Spatial and temporal variation in malaria transmission in a low endemicity area in northern Tanzania

Background

Current detection or screening for malaria infection necessitates drawing blood by fingerprick or venipuncture, which poses risks and limitations for repeated measurement. This study presents PCR detection of Plasmodium falciparum in human urine and saliva samples, and illustrates this potential application in genotyping malaria infections.

Methods

Urine and saliva were obtained from 47 thick film positive and 4 negative individuals one day after collection of blood slides and filter paper blood spots. P. falciparum DNA was extracted from blood, urine and saliva, in separate groups, using the Chelex method or Qiagen DNEasy^® kit (urine and saliva only). Blood, urine and saliva extracts were subjected to PCR in separate batches. Amplicons from the various sample types were examined for MSP2 polymorphisms and restriction fragment patterns on DHFR amino acid codon 59.

Results and discussion

Malaria infections exhibited primarily low-grade parasite densities, with a geometric mean of 775 asexual parasites/μl. Regularly matching polymorphic MSP2 genotypes were found between the corresponding urine, saliva and peripheral blood amplicons of each individual, with different inter-individual polymorphic genotypes. Amplicon yields were significantly dependent on DNA extraction method, parasite density and primer set (p < 0.001). A Qiagen^® kit extraction had more than 2× higher amplicon yield than the Chelex method, for both urine and saliva. Amplicon yields were 1.6 fold higher from saliva than urine. For each unit increase in log parasite density, the probability of amplicon enhanced 1.8 fold. Highest amplicon yields were obtained from the primer set with the shortest PCR product.

Conclusion

P. falciparum infection is detectable by PCR on human urine and saliva samples. Subject to further refinement of extraction technique and amplicon yields, large-scale malaria parasite screening and epidemiological surveys could be possible without the need to collect blood and use of needles or sharps.     

ADP-ribosyl cyclase and abscisic acid are involved in the seasonal growth and in post-traumatic tissue regeneration of Mediterranean sponges

In previous papers it has been demonstrated that the plant hormone abscisic acid (ABA) is responsible for the stimulation of water filtration and oxygen consumption elicited by a temperature increase in the Mediterranean demosponge Axinella polypoides. The signal transduction pathway triggered by ABA involves activation of ADP-ribosyl cyclase (ADPRC), leading to an increase of the intracellular concentration of cyclic ADP-ribose (cADPR), a universal and potent intracellular calcium mobilizer. These data prompted us to investigate the possible involvement of the ABA/ADPRC/cADPR system in the sponge life cycle and in post-traumatic tissue regeneration of Mediterranean sponges. ADPRC activity was detected in the cell lysate from several common Mediterranean sponge species, including Calcarea and Demospongiae. Specimens were collected monthly over a 2-year period, from January 2002 to April 2004. All species studied showed a peak of ADPRC activity during July and August 2003, concomitant with an anomalous heat wave that struck the whole Mediterranean basin during these months. In the aquarium, during spontaneous tissue regeneration, an increase of the [ABA]_i and of the ADPRC activity over time zero values was consistently observed. In conclusion, these results indicate that an increase of ABA content and of ADPRC activity correlates with the growth and with post-traumatic tissue regeneration in several Mediterranean sponge species, indicating that the ABA/ADPRC/cADPR system is involved in the response to environmental stress in sponges. Determination of ADPRC activity/ABA content may provide a means to assess metabolic activation of sponge populations under conditions of environmental stress.     

Salinity stress and cytoplasmic factors. A comparison of cell permeability and lipid partiality in salt sensitive and salt resistant cultivars and lines of Triticum aestivum and Hordeum vulgare

Salinity effects on the cell membranes of four lines of wheat ( Triticum aestivum L.). and two cultivars of barley ( Hordeum vulgare L.), differing in salt resistance were investigated. Plants were grown for 10 days in 1/4-strength Hoagland solution and then for 5 more days in 1/4-strength Hoagland with and without NaCl (100 m M ) or (for Hordeum only) polyethylene glycol (PEG). Permeability to three non-electrolytes (urea, methylurea and ethylurea) of subepidermal cells of leaf sheaths ( Triticum ) and coleoptiles ( Hordeum ) was determined and membrane partiality calculated, a parameter which numerically indicates the degree of lipophilicity of a membrane. Non-electrolyte permeability significantly increased and membrane partiality decreased in the salt sensitive cultivars or lines under salt stress. Neither parameter changed significantly in the salt resistant lines and cultivar in a saline environment. Osmotic stress in Hordeum by PEG 10000 had no significant effect on permeability and thus membrane partiality neither in sensitive nor in resistant cultivars.
The osmotic component of salinity stress did not seem to be a major factor causing injury, rather ion toxicity may be a cause of cell damage. The results indicate differences in the membrane between salt sensitive and salt resistant genotypes. Salt resistance seems to be controlled by genetic factors independent of external salinity levels.