Pathogenicity for several laboratory animals of toxoplasma oocysts originated from naturally infected cats.

The pathogenicity of four strains, O-1, O-2, O-3, and O-4, of Toxoplasma isolated in the form of oocyst from the feces of naturally infected cats was examined for such laboratory animals as mice, rats, rabbits, guinea pigs, and dogs, in comparison with that of the Beverley strain. Suspensions of seven graded doses of oocysts of each strain ranging from 1.0 X 10(-1) to 1.0 X 10(5) were inoculated orally into seven groups of five mice each. The O-1, O-2, and O-3 strains were as pathogenic for mice as the Beverley strain, but the O-4 strain was not so pathogenic as any other strain. Rats, rabbits, guinea pigs, and dogs were inoculated orally with around 1.0 X 10(5) oocysts. The four O strains were not so severly pathogenic for rats and rabbits as to cause death. The O-2 and O-3 strains showed strong pathogenicity for guinea pigs, almost all of which, when inoculated with them, died after manifesting severe clinical symptoms. The pathogenicity of the O-1 and O-2 strains showed essentially the same tendency for dogs as for any other animal. In inoculation with oocysts, as well as with proliferative forms or cysts, the same pathogenicity was not observed in different strains, even if the same species of host animals was used. On the contrary, the same pathogenicity was not always found even in one strain when a different species of animals was used.     

On the re-isolation and taxonomic study of Candida viswanathii Viswanathan et Randhawa 1959

Summary A detailed taxonomic study of a new isolate ofCandida viswanathii from sputum is reported.     

Experimental models for the study of diabetogenesis in laboratory animals.

The normal process of glucose-induced insulin release involves three major steps. First, glucose is identified by the pancreatic B-cell as an insulinotropic factor. Second, calcium accumulation in a critical cellular site triggers the release process. Third, a microtubular-microfilamentous system serves as the effector system for the translocation and eventual extrusion of secretory granules. It is possible to interfere rather specifically with each of these events. For instance, fasting results in an impairment of the process of glucose identification. Various pharmacological agents, including organic calcium-antagonists may uncouple the metabolic process of glucose recognition form the effector response. Last, experimental alterations of the B-cell microtubular-microfilamentous system cause severe disturbances in the dynamics of insulin release. It is proposed that such experimental models may help to elucidate the primary lesion in different types of spontaneous diabetes mellitus in laboratory animals.     

Enantioselective reduction of aryl ketones using immobilized cells of Candida viswanathii

Enantioselective reduction of 1-acetonapthone to S(−)-1-(1-naphthyl) ethanol, a key intermediate for the synthesis of HMG Co-A reductase inhibitor, was successfully carried out using immobilized cells of a newly isolated carbonyl reductase producing yeast strain Candida viswanathii MTCC 5158. Calcium alginate (1.5%, w/v) gave the best immobilization efficiency. Among different organic solvents and ionic liquids tried as reaction media, isopropanol gave the best enantioselectivity with moderate conversion. The immobilized cells (100 mg/ml in 50 mM Tris buffer pH 9) showed best results at a substrate concentration of 0.2 mg/ml at 30 °C. After twelve cycles of reaction, no significant decrease in bioreduction efficiency of the immobilized cells was observed as compared to the free cells.     

Optimization of physicochemical parameters for the enhancement of carbonyl reductase production by Candida viswanathii

Culture conditions have been optimized for a newly isolated yeast strain Candida viswanathii PBR2 which is capable of reducing a wide variety of aryl ketones with high stereospecificity. Studies on the culture conditions and catalytic performance of this microorganism showed that the carbonyl reductase occurs constitutively in the cells and its production is enhanced by feeding with acetophenone (2 mM) during the early period of cultivation. Mannitol (1%, wv⁻¹) was found to be beneficial both for growth and enzyme production. Supplementation of the media with yeast extract (1.0%, wv⁻¹) and Ca²⁺ (4 mM) enhanced the enzyme production. The optimal temperature and pH for the growth and enzyme production were 25 °C and 9.0, respectively. Excellent conversions along with almost absolute enantioselectivity were observed when the resting cells of this yeast strain were exploited to carry out the stereoselective reduction of a number of aryl ketones.     

Some aspects of the pathogenicity of Candida albicans in laboratory animals

Summary A study of nervous and hemorrhagic signs of experimental moniliasis and data on the comparative susceptibility of laboratory animals toC. albicans are presented.Paresis, ataxia, choreatic movements, unilateral neck muscle contractures, etc. were observed in every animal species. Hemorrhagic signs were also common and consisted of epistaxis and bloody eyes (only in rats).The susceptibility toC. albicans is in the mentioned order most outspoken in the rat, than the rabbit, guinea pig and mouse.A special selectivity for prostatic localization was observed in rats, but was absent in the other species.The possibility of toxic endothelial damage is mentioned.     

Enhancing the biocatalytic potential of carbonyl reductase of Candida viswanathii using aqueous-organic solvent system

In the present work, the toxic effect of various solvents with different Log P values was studied on the whole cells of Candida viswanathii. Experiments showed that the lower concentrations of some solvent increased both the activity retention and enzyme activity as compared to the control while this was not the case with higher concentrations of the same solvents. The model compound taken in the present study was 1-acetophenone. The percentage conversion improved from 76 to 94%. Addition of 2-propanol increased the substrate tolerance, giving the conversion of 90% compared to 9% in control at a substrate concentration of 70 mM in 1h. The operational stability increased at higher temperatures with the addition of 2-propanol in the reaction mixture with good conversion (90%) and enantiomeric excess (>99%) at 45 degrees C and 50 degrees C. The effect was also found to be prominent in other tested substrates. In order to further stabilize the cells for long term use in higher concentration of organic solvents, the cells were further immobilized, and were found to have higher activity retention than that of free cells.     

Pathogenicity of Nocardia transvalensis for laboratory mice

Nocardia transvalensis was found to be virulent for laboratory mice both by intraperitoneal and intravenous routes of inoculation, the latter route producing a more progressive and disseminating infection. Cortisone administration was found to enhance the susceptibility of mice, the LD₅₀ for the cortisone treated mice being five times less than that for the untreated animals. In the tissues of cortisone treated mice, N. transvalensis grew as dispersed filaments with coccobacillary forms or sometimes their loose aggregates, whereas in normal animals granule formation was a conspicuous feature. The pathogenicity of N. transvalensis is compared with that of N. asteroides, N. brasiliensis and N. caviae from published reports.     

An anesthetic system for small laboratory animals.

A non-rebreathing anesthetic system for administering volatile anesthetic mixtures to small laboratory animals was designed. The device is easily constructed and simple to operate, yet permits the anesthetic management of small animals by technics similar to those used for man and larger species.     

An apparatus for anesthetizing small laboratory animals.

A simple apparatus was designed for simultaneous general anesthesia of a number of small laboratory animals with spontaneous respiration. Anesthesia is consistent over many hr. The apparatus consists of an oxygen tank and vaporizer, a glass distribution bottle, and a non-return circuit of separate inspiratory and expiratory valves for each animal. The equipment is inexpensive to construct and can be rapidly adjusted for exact control of gas flow and anesthetic depth.     

A new airway device for small laboratory animals

There is a need for a device for improved management of the airway of small laboratory animals during general anaesthesia. This report introduces such a device, referred to here as the airway device (AD). The AD has some similarity to the laryngeal mask airway (LMA) developed for human patients, but the mask portion of the device is specifically designed for small laboratory animals. In addition, the device has an oesophageal extension and unlike the LMA does not have a cuff associated with the mask. This report also shares experience of tests of one prototype AD with six New Zealand white rabbits. The AD was used for administering isoflurane and its effectiveness was evaluated during conditions of spontaneous and controlled intermittent positive pressure ventilation. The results provide encouragement for further development of the AD for airway management of small laboratory animals.