Rapid detection of microbial contamination in Ghanaian herbal medicines by PCR nanalysis
Rahman, Mohammed, Amuna, Paul and Dei-Tutuwa, Delali (2014) Rapid detection of microbial contamination in Ghanaian herbal medicines by PCR nanalysis. Ghana Medical Journal, 48 (2). pp. 106-111. ISSN 0016-9560 (doi:https://doi.org/10.4314/gmj.v48i2.9)
|
PDF (Publisher PDF)
12111_Rahman_Rapid_detection_of_microbial_contamination_(pub_PDF)_2014.pdf - Published Version Download (243kB) |
|
PDF (Copyright permission)
12111_Rahman_Permission_to_upload_to_GALA_(2016).pdf - Additional Metadata Restricted to Repository staff only Download (110kB) |
Abstract
Background: There is widespread use of herbal medicines across the world and the need for regulatory measures to ensure their safety, efficacy and quality is therefore imperative. Conventional microbiological methods are used in carrying out quality control analysis of herbal medicines but these are often slow, may be less sensitive or specific and labour-intensive. In this study we investigated the ability to use Polymerase Chain Reaction (PCR) as a fast, accurate and inexpensive novel method to detect the presence of common pathogens in herbal medicines from Ghana.
Methods: We employed different DNA extraction techniques including TE buffer, boiling method for DNA extraction as well as commercially available DNA extraction kits from Qiagen, UK: Gentra Puregene Yeast/Bact. Kit and DNeasyTM Tissue Kit which is column based to identify Escherichia coli, Staphylococcus aureus and Salmonella sp. in herbal products from Ghana in local African shops on the UK market.
Results: The TE buffer and boiling methods did not yield any bacterial DNA, however both commercial kits yielded significant amounts of DNA. PCR was able to detect pathogens present in the samples directly. Escherichia coli could be detected at 10 cfu/ml whilst Staphylococcus aureus was detectable at a threshold of up to 103 cfu/ml when samples were enriched overnight. Salmonella sp. could not be detected in DNA samples extracted from herbal medicines.
Conclusion: We conclude that PCR and similar new molecular techniques such as Real Time PCR have the potential as rapid microbiological analytical techniques especially in busy clinical settings and for quality control of herbal medicines.
Item Type: | Article |
---|---|
Additional Information: | © Ghana Medical Association |
Uncontrolled Keywords: | Herbal medicine, Microbial contamination, PCR, Ghana |
Faculty / School / Research Centre / Research Group: | Faculty of Education, Health & Human Sciences > School of Human Sciences (HUM) |
Last Modified: | 09 Oct 2021 04:46 |
URI: | http://gala.gre.ac.uk/id/eprint/12111 |
Actions (login required)
View Item |
Downloads
Downloads per month over past year