Prevalence of malaria, typhoid and co-infection in District DIR (lower), Pakistan / Prevalência de malária, febre tifóide e co-infecção no distrito dir (inferior), Paquistão

Malaria and typhoid fever are among the most endemic diseases in the tropical and developing countries. Both diseases share similar transmission factor and often have the similar symptom. Based on this reason, much medical personnel try to cure both malaria and typhoid instantaneously in each case of suspected Salmonella infection and vice versa. The District Dir (Lower) is a favorable location for the protozoan nourishment and secondly mostly reported cases of malaria and typhoid co-infections. The main objective of this study was to find out the prevalence of malaria and typhoid co-infection in the District Dir (Lower), Khyber Pakhtunkhwa (KPK), Pakistan. The blood samples of 1889 patients were examined from September 2012 to April 2013, out of which 311 (16.46%) were positive for malaria and typhoid. Out of these infected, 117 (38%) sample was positive for malaria, 183 (58%) sample were positive for typhoid while co-infected cases were only 11 (4%). The current results indicate that this area is endemic for malaria and typhoid and co-infection. Its infection is prevalent in both the genders at varying degrees.

A malária e a febre tifóide estão entre as doenças mais endêmicas nos países tropicais e em desenvolvimento. Ambas as doenças compartilham fator de transmissão semelhante e muitas vezes têm sintomas semelhantes. Com base nessa razão, muitos profissionais da saúde tentam curar a malária e a febre tifóide ao mesmo tempo em cada caso de suspeita de infecção por Salmonella e vice-versa. O Distrito Dir (inferior) é um local favorável para a nutrição de protozoários e o segundo local com mais casos reportados de malária e co-infecções tifoides. O principal objetivo deste estudo foi descobrir a prevalência da malária e da co-infecção tifóide nos distritos de Dir (Lower), Khyber Pakhtunkhwa (KPK), Paquistão. As amostras de sangue de 1889 pacientes foram examinadas de setembro de 2012 a abril de 2013, das quais 311 (16,46%) foram positivas para malária e febre tifóide. Destes infectados, 117 (38%) amostras foram positivas para a malária, 183 (58%) amostras foram positivas para a febre tifóide, enquanto os casos co-infectados foram apenas 11 (4%). Os resultados atuais indicam que esta área é endêmica para malária e febre tifóide e co-infecção. Sua infecção é prevalente em ambos os sexos em diferentes graus.

Significance of anti-HBc screening of blood donors & its association with occult hepatitis B virus infection: Implications for blood transfusion.

Background & objective: Expansions of blood donor screening and improved laboratory detection of viral markers have remarkably reduced the risk for infection with transfusion-transmitted viruses. This study was aimed to evaluate the presence of anti-HBc and to determine the presence or absence of HBV DNA in the serum samples from HBsAg negative, anti-HBc positive blood donors in a tertiary care hospital blood bank from Delhi. Methods: A total of 2175 HBsAg negative, first time volunteer blood donors were included in the study from blood bank, Lok Nayak Hospital, New Delhi. The blood specimens from all these subjects were evaluated for anti-HBV-core antigen (anti-HBc) serology, anti-HBV-surface antigen (anti-HBs) titres and HBeAg. The presence of HBV DNA was evaluated by testing, through polymerase chain reaction (PCR) techniques. Results: Of the 2175 HBsAg negative voluntary blood donors, 413 (19.8%) were tested to be positive for anti-HBc alone. Of these, 153 (group-I) were anti-HBs negative whereas group-II comprises a total of 260 anti-HBs positive cases i.e. 89 out of 413 had anti-HBs titres of 10-99 IU/l and the remaining 171 had anti-HBs titres of 100-500 IU/l. HBV DNA was detected in 7.5 per cent anti-HBc positive samples irrespective of anti-HBs status. Interpretation & conclusions: Our results showed that 18.9 per cent of our donor population was anti-HBc reactive, and hence inclusion of anti-HBc testing will lead to a high discard rate. The presence of HBV DNA in fairly high percentage of anti-HBc positive samples highlighted the need for a stringent and better screening system to prevent occult HBV infection.

Effect of sodium nitroprusside on H+-ATPase activity and ATP concentration in Candida albicans.

ATP hydrolysis by plasma membrane H+-ATPase from Candida albicans has been investigated in presence of nitric oxide and various nutrients (sugars and amino acids). Sodium nitroprusside (SNP) was used as nitric oxide donor. It was found that ATP concentration decreased in SNP treated cells which was more in presence of sugars like glucose, xylose and 2-deoxy-D-glucose and amino acids as compared to their respective controls. The activity of H+-ATPase from plasma membrane decreased by 70 % in SNP treated cells. Both in vivo and in vitro treatments of SNP showed almost similar effects of decrease in ATPase activity. Effect of SNP was more pronounced in presence of nutrients. Interestingly, it was observed that vanadate did not show any independent effect in presence of nitric oxide. Several workers have reported similar type of results with other P-type ATPases. For the first time, it was observed in the present study that in presence of nitric oxide, H+-ATPase activity decreased like other P-type ATPases. Our study indicated that NO had a significant effect on ATP synthesis and activity of H+- ATPase. In the presence of NO, the ATP concentration was decreased indicating it affected mitochondrial electron transport chain. It may be concluded that NO, not only affects (inhibit) mitochondrial electron transport chain but also interferes with H+- ATPase of plasma membrane by changing its conformation resulting in decreased activity.

Effect of nitric oxide on H+ -efflux in presence of various nutrients in Candida albicans.

In the present study tentative link has been established between H+ -efflux and effect of NO in presence of various nutrients (glucose, 2-deoxy-D-glucose, xylose, proline, glutamic acid and lysine) in C. albicans using sodium nitroprusside (SNP) as a potent source of NO. It was observed that there was a decreasing trend in pH with time, in control, while SNP treated cells showed an initial decline in pH for 10-15 min, followed by an increase in pH up to 30 min. In presence of glucose there was an enhancement in H+ -efflux by 9-fold whereas proline, glutamic acid and lysine showed enhancement by 3, 6 and 1.5-fold respectively. Similar trends in increase in pH after 15 min in SNP treated cells of Candida was observed in presence of all nutrients used. It was demonstrated for the first time that H+ -ATPase of C. albicans was affected by NO.

Effect of phosphocreatine on H+ extrusion, pHi and dimorphism in Candida albicans.

Candida albicans is an opportunistic pathogen. Its proliferation in human hosts is believed to be controlled by immunologic mechanisms. The plasma membrane of the fungus possesses an H(+)-ATPase (PM-ATPase) which actively extrudes protons to generate an electrochemical gradient which is used in co-transport of nutrients. This ATPase is associated with the growth, dimorphism and pathogenicity of the fungus. The physiological concentration of phosphocreatine (PCr) is 20-35 mM in skeletal muscles. H(+)-extrusion in Candida cells was strongly inhibited by PCr; 44% at 20 mM and 69% at 40 mM. H(+)-extrusion was stimulated 6.2-fold in the presence of 10 mM glucose. This glucose stimulated extrusion was inhibited significantly by PCr; 36% at 20 mM and 53% at 40 mM. The intracellular pH pattern of cells destined to differentiate was greatly altered in the presence of PCr. Evagination time for control cells was between 90-120 min. PCr, delayed dimorphism, reduced the population of cells differentiating to hyphae and also reduced the length of hyphae after each time interval. Only 60% differentiation was observed with 10 mM PCr and 40% for higher PCr concentration even after 210 min. Direct interaction of PM-ATPase and PCr has been demonstrated by difference spectrum measurement employing stopped flow spectrophotometer. It can be concluded that PCr may be playing a significant role in checking growth and pathogenesis of C. albicans.