoides midges available in the region in their breeding season with conducive environmental factors, if any. MATERIALS AND METHODS: A total of 1509 (sheep-504, goat-1005) samples were collected from three different agroclimatic zones of South Bengal viz. new alluvial, red laterite and coastal saline. To detect anti-BT antibodies in the collected serum samples, indirect-enzyme-linked immunosorbent assay (i-ELISA) was performed. Culicoides midges were collected from those agro-climatic zones of South Bengal for species identification. The meteorological parameters, viz. temperature (maximum and minimum), rainfall and relative humidity of three agro-climatic zones of South Bengal were analyzed for the months of July to December during 2010-2013. RESULTS: The overall seropositivity was 33.13% and 30.24% in sheep and goat, respectively as assessed by i-ELISA. In South Bengal, the predominant species of Culicoides found were Culicoides schultzei, Culicoides palpifer and Culicoides definitus. CONCLUSION: Since virus transmitting species of Culicoides midges could be detected in South Bengal, besides high seropositivity in ruminants, the possibility of circulating BT virus in South Bengal is quite imminent.

2.
Vet World ; 8(3): 346-9, 2015 Mar.
Article in English | MEDLINE | ID: mdl-27047095

ABSTRACT

AIM: This study was carried out to assess the presence of anti-bluetongue (BT) antibodies in sheep, goat and cattle of different agro-climatic zones of Jharkhand. MATERIALS AND METHODS: Serum samples were collected from apparently healthy as well as suspected sheep, goat and cattle from different districts of Jharkhand covering different agro-climatic zones. Serum samples were screened by indirect enzyme linked immunosorbent assay (iELISA) for detecting anti-BT antibodies. RESULTS: Out of a total of 480 animal serum samples (sheep-190, goats-210 and cattle-80) screened, 83 (43.68%) of sheep, 91 (43.33%) of goat and 46 (57.50%) of cattle sera were found positive. The % positivity ranged between 41% and 51% in different agro-climatic zones. The results showed slight higher seroprevalence, although not significantly, in cattle than sheep and goats in different agro-climatic zones of Jharkhand. CONCLUSIONS: The above data indicate widespread prevalence of BT virus antibodies in studied areas. The incidence of BT is not detected officially, so far. The present seroprevalence status of BT in Jharkhand indicates presence of BT infection in the state for the first time.

3.
Asian Pac J Trop Med ; 6(4): 315-9, 2013 Apr 13.
Article in English | MEDLINE | ID: mdl-23608335

ABSTRACT

OBJECTIVE: To evaluate the antimicrobial efficacy of berberine, a plant alkaloid. METHODS: Five multi-drug resistant (MDR) STEC/EPEC and five MDR ETEC isolates from yaks with haemorrhagic diarrhoea were selected for the study. Antibacterial activity of berberine was evaluated by broth dilution and disc diffusion methods. The binding kinetics of berberine to DNA and protein was also enumerated. RESULTS: For both categories of enterovirulent Escherichia coli (E. coli) isolates, berberine displayed the antibacterial effect in a dose dependent manner. The MIC(50) of berberine chloride for STEC/EPEC isolates varied from 2.07 µM to 3.6 µM with a mean of (2.95 ± 0.33) µM where as for ETEC strains it varied from 1.75 to 1.96 µM with a mean of (1.87 ± 0.03) µM. Berberine bind more tightly with double helix DNA with Bmax and Kd of (24.68±2.62) and (357.8±57.8), respectively. Berberine reacted with protein in comparatively loose manner with Bmax and Kd of (18.9±3.83) and (286.2±113.6), respectively. CONCLUSIONS: The results indicate clearly that berberine may serve as a good antibacterial against multi drug resistant E. coli.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Berberine/therapeutic use , Cattle Diseases/drug therapy , Diarrhea/drug therapy , Escherichia coli Infections/drug therapy , Animals , Berberine/metabolism , Cattle , DNA, Bacterial/metabolism , Diarrhea/veterinary , Drug Resistance, Multiple, Bacterial , Enteropathogenic Escherichia coli , Enterotoxigenic Escherichia coli , Escherichia coli Infections/veterinary , Microbial Sensitivity Tests , Protein Binding , Shiga-Toxigenic Escherichia coli
4.
Trop Anim Health Prod ; 44(5): 1063-72, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22228494

ABSTRACT

Of 273 samples (rectal swab) collected from free-ranging yaks of Tawang district, Arunachal Pradesh, 42 Shiga toxin-producing Escherichia coli (STEC), six enteropathogenic E. coli (EPEC) and 27 enterotoxigenic E. coli (ETEC) strains were isolated. All the STEC and EPEC strains were further investigated for respective stx variants (for STEC only) and additional putative virulence factors. The 27 ETEC strains were also screened for characteristic enterotoxin gene(s) and colonization factors. Occurrence of ETEC was significantly (p < 0.05) higher in the diarrheic yaks and yaks of less than 1 year of age. Majority of enterovirulent E. coli isolates were resistant to amikacin, azithromycin, chloramphenicol, colistin, doxycycline, furazolidone, nalidixic acid, nitrofurantoin, streptomycin and tetracycline. Dendrogram, constructed with molecular fingerprinting profiles obtained from RAPD (Randomly Amplified Polymorphic DNA) and ERIC (Enterobacterial Repetitive Intergenic Consensus) PCR, placed the isolates in different clusters irrespective of their serotypes, virulence gene and drug resistance pattern. Collectively, the study indicates that yaks, being a potential reservoir of multidrug resistant STEC and EPEC, may represent significant risk to public health in this region. Higher recovery of ETEC isolates from yaks with diarrhea points out that ETEC may be a major determinant for repeated occurrence of diarrhea in yaks.


Subject(s)
Cattle Diseases/epidemiology , Diarrhea/veterinary , Drug Resistance, Multiple, Bacterial , Enteropathogenic Escherichia coli/genetics , Enterotoxigenic Escherichia coli/genetics , Escherichia coli Infections/veterinary , Shiga-Toxigenic Escherichia coli/genetics , Animals , Cattle , Cattle Diseases/microbiology , DNA Fingerprinting/veterinary , DNA, Bacterial/genetics , Diarrhea/epidemiology , Diarrhea/microbiology , Enteropathogenic Escherichia coli/classification , Enteropathogenic Escherichia coli/isolation & purification , Enteropathogenic Escherichia coli/pathogenicity , Enterotoxigenic Escherichia coli/classification , Enterotoxigenic Escherichia coli/isolation & purification , Enterotoxigenic Escherichia coli/pathogenicity , Escherichia coli Infections/epidemiology , Escherichia coli Infections/microbiology , India , Phylogeny , Polymerase Chain Reaction/veterinary , Prevalence , Random Amplified Polymorphic DNA Technique/veterinary , Sequence Analysis, DNA/veterinary , Shiga-Toxigenic Escherichia coli/classification , Shiga-Toxigenic Escherichia coli/isolation & purification , Shiga-Toxigenic Escherichia coli/pathogenicity , Virulence Factors/genetics , Virulence Factors/isolation & purification
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