Enoch Aninagyei , Comfort Addo Boatey , Joshua Nkunim Arthur-Asmah , Gifty Larbi , Benjamin Sarfo-Bempong , Wilson Bright Tsidi , Charity Asantewaa Ankomah , Regina Yayra Menu , Keren Trishia Yemofio , Desmond Omane Acheampong
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引用次数: 0
Abstract
The Self-Lollisponge® device was used to collect saliva in children with malaria. Malaria antigens, namely, P. falciparum histidine-rich proteins 2 (PfHRP2) and Plasmodium lactate dehydrogenase (pLDH) were detected in blood and saliva samples. Subsequently, replicate samples with malaria antigens were stored at room temperature (28 °C) and 6 °C for 7 days. Malaria antigens were detected on days 1, 3, and 7. In the blood, PfHRP2 was detected in all 212 malaria samples, while pLDH was detected in 117 of the 212 samples (55.2 %). In the saliva, PfHRP2 was detected in 99/212 (46.7 %) samples while pLDH was detected in 111 of the 117 (94.8 %) samples whose corresponding blood had the pLDH detected. Compared to the blood samples, the overall sensitivity and accuracy of using saliva to detect PfHRP2 antigens were 46.7 % (95 % CI: 39.8–53.7 %) and 56.9 % (95 % CI: 50.6–63 %), respectively. Further, the overall sensitivity and accuracy for the detection of saliva-pLDH were 94.8 % (95 % CI: 89.2–98.1 %) and 96.4 % (95 % CI: 92.3–98.7 %), respectively. The PfHRP2 antigens were preserved for three days at 6 °C but at room temperature, the stability was for just a day. Nonetheless, the pLDH reduced comparatively faster, irrespective of the storage temperature.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.