An illustration of human sperm morphology and their functional ability among different group of subfertile males.

Condensed sperm chromatin is a prerequisite for natural fertilization. Some reports suggested the prevalence of chromatin condensation defects in teratozoospermia cases with head anomalies; conversely, earlier studies exemplified its occurrence in morphologically normal spermatozoa too. The aim of this study was to compare the condensation defects in correlation with head anomalies among different groups of subfertile males and its impact on the rate of fertilization in assisted reproduction procedures. Ultrastructure analysis of spermatozoa through scanning electron microscopy and atomic force microscopy could facilitate an in-depth evaluation of sperm morphology. Nuclear condensation defects (%) in spermatozoa were analyzed in 666 subjects, and its effect on the rate of fertilization was analyzed in 116 IVF and 90 intracytoplasmic sperm injection cases. There was no correlation of condensation defects with head anomalies (%). Student's t-test showed no significant changes in mean values of condensation defects in abnormal semen samples in comparison with the normal group. Condensation defects were observed in normal spermatozoa too, which was negatively associated with the rate of fertilization in IVF (p < 0.01), but intracytoplasmic sperm injection outcome remained unaffected. Ultrastructure study revealed sperm morphological features in height, amplitude, and three-dimensional views in atomic force microscopy images presenting surface topography, roughness property of head, and compact arrangement of mitochondria over axoneme with height profile at nanoscale. In pathological forms, surface roughness and nuclear thickness were marked higher than the normal spermatozoa. Thus, percentage of normal spermatozoa with condensation defects could be a predictive factor for the rate of fertilization in IVF. From diverse shapes of nucleus in AFM imaging, it could be predicted that defective nuclear shaping might be impeding the activity of some proteins/ biological motors, those regulate the proper Golgi spreading over peri-nuclear theca.

Bayesian analysis of two diagnostic methods for paediatric ringworm infections in a teaching hospital.

Quantitatively, conventional methods of diagnosis of tinea capitis or paediatric ringworm, microscopic and culture tests were evaluated with Bayes rule. This analysis would help in quantifying the pervasive errors in each diagnostic method, particularly the microscopic method, as a long-term treatment would be involved to eradicate the infection by the use of a particular antifungal chemotherapy. Secondly, the analysis of clinical data would help in obtaining digitally the fallible standard of the microscopic test method, as the culture test method is taken as gold standard. Test results of 51 paediatric patients were of 4 categories: 21 samples were true positive (both tests positive), and 13 were true negative; the rest samples comprised both 14 false positive (microscopic test positivity with culture test negativity) and 3 false negative (microscopic test negativity with culture test positivity) samples. The prevalence of tinea infection was 47.01% in the population of 51 children. The microscopic test of a sample was efficient by 87.5%, in arriving at a positive result on diagnosis, when its culture test was positive; and, this test was efficient by 76.4%, in arriving at a negative result, when its culture test was negative. But, the post-test probability value of a sample with both microscopic and culture tests would be correct in distinguishing a sample from a sick or a healthy child with a chance of 71.5%. However, since the sensitivity of the analysis is 87.5%, the microscopic test positivity would be easier to detect in the presence of infection. In conclusion, it could be stated that Trychophyton rubrum was the most prevalent species; sensitivity and specificity of treating the infection, by antifungal therapy before ascertaining by the culture method remain as 0.8751 and 0.7642, respectively. A correct/coveted diagnostic method of fungal infection would be could be achieved by modern molecular methods (matrix-assisted laser desorption ionisation-time of flight mass spectrometry or fluorescence in situ hybridization or enzyme-linked immunosorbent assay [ELISA] or restriction fragment length polymorphism or DNA/RNA probes of known fungal taxa) in advanced laboratories.

Toxicity of two carbamate insecticides to the cyanobacterium Anabaena PCC 7120 and computations of partial lethal concentrations by the probit method.

Toxicity studies of two commercial carbamate insecticides, carbaryl and carbofuran with the nitrogen-fixing filamentous cyanobacterium Anabaena PCC 7120, are described. Under nitrogen-fixing conditions and with calcium nitrate supplementation, 100 and 120 ppm carbaryl were the respective lethal concentrations (LC100), while 20 to 80 ppm (nitrogen-fixing conditions) and 20 to 100 ppm (with nitrate supplementation) were the partial lethal doses (

Monitoring of chemical fertilizers on toxicity of two carbamate insecticides to the cyanobacterium Anabaena PCC 7120.

The effects of individual chemical fertilizers (urea, superphosphate and potash) on the toxicity of two carbamate insecticides (carbaryl and carbofuran) to the nitrogen-fixing cyanobacterium Anabaena PCC 7120, were studied in vitro at partial lethal levels of each insecticide. Urea at 10 and 50 ppm levels reduced the toxicity due to carbaryl at 50 ppm partial lethal dose and due to carbofuran at 100 and 250 ppm partial lethal doses. Urea at 100 ppm enchanced the toxicity of both insecticides. Superphosphate at 10 ppm reduced the toxicity of carbaryl at 50 ppm and carbofuran at 100 and 250 ppm, but it enhanced the toxicity due to both insecticides at 50 ppm superphosphate. The toxicity due to carbaryl at 40 and 60 ppm were reduced by 100 and 200 ppm potash, but higher potash levels caused enhancement of toxicity. Carbofuran toxicity at 100 ppm was reduced but at 250 ppm the toxicity was enhanced with 100 ppm potash. Urea, superphosphate and potash caused no significant change in number of vegetative cells between the successive heterocysts at 10 and 50 ppm of urea and superphosphate, respectively, and 100 ppm of potash.

Restriction analysis and quantitative estimation of methylated bases of filamentous and unicellular cyanobacterial DNAs.

The DNAs of strains of three cyanobacterial genera (Anabaena, Plectonema, and Synechococcus) were found to be partially or fully resistant to many restriction endonucleases. This could be due to the absence of specific sequences or to modifications, rendering given sequences resistant to cleavage. The latter explanation is substantiated by the content of N6-methyladenine and 5-methylcytosine in these genomes, which is high in comparison with that in other bacterial genomes. dcm- and dam-like methylases are present in the three strains (based on the restriction patterns obtained with the appropriate isoschizomeric enzymes). Their contribution to the overall content of methyladenine and methylcytosine in the genomes was calculated. Partial methylation of GATC sequences was observed in Anabaena DNA. In addition, the GATC methylation patterns might not have been random in the three cyanobacterial DNA preparations, as revealed by the appearance of discrete fragments (possibly of plasmid origin) withstanding cleavage by DpnI (which requires the presence of methyladenine in the GATC sequence).

Effects of host aging, ions, and pH on the adsorption of the cyanovirus N-1 to Nostoc muscorum.

The adsorption rate of the cyanovirus N-1 infecting the nitrogen-fixing blue-green alga Nostocmuscorum decreased with aging of algal cultures and the virus failed to adsorb to the dead host cells. The adsorption rate declined in saline magnesium chloride solution compared to that in algal growth medium. The addition of amino acids like L-tryptophan and L-phenylalanine failed to enhance the adsorption rate of the virus. Optimal pH of adsorption was 7.6 to 8;1.

Effect of temperature on the adsorption and one-step growth of the Nostoc virus N-1.

This study was an attempt to observe the effects of temperature on adsorption and one-step growth of the virus N-1 infecting the nitrogen-fixing cyanobacterium Nostoc muscorum. Adsorption rate was found to maximum at 40 degrees C whereas no adsorption occurred at 10 degrees C. The Q10 value was about 2.03 and the energy of activation, Ea was 16.3 kcal/mole for the adsorption process. The development cycle of the virus was temperature sensitive. With increase in temperature, a gradual increase in inhibition of virus yield i.e. 8.33% at 30 degrees C, 35.3% at 35 degrees C and complete inhibition at 40 degrees C was observed. Out of 7 h latent period, the early 4 h were temperature sensitive and heat treatment had a reversible inhibitory effect on virus development. The temperature treatment did not affect the rise period but burst-size was reduced.

Effect of physical and chemical agents on the blue-green algal virus N-1.

The stability of the blue-green algal virus N-1, infecting the blue-green alga Nostoc muscorum, against temperature, EDTA and pH was studied. Ninety per cent thermal inactivation of virus occured at 55 degrees C in 20 minutes with an average inactivation rate constant of 0.07 per minute; at 60 degrees C the virus was completely inactivated within 5 minutes. 10(-4) M EDTA inactivated 30 per cent of free virus in 60 minutes; 10(-3) M EDTA was completely lethal. Intracellular virus was comparatively resistant to EDTA. The virus was stable in the pH range from 6.7 to 10.5 and was inactivated at acidic pH.

Mutation to resistance for virus N-1 in the blue-green alga Nostoc muscorum.

The spontaneous and nitrosoguanidine induced N-1 virus resistant mutants of the blue-green alga Nostoc muscorum were isolated with the average mutation frequency of 3.55 X 10(-5) and 6.08 X 10(-4) respectively. Of the surviving colonies 8 per cent became virus sensitive,whereas out of the remaining 92 per cent 9.3 per cent showed lysogenic behaviour and 13.3 per cent showed poor or no nitrogen fixing ability. Mutation to virus-resistance was independent of the presence of the virus.Spontaneous host range mutants of virus were not found in repeated experiments.