Title of article :
Sugar-Rich Foods Carry Osmotolerant Yeasts with Intracellular Helicobacter Pylori and Staphylococcus spp
Author/Authors :
Siavoshi, Farideh Department of Microbiology - School of Biology - University College of Sciences - University of Tehran, Tehran, Iran , Sahraee, Marzieh Department of Microbiology - School of Biology - University College of Sciences - University of Tehran, Tehran, Iran , Heydari, Samira Department of Microbiology - School of Biology - University College of Sciences - University of Tehran, Tehran, Iran , Sarrafnejad, Abdolfattah Department of Immunology - School of Public Health - Tehran University of Medical Sciences, Tehran, Iran , Saniee, Parastoo Department of Microbiology and Microbial Biotechnology - Faculty of Life Science and Biotechnology - Shahid Beheshti University G.C, Tehran, Iran , Tavakolian, Atefeh Department of Microbiology and Microbial Biotechnology - Faculty of Life Science and Biotechnology - Shahid Beheshti University G.C, Tehran, Iran , Heidarian, Sheida Department of Microbiology - School of Biology - University College of Sciences - University of Tehran, Tehran, Iran
Abstract :
BACKGROUND
Sugar-rich foods are of the main components of daily human meals. These foods with high
sugar and low water content kill bacteria. However, osmotolerant yeasts survive and multiply. The
aim of this study was to examine the occurrence of intracellular Helicobacter pylori (H. pylori)
and Staphylococcus spp. in yeast isolates from sugar-rich foods.
METHODS
Thirty-two yeast isolates from fresh fruits, dried fruits, commercial foods, and miscellaneous
foods were identified by the sequencing of amplified products of 26S rDNA. Fluorescence microscopy
and LIVE/DEAD bacterial viability kit were used to examine the occurrence of live bacteria inside
the yeast’s vacuole. Immunofluorescence assay was used to confirm the identity of intracellular
bacteria as H. pylori and Staphylococcus. Polymerase chain reaction (PCR) was used for the detection
of 16S rDNA of H. pylori and Staphylococcus in the total DNA of yeasts.
RESULTS
Yeasts were identified as members of seven genera; Candida, Saccharomyces, Zygosaccharomyces,
Pichia, Meyerozyma, Metschnikowia, and Wickerhamomyces. Intravacuolar bacteria were stained
green with a bacterial viability kit, revealing that they were alive. Immunofluorescence assay confirmed
the identity of intracellular H. pylori and Staphylococcus spp. PCR results revealed that among the
32 isolated yeasts, 53% were H. pylori-positive, 6% were Staphylococcus-positive, 18.7% were
positive for both, and 21.8% were negative for both.
CONCLUSION
Detection of H. pylori- and Staphylococcus-16S rDNA in yeast isolates from dried fruits, and
commercial foods showed the occurrence of more than one kind of endosymbiotic bacterium in
yeasts’ vacuoles. While the establishment of H. pylori and Staphylococcus in yeast is a sophisticated
survival strategy, yeast serves as a potent bacterial reservoir
Keywords :
Sugar-rich foods , Yeast , Intracellular bacteria , Helicobacter pylori , Staphylococcus spp
Journal title :
Middle East Journal of Digestive Diseases(MEJDD)