000			04362nam a22003137a 4500
999			_c112499 _d112499
003			IE-CoIT
005			20181017150047.0
008			181016s2018 ie ||||| |||| 00| 0|eng||
040			_aIE-CoIT
082			_aTHESES PRESS
100	1		_9125473 _aOleksy, Patrycja _eauthor
245	1	0	_aInhibition of Listeria monocytogenes by human gut bacteria / _cPatrycja Oleksy
264		1	_aCork : _bCork Institute of Technology, _c2018.
300			_av, 141 pages : _billustrations (some color), tables ; _c30 cm
336			_atext _btxt _2rdacontent
337			_aunmediated _bn _2rdamedia
338			_avolume _bnc _2rdacarrier
490	0		_aM.Sc. - Biological Sciences
502			_aThesis _b(M.Sc.) - _cCork Institute of Technology, _d2018.
504			_aBibliography: (pages 108-138)
520	3		_a"Listeria monocytogenes is a foodborne pathogen, which continues to be problematic to the food industry due to its ability to survive within food products and persist within food processing environments. The growing trend towards natural food preservatives and antimicrobial agents increases the need for the development of novel, natural anti-Listeria agents. Evidence presented in the literature suggests that the human gut microbiota is a reservoir of novel antimicrobial agents. It was therefore hypothesized that novel anti-Listeria agents are produced by human gut-derived bacteria. The object of this study was to isolate and characterize gut bacteria with anti-Listeria monocytogenes activity. A total of 23 fecal banks of human origin were screened for antagonistic activity against L.monocytogenes 10403S. The results of the initial screening have shown that 1,569 gut-derived isolates have demonstrated various levels of anti-Listeria activity. Following an extensive screen 59 gut-derived isolates were initially shortlisted and were identified mostly as Enterococcus spp. By a combination of MALDI-TOF MS analysis and 16S rRNA gene sequencing. The data collected allowed a further shortlisting of strains from 59 to 16 based on differences observed in the colony morphology, the size and appearance of the zones of inhibition observed in the deferred antagonism assays and well diffusion assays as well as spectrum of activity of each isolate against a umber of indicator strains. The antimicrobials produced by 11 out of 16 shortlisted gut derived isolates were identified as peptides using a proteinase K assay. The anti-Listeria activity of the shortlisted isolates were examined in a model broth co-culture experiment. Based on the results obtained the antimicrobials produced by two Enterococcus faecium isolates were selected for further investigation. The activity of the antimicrobials were investigated in dairy food homogenate models and stainless steel biofilm assays. The findings of the food trials have shown a reduction of Listeria numbers by ~0.6 log CRFU/mL in natural yogurt treated with cell free supernatent (CFS) and a reduction of ~1.5 log CFU/mL observed in cheddar cheese treated with whole cell extract (WCE) following a 3 hr incubation. The anti-biofilm assays demonstrated a reduction in biofilm formation of stainless steel by 70% when treated with CFS and 92.42% when treated with (WCE). The experiments presented in this thesis confirm that bacteria from the human gut produce anti-Listeria compounds which can control or reduce the numbers of Listeria in model co-cultures and in food homogenates. The antimicrobials isolated in this study have also shown the ability to reduce Listeria biofilm formation. Future efforts should focus on identifying the antimicrobials produced by all of the shortlisted strains (through a combination of genome sequencing and peptide purifications). It is hoped that any novel antimicrobial that is discovered have an application in the food industry to reduce the significant threat posed by L. monocytogenes. These antimicrobials could be used as a natural preservative in food products and packaging or incorporated into a spray to control biofilm in the food processing environment". Abstract
650		0	_944779 _aListeria monocytogenes
650		0	_944778 _aListeria
650		0	_944765 _aFoodborne diseases
650		0	_937454 _aFood industry and trade
650		0	_939915 _aMicrobial metabolism
650		0	_937714 _aGastrointestinal system
942			_2ddc