<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2020.119061</article-id><article-id pub-id-type="publisher-id">FNS-102955</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Antimicrobial Effects of Berries on Listeria monocytogenes
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Elisaveta</surname><given-names>Sandulachi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Daniela</surname><given-names>Cojocari</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Greta</surname><given-names>Balan</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Liliana</surname><given-names>Popescu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aliona</surname><given-names>Ghendov-Moșanu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rodica</surname><given-names>Sturza</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>"Nicolae Testemitanu" State University of Medicine and Pharmacies, Chisinau, Republic of Moldova (RM)</addr-line></aff><aff id="aff1"><addr-line>Technical University of Moldova, Chisinau, Republic of Moldova (RM)</addr-line></aff><pub-date pub-type="epub"><day>21</day><month>09</month><year>2020</year></pub-date><volume>11</volume><issue>09</issue><fpage>873</fpage><lpage>886</lpage><history><date date-type="received"><day>7,</day>	<month>July</month>	<year>2020</year></date><date date-type="rev-recd"><day>18,</day>	<month>September</month>	<year>2020</year>	</date><date date-type="accepted"><day>21,</day>	<month>September</month>	<year>2020</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The purpose of this study was to first evaluate the antimicrobial effects of powder and extracts of berries (rose-hip, aronia, sea buckthorn and hawthorn) on the development of antibiotic-resistant 
  L
  . 
  monocitogenes
  . 
  Listeria 
  monocytogenes
   is considered one of the most important pathogens responsible for food-borne infection. Antimicrobial properties were evaluated using the standard Kirby-Bauer disk diffusion method. Bacterial inactivation networks were determined and compared, as well as the possibility of using powders and extracts of berries to control the risk of 
  Listeria 
  monocytogees
   infestation in the milk and dairy industry as well as in the meat industry. The effect of pH (4.78 - 4.43) and water activity (0.90 - 0.80) on the relationship between optical density (OD) at 600 nm and the plate count (CFU ml<sup>-</sup>
  <sup>1</sup>
  ) was investigated for 
  Listeria 
  monocytogenes
  . It was determined Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC) 
  of berries for
   
  L. monocytogenes
  . 
  The most relevant bacteriostatic and bactericidal 
  effect on L. monocytogenes in the tested berries demonstrated sea buckthorn and rosehip.
 
</p></abstract><kwd-group><kwd>L. monocitogenes</kwd><kwd> Berries</kwd><kwd> Kirby-Bauer Test</kwd><kwd> Minimum Inhibitory Concentration (MIC)</kwd><kwd> Minimum Bactericidal Concentration (MBC)</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Listeria monocytogenes is considered one of the most important pathogens responsible for food-borne infection. It is often incriminated in outbreaks of human listeriosis [<xref ref-type="bibr" rid="scirp.102955-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref2">2</xref>]. Listeria monocytogenes is a foodborne pathogen that can cause invasive severe human illness (listeriosis) in susceptible patients. Most human listeriosis cases appear to be caused by consumption of refrigerated ready-to-eat foods [<xref ref-type="bibr" rid="scirp.102955-ref3">3</xref>]. In the European Union (EU), 1763 confirmed human cases of listeriosis were reported in 2013 by 27 member states. The EU notification rate was 0.44 cases per 100,000 population which represented an 8.6% increase compared to 2012 [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>]. In 2013, there were 191 deaths caused by listeriosis in the EU. The highest number of fatal cases (64) was reported in France. Mortality rate in the EU was established at 15.6% among cases with known outcome. In 2013, a total of 13 outbreaks caused by L. monocytogenes were reported by seven MS and one non-MS. It was observed that the number of listeriosis in 2013 was slightly higher than in the previous years [<xref ref-type="bibr" rid="scirp.102955-ref5">5</xref>]. The European Food Safety Authority (EFSA) reported, in Europe, from 2008 to 2015, 37 food-borne outbreaks caused by L. monocytogenes that lead to 37 deaths [<xref ref-type="bibr" rid="scirp.102955-ref6">6</xref>]. Just from June of 2018, 47 cases have been reported, and nine patients have died due to or with the infection [<xref ref-type="bibr" rid="scirp.102955-ref7">7</xref>]. L. monocytogenes is an opportunistic bacterial pathogen that has the capacity to survive under extreme environmental conditions encountered in nature and in the food chain, such as high salt concentrations [<xref ref-type="bibr" rid="scirp.102955-ref8">8</xref>], large range of pH [<xref ref-type="bibr" rid="scirp.102955-ref9">9</xref>], desiccation [<xref ref-type="bibr" rid="scirp.102955-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref11">11</xref>] and low temperatures [<xref ref-type="bibr" rid="scirp.102955-ref12">12</xref>].</p><p>In dairy industry, Listeria can contaminate directly or indirectly the products and the environment through contaminated raw milk, resulting in huge losses both in terms of public health and economy [<xref ref-type="bibr" rid="scirp.102955-ref2">2</xref>]. The presence of Listeria in yogurt may be a result of very bad quality of raw milk, inadequate heat treatment of milk or re-contamination as a result of using contaminated additives and poor hygiene during processing and packaging [<xref ref-type="bibr" rid="scirp.102955-ref13">13</xref>]. The pasteurization of milk has been recognized to ensure effective consumer safety against L. monocytogenes [<xref ref-type="bibr" rid="scirp.102955-ref14">14</xref>]. A study in Morocco [<xref ref-type="bibr" rid="scirp.102955-ref2">2</xref>] shows that out of 288 samples of dairy products examined, 17 (5.90%) were found to be contaminated with L. monocytogenes. Boubendir et al. [<xref ref-type="bibr" rid="scirp.102955-ref15">15</xref>] reported 5.76% prevalence of L. monocytogenes in bovine raw milk produced in the North Eastern Algeria. Similar results found by Guerra et al. [<xref ref-type="bibr" rid="scirp.102955-ref16">16</xref>], where the incidence of contamination was 5% in milk and dairy products sold in mainland Portugal. Gaya et al. [<xref ref-type="bibr" rid="scirp.102955-ref17">17</xref>] reported also a low incidence of 3.6% of L. monocytogenes in raw milk produced in Spain. Whereas in China, the prevalence of L. monocytogenes in raw milk is very low (0.23% to 1.2%) [<xref ref-type="bibr" rid="scirp.102955-ref18">18</xref>]. Benkerroum et al. [<xref ref-type="bibr" rid="scirp.102955-ref19">19</xref>] reported that bacteriocins produced by the lactic acid bacteria reduce counts of L. monocytogenes in cheese and yoghurt. Furthermore, several authors have confirmed that the growth or survival of L. monocytogenes in a food product depends on a variety of physico-chemical parameters, including pH, a<sub>w</sub> and NaCl content [<xref ref-type="bibr" rid="scirp.102955-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref21">21</xref>].</p><p>Listeria monocytogenes is a psychrotrophic microorganism (able to grow and multiply during cold storage) and even a few cells present in the final product can multiply to a level that is dangerous to consumers [<xref ref-type="bibr" rid="scirp.102955-ref22">22</xref>]. On the basis of literature data [<xref ref-type="bibr" rid="scirp.102955-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref24">24</xref>], it can be concluded that L. monocytogenes has unfavourable conditions for growth in yogurt. However, these bacteria may survive in the final product for definite time depending on the type of product, its characteristics (e.g. pH, competitive microflora), storage conditions (temperature) and other environmental circumstances. Previous studies have specifically shown that L. monocytogenes does not grow at a pH below 5.3 when the a<sub>w</sub> is lower than 0.93 [<xref ref-type="bibr" rid="scirp.102955-ref25">25</xref>], or at a pH below 4.46 regardless of the a<sub>w</sub> [<xref ref-type="bibr" rid="scirp.102955-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref26">26</xref>]. In our study, the average physicochemical parameters associated with Lben and Jben are as such that they should limit (if not prevent) the growth of L. monocytogenes. The poor hygienic conditions during milking, transport, storage of milk and its use in the manufacture of Lben and Jben in traditional dairies, which do not respect the principles of food hygiene, can also be in favor of the contamination with L. monocytogenes [<xref ref-type="bibr" rid="scirp.102955-ref2">2</xref>]. When L. monocytogenes is present in a large number in raw milk some cells may survive the production process of yogurt and pose a serious hazard for consumers health [<xref ref-type="bibr" rid="scirp.102955-ref23">23</xref>]. Control of the feeding cattle, the general principles of food hygiene and milk pasteurization limit the contamination with L. monocytogenes [<xref ref-type="bibr" rid="scirp.102955-ref2">2</xref>]. Understanding the behavior of Listeria monocytogenes in fermented dairy products constitute sa crucial knowledge for Microbiological Risk Assessment (MRA) process, as well as Hazard Analysis and Critical Control Point (HACCP) system [<xref ref-type="bibr" rid="scirp.102955-ref23">23</xref>]. The experimental data regarding survival or inactivation of this foodborne pathogen during production and cold storage of yogurt at different temperatures can be described mathematically by predictive models [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref29">29</xref>].</p><p>Predictive microbiology is based on the premise that the response of microorganisms to environmental factors is reproducible [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>]. By defining the parameters that have the strongest effect on the behavior of microorganisms, it is possible to predict the response of microorganisms based on the performed observations [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref31">31</xref>]. L. monocytogenes is a Gram-positive, non-sporeforming foodborne pathogen, which is cold tolerant, widespread in the environment, and has the capability to grow under harsh conditions, including at elevated salt levels (up to 14%). Listeria has been known to persist in the food production environment for prolonged periods, despite regular sanitation [<xref ref-type="bibr" rid="scirp.102955-ref32">32</xref>]. The gram-positive bacterium Listeria monocytogenes is recognized as a food-borne pathogen with significance for humans [<xref ref-type="bibr" rid="scirp.102955-ref33">33</xref>], and major outbreaks of infection have been linked to the consumption of contaminated coleslaw [<xref ref-type="bibr" rid="scirp.102955-ref34">34</xref>], cheeses [<xref ref-type="bibr" rid="scirp.102955-ref35">35</xref>] and pasteurized milk [<xref ref-type="bibr" rid="scirp.102955-ref36">36</xref>]. The innate resistance of L. monocytogenes to many of the food preservation systems that are effective against other food-borne pathogens has prompted research aimed at developing combination systems for more effective control of this pathogen [<xref ref-type="bibr" rid="scirp.102955-ref37">37</xref>]. The purpose of the study was to determine the antibacterial activity of powder and extracts of berries (rose-hip, aronia, sea buckthorn and hawthorn) on L. monocytogenes.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>Materials: extracts and powder berries—sea buckthorn, rose-hip, aronia and hawthorn. The test products were dissolved: 1 g produced in 4 ml of physiological solution, After which dilutions were made. Concentration of test substances: 1 - 250 mg/ml; 2 - 125 mg/ml; 3 - 62.5 mg/ml; 4 - 31.25 mg/ml.</p><p>Initial concentration of preparations (liquids) of berries: sea buckthorn—0.12 mg/100ml; rose-hip—0.15 mg/100ml; aronia—0.18 mg/100ml; hawthorn—0.20 mg/100ml.</p><p>Product: Experimental samples (yogurt control and yogurt with addition (extracts and powder) of aronia were prepared in laboratory conditions in the Food Technology Department. Raw cow milk, obtained from local farm was received according to Governmental Decision No. 158, on 07.03.2019 with regard to the approval of the Technical Regulation “Milk and dairy products” that included technical conditions for the quality of raw cow milk collected for industrial processing [<xref ref-type="bibr" rid="scirp.102955-ref38">38</xref>]. The milk was pasteurized and standardized to a fat content of 2.5%. The milk was pasteurized (95˚C/30min), cooled to 45˚C and inoculated with 1.5% starter culture consisting of Lactobacillus delbrueckii ssp. bulgaricus and Streptococcus salivarius spp. Thermophiles (yogurt control) and yogurt with the addition (extracts and powder)—different concentrations of aronia. Notify the probe: Y—yogurt (control); YA 0.5—yogurt with 0.5% aronia powder; YA 0.75—yogurt with 0.75% aronia powder; YA 1.0—yogurt with 1.0% aronia powder.</p><p>Test strain: L. monocytogenes ATCC 19118; Listeria monocytogenes EGDe Mc Farland 0.5 (10<sup>5</sup>) of L. monocytogenes strain ATCC 19118. Triptone Soya Broth (Oxoid) 6%, TSA—Triptone Soya Agar (Oxoid).</p><p>Methods: Antimicrobial Testing of extracts and powder berries</p><p>Well diffusion method:</p><p>In this study we used the agar diffusion procedure, called well diffusion method, it is a qualitative method used to determine antibacterial activity of the tested substances (extracts and powder from berries) on tested strain. Previously, the tested strain of listeria was spread with the swab on the surface of the plate. Then, 8 mm diameter wells were made in the Mueller Hinton agar plate. The dissolved extracts were introduced into each well. If the bacterial strain is susceptible to the antimicrobial agent, then a transparent area is observed around the well. This area represents the inhibition zone of growth. If the bacteria is resistant to the antimicrobial agent around the well will be observed growth. The sensitivity or resistance of bacteria were calculated by measuring the inhibition zone diameter around the wells. The antimicrobial activity is calculated in millimeter: the total diameter of growth inhibited zone minus diameter of the well [<xref ref-type="bibr" rid="scirp.102955-ref39">39</xref>].</p><p>1 g of yogurt was added 1 - 2 drops of microbial suspension according to the Mc Farland 0.5 (10<sup>5</sup>) turbidity standard from L. monocytogenes strain ATCC 19118. The infected samples were incubated in thermostat at 37˚C for 24, 48 hours and respectively 15 days.</p><p>Identification of minimum inhibitory concentration (MIC) The methodology for this experiment is based on the work of Lambert and others [<xref ref-type="bibr" rid="scirp.102955-ref40">40</xref>]. Ten μL of inoculum were dispensed in each well. After inoculation, the plate was incubated at 25˚C for 24 h and the optical density (O.D.) of each well was recorded at 600 nm every 20 min after shaking [<xref ref-type="bibr" rid="scirp.102955-ref41">41</xref>].</p><p>Identification of minimum bactericidal concentration (MBC)</p><p>The methodology described below is an adaptation of the Minimum Bactericidal Concentration Testing from the Clinical Microbiology Procedures Handbook [<xref ref-type="bibr" rid="scirp.102955-ref42">42</xref>]. L. monocytogenes was cultured on tryptone soya (TS) agar plate at 37˚C for 18 h, and a cellular suspension was prepared in sterile distilled water.</p></sec><sec id="s3"><title>3. Results and Discussions</title><p>Listeria monocytogenes is considered one of the most important pathogens responsible for foodborne infection. It is often incriminated in outbreaks of human listeriosis [<xref ref-type="bibr" rid="scirp.102955-ref1">1</xref>]. A number of studies have demonstrated that L. monocytogenes is more acid tolerant than most food-borne pathogens, although the sensitivity of the organism to organic acids varies with the nature of the acidulant used [<xref ref-type="bibr" rid="scirp.102955-ref43">43</xref>], Listeria spp. prefers to grow at pH 7 -8 but they will grow in the range pH 5 - 10 and may survive and grow in material with a pH as low as 4.4 (<xref ref-type="table" rid="table1">Table 1</xref>). Results of another study demonstrate a high risk associated with consumption of bulked raw milk and fermented dairy products in due to occurrence of Listeria spp. [<xref ref-type="bibr" rid="scirp.102955-ref44">44</xref>].</p><p>In previous studies [<xref ref-type="bibr" rid="scirp.102955-ref46">46</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref47">47</xref>] it has been found that sea buckthorn, rose-hip, aronia and hawthorn have antimicrobial effects on pathogenic microorganisms. Following the tests, the authors established that the additives of rose and hawthorn in the sausage recipe can control the growth rate of microorganisms, including pathogens. By studying the Lag and Logarithmic growth phases of pathogenic microbial strains we determined that the hawthorn has a greater bacteriostatic effect on strains of S. aureus ATCC 25923 and E. coli ATCC 25922 and the rose-hip has a greater bacteriostatic effect on Salmonella strains Abony ATCC 6017, Klebsiella pneumoniae ATCC 13883. The most relevant antimicrobial effect was seen for berry powders on E. coli strains inoculated in tested cream cheese samples. The additions of rose-hip and aronia powders manifested major antimicrobial effect on Salmonella strains. The addition of hawthorn powder manifested major antimicrobial effect on Staphylococcus aureus [<xref ref-type="bibr" rid="scirp.102955-ref46">46</xref>].</p><p>The results of the minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) for L. monocitogenes strain are presented in <xref ref-type="table" rid="table2">Table 2</xref>, <xref ref-type="table" rid="table3">Table 3</xref>. The results of the study showed that aronia and hawthorn have no antimicrobial activity against L. monocytogenes. Significant positive results showed the extracts and powders of sea buckthorn and rose-hip.</p><p>It has been studied whether berries have bactericidal effect on L. monocytogenes in food (yogurt). Yogurt samples (I) were infected with L. monicytogenes, the initial concentration being 10<sup>5</sup> cells. After 24, 48 hours a decrease in bacteria was found in all samples, including in the control sample, without the addition of berries. After 15 days the samples were tested and it was found that L. monocytogenes was not present (<xref ref-type="table" rid="table4">Table 4</xref>). In the samples where additions of berries (extracts and powders) were introduced, the rate of reduction was much higher. The bactericidal effect of berries has been demonstrated.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Factors identified to have an impact on the growth and survival of L. monocytogenes<sup>a</sup>(adapted from SANCO [<xref ref-type="bibr" rid="scirp.102955-ref45">45</xref>] )</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Factor</th><th align="center" valign="middle" >Lower Growth Limit</th><th align="center" valign="middle" >Optimum<sup>b</sup></th><th align="center" valign="middle" >Upper Growth Limit</th><th align="center" valign="middle" >Can Survive<sup>c</sup> (No Growth)</th></tr></thead><tr><td align="center" valign="middle" >Temperature (˚C)</td><td align="center" valign="middle" >−1.5 to +3.0</td><td align="center" valign="middle" >30.0 to 37.0</td><td align="center" valign="middle" >45.0</td><td align="center" valign="middle" >−18.0</td></tr><tr><td align="center" valign="middle" >pH<sup>d</sup></td><td align="center" valign="middle" >4.2 to 4.3</td><td align="center" valign="middle" >7.0</td><td align="center" valign="middle" >9.4 to 9.5</td><td align="center" valign="middle" >3.3 to 4.2</td></tr><tr><td align="center" valign="middle" >Water Activity (a<sub>w</sub>)</td><td align="center" valign="middle" >0.90 to 0.93</td><td align="center" valign="middle" >0.99</td><td align="center" valign="middle" >&gt;0.99</td><td align="center" valign="middle" >&lt;0.90</td></tr><tr><td align="center" valign="middle" >Salt Concentration <sup>e</sup>(%)</td><td align="center" valign="middle" >&lt;0.5</td><td align="center" valign="middle" >0.7</td><td align="center" valign="middle" >12 - 16</td><td align="center" valign="middle" >≥20</td></tr><tr><td align="center" valign="middle" >Atmosphere</td><td align="center" valign="middle"  colspan="4"  >Facultative anaerobe (it can grow in the presence or absence of oxygen, e.g. in a vacuum or modified atmosphere package)</td></tr><tr><td align="center" valign="middle" >Heat Treatment during Food Processing</td><td align="center" valign="middle"  colspan="4"  >A temperature/time combination e.g. of 70˚C and 2 min is required for a D6 (i.e. 106 or 6 decimal) reduction in numbers of L. monocytogenes cells. Other temperature/time combinations may also provide the same reduction</td></tr></tbody></table></table-wrap><p><sup>a</sup>Based on experimental data and hence provide only a rough estimate; <sup>b</sup>Optimum indicates when the growth of L. monocytogenes is fastest; <sup>c</sup>Survival period will vary depending on nature of food and other factors; <sup>d</sup>Inhibition of L. monocytogenes is dependent on type of acid present; <sup>e</sup>Based on percent sodium chloride, water phase.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> MIC and MBC L. monocytogenes ATCC 19118</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Nr.</th><th align="center" valign="middle"  rowspan="2"  >Berries</th><th align="center" valign="middle"  colspan="4"  >Diameter of the complete growth inhibition zone (mm)</th></tr></thead><tr><td align="center" valign="middle" >250 mg/ml</td><td align="center" valign="middle" >125 mg/ml</td><td align="center" valign="middle" >62.5 mg/ml</td><td align="center" valign="middle" >31.25 mg/ml</td></tr><tr><td align="center" valign="middle" >1.</td><td align="center" valign="middle" >Sea buckthorn (extract)</td><td align="center" valign="middle" >22.5 &#177; 0.25</td><td align="center" valign="middle" >19.25 &#177; 0.22</td><td align="center" valign="middle" >14.25 &#177; 0.22</td><td align="center" valign="middle" >10.75 &#177; 0.22</td></tr><tr><td align="center" valign="middle" >2.</td><td align="center" valign="middle" >Sea buckthorn (powder)</td><td align="center" valign="middle" >16.33 &#177; 0.26</td><td align="center" valign="middle" >12.5 &#177; 0.25</td><td align="center" valign="middle" >10.75 &#177; 0.22</td><td align="center" valign="middle" >0.0 &#177; 0.0</td></tr><tr><td align="center" valign="middle" >5.</td><td align="center" valign="middle" >Rose-hip (extract)</td><td align="center" valign="middle" >16.33 &#177; 0.26</td><td align="center" valign="middle" >12.25 &#177; 0.22</td><td align="center" valign="middle" >10.25 &#177; 0.22</td><td align="center" valign="middle" >0.0 &#177; 0.0</td></tr><tr><td align="center" valign="middle" >6.</td><td align="center" valign="middle" >Rose-hip (powder)</td><td align="center" valign="middle" >17.75 &#177; 0.42</td><td align="center" valign="middle" >15.75 &#177; 0.22</td><td align="center" valign="middle" >11.75 &#177; 0.22</td><td align="center" valign="middle" >0.0 &#177; 0.0</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The diameter of the complete growth inhibition zone of different species of L. monocytogenes under the action of the extract and powder of sea buckthorn rose-hip</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="3"  >Nr.</th><th align="center" valign="middle"  rowspan="3"  >Berries</th><th align="center" valign="middle" >L. monocytogenes ATCC 19118</th><th align="center" valign="middle"  rowspan="3"  >Berries</th><th align="center" valign="middle" >L. monocytogenes EGDe</th></tr></thead><tr><td align="center" valign="middle" >Diameter of the complete growth inhibition zone (mm)</td><td align="center" valign="middle" >Diameter of the complete growth inhibition zone (mm)</td></tr><tr><td align="center" valign="middle" >250 mg/ml</td><td align="center" valign="middle" >250 mg/ml</td></tr><tr><td align="center" valign="middle" >1.</td><td align="center" valign="middle" >Sea buckthorn (extract)</td><td align="center" valign="middle" >22.25 … 22.75</td><td align="center" valign="middle" >Sea buckthorn C<sub>1</sub>, C<sub>2</sub> (concentrated hydroalcoholic extract)</td><td align="center" valign="middle" >30 … 32</td></tr><tr><td align="center" valign="middle" >2.</td><td align="center" valign="middle" >Sea buckthorn (powder)</td><td align="center" valign="middle" >16.07 … 16.59</td><td align="center" valign="middle" >Sea buckthorn H<sub>1</sub>, H<sub>2</sub> (hydroalcoholic extract)</td><td align="center" valign="middle" >29 … 30</td></tr><tr><td align="center" valign="middle" >5.</td><td align="center" valign="middle" >Rose-hip (extract)</td><td align="center" valign="middle" >16.07 … 16.59</td><td align="center" valign="middle" >Rose-hip C<sub>1</sub>, C<sub>2</sub> (concentrated hydroalcoholic extract)</td><td align="center" valign="middle" >20 … 21.5</td></tr><tr><td align="center" valign="middle" >6.</td><td align="center" valign="middle" >Rose-hip (powder)</td><td align="center" valign="middle" >17.33 … 18. 17</td><td align="center" valign="middle" >Rose-hip H<sub>1</sub>, H<sub>2</sub> (hydroalcoholic extract)</td><td align="center" valign="middle" >22 … 22</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> The influence of different concentrations of aronia on the bactericidal effect (L. monocitogenes) in yogurt</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >The product tested</th><th align="center" valign="middle"  colspan="4"  >L. monocytogenes, ln N</th></tr></thead><tr><td align="center" valign="middle" >initially infected with bacteria</td><td align="center" valign="middle" >1 day</td><td align="center" valign="middle" >2 days</td><td align="center" valign="middle" >15 days</td></tr><tr><td align="center" valign="middle" >Y</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >6.40</td><td align="center" valign="middle" >6.55</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 0.5</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >4.80</td><td align="center" valign="middle" >5.58</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 0.75</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >3.61</td><td align="center" valign="middle" >4.16</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 1.0</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >5.58</td><td align="center" valign="middle" >5.24</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 0.5</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >4.88</td><td align="center" valign="middle" >3.61</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 0.75</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >5.46</td><td align="center" valign="middle" >4.30</td><td align="center" valign="middle" >−9.21</td></tr><tr><td align="center" valign="middle" >YA 1.0</td><td align="center" valign="middle" >11.51</td><td align="center" valign="middle" >5.02</td><td align="center" valign="middle" >2.20</td><td align="center" valign="middle" >−9.21</td></tr></tbody></table></table-wrap><disp-formula id="scirp.102955-formula1"><graphic  xlink:href="//html.scirp.org/file/1-2702891x2.png"  xlink:type="simple"/></disp-formula><p>Results have been obtained that have been reported in other research studies. The main mechanism of bactericidal effect of yogurt on foodborne pathogens seems to be the decline in pH due to lactose fermentation by Lactobacillus delbrueckii ssp. bulgaricus and Streptococcus salivarius ssp. thermophilus added to milk as a starter culture, as well as the production of organic acids, mainly lactic acid [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref48">48</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref49">49</xref>]. The researchers found that lag phase and growth rate of Listeria were affected not only by storage temperature but also by lactic acid concentration and pH of product ranged from 5.2 do 5.8. J. Kowalik et al. [<xref ref-type="bibr" rid="scirp.102955-ref50">50</xref>] observed more dynamic growth of L. monocytogenes in milk samples, having a pH of 6.6, and stored under conditions identical to those applied for the samples of the cottage cheese. Some authors have suggested that antimicrobial activity of yogurt is not exclusively due to accumulation of lactic acid and may be also the effect of lactic acid and other compounds such as hydrogen peroxide, carbon dioxide, acetaldehyde, polysaccharide and bacteriocins [<xref ref-type="bibr" rid="scirp.102955-ref51">51</xref>]. The pH value of 4.6 is usually considered as a minimum pH permitting the growth of L. monocytogenes in food [<xref ref-type="bibr" rid="scirp.102955-ref52">52</xref>]. However, pH minimum as low as 4.39 has also been reported [<xref ref-type="bibr" rid="scirp.102955-ref53">53</xref>]. Low pH of the environment is an important factor responsible for the reduction of Listeria population in yogurt, the correlation between the number of L. monocytogenes and pH amounted to 0.832 [<xref ref-type="bibr" rid="scirp.102955-ref4">4</xref>]. Listeria is one of the few foodborne pathogens that can multiply at low water activity. Studies have shown that this organism can multiply at a<sub>w</sub> below 0.93 [<xref ref-type="bibr" rid="scirp.102955-ref54">54</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref55">55</xref>].</p><p>In the food industry, salting is a food preservation method designed primarily to obtain lower water activity. However, L. monocytogenes is able to survive high concentration of salt and is thus not an easy pathogen to control by osmotic stress alone. Osmo-adaptation in bacteria can involve both physiological changes and as well as regulation at the gene expression level [<xref ref-type="bibr" rid="scirp.102955-ref56">56</xref>].</p><p>The low counts observed in Bongo may be attributed to the low pH and other antimicrobial compounds such as bacteriocins produced by lactic acid bacteria. Also, the type of acid and the storage temperature have a marked effect on the ability of Listeria to survive and grow at low pH. On the other hand, the presence of Listeria spp. in Bongo may be attributed to contamination from raw milk, the starter culture inoculum and slow rate of acid formation and pH decline [<xref ref-type="bibr" rid="scirp.102955-ref44">44</xref>].</p><p>A number of studies have demonstrated the inhibitory activity of organic acids against L. monocytogenes and have shown that the effects are mainly related to the amount of undissociated acid [<xref ref-type="bibr" rid="scirp.102955-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref59">59</xref>]. Benzoate and formate (used alone) they were highly effective at killing L. monocytogenes at pH 3. Nevertheless, in all cases addition of ethanol resulted in shorter killing times. The most effective bactericidal combination, 5% ethanol and 50 mM formate, resulted in 5 log units of killing in just 4 min [<xref ref-type="bibr" rid="scirp.102955-ref43">43</xref>]. A number of studies have demonstrated the inhibitory activity of organic acids against L. monocytogenes and have shown that the effects are mainly related to the amount of undissociated acid [<xref ref-type="bibr" rid="scirp.102955-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref59">59</xref>]. The most common way to assess microbial growth in solution is the measurement of the optical density at 600 nm, or short OD<sub>600</sub>. The method is based on absorbance detection mode and basically determines which portion of light passes through a sample, more specifically through a suspension of microorganisms [<xref ref-type="bibr" rid="scirp.102955-ref60">60</xref>]. The calibration lines obtained by plotting log OD<sub>600nm</sub> values vs. log plate counts showed high determination coefficients for all the tested strains in the range of OD<sub>600nm</sub> values 0.1 - 1.5 corresponding to approximately 10<sup>6</sup> - 10<sup>9</sup> CFU/ml [<xref ref-type="bibr" rid="scirp.102955-ref61">61</xref>].</p><p>A case study was performed to determine the minimum inhibitory concentration (MIC) and the minimum bactericidal concentrations (MBC) of the extracts and powders of the dogwood and mulberry on L. monotogenes. The results of the study are presented in <xref ref-type="table" rid="table5">Table 5</xref>.</p><p>The results of the study showed that hydroalcoholic extracts of sea buckthorn and rosehip showed beneficial results on the inhibitory and bactericidal effect of L. monocytogenes. The sea buckthorn has shown antimicrobial properties for L.monocytogenes more pronounced than rose-hip. Probably these properties are due to the chemical composition of sea buckthorn and rosehip. These berries are rich in organic acids. Determining the chemical composition of the rosehip, used in the case study, we found that the fruit contains: malic acid—154.3; citric</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC) for L. monocytogenes EGDe</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >The tested material</th><th align="center" valign="middle"  colspan="2"  >Sea buckthorn</th><th align="center" valign="middle"  colspan="2"  >Rose-hip</th></tr></thead><tr><td align="center" valign="middle" >OD, Λ<sub>600</sub></td><td align="center" valign="middle" >Minimum Inhibitory Concentration (MIC), mg/ml</td><td align="center" valign="middle" >OD, Λ<sub>600</sub></td><td align="center" valign="middle" >Minimum Inhibitory Concentration (MIC), mg/ml</td></tr><tr><td align="center" valign="middle" >C<sub>1</sub></td><td align="center" valign="middle" >0.071</td><td align="center" valign="middle" >2.6</td><td align="center" valign="middle" >0.059</td><td align="center" valign="middle" >4.2</td></tr><tr><td align="center" valign="middle" >C<sub>2</sub></td><td align="center" valign="middle" >0.047</td><td align="center" valign="middle" >5.2</td><td align="center" valign="middle" >0.053</td><td align="center" valign="middle" >16.7</td></tr><tr><td align="center" valign="middle" >H<sub>1</sub></td><td align="center" valign="middle" >0.061</td><td align="center" valign="middle" >2.6</td><td align="center" valign="middle" >0.020</td><td align="center" valign="middle" >4.2</td></tr><tr><td align="center" valign="middle" >H<sub>2</sub></td><td align="center" valign="middle" >0.072</td><td align="center" valign="middle" >2.6</td><td align="center" valign="middle" >0.024</td><td align="center" valign="middle" >4.2</td></tr></tbody></table></table-wrap><p>C<sub>1</sub>, C<sub>2</sub>—concentrated hydroalcoholic extract; H<sub>1</sub>, H<sub>2</sub>—hydroalcoholic extract; DO—optical density.</p><p>acid—1684; succinic acid—56.89; lactic acid—30.54; acetic acid—23.85, including L-ascorbic acid—72 mg/100 g s.u. Data recorded over the world, over time, show that dried rose hips contain ascorbic acid between 0.1%, 0.5% and 1.0%, and some varieties even up to 9% [<xref ref-type="bibr" rid="scirp.102955-ref62">62</xref>].</p><p>In the study conducted by Ţifrea Anca it was found that the addition of sea buckthorn pulp positively influences the increase of lactic acid content in yogurt [<xref ref-type="bibr" rid="scirp.102955-ref63">63</xref>]. The increase in lactic acid content may be due in part to the addition of sea buckthorn pulp due to the content of organic acids in it. Compared with the control sample which initially had 4.6 and finally 4.2 it can be seen that the addition of sea buckthorn influenced the pH by a greater decrease in the samples with higher addition of sea buckthorn in a similar way to acidity.</p><p>Another factor that would control the microbiological risk in food is water activity. Most bacterial species, including L. monocytogenes grow optimally at a water activity (a<sub>w</sub>) of 0.97 [<xref ref-type="bibr" rid="scirp.102955-ref45">45</xref>] [<xref ref-type="bibr" rid="scirp.102955-ref64">64</xref>]. Listeria monocytogenes is one of the few food-borne pathogens that can grow at an a<sub>w</sub> value below 0.93 [<xref ref-type="bibr" rid="scirp.102955-ref65">65</xref>]. However, L. monocytogenes also has the ability to grow to a level of a<sub>w</sub> 0.90 [<xref ref-type="bibr" rid="scirp.102955-ref66">66</xref>]. In our case study it was found that in yogurt with the addition of powder rose hip the value a<sub>w</sub> was in the range of 0.876 … 0.877. The reduction in aw was also found in the samples of yogurt with the addition of sea buckthorn powder, compared to the control samples. This can probably be explained by the fact that bactericide was more prominent in yogurt with the addition of berries compared to classic yogurt. The cumulative effect of the quantitative and qualitative content of acids in the composition of sea buckthorn and rosehip extracts and powders and the property of reducing the pH and activity of water, make berries have bacteriostatic and bactericidal properties on Listeria monocytogenes.</p></sec><sec id="s4"><title>4. Conclusions</title><p>Based on the study, sea buckthorn and rose-hip (extract and powder) were found to be excellent remedies for controlling the risk of L. monocytogenes infestation of food. This is due to the cumulative effect of the chemical composition of these berries (antioxidant content, organic acids, etc.), increased acidity, reduced pH and water activity of the food environment in which they were introduced below the development values of L. monocytogenes.</p><p>The minimum dose of inhibition and the minimum bactericidal dose of berries were determined. The use of added berry powders in the recipe for the production of dairy products can have two meanings: improving the nutritional value of the food and increasing the product shelf-life by keeping the microbiological risk under control, including L. monocytogenes.</p></sec><sec id="s5"><title>Acknowledgements</title><p>The research was funded by State Project 20.80009.5107.09 “Improving of food quality and safety through biotechnology and food engineering”, running at Technical University of Moldova.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Sandulachi, E., Cojocari, D., Balan, G., Popescu, L., Ghendov- Moșanu, A. and Sturza, R. (2020) Antimicrobial Effects of Berries on Listeria monocytogenes. Food and Nutrition Sciences, 11, 873-886. https://doi.org/10.4236/fns.2020.119061</p></sec></body><back><ref-list><title>References</title><ref id="scirp.102955-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ryser, E.T. and Marth, E. (2007) Listeria, Listeriosis and Food Safety. 3rd Edition, Taylor and Francis,Raton. https://doi.org/10.1201/9781420015188</mixed-citation></ref><ref id="scirp.102955-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">El Marnissi, B., Bennani, L., Cohen, N., et al. (2013) Presence of Listeria monocytogenes in Raw Milk and Traditional Dairy Products Marketed in the North-Central Region of Morocco. African Journal of Food Science, 7, 87-91. https://doi.org/10.5897/AJFS2013.0992</mixed-citation></ref><ref id="scirp.102955-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Santos, T., et al. 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