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Journal Publication
Title of Article Analysis of xanthyletin and secondary metabolites from Pseudomonas stutzeri ST1302 and Klebsiella pneumoniae ST2501 against Pythium insidiosum 
Date of Acceptance 2 April 2019 
Journal
     Title of Journal BMC Microbiology 
     Standard SCOPUS 
     Institute of Journal BioMed Central Ltd unless otherwise stated. Part of Springer Nature. 
     ISBN/ISSN 1471-2180 
     Volume 2019 
     Issue
     Month April
     Year of Publication 2020 
     Page 78 
     Abstract Background: Pythium insidiosum is a member of the oomycetes class of aquatic fungus-like microorganisms. It can infect humans and animals through skin wounds and the eyes, causing pythiosis, an infectious disease with high morbidity and mortality rates. Antifungal agents are ineffective as pythiosis treatments because ergosterol, the target site of most antifungal agents, is not found in the P. insidiosum cytoplasmic membrane. The best choice for treatment is surgical removal of the infected organ. While natural plant products or secretory substances from bacterial flora have exhibited in vitro anti-P. insidiosum activity, their mechanism of action remains unknown. Therefore, this study hypothesized that the mechanism of action could be related to changes in P. insidiosum biochemical composition (such as lipid, carbohydrate, protein or nucleic acid) following exposure to the inhibitory substances. The biochemical composition of P. insidiosum was investigated by Synchrotron radiation-based Fourier- transform infrared (FTIR) microspectroscopy. Results: Fraction No.6 from the crude extract of P. stutzeri ST1302, fraction No.1 from the crude extract of K. pneumoniae ST2501 and xanthyletin were used as anti-P. insidiosum substances, with MFCs at 3.125, 1.57–1.91, 0. 003 mg/ml, respectively. The synchrotron FTIR results show that the deconvoluted peak distributions in the amide I, amide II, and mixed regions were significantly different between the treatment and control groups. Conclusions: Xanthyletin and the secondary metabolites from P. stutzeri ST1302 and K. pneumoniae ST2501 exerted anti-P. insidiosum activity that clearly changed the proteins in P. insidiosum. Further study, including proteomics analysis and in vivo susceptibility testing, should be undertaken to develop a better understanding of the mechanism of anti-P. insidiosum activity. 
     Keyword P. insidiosum, P. stutzeri ST1302, K. pneumoniae ST2501, Xanthyletin, Synchrotron radiation-based Fourier- transform infrared (FTIR) microspectroscopy 
Author
577090005-7 Miss KITTIYA WITTAYAPIPATH [Main Author]
Associated Medical Sciences Doctoral Degree

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Level of Publication นานาชาติ 
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