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1.
Rev Environ Health ; 26(2): 127-33, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21905456

RESUMO

We undertook this study to identify the risk factors and prevalence of Cryptosporidium spp. in HIV-positive and HIV-negative diarrhea patients in the Alice rural settlement in the Eastern Cape Province of South Africa. A total of 180 stool specimens (35 HIV-positive diarrhea, 125 HIV-negative diarrhea patients, and 20 apparently healthy subjects) were screened for cryptosporidiosis using an ELISA-based approach. Sociodemographic information, water supply, and animal contact were recorded for diarrhea-positive patients. The data were analyzed using Pearson's chi2-test and Fisher's exact test. Cryptosporidium antigen was detected in 122 of 180 specimens (overall prevalence=67.8%). In HIV-positive diarrhea patients, the age groups 31-43 years (mean age 36.5 years) and 70-82 years (mean age 75.8 years) had a higher prevalence (100%) of the antigen than age groups 18-30 years (mean age 23.2 years) and 83-95 years (mean age 88.8 years) (50.0%). In HIV-negative diarrhea patients, the prevalence was highest (87.5%) at ages 18-30 years (mean age 23.2 years) and lowest (35.7%) at ages 83-95 years (mean age 88.8 years). Cryptosporidium antigenemia was slightly higher in females (78.2%, mean age 46.7 years) than in males (71.1%, mean age 42.6 years), but the difference was not significant (p>0.05). No apparently healthy control subject was infected with Cryptosporidium. HIV-negative patients had a significantly higher prevalence of antigen than HIV-positive patients, with farm animals considered a possible risk factor. In HIV-positive diarrhea patients, the prevalence peak was detected in more low income patients (85.7%) than in high income patients (32%). The high infection rate of specific groups was associated with exposure to a contaminated water supply. The results indicate that Cryptosporidium infection is highly prevalent in adult fecal specimens from the Nkonkobe Municipality, an indication of active infection that is likely to emerge as a major human pathogen in this locality owing to socioeconomic changes that favor transmission.


Assuntos
Criptosporidiose/epidemiologia , Cryptosporidium/fisiologia , Diarreia/epidemiologia , Exposição Ambiental , Adulto , Idoso , Idoso de 80 Anos ou mais , Antígenos de Protozoários/análise , Criptosporidiose/complicações , Criptosporidiose/diagnóstico , Criptosporidiose/parasitologia , Demografia , Diarreia/complicações , Diarreia/diagnóstico , Diarreia/parasitologia , Fezes/parasitologia , Feminino , Soropositividade para HIV/complicações , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Prevalência , Fatores de Risco , População Rural , África do Sul/epidemiologia , Abastecimento de Água , Adulto Jovem
2.
Arch Med Res ; 45(7): 540-6, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25240315

RESUMO

BACKGROUND AND AIMS: Pathogenic effects associated with Helicobacter pylori infection include peptic ulcer. Pathogenicity is mediated by the bacteria ureases. The emerging resistance of H. pylori to clarithromycin used in combination with amoxicillin in the treatment of H. pylori infection has necessitated the search for other means of combating the scourge of H. pylori, hence the search for potent H. pylori urease inhibitor. The aim of the study was to evaluate honey fractions obtained from different geographic zones for H. pylori urease inhibitory potentials. METHODS: Chloroform and diethyl-ether were used to extract honey fractions (HS) and Manuka honey (HM). H. pylori ureases were obtained from a 48-h culture through sonication. Urease activity was measured spectrophotometrically by assaying the reduction in NADH in coupled urease-glutamate dehydrogenase (GDH) system, whereas urease inhibition was calculated by comparing the NADH oxidation rate before and after incubation with honey fractions. RESULTS: Urease inhibition by the HS and HM were time and concentration independent. Chloroform extract of HS showed 48 and 42% inhibitory activities against urease from H. pylori (369C) and H. pylori (ATCC 43526), respectively, wheeras diethyl ether extract of HM showed 45 and 51% inhibitory activities against urease from H. pylori (369C) and H. pylori (ATCC 43526), respectively. Dixon plot revealed that HM extract showed mixed inhibition pattern in a reversible inhibition kinetics. CONCLUSIONS: Honey fractions were good inhibitors of H. pylori urease and may serve as a template in the development of urease inhibitors in pharmaceuticals.


Assuntos
Antibacterianos/farmacologia , Infecções por Helicobacter/tratamento farmacológico , Helicobacter pylori/enzimologia , Mel , Urease/antagonistas & inibidores , Amoxicilina/farmacologia , Fracionamento Químico , Clorofórmio/química , Claritromicina/farmacologia , Farmacorresistência Bacteriana , Infecções por Helicobacter/microbiologia , Helicobacter pylori/efeitos dos fármacos
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