Studies on the nutrition of the genus Pestalotiopsis II. Chromatographic analysis of the medium during the utilization of various carbohydrates

The utilization of 17 different carbohydrates by four isolates ofPestalotiopsis was studied by the paper chromatographic technique.Among the pentoses, xylose, which was recorded as a poor source, was not consumed even in 15 days by any of the isolates. L-arabinose was exhausted in 6–8 days while L-rhamnose was used up in 9–10 days, both supporting growth equal to glucose as a source. There was a good correlation between the efficiency and the rate of utilization of the three pentose sugars.The utilization of the hexoses had no correlation with dry weight output as was in the case of the pentoses. Glucose from the medium was exhausted between 4–9 days; fructose required 7–10 days. Fructose was much superior than glucose but was consumed slowly as compared to glucose. D-galactose which was a poor source was used up only in 7 days byP. royneae but the other three isolates took longer time, 11–14 days to exhaust the sugar. L-sorbose was used up in 10–15 days. D-mannose, which was a good source for mycelial attainment required 6–12 days for complete utilization.Hydrolytic pathway of utilization of oligosaccharides was recorded for all the isolates; in lactose, however, the component sugars could not be detected and the disaccharide was present up to the end of the incubation period. This was obviously due to slow rate of its breakdown. Sucrose was hydrolysed in the shortest period of 2 days in all cases. Glucose was utilized faster than the other hydrolytic products by three isolates.P. royneae, however, finished both in equal time of 6 days. Maltose, cellobiose and trehalose were used slowly. In maltose, one or two transient oligosaccharides were also detected. Trehalose persisted for the longest time. Melibiose was present till the end of the incubation period during the growth ofP. gracilis andP. paeoniae isolate I. The isolate II ofP. paeoniae andP. royneae consumed it in 9 days. Only one of its hydrolytic products, i.e. glucose was detected in the medium, on raffinose solution only fructose and galactose were spotted.The hydrolytic products of starch could not be detected in the medium. In dextrin, however, glucose was detected in the medium used by three isolates other thanP. paeoniae isolate I.Oligosaccharide synthesis was accomplished by all the isolates ofPestalotiopsis under study. On maltose medium,P. gracilis andP. paeoniae isolate I synthesised two such transient oligosaccharides,P. royneae andP. paeoniae II formed only one.     

Proteomic approach for identification and characterization of novel immunostimulatory proteins from soluble antigens of Leishmania donovani promastigotes

Visceral leishmaniasis (VL) caused by Leishmania donovani is a major parasitic disease prevalent in endemic regions of Bihar in India. In the absence of good chemotherapeutic options, there is a need to develop an effective vaccine against VL which should be dependent on the generation of a T helper type 1 (Th1) immune response. We have shown that soluble proteins from promastigote of a new clinical isolate of L. donovani (2001) ranging from 68 to 97.4 kDa (F2 fraction), induce Th1 responses in the peripheral blood mononuclear cells of cured Leishmania patients and hamsters and also showed significant prophylactic potential. To understand the nature of F2 proteins, it was further characterized using 2-DE, MALDI-TOF and MALDI-TOF/TOF-MS. In all, 63 spots were cut from a CBB stained gel for analysis and data was retrieved for 52 spots. A total of 33 proteins were identified including six hypothetical/unknown proteins. Major immunostimulatory proteins were identified as elongation factor-2, p45, heat shock protein (HSP)70, HSP83, aldolase, enolase, triosephosphate isomerase, protein disulfideisomerase and calreticulin. This study substantiates the usefulness of proteomics in characterizing a complex protein fraction (F2) map of soluble L. donovani promastigote antigen identified as Th1 stimulatory for its potential as vaccine targets against VL.     

Lateral hydrological connectivity differentially affects the community characteristics of multiple groups of aquatic invertebrates in tropical wetland pans in South Africa

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Modelling the distribution of the invasive Ziziphus mauritiana along road corridors in Zimbabwe

We investigate how human fruit consumption affects the spread of the alien invasive Ziziphus mauritiana along road corridors in northern Zimbabwe. A field survey was conducted to identify and map Z. Mauritiana stems at 25 randomly located 6‐ha plots placed along two main roads connecting the Zambezi Valley to the Highveld region. The L‐function was used to test for evidence of significant spatial clustering of the stems. The inhomogeneous point model fitted by maximum likelihood was also applied to check whether distance from the road explains variation in the number of stems per unit area. Finally, a t test was executed on log‐transformed abundance data to test for significant differences in the mean number of saplings and adults between the Zambezi Valley and the Highveld. Results of the L‐function indicated that Z. mauritiana had a clustered and linear distribution along roads both in the Zambezi Valley and Highveld regions. Results of the t test showed that the mean number of saplings per plot in the Zambezi Valley (μ₁ = 275) was three times higher than in the Highveld (μ₂ = 78), with p < 0.01. The mean number of adult trees was also significantly higher in the Zambezi Valley than in the Highveld.     

Southern blot analysis with synthetic oligonucleotides. Application to prostatic protein genes.

1. An ethanol precipitation procedure was developed to purify radiolabeled DNA and oligonucleotide probes to be used in Southern blots. 2. The radiolabeled probes produced strong hybridization signals on a clear background on Southern blot analysis of single gene copies even after 5 days of exposure on X-ray films. 3. An oligonucleotide probe complementary to human glandular kallikrein-1 coding region (amino acids 161-167) detected a single DNA fragment after digestion with Bam H1, Hind III or Pst 1. 4. Another oligonucleotide probe coding for the same region of human prostate-specific antigen detected 3 DNA fragments on Southern blots by contrast to a 1.5 kb full length cDNA probe which detected the presence of only one strong hybridization signal. 5. Oligonucleotide probes appear to be excellent tools for gene mapping. Their sensitivity, specificity and limitations can be compared to the one of monoclonal antibodies used in epitope mapping of proteins.     

Haemoglobin variants and Plasmodium falciparum malaria in children under five years of age living in a high and seasonal malaria transmission area of Burkina Faso

ABSTRACT: BACKGROUND: Genetic factors play a key role in determining resistance/susceptibility to infectious disease. Susceptibility of the human host to malaria infection has been reported to be influenced by genetic factors, which could be confounders if not taken into account in the assessment of the efficacy of interventions against malaria. This study aimed to assess the relationship between haemoglobin genotypes and malaria in children under five years in a site being characterized for future malaria vaccine trials. METHODS: The study population consisted of 452 children living in four rural villages. Hb genotype was determined at enrolment. Clinical malaria incidence was evaluated over a one-year period using combined active and passive surveillance. Prevalence of infection was evaluated via bi-annual cross-sectional surveys. At each follow-up visit, children received a brief clinical examination and thick and thin blood films were prepared for malaria diagnosis. A clinical malaria was defined as Plasmodium falciparum parasitaemia >2,500 parasites/ul and axillary temperature [greater than or equal to]37.5degreesC or reported fever over the previous 24 hours. RESULTS: Frequencies of Hb genotypes were 73.2% AA; 15.0% AC; 8.2% AS; 2.2% CC; 1.1% CS and 0.2% SS. Prevalence of infection at enrolment ranged from 61.9%-54.1% among AA, AC and AS children. After one year follow-up, clinical malaria incidence (95% CI) (episodes per person-year) was 1.9 (1.7-2.0) in AA, 1.6 (1.4-2.1) in AC, and 1.7 (1.4-2.0) in AS children. AC genotype was associated with lower incidence of clinical malaria relative to AA genotype among children aged 1-2 years [rate ratio (95% CI) 0.66 (0.42-1.05)] and 2-3 years [rate ratio (95% CI) 0.37 (0.18-0.75)]; an association of opposite direction was however apparent among children aged 3-4 years. AS genotype was associated with lower incidence of clinical malaria relative to AA genotype among children aged 2-3 years [rate ratio (95% CI) 0.63 (0.40-1.01)]. CONCLUSIONS: In this cohort of children, AC or AS genotype was associated with lower risk of clinical malaria relative to AA genotype only among children aged one to three years. It would be advisable for clinical studies of malaria in endemic regions to consider haemoglobin gene differences as a potentially important confounder, particularly among younger children.     

A GABA-neuropeptide Y (NPY) interplay in LH release

Neuropeptide Y (NPY) stimulates and gamma-amino butyric acid (GABA) inhibits LH release in the rat. Since a sub-population of NPY-producing neurons in the arcuate nucleus (ARC) of the hypothalamus co-express GABA, the possibility of an interplay between NPY and GABA in the release of LH was investigated in two ways. First by employing light and electron microscopic double staining for NPY and GABA, using pre and post-immunolabeling on rat brain sections, we detected GABA in NPY immunoreactive axon terminals in the MPOA, one of the primary sites of action of these neurotransmitters/neuromodulators in the regulation of LH release. These morphological findings raised the possibility that inhibitory GABA co-released with NPY may act to restrain the excitatory effects of NPY on LH release. Muscimol (MUS, 0.44 or 1.76 nmol/rat), a GABA(A) receptor agonist, administered intracerebroventricularly (icv), alone failed to affect LH release, but NPY (0.47 nmol/rat icv) alone stimulated LH release in ovarian steroid-primed ovariectomized rats. On the other hand, administration of MUS blocked the NPY-induced stimulation of LH release in a dose-dependent manner. Similarly, administration of MUS abolished the excitatory effects on LH release of 1229U91, a selective NPY Y4 receptor agonist. These results support the possibility that in the event of co-release of these neurotransmitters/neuromodulators, GABA may act to restrain stimulation of LH release by NPY during the basal episodic and cyclic release of LH in vivo.