Designing primers potentially specific to Entamoeba gingivalis genes
DOI:
https://doi.org/10.1515/cipms-2015-0064Słowa kluczowe:
actin, cysteine proteinase, Entamoeba gingivalis, 18S-rRNA, 5.8S-rRNA, PCR primersAbstrakt
Entamoeba gingivalis normally exists in the human oral cavity, namely in the gums, and brings about some specific diseases. However, it can also trigger some more serious illnesses. Among these are infections of the genital tract, acute osteomyelitis of the mandible and pulmonary abscess. Entamoeba gingivalis identification by light microscopy is difficult, hence polymerase chain reaction (PCR) is used. The contemporary primers for PCR are complement to 18S rRNA. This article informs the reader of the process that was involved in designing new primers for three genes which were thought to be present on the Entamoeba gingivalis genome, but their sequences were unknown. The newly obtained sequences of primers have better properties for identification purposes, compared to these which are currently used.
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Prawa autorskie (c) 2015 Autorzy
Praca jest udostępniana na licencji Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 Unported License.
