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2.
Transbound Emerg Dis ; 65(1): e63-e69, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28707820

ABSTRACT

Foot-and-mouth disease (FMD) is a contagious disease of cloven-hoofed animals that causes substantial and perpetual economic loss. Apart from the contagious nature of the disease, the FMD virus can establish in a "carrier state" among all cloven-hoofed animals. The Mithun (Bos frontalis), popularly called the "Cattle of Mountain," is found in the geographically isolated, hilly region of north-east India: Arunachal Pradesh, Nagaland, Manipur and Mizoram. Despite the geographical inaccessibility, infection by FMD virus has emerged as the single most devastating disease among Mithun after the eradication of rinderpest from this region. Samples from outbreaks of FMD in Mithun were analysed by sandwich ELISA, multiplex RT-PCR (MRT-PCR) and liquid-phase blocking enzyme-linked immunosorbent assay and isolated in the BHK-21 cell line. The results indicate the presence of FMDV serotype "O." The sequencing and molecular phylogenies have revealed close relationships in the lineage of type "O" isolates from Bangladesh. The findings will provide useful information for further research and development of a sustainable programme for the progressive control of FMD in the Mithun population.


Subject(s)
Cattle Diseases/virology , Disease Outbreaks/veterinary , Foot-and-Mouth Disease Virus/isolation & purification , Foot-and-Mouth Disease/virology , Amino Acid Sequence , Animals , Carrier State , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/epidemiology , Cattle Diseases/prevention & control , Enzyme-Linked Immunosorbent Assay/veterinary , Foot-and-Mouth Disease/diagnosis , Foot-and-Mouth Disease/epidemiology , Foot-and-Mouth Disease/prevention & control , Geography , India/epidemiology , Multiplex Polymerase Chain Reaction/veterinary , Retrospective Studies , Sequence Alignment/veterinary , Serogroup
4.
Vet World ; 9(2): 123-7, 2016 Feb.
Article in English | MEDLINE | ID: mdl-27051196

ABSTRACT

AIM: The purpose of this study was to determine the virulence genes and serotype of Shiga toxin producing Escherichia coli (STEC) strains isolated from animals and birds. MATERIALS AND METHODS: A total of 226 different samples viz., fecal, intestinal content, rectal swab and heart blood were collected from different clinically affected/healthy animals and birds and were streaked on McConkeys' lactose agar and eosin methylene blue agar for isolation of E. coli, confirmed by staining characteristics and biochemical tests. By polymerase chain reaction (PCR) all the E. coli isolates were screened for certain virulence genes, viz., Shiga toxin 1 (stx1), stx2 and eae and enterohemolytic (Ehly) phenotype was observed in washed sheep blood agar plate. All the isolated E. coli strains were forwarded to the National Salmonella and Escherichia Centre, Central Research Institute, Kasauli (Himachal Pradesh) for serotyping. RESULTS: Out of 226 samples 138 yielded E. coli. All the isolates were screened for molecular detection of different virulent genes, viz. stx1, stx2 and eae, based on which 36 (26.08%) were identified as STEC. Among those STEC isolates, 15 (41.67%), 14 (38.89%), 1 (2.78%) exhibited eae, stx2, stx1 alone, respectively, whereas 4 (11.11%) and 2 (5.56%) carried both stx1 and stx2, stx2 and eae, respectively. Among the STEC isolates 22 were belonged to 15 different sero-groups, viz., O2, O20, O22, O25, O43, O60, O69, O90, O91, O95, O106, O118, O130, O162 and O170 and others were untypable. Ehly phenotype was observed in 10 (27.78%) the STEC isolates. CONCLUSION: The present study concluded that STEC could be isolated from both clinically affected as well as healthy animals and birds. Regular monitoring of more samples from animal and bird origin is important to identify natural reservoir of STEC to prevent zoonotic infection.

5.
Phys Rev Lett ; 108(12): 127201, 2012 Mar 23.
Article in English | MEDLINE | ID: mdl-22540618

ABSTRACT

We report magnetic, dielectric, and magnetodielectric responses of the pure monoclinic bulk phase of partially disordered La2NiMnO6, exhibiting a spectrum of unusual properties and establish that this compound is an intrinsically multiglass system with a large magnetodielectric coupling (8%-20%) over a wide range of temperatures (150-300 K). Specifically, our results establish a unique way to obtain colossal magnetodielectricity, independent of any striction effects, by engineering the asymmetric hopping contribution to the dielectric constant via the tuning of the relative-spin orientations between neighboring magnetic ions in a transition-metal oxide system. We discuss the role of antisite (Ni-Mn) disorder in emergence of these unusual properties.

6.
Toxicology ; 165(2-3): 87-95, 2001 Aug 28.
Article in English | MEDLINE | ID: mdl-11522367

ABSTRACT

Anilofos and isoproturon are important herbicides of organophosphorus and substituted phenylurea groups, respectively. Isoproturon is an inducer of hepatic drug-metabolizing enzymes. Animals and humans have the potential to be exposed to the mixture of these intentionally introduced environmental xenobiotics, but toxicological interactions between these herbicides are not known. Effects of isoproturon pretreatment (675 mg/kg/day for 3 consecutive days) on the toxic actions of anilofos administered orally as a single dose (850 mg/kg) were evaluated by determining some biochemical attributes in blood (erythrocyte/plasma), brain and liver of rats. Anilofos or isoproturon alone or in combination failed to produce any noticeable signs of cholinergic hyperactivity and behavioural alterations. Isoproturon did not potentiate the anticholinesterase action of anilofos in blood and liver. Inhibition of brain acetylcholinesterase was significantly protected. No significant alteration in anilofos-mediated production of lipid peroxidation was observed in erythrocyte and brain of isoproturon-pretreated rats, but it was significantly increased in liver. Anilofos did not affect GSH and GST. The isoproturon-mediated increase in GSH levels of brain (threefold) and liver (3.6-fold) was also not affected following combined administration. GST activity was increased in liver of rats given isoproturon alone (fourfold) or in combination with anilofos (2.8-fold). Activities of total ATPase, Mg2+-ATPase and Na+-K+-ATPase were not affected in rats given either anilofos alone or herbicides in sequence. With these treatments, there were no alterations in the protein content of plasma, brain and liver. Overall findings of the study indicate that isoproturon pretreatment does not alter the toxicity of anilofos, the GSH-GST metabolic pathway may not have a significant implication in the detoxification of anilofos and the production of a reactive oxygen species may be a factor in mediating anilofos toxicity.


Subject(s)
Herbicides/toxicity , Methylurea Compounds/toxicity , Organophosphorus Compounds/toxicity , Phenylurea Compounds , Adenosine Triphosphatases/metabolism , Animals , Blood Proteins/metabolism , Brain/drug effects , Brain/enzymology , Brain/metabolism , Cholinesterase Inhibitors/toxicity , Drug Interactions , Erythrocytes/drug effects , Erythrocytes/enzymology , Erythrocytes/metabolism , Glutathione/metabolism , Glutathione Transferase/metabolism , Lipid Peroxidation/drug effects , Liver/drug effects , Liver/enzymology , Liver/metabolism , Male , Nerve Tissue Proteins/metabolism , Rats , Rats, Wistar
7.
Indian J Exp Biol ; 39(11): 1107-12, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11906102

ABSTRACT

In acute toxicity study, rats showed dose-dependent signs of cholinergic hyperactivity and behavioural alterations. Maximum intensity of symptoms was not associated with mortality. Oral LD50 was 1681 mg/kg. In subacute toxicity study, rats were orally administered 50, 100 or 200 mg/kg of anilofos once daily for 28 days. Signs and symptoms were observed mainly with 200mg/kg. At this dose, anilofos induced hypothermia and progressive weight loss. None of the anilofos-treated rats died. Weight of brain, lung, testis was not altered, while of liver, heart, spleen and kidney increased. Anilofos inhibited cholinesterase (ChE) activities of erythrocyte (41-67%), plasma (36%), blood (37-64%), brain (63-73%) and liver (28-48%). Total protein was decreased in plasma and liver. Results indicate moderate toxic potential of anilofos in mammals, substantial contribution of CNS-mediated effects in causing anilofos toxicity and no direct relationship between hypothermia and level of ChE inhibition.


Subject(s)
Herbicides/toxicity , Organophosphorus Compounds/toxicity , Acetylcholinesterase/blood , Acetylcholinesterase/metabolism , Animals , Brain/drug effects , Brain/enzymology , Cholinesterase Inhibitors/toxicity , Lethal Dose 50 , Liver/drug effects , Liver/enzymology , Male , Organ Size/drug effects , Rats , Rats, Wistar
8.
Indian J Exp Biol ; 39(11): 1113-7, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11906103

ABSTRACT

Effects of anilofos on lipid peroxidation--an index of oxidative stress, ATPase activity--an integral part of active transport mechanisms for cations, GSH level and GST activity were evaluated in blood (erythrocyte/plasma), brain and liver of male rats after daily oral exposure to 50, 100 or 200 mg/kg for 28 days. None of the doses increased lipid peroxidation. The lowest dose, rather, produced marginally significant decrease in peroxidation in liver. Different doses of anilofos decreased GSH content and activities of GST and ATPases. Inhibition of total ATPase (34-44%) and Na+-K+-ATPase (45-52%) activities was maximum in liver, while that of Mg2+-ATPase (46-56%) was more in erythrocyte. Results indicate that anilofos may not cause oxidative damage to cell membrane in repeatedly exposed animals and may cause neuronal/cellular dysfunction by affecting ionic transport across cell membrane.


Subject(s)
Adenosine Triphosphatases/metabolism , Herbicides/toxicity , Lipid Peroxidation/drug effects , Organophosphorus Compounds/toxicity , Adenosine Triphosphatases/blood , Animals , Brain/drug effects , Brain/metabolism , Liver/drug effects , Liver/metabolism , Male , Oxidative Stress/drug effects , Rats , Rats, Wistar
9.
J Commun Dis ; 27(1): 15-8, 1995 Mar.
Article in English | MEDLINE | ID: mdl-7636146

ABSTRACT

Serum samples of 9350 individuals belonging to different high risk groups were tested for HIV Infection by ELISA and western blot technique. 9 samples were found to be positive. Two of them belonged to indigenous people of Assam and the infection was transfusion/transplant associated and acquired outside the state during the course of medical treatment. Two were IDUs from Nagaland requiring treatment in a local hospital at Dibrugarh, Assam. Five were from floating population temporarily residing in Assam with history of heterosexual promiscuity. Overall seropositivity rate was 0.97/1000. It is felt that HIV infection in Upper Assam has not penetrated deeply and is at a manageable level and the spread of infection can be prevented through IEC programmes.


Subject(s)
HIV Seropositivity/epidemiology , Adult , Age Distribution , Female , HIV Seropositivity/blood , HIV Seropositivity/transmission , Humans , India/epidemiology , Male , Population Surveillance , Risk Factors , Seroepidemiologic Studies , Sex Distribution
10.
Biotechnol Bioeng ; 25(12): 2945-56, 1983 Dec.
Article in English | MEDLINE | ID: mdl-18548629

ABSTRACT

Using two species of yeast and one of bacterium, evidence has ben obtained which indicates that the microbial uptake of solid alkane powders occurs primarily through a substrate solubilization mechanism. EDTA, a strong inhibitor of hydrocarbon solubilization by the cells, inhibited the growth of these organisms on alkane powder; the inhibition could be removed vai a supply of artificially solubilized alkane. One of the yeast strians, which was a mutant incapable of growing on solid alkane powder and liquid alkane, could grow very well on artifically solubilized alkanes. It was demonstrated that the solid alkane solubilization rate during microbial growth could satisfactorily account for the maximal alkane uptake rate actully observed during growth. The specificity of solubilization for the solid alkane used as the growth substrate was demonstrated.

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