PL EN
MORPHOSTRUCTURAL DAMAGE OF FOODBORNE BACTERIAL PATHOGENS INFLUENCED BY SWAMP CRANBERRY (VACCINIUM OXYCOCCOS L.) POMACE EXTRACT REVEALED BY TRANSMISSION ELECTRON MICROSCOPY (TEM)
 
More details
Hide details
1
Central Institute for Labour Protection – National Research Institute, Laboratory of Biohazards
 
2
WULS-SGGW, Institute of Food Sciences
 
 
Publication date: 2021-06-28
 
 
2019;(598):41-50
 
KEYWORDS
ABSTRACT
Foodborne pathogens are a serious threat to human health when they contaminate food products. Nowadays, consumers are interested in natural, safe, multi-health benefits food and at the same time increasingly concerned about food chemical preservatives and additives. Due to this fact, it is important to focus on natural alternatives for food products preservation. Data related to antimicrobial properties of cranberry fruit are available; however, information regarding morphostructural damage due to foodborne pathogens, due to the natural extracts is still scarce. This study was performed to evaluate the morphostructural effects of swamp cranberry water–ethanol pomace extract (WEPE) on selected Gram-positive (Staphylococcus aureus and Listeria monocytogenes) and Gram-negative (Escherichia coli and Salmonella Enteritidis) foodborne bacterial pathogens. The morphological and ultrastructural alterations of extract-treated bacteria cells were observed using transmission electron microscopy technique (TEM). In our study, TEM revealed changes in the cell structure and the integrity of cells both for Gram-positive and Gram-negative strains. Our investigation revealed substantial structural damage at the cellular level and irreversible cell membrane rupture with the apparent leakage of intracellular contents. Present results indicate that WEPE is highly effective against foodborne pathogens, so as the antimicrobial effect of WEPE, including destructive influence on bacterial cells proved in this study, suggests promising potential use of cranberry extract as a natural preservative in food products. Influence of WEPE on other processes, such as inhibition of nucleic acid synthesis, inhibition of cell wall and membrane protein synthesis or disturbance of cellular energy metabolism, should be the subject of further research.
 
REFERENCES (23)
1.
Côté J.P., Caillet S., Doyon G., Dussault D., Sylvain J.F., Lacroix M., 2011. Antimicrobial effect of cranberry juice and extracts. Food Control 22, 1413–1418.
 
2.
Erdem B., Kariptas E., Kaya T., Tulumoglu S., Gorgulu O., 2016. Factors influencing antibacterial activity of chitosan against Aeromonas hydrophila and Staphylococcus aureus. Int. Curr. Pharm. J. 5(5), 45–48.
 
3.
Ghuysen J.M., Hakenbeck R. (Eds.), 1994. Bacterial Cell Wall. Elsevier Science, Amsterdam.
 
4.
Gniewosz M., Stobnicka A., 2017. Bioactive components content, antimicrobial activity, and foodborne pathogen control in minced pork by cranberry pomace extracts. J. Food Saf. 38(1), e12398. https://doi.org/10.1111/jfs.12....
 
5.
Gould G.W., 1996. Industry perspectives on the use of natural antimicrobials and inhibitors for food applications. J. Food Prot. 59(13), 82–86.
 
6.
Hartmann M., Berditsch M., Hawecker J., Ardakani M.F., Gerthsen D., Ulrich A.S., 2010. Damage of the bacterial cell envelope by antimicrobial peptides gramicidin S and PGLa as revealed by transmission and scanning electron microscopy. Antimicrob. Agents and Chemother. 54(8), 3132–3142.
 
7.
Haslam E., 1996. Natural polyphenols (vegetable tannins) as drugs: possible modes of action. J. Nat. Prod. 59(2), 205–215.
 
8.
Kaviya Srinidhi A.J., 2014. Cranberry and its Antibacterial Activity – A Review. J. Pharm. Sci. & Res. 6(1), 41–44.
 
9.
Kim Y.H., Chung H.J., 2011. The effects of Korean propolis against foodborne pathogens and transmission electron microscopic examination. N. Biotechnol. 28(6), 713–718.
 
10.
Lacombe A., Wu V.C., Tyler S., Edwards K., 2010. Antimicrobial action of the American cranberry constituents; phenolics, anthocyanins, and organic acids, against Escherichia coli O157:H7. Int. J. Food Microbiol. 139(1–2), 102–107.
 
11.
Li B., Wang X., Chen R.X., Huangfu W.G., Xie G.L., 2008. Antibacterial activity of chitosan solution against Xanthomonas pathogenic bacteria isolated from Euphorbia pulcherrima. Carbohydr. Poly. 72(2), 287–292.
 
12.
Lou Z., Wang H., Zhu S., Ma C., Wang Z., 2011. Antibacterial activity and mechanism of action of chlorogenic acid. J. Food Sci. 76(6), 398–403.
 
13.
Malinowska-Pańczyk E., Sztuka K., Kołodziejska I., 2010. Substancje o działaniu przeciwdrobnoustrojowym jako składniki biodegradowalnych folii z polimerów naturalnych [Active antimicrobial agents as components for naturally occurring biodegradable polymers]. Polimery 9, 625–706.
 
14.
Mirzoeva O.K.L., Grishanin R.N., Calder P.C., 1997. Antimicrobial action of propolis and some of its components: the effects on growth, membrane potential and motility of bacteria. Microbiol. Res. 152(3), 239–246.
 
15.
Puupponen-Pimiä E.R., Nohynek L., Meier C., Kähkönen M., Heinonen M., Hopia A., Oksman-Caldentey K.M., 2001. Antimicrobial properties of phenolic compounds from berries. J. Appl. Microbiol. 90, 494–507.
 
16.
Reimer L. (Ed.), 1995. Energy-Filtering Transmission Electron Microscopy. Optical Sciences Series. Vol. 71. Springer, Berlin-Heidelberg.
 
17.
Ricke S.C., 2003. Perspectives on the use of organic acids and short chain fatty acids as antimicrobials. Poult. Sci. 82(4), 632–639.
 
18.
Stewart P.S., Mukherjee P.K., Ghannoum M.A., 2004. Biofilm antimicrobial resistance. In: M.A. Ghannoum, G.A. O’Toole (Eds.), Microbial Biofilms. ASM Press, Washington, DC, 250–268.
 
19.
Stobnicka A., Gniewosz M., 2017. Antimicrobial protection of minced pork meat with the use of Swamp Cranberry (Vaccinium oxycoccos L.) fruit and pomace extracts. JFST 55. https://doi.org/10.1007/s13197....
 
20.
Tyagi A.K., Malik A., 2010. In situ SEM, TEM and AFM studies of the antimicrobial activity of lemon grass oil in liquid and vapour phase against Candida albicans. Micron 41(7), 797–805.
 
21.
Wu V.C.H., Qiu X., Bushway A., Harper L., 2008. Antibacterial effects of American cranberry (Vaccinium macrocarpon) concentrate on foodborne pathogens. LWT-Sci Technol. 41(10), 1834–1841.
 
22.
Yi S.M., Zhu J.L., Fu L.L., Li J.R., 2010. Tea polyphenols inhibit Pseudomonas aeruginosa through damage to the cell membrane. Int. J. Food Microbiol. 144(1), 111–117.
 
23.
Yinfeng Lyu Y., Yang Y., Lyu X., Dong N., Shan A., 2016. Antimicrobial activity, improved cell selectivity and mode of action of short PMAP-36-derived peptides against bacteria and Candida. Scientific Reports 6, 27258. https://doi.org/10.1038/srep27....
 
ISSN:0084-5477
Journals System - logo
Scroll to top