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Antibacterial, antibiofilm activity and cytotoxicity of crude extracts of Ptaeroxylon obliquum (Ptaeroxylaceae) used in South African ethnoveterinary medicine against Bacillus anthracis Sterne vaccine strain
Author(s) -
Famuyide Ibukun Michael,
Eloff Jacobus Nicolaas,
McGaw Lyndy Joy
Publication year - 2020
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2020.34.s1.00560
Subject(s) - bacillus anthracis , antimicrobial , broth microdilution , antibacterial activity , microbiology and biotechnology , antibiotics , minimum inhibitory concentration , traditional medicine , bark (sound) , cytotoxicity , chemistry , biology , bacteria , in vitro , medicine , biochemistry , genetics , ecology
Anthrax, a zoonotic disease and a potential biological weapon for terrorism is caused by Bacillus anthracis , a Gram‐positive, sporulating bacterium. Anthrax is endemic in South Africa and primarily affects livestock and wildlife species. Problems with the control of anthrax include growing resistance to present antibiotics and disinfectants or decontaminants coupled with low antibiotic access in rural and poor settings. Therefore, it is imperative to search for new antimicrobials, especially from natural sources that could offer effective and potent alternatives. Medicinal plants are putative sources of new antimicrobials. Ptaeroxylon obliquum (Ptaeroxylaceae) is used traditionally in South Africa as an anthrax remedy in livestock. Here, the antibacterial and antibiofilm activity as well as cytotoxicity of the bark and fresh leaf crude extracts of P. obliquum was determined. A two‐fold serial microdilution assay was used to determine the minimum inhibitory concentration (MIC) of the acetone and chloroform extracts of bark and the chloroform extract of fresh leaves of the plant against B. anthracis Sterne vaccine strain. The crystal violet assay was used to determine antibiofilm activity while cytotoxicity was determined using a tetrazolium‐based colorimetric (MTT) assay against Caco‐2 intestinal cells. The MIC of the extracts ranged from 0.005 – 0.039 mg/mL compared to the positive control gentamicin (MIC = 4.9 × 10 −5 ) with acetone bark extract being the most active (MIC = 0.005 mg/mL). Activity of extracts against B. anthracis biofilms was high (>50 % antibiofilm activity) at 0 h (prevention of biofilms; ranged between 87–99 %), and 24 h (destruction of pre‐formed biofilms; ranged between 58–93 %). The chloroform fresh leaf extract had the best antibiofilm activity. The acetone bark extract had the best total antibacterial activity (yield (mg/g)/MIC (mg/mL)) of 21 500 g/mL. This means that the mass extracted from 1 g of the acetone extract can be diluted by 21 500 times and still inhibit bacterial growth. The 50% lethal concentration (LC 50 ) of the extracts against Caco‐2 cells ranged between 0.03–0.19 mg/mL with the chloroform fresh leaf extract being relatively the safest (LC 50 = 0.19 mg/mL). The acetone bark extract had the best selectivity index (LC 50 /MIC) of 6. This shows that the extract has higher toxicity against the bacteria than to mammalian cells. The results support the use of the plant against anthrax in South African ethnoveterinary medicine. The extracts may be potential alternatives to chemicals as disinfectants or decontaminants, especially in rural areas where chemicals are not accessible to the farmers. The compounds responsible for anti‐ B. anthracis activity, and their mechanism(s) of action, is the focus of future studies. Support or Funding Information The University of Pretoria is thanked for providing research support

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