<?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">AiM</journal-id><journal-title-group><journal-title>Advances in Microbiology</journal-title></journal-title-group><issn pub-type="epub">2165-3402</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/aim.2017.711058</article-id><article-id pub-id-type="publisher-id">AiM-80419</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>
 
 
  Assessment of the Effect of Environmental Factors on the Antagonism of &lt;i&gt;Bacillus amyloliquefaciens&lt;/i&gt; and &lt;i&gt;Trichoderma harzianum&lt;/i&gt; to &lt;i&gt;Colletotrichum acutatum&lt;/i&gt;
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rababe</surname><given-names>Es-Soufi</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>Brahim</surname><given-names>El Bouzdoudi</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>Mounia</surname><given-names>Bouras</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>Mohammed</surname><given-names>L’Bachir El Kbiach</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>Alain</surname><given-names>Badoc</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>Ahmed</surname><given-names>Lamarti</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Laboratory of Plant Biotechnology, Biology Department, Faculty of Sciences, Abdelmalek Essaadi University, Tetouan, Morocco</addr-line></aff><aff id="aff2"><addr-line>Axe MIB (Molécules d’Intérêt Biologique), Unité de Recherche CEnologie EA 4577, USC 1366 INRA, UFR des Sciences Pharmaceutiques, Université de Bordeaux, ISVV (Institut des Sciences de la Vigne et du Vin), Villenave-d’Ornon, France</addr-line></aff><pub-date pub-type="epub"><day>10</day><month>11</month><year>2017</year></pub-date><volume>07</volume><issue>11</issue><fpage>729</fpage><lpage>742</lpage><history><date date-type="received"><day>13,</day>	<month>October</month>	<year>2017</year></date><date date-type="rev-recd"><day>17,</day>	<month>November</month>	<year>2017</year>	</date><date date-type="accepted"><day>20,</day>	<month>November</month>	<year>2017</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 effect of temperature (18&#176;C - 30&#176;C), water activity (0.85 - 1) and pH (4 - 9) was studied by dual culture technique on the antagonism of 
   Bacillus amyloliquefaciens and 
   Trichoderma harzianum to 
   Colletotrichum acutatum, responsible of strawberry (
   Fragaria x ananassa (Weston) Duchesne ex Rozier) anthracnose. The antagonistic bacteria’s strains behave significantly and differently according to the parameters studied. These results reveal useful information about the applicability of their biocontrol in agricultural culture with the change of environmental factors. 
  
 
</p></abstract><kwd-group><kwd>Antagonism</kwd><kwd> Anthracnose</kwd><kwd> Biocontrol</kwd><kwd> Environmental Factors</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Strawberry (Fragaria x ananassa (Weston) Duchesne ex Rozier) is an important fruit crop, grown in Morocco in the areas of Souss, Gharb and Loukkos. A major constraint to the culture of strawberry is the low tolerance of this species to fungal diseases [<xref ref-type="bibr" rid="scirp.80419-ref1">1</xref>] . The number of phytopathogenic fungi attacking this culture is vast, more than 50 genera [<xref ref-type="bibr" rid="scirp.80419-ref2">2</xref>] , resulting in severe economic losses. Fungal diseases can affect all parts of strawberry, but there are those who produce the crown rot, resulting in death of the plant, as anthracnose caused by Colletotrichum spp. [<xref ref-type="bibr" rid="scirp.80419-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref5">5</xref>] , especially C. acutatum, considered among the more devastating phytopathogens. The control of fungal diseases attacking strawberry plants is mainly done by treatment of the soil and the plants using chemical pesticides. The intensive use of fungicides leads to the accumulation of toxic compounds potentially dangerous for humans and the environment, as well as in the induction of the resistance of phytopathogenic agents [<xref ref-type="bibr" rid="scirp.80419-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref8">8</xref>] . Biological control has received great attention as one of the non-hazardous pest management techniques against diseases caused by phytopathogenic fungi, including anthracnose [<xref ref-type="bibr" rid="scirp.80419-ref9">9</xref>] . The selection of the antagonists planned for the biological control of plant diseases usually involves examining a large number of microbial isolates to increase the probability of discovering a strain highly effective. The natural antagonists on the surfaces of the host are promising components of protection of organic crops [<xref ref-type="bibr" rid="scirp.80419-ref10">10</xref>] . Antagonistic bacteria such as Bacillus subtilis [<xref ref-type="bibr" rid="scirp.80419-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref11">11</xref>] , B. amyloliquefaciens [<xref ref-type="bibr" rid="scirp.80419-ref9">9</xref>] and Pseudomonas fluorescens [<xref ref-type="bibr" rid="scirp.80419-ref12">12</xref>] or fungi such as Trichoderma harzianum [<xref ref-type="bibr" rid="scirp.80419-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref14">14</xref>] or yeast such as Saccharomyces cerevisiae [<xref ref-type="bibr" rid="scirp.80419-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref15">15</xref>] have been found effective for the control of the anthracnose disease under controlled research conditions.</p><p>Some environmental factors can strongly influence the biological effectiveness of the antagonist against plant pathogens. Climate change and water conditions are among the crucial factors influencing microbial activity in natural systems [<xref ref-type="bibr" rid="scirp.80419-ref16">16</xref>] . Therefore it is reasonable to study the influence of temperature, pH and water activity on the in vitro antagonism of Bacillus amyloliquefaciens and Trichoderma harzianum. However, there is a lack of comparative information on the effects of these factors on potential biocontrol of B. amyloliquefaciens and T. harzianum against plant diseases.</p><p>The objective of this study is to evaluate the effect of temperature, pH and water activity on the antagonism of Bacillus amyloliquefaciens and Trichoderma harzianum to Colletotrichum acutatum.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Fungal Pathogen Strain</title><p>Strain Ca6 of Colletotrichum acutatum was isolated from naturally infected strawberry fruits presenting anthracnose symptoms. It was selected for its aggressiveness among several isolates found in different strawberry cultivars. C. acutatum Ca6 originated from fields of strawberry plants of Loukkos (Larache, Morocco), developed well in Potato Dextrose Agar and was incubated ten days in 25˚C &#177; 2˚C before use. The identification was carried out by macroscopic and microscopic observations of the isolates using determination keys [<xref ref-type="bibr" rid="scirp.80419-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref18">18</xref>] .</p></sec><sec id="s2_2"><title>2.2. Isolation of Antagonistic Bacterial Strains</title><p>Nine bacterial strains were isolated by the method of serial dilutions from rhizosphere soil and roots of strawberry plants taken from various agricultural zones of the Loukkos region (Larache, Morocco), and identified by Hamdache et al.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Identification of antagonistic strains of Bacillus amyloliquefaciens [<xref ref-type="bibr" rid="scirp.80419-ref19">19</xref>] </title></caption><table><tbody><thead><tr><th align="center" valign="middle" >First name of strain</th><th align="center" valign="middle" >Code of strain after identification</th><th align="center" valign="middle" >Percentage of similarity</th><th align="center" valign="middle" >Strain reference</th></tr></thead><tr><td align="center" valign="middle" >I1</td><td align="center" valign="middle" >B. amyloliquefaciens Bc1</td><td align="center" valign="middle" >99.8% (1014/1016 pb)</td><td align="center" valign="middle" >LMG 22478</td></tr><tr><td align="center" valign="middle" >I2</td><td align="center" valign="middle" >B. amyloliquefaciens Bc2</td><td align="center" valign="middle" >99.8% (1033/1035 pb)</td><td align="center" valign="middle" >CR-502</td></tr><tr><td align="center" valign="middle" >I3</td><td align="center" valign="middle" >B. amyloliquefaciens Bc3</td><td align="center" valign="middle" >100% (1030/1030 pb)</td><td align="center" valign="middle" >CR-502</td></tr><tr><td align="center" valign="middle" >I18</td><td align="center" valign="middle" >B. amyloliquefaciens Bc4</td><td align="center" valign="middle" >100% (1035/1035 pb)</td><td align="center" valign="middle" >CR-502</td></tr><tr><td align="center" valign="middle" >B3</td><td align="center" valign="middle" >B.amyloliquefaciens Bc5</td><td align="center" valign="middle" >99.9% (1020/1022 pb)</td><td align="center" valign="middle" >LMG 22478</td></tr><tr><td align="center" valign="middle" >B12</td><td align="center" valign="middle" >B. amyloliquefaciens Bc6</td><td align="center" valign="middle" >99.9% (1021/1022 pb)</td><td align="center" valign="middle" >LMG 22478</td></tr><tr><td align="center" valign="middle" >B24</td><td align="center" valign="middle" >B. amyloliquefaciens Bc7</td><td align="center" valign="middle" >99.9% (1019/1020 pb)</td><td align="center" valign="middle" >LMG 22478</td></tr><tr><td align="center" valign="middle" >RA9</td><td align="center" valign="middle" >B. amyloliquefaciens Bc8</td><td align="center" valign="middle" >99.9% (778/779 pb)</td><td align="center" valign="middle" >LMG 22478</td></tr><tr><td align="center" valign="middle" >RA12</td><td align="center" valign="middle" >B. amyloliquefaciens Bc9</td><td align="center" valign="middle" >99.9% (1035/1036 pb)</td><td align="center" valign="middle" >CR-502</td></tr></tbody></table></table-wrap><p>[<xref ref-type="bibr" rid="scirp.80419-ref19">19</xref>] . A molecular identification revealed that the nine antagonistic bacterial isolates belong to the species Bacillus amyloliquefaciens. Strains at the beginning were noted by an arbitrary notation I1, I2, I3, I18, B3, B12, RA9 and RA12 (<xref ref-type="table" rid="table1">Table 1</xref>).</p></sec><sec id="s2_3"><title>2.3. Fungal Antagonist Strain</title><p>Trichoderma harzianum (TR) strain was isolated from soil into PDA (Potato Dextrose Agar) plates using spread plate technique. Litter materials were cultured in PDA plates for the isolation. The TR strain was isolated into pure culture on PDA. The identification was carried out by macroscopic and microscopic observations [<xref ref-type="bibr" rid="scirp.80419-ref20">20</xref>] .</p></sec><sec id="s2_4"><title>2.4. Effect of Environmental Factors</title><p>The potential of biological control of the nine strains of Bacillus amyloliquefaciens and the strain of Trichoderma harzianum was assessed. The inhibition of Colletotrichum acutatum Ca6 according to the variation of some factors (temperature, pH, activity of the water) was evaluated by calculating the percentage of inhibition of mycelial growth on Petri dishes by dual culture technique on PDA. The antagonist and the phytopathogen were put on the opposite sides of Petri dish at the same distance from the periphery. A completely randomized experimental device was used with three replicates for each antagonist.</p><sec id="s2_4_1"><title>2.4.1. Effect of Temperature</title><p>The inoculated dishes were incubated in the dark at 18˚C; 23˚C; 25˚C; 27˚C and 30˚C for 7 days.</p></sec><sec id="s2_4_2"><title>2.4.2. Effect of Water Activity</title><p>The water activity (aw) represents the availability in open water for the biochemical reactions for the development of microorganisms. Different values of activity of the water have been tested (1; 0.95; 0.90 and 0.85) by the addition of glycerol in PDA [<xref ref-type="bibr" rid="scirp.80419-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref21">21</xref>] , which will attach a part of the water and make it unusable to microorganisms. The same technique of dual culture has been fol-</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> pH values and buffers used [<xref ref-type="bibr" rid="scirp.80419-ref19">19</xref>] </title></caption><table><tbody><thead><tr><th align="center" valign="middle" >pH</th><th align="center" valign="middle" >4</th><th align="center" valign="middle" >4.5</th><th align="center" valign="middle" >5</th><th align="center" valign="middle" >5.5</th><th align="center" valign="middle" >6</th><th align="center" valign="middle" >6.5</th><th align="center" valign="middle" >7</th><th align="center" valign="middle" >7.5</th><th align="center" valign="middle" >8</th><th align="center" valign="middle" >9</th></tr></thead><tr><td align="center" valign="middle" >Buffer</td><td align="center" valign="middle"  colspan="2"  >Trizma</td><td align="center" valign="middle"  colspan="2"  >MES</td><td align="center" valign="middle"  colspan="2"  >Pipes</td><td align="center" valign="middle"  colspan="2"  >Mops</td><td align="center" valign="middle"  colspan="2"  >Bicine</td></tr></tbody></table></table-wrap><p>lowed. After seven days of incubation in the dark at 25˚C, the PIGR (Percentage of Radial Growth Inhibition) has been calculated.</p></sec><sec id="s2_4_3"><title>2.4.3. Effect of pH</title><p>To assess the effect of pH on the inhibition of mycelial growth by antagonistic bacteria, the following pH, acid, neutral, and basic, have been tested: 4; 4.5; 5; 5.5; 6; 6.5; 7; 7.5; 8 and 9 (<xref ref-type="table" rid="table2">Table 2</xref>). The medium PDA has been stamped, according to the desired pH, by different buffers. Using a pH meter, the pH has been adjusted by addition of HCl to the pH acids and NaOH to the basic pH. The boxes were incubated at 25˚C. The PICR is calculated after seven days of incubation.</p></sec><sec id="s2_4_4"><title>2.4.4. Percentage of Inhibition of Radial Growth</title><p>After the incubation period, the radial growth of the pathogens was measured and the percent inhibition (1) of mean radial growth was calculated relative to the control as follows:</p><p>P I G R = ( T − C ) / T &#215; 100 (1)</p><p>PIRG: Percent Inhibition of Radial Growth of pathogen’s mycelium;</p><p>T: Radial growth of control agent;</p><p>C: Radial growth of the pathogen in the presence of the antagonist.</p></sec><sec id="s2_4_5"><title>2.4.5. Statistical Analysis</title><p>All analyses were conducted in triplicates. The percent of inhibition of mycelial growth of the phytopathogenic agent by the antagonists have been subjected to an analysis of variance (ANOVA) using the software STATISTICA for Windows v.6. The statistical significance of the results was determined by performing a test of Duncan’s multiple range (p &lt; 0.05). Results were expressed as mean &#177; standard deviation.</p></sec></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Dual Culture Technique</title><p>Bacillus amyloliquefaciens strains and Trichoderma harzianum provide inhibitory effects on the mycelial growth of the phytopathogenic strain (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The inhibition of development of Colletotrichum acutatum isolate varies within B. amyloliquefaciens strains.</p></sec><sec id="s3_2"><title>3.2. Effect of Temperature</title><p>The percent inhibition of mycelial growth by Bacillus amyloliquefaciens differs according the isolates and the temperatures studied. Isolate Bc2 is the most effective and presents the highest percent inhibition (<xref ref-type="fig" rid="fig2">Figure 2</xref>), whereas Bc5 has the lowest percent inhibition at all tested temperatures. Trichoderma harzianum</p><p>presents a very high efficiency on the inhibition of radial growth of Colletotrichum acutatum with an inhibitory effect exceeding 70% at all tested temperatures (<xref ref-type="fig" rid="fig3">Figure 3</xref>).</p></sec><sec id="s3_3"><title>3.3. Effect of Water Activity</title><p>The inhibition of mycelial growth of Colletotrichum acutatum is important in the presence of the isolate Bc2 and low in the presence of Bc5 (<xref ref-type="fig" rid="fig4">Figure 4</xref>). Trichoderma harzianum has a high potential of radial growth inhibition of the phytopathogenic agent that increases with the water activity (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p></sec><sec id="s3_4"><title>3.4. Effect pH</title><p>The pH presents a large effect on the antagonistic potential of Trichoderma harzianum (<xref ref-type="fig" rid="fig6">Figure 6</xref>) and Bacillus amyloliquefaciens (<xref ref-type="fig" rid="fig7">Figure 7</xref>). Among the bacterial isolates, Bc2 shows a large inhibitory effect on the growth of Colletotrichum acutatum; contrariwise, Bc5 has the lowest inhibitory effect (<xref ref-type="fig" rid="fig7">Figure 7</xref>).</p><p>The percent of growth inhibition of the phytopathogen by the fungal antagonist increase by the pH values up to neutral pH 7, and then start to decrease in alkaline pH (<xref ref-type="fig" rid="fig6">Figure 6</xref> and <xref ref-type="fig" rid="fig7">Figure 7</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Biological control is an alternative to the use of phytochemicals in involving biological products in the control of plant diseases. In this study, we found that Bacillus amyloliquefaciens and Trichoderma harzianum provide inhibitory effects on the development of Colletotrichum acutatum, the phytopathogenic agent of the anthracnose of strawberry (Fragaria x ananassa). Biological control of Colletotrichum species has been demonstrated in other studies using Trichoderma species [<xref ref-type="bibr" rid="scirp.80419-ref13">13</xref>] and Bacillus species [<xref ref-type="bibr" rid="scirp.80419-ref9">9</xref>] . This study shows that T. harzianum grows faster than C. acutatum Ca6 strain. This rapid growth suggests a mycoparasitism, at least in the experimental conditions tested, and gives Trichoderma an important advantage in the competition for nutrients and space with phytopathogenic fungi [<xref ref-type="bibr" rid="scirp.80419-ref22">22</xref>] . Biological control is important in crop production disease control [<xref ref-type="bibr" rid="scirp.80419-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref24">24</xref>] . Bacillus subtilis and B. amyloliquefaciens have been used in commercial biological control products due to their potential of biocontrol and high stability in harsh environmental conditions caused by spore forms [<xref ref-type="bibr" rid="scirp.80419-ref25">25</xref>] .</p><p>The environmental factors play an important role, since they affect the biological life of the microbial species and the physiology/metabolism of pathogen antagonist and host plant [<xref ref-type="bibr" rid="scirp.80419-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref27">27</xref>] . Several species antagonists of Bacillus spp. have shown efficiency in the fight against the anthracnose of multiple hosts [<xref ref-type="bibr" rid="scirp.80419-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref31">31</xref>] .</p><p>The inhibition of mycelial growth of Colletotrichum acutatum by the Bacillus amyloliquefaciens strains tested and by changing the temperature, water activity and pH, shows that the potential of biological control varies from an isolate to the other. Bacillus amyloliquefaciens isolates have a different effect on mycelial growth of the phytopathogen. Bc2 shows a great effect compared to other isolates, Bc5 has a weak influence on radial growth. Trichoderma harzianum has a large antagonistic effect on the mycelial growth of the phytopathogenic agent. Hamdache et al. [<xref ref-type="bibr" rid="scirp.80419-ref19">19</xref>] have worked on the same bacterial strains to fight against Botrytis cinerea and have found that strain Bc7 has an efficiency of upper control against Botrytis cinerea compared to other strains to the different conditions tested, while strain Bc4 is the least effective. For the control against Colletotrichum acutatum we found that the isolate Bc2 is the more efficient compared to other isolates and Bc5 the less effective to the different conditions tested.</p><p>B. amyloliquefaciens show good antifungal activity on various plant pathogens, can be effectively used for controlling phytopathogens including Colletotrichum acutatum [<xref ref-type="bibr" rid="scirp.80419-ref32">32</xref>] . Trichoderma harzianum also has a great potential of biocontrol against anthracnose caused by C. acutatum [<xref ref-type="bibr" rid="scirp.80419-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref34">34</xref>] .</p><p>Temperature has a great influence on the development of microorganisms as well as their biological activity. All bacterial isolates represent a large inhibitory effect of radial growth at 25˚C. Studies have been made on the influence of environmental parameters on the development of Colletotrichum acutatum and have found that the optimal values of the temperature is 25˚C &#177; 2˚C [<xref ref-type="bibr" rid="scirp.80419-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref36">36</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref37">37</xref>] , Bc2 is the most effective among the other isolates and Bc5 the least effective. The fungal antagonist has a great inhibitory effect at all temperatures studied, and rises by increasing the temperature. Trichoderma harzianum has high efficacy at 33˚C or lower against Sclerotium rolfii, another phytopathogenic agent, and produces secondary metabolites and mycotoxins at high temperatures that will help control plant pathologies [<xref ref-type="bibr" rid="scirp.80419-ref38">38</xref>] . Antagonistic activity in vitro of T. harzianum to B. cinerea is more effectively at a near-optimal 25˚C is consistent with a more rapidly increasing conidial respiratory rate at the higher temperature [<xref ref-type="bibr" rid="scirp.80419-ref39">39</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref40">40</xref>] . The optimum temperature for radial growth of Trichoderma spp. is between 25˚C and 30˚C [<xref ref-type="bibr" rid="scirp.80419-ref41">41</xref>] .</p><p>The water activity has a remarkable way on the mycelial growth, which is optimal between 0.95 and 1. The activity of water has also been favorable to inhibit the growth of Verticillium dahliae and Rhizoctonia solani by Trichoderma harzianum [<xref ref-type="bibr" rid="scirp.80419-ref42">42</xref>] . At 37˚C the optimal growth of B. amyloliquefaciens was at aw 0.960 [<xref ref-type="bibr" rid="scirp.80419-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref44">44</xref>] , this antagonist has inhibited the growth of A. flavus and F. verticillioides at aw = 0.99; 0.97; 0.95 and 0.93 [<xref ref-type="bibr" rid="scirp.80419-ref45">45</xref>] and inhibited the growth and aflatoxin B1 production by Aspergillus section Flavi at aw = 0.982 [<xref ref-type="bibr" rid="scirp.80419-ref46">46</xref>] . Maximal growth rates of T. harzianum were observed at aw 0.997 [<xref ref-type="bibr" rid="scirp.80419-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref47">47</xref>] , the optimal aw values for mycelial growth and in vitro enzyme activities were similar [<xref ref-type="bibr" rid="scirp.80419-ref16">16</xref>] . The in vitro enzyme activities of T. harzianum were also affected by aw, but significant enzyme activities were measured for most of the enzymes even at aw values less than the limit of mycelial growth [<xref ref-type="bibr" rid="scirp.80419-ref48">48</xref>] .</p><p>Bacillus amyloliquefaciens and Trichoderma harzianum were influenced by pH, which was low at acid pH, and increased by increasing pH values to 7 (neutral pH) and then began to decrease in alkaline pH. Colletotrichum musae, agent to anthracnose of the banana tree, develops at an optimal pH equal to 4.5 [<xref ref-type="bibr" rid="scirp.80419-ref49">49</xref>] . The tolerance of B. amyloliquefaciens to grow under different pH-temperature was studied by Gotor-Vila et al. [<xref ref-type="bibr" rid="scirp.80419-ref43">43</xref>] ; they have found that the optimum growth was observed at 37˚C and pH 5-7 [<xref ref-type="bibr" rid="scirp.80419-ref50">50</xref>] . B. amyloliquefaciens has exhibited significantly low activities of starch-degrading enzymes and high resistance to low pH [<xref ref-type="bibr" rid="scirp.80419-ref51">51</xref>] . The crude lipopeptides of B. amyloliquefaciens were insensitive to pH variation. The activity was not affected at pH 2 to 11, and was reduced at pH 12 [<xref ref-type="bibr" rid="scirp.80419-ref52">52</xref>] [<xref ref-type="bibr" rid="scirp.80419-ref53">53</xref>] which means variation of pH affect the antifungal activity of this antagonist. T. harzianum were able to grow on a wide range of pH from 2 to 6, and the optimal growth was observed at pH 4, the mycelial growth ceased at pH 8 and 7, also pH had an effect on the in vitro of enzymes activities of T. harzianum [<xref ref-type="bibr" rid="scirp.80419-ref16">16</xref>] . Jackson et al. [<xref ref-type="bibr" rid="scirp.80419-ref54">54</xref>] have found that optimum biomass production Trichoderma harzianum occurred at pH 4.6 - 6.8.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The antagonists behave differently depending on the environmental parameters. We found that isolate Bc2 show more efficiency compared to other bacterial strains, and that Trichoderma harzianum always inhibits the development of the pathogen despite the change in the factors studied. However, other parameters could be considered to develop and improve the control efficiency by these antagonists in order to acquire a viable biological control system against the brown spot disease caused by Colletotrichum acutatum. Adaptation of biocontrol potential of the antagonists studied to environments with different temperature; aw and pH characteristics seems to be an important mechanism of evolution enabling the effective competition for nutrients under a wider range of these environmental parameters.</p></sec><sec id="s6"><title>Cite this paper</title><p>Es-Soufi, R., El Bouzdoudi, B., Bouras, M., El Kbiach, M.L., Badoc, A. and Lamarti, A. (2017) Assessment of the Effect of Environmental Factors on the Antagonism of Bacillus amyloliquefaciens and Trichoderma harzianum to Colletotrichum acutatum. Advances in Microbiology, 7, 729-742. https://doi.org/10.4236/aim.2017.711058</p></sec></body><back><ref-list><title>References</title><ref id="scirp.80419-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Garrido, C., Carbú, M., Fernández-Acero F.J., González-Rodríguez, V.E. and Cantoral, J.M. (2011) New Insights in the Study of Strawberry Fungal Pathogens. Genes. Genomes, Genomics 5 (Spec. Iss. 1), 24-39.</mixed-citation></ref><ref id="scirp.80419-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Maas, J.L. (1998) Compendium of Strawberry Diseases. Second Edition, St Paul, Minn.: APS Press, 98 p.</mixed-citation></ref><ref id="scirp.80419-ref3"><label>3</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Barclay Poling</surname><given-names> E. </given-names></name>,<etal>et al</etal>. (<year>2008</year>)<article-title>Anthracnose on Strawberry: Its Etiology, Epidemiology, and Pathology, Together with Management Strategies for Strawberry Nurseries: Introduction to the Workshop</article-title><source> HortScience</source><volume> 43</volume>,<fpage> 59</fpage>-<lpage>65</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.80419-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Tanaka, M.A.S. and Passos, F.A. (2002) Caracteriza&amp;atilde;o patogênica de Colletotrichum acutatum e C. fragariae associados à antracnose do morangueiro. [Characterization of the Pathogenic: Colletotrichum acutatum and C. fragariae Associated with Strawberry Anthracnose.] Fitopatologia Brasileira, 27, 484-488.  
https://doi.org/10.1590/S0100-41582002000500008</mixed-citation></ref><ref id="scirp.80419-ref5"><label>5</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Smith</surname><given-names> B.J. </given-names></name>,<etal>et al</etal>. (<year>2008</year>)<article-title>Epidemiology and Pathology of Strawberry Anthracnose: A North American Perspective</article-title><source> HortScience</source><volume> 43</volume>,<fpage> 69</fpage>-<lpage>73</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.80419-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Mari, M. and Guizzardi, M. (1998) The Postharvest Phase: Emerging Technologies for the Control of Fungal Diseases. Phytoparasitica, 26, 59-66.  
https://doi.org/10.1007/BF02981267</mixed-citation></ref><ref id="scirp.80419-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Janisiewicz, W.J. and Korsten, L. (2002) Biological Control of Postharvest Diseases of Fruits. Annual Review of Phytopathology, 40, 411-441.  
https://doi.org/10.1146/annurev.phyto.40.120401.130158</mixed-citation></ref><ref id="scirp.80419-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Conway, W.S., Leverentz, B., Janisiewicz, W.J., Blodgett, A.B., Saftner, R.A. and Camp, M.J., (2004) Integrating Heat Treatment, Biocontrol and Sodium Bicarbonate to Reduce Postharvest Decay of Apple Caused by Colletotrichum acutatum and Penicillium expansum. Postharvest Biology and Technology, 34, 11-20.  
https://doi.org/10.1016/j.postharvbio.2004.05.011</mixed-citation></ref><ref id="scirp.80419-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Mochizuki, M., Yamamoto, S., Aoki, Y. and Suzuki, S. (2012) Isolation and Characterisation of Bacillus amyloliquefaciens S13-3 as a biological Control Agent for Anthracnose Caused by Colletotrichum gloeosporioides. Biocontrol Science and Technology, 22, 697-709. https://doi.org/10.1080/09583157.2012.679644</mixed-citation></ref><ref id="scirp.80419-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">De Costa, D.M. and Erabadupitiya, H.R.U.T. (2005) An Integrated Method to Control Postharvest Diseases of Banana Using a Member of the Burkholderia cepacia Complex. Postharv. Postharvest Biology and Technology, 36, 31-39.  
https://doi.org/10.1016/j.postharvbio.2004.11.007</mixed-citation></ref><ref id="scirp.80419-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Ashwini, N. and Srividya, S. (2014) Potentiality of Bacillus subtilis as Biocontrol Agent for Management of Anthracnose Disease of Chilli Caused by Colletotrichum gloeosporioides OGC1. 3 Biotech, 4, 127-136.  
https://doi.org/10.1007/s13205-013-0134-4</mixed-citation></ref><ref id="scirp.80419-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Vivekananthan, R., Ravi, M., Ramanathan, A. and Samiyappan, R. (2004) Lytic Enzymes Induced by Pseudomonas fluorescens and Other biocontrol Organisms Mediate Defence against the Anthracnose Pathogen in Mango. World Journal of Microbiology and Biotechnology, 20, 235-244.  
https://doi.org/10.1023/B:WIBI.0000023826.30426.f5</mixed-citation></ref><ref id="scirp.80419-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Freeman, S., Minz, D., Kolesnik, I., Barbul, O., Zveibil, A., Maymon, M., Nitzani, Y., Kirshner, B., Rav-David, D., Bilu, A., Dag, A., Shafir, S. and Elad, Y. (2004) Trichoderma Biocontrol of Colletotrichum acutatum and Botrytis cinerea and Survival in Strawberry. European Journal of Plant Pathology, 110, 361-370.  
https://doi.org/10.1023/B:EJPP.0000021057.93305.d9</mixed-citation></ref><ref id="scirp.80419-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Shovan, L.R., Bhuiyan, M.K.A., Begum, J.A. and Pervez, Z. (2008) In Vitro Control of Colletotrichum dematium Causing Anthracnose of Soybean by Fungicides, Plant Extracts and Trichoderma harzianum. International Journal of Sustainable Crop Production, 3, 10-17.</mixed-citation></ref><ref id="scirp.80419-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Palaniyandi, S.A., Yang, S.H., Cheng, J.H., Meng, L. and Suh, J.W. (2011) Biological Control of Anthracnose (Colletotrichum gloeosporioides) in Yam by Streptomyces sp. MJM5763. Journal of Applied Microbiology, 111, 443-455.  
https://doi.org/10.1111/j.1365-2672.2011.05048.x</mixed-citation></ref><ref id="scirp.80419-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Kredics, L., Manczinger, L., Antal, Z., Pénzes, Z., Szekeres, A., Kevei, F. and Nagy, E. (2004) In Vitro Water Activity and pH Dependence of Mycelial Growth and Extracellular Enzyme Activities of Trichoderma Strains with Biocontrol Potential. Journal of Applied Microbiology, 96, 491-498.  
https://doi.org/10.1111/j.1365-2672.2004.02167.x</mixed-citation></ref><ref id="scirp.80419-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Smith, B.J. and Black, L.L. (1990) Morphological, Cultural, and Pathogenic Variation among Colletotrichum Species Isolated from Strawberry. Plant Disease, 74, 69-76. https://doi.org/10.1094/PD-74-0069</mixed-citation></ref><ref id="scirp.80419-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Talhinhas, P., Sreenivasaprasad, S., Neves-Martins, J. and Oliveira, H. (2002) Genetic and Morphological Characterization of Colletotrichum acutatum Causing Anthracnose of Lupins. Phytopathology, 92, 986-996.  
https://doi.org/10.1094/PHYTO.2002.92.9.986</mixed-citation></ref><ref id="scirp.80419-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Hamdache, A., Ezziyyani, M., Badoc, A. and Lamarti, A. (2012) Effect of pH, Temperature and Water Activity on the Inhibition of Botrytis cinerea by Bacillus amyloliquefaciens Isolates. African Journal of Biotechnology, 11, 2210-2217.</mixed-citation></ref><ref id="scirp.80419-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Flegel, T.W. (1980) Semipermanent Microscope Slides of Microfungi using a Sticky Tape Technique. Canadian Journal of Microbiology, 26, 551-553.  
https://doi.org/10.1139/m80-095</mixed-citation></ref><ref id="scirp.80419-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Maouni, A. (2002) Principaux Agents Fongiques des poires pourries en conservation: Biologie, physiologie et application de quelques moyens de lutte chimique. [Main Fungal Agents of Rotting Conserved Pears: Biology, Physiology and Application of Some Techniques of Chemical Control.] Thèse Doct. Phytopathol. Fac. Sci. Tétouan, Maroc, 152 p.</mixed-citation></ref><ref id="scirp.80419-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Barbosa, M.A.G., Rehn, K.G., Menezes, M. and Mariano, R.L.R. (2001) Antagonism of Trichoderma Species on Cladosporium herbarum and Their Enzymatic Characterization. Brazilian Journal of Microbiology, 32, 98-104.  
https://doi.org/10.1590/S1517-83822001000200005</mixed-citation></ref><ref id="scirp.80419-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Han, K.S., Kim, B.R., Kim, J.T., Hahm, S.S., Hong, K.H., Chung, C.K., Nam, Y.G., Yu, S.H. and Choi, J.E. (2013) Biological Control of White Rot in Garlic using Burkholderia pyrrocinia CAB08106-4. Research in Plant Disease, 19, 21-24.  
https://doi.org/10.5423/RPD.2013.19.1.021</mixed-citation></ref><ref id="scirp.80419-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Kim, S.T. and Yun, S.C. (2011) Biocontrol Activity of Myxococcus sp. KYC 1126 against Phytophthora Blight on Hot Pepper. Research in Plant Disease, 17, 121-128.  
https://doi.org/10.5423/RPD.2011.17.2.121</mixed-citation></ref><ref id="scirp.80419-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Kwak, Y.K., Kim, I.S., Cho, M.C., Lee, S.C. and Kim, S. (2012) Growth Inhibition Effect of Environment-Friendly Farm Materials in Colletotrichum acutatum in Vitro. Journal of Bio-Environment Control, 21, 127-133.</mixed-citation></ref><ref id="scirp.80419-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">El-Ghaouth, A., Smilanick, J.L., Brown, G.E., Ippolito, A. and Wilson, C.L. (2001) Control of Decay of Apple and Citrus Fruits in Semicommercial Tests with Candida Saitoana and 2-Deoxy-D-Glucose. Biological Control, 20, 96-101.  
https://doi.org/10.1006/bcon.2000.0894</mixed-citation></ref><ref id="scirp.80419-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Lahlali, R., Hamadi, Y., El Guilli, M. and Jijakli, M.H. (2011) Efficacy Assessment of Pichia guilliermondii Strain Z1, a New Biocontrol Agent, against Citrus Blue Mould in Morocco under the Influence of Temperature and Relative Humidity. Biological Control, 56, 217-224.</mixed-citation></ref><ref id="scirp.80419-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Govender, V., Korsten, L. and Sivakumar, D. (2005) Semi-Commercial Evaluation of Bacillus licheniformis to Control Mango Postharvest Diseases in South Africa. Postharvest Biology and Technology, 38, 57-65.</mixed-citation></ref><ref id="scirp.80419-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Kim, P.I., Ryu, J., Kim, Y.H. and Chi, Y.T. (2010) Production of Biosurfactant Lipopeptides Iturin A, Fengycin, and Surfactin A from Bacillus subtilis CMB32 for Control of Colletotrichum gloeosporioides. Journal of Microbiology and Biotechnology, 20, 138-145.</mixed-citation></ref><ref id="scirp.80419-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Zheng, M., Shi, Z., Shi, J., Wang, Q. and Li, Y. (2013) Antimicrobial Effects of Volatiles Produced by Two Antagonistic Bacillus Strains on the Anthracnose Pathogen in Postharvest Mangos. Biological Control, 65, 200-206.</mixed-citation></ref><ref id="scirp.80419-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Zivkovic, S., Stojanovic, S., Ivanovic, Z., Gavrilovic, V., Popovic, T. and Jelica, B. (2010) Screening of Antagonistic Activity of Microorganisms against Colletotrichum acutatum and Colletotrichum gloeosporioides. Archives of Biological Sciences, 62, 611-623. https://doi.org/10.2298/ABS1003611Z</mixed-citation></ref><ref id="scirp.80419-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Martinez, A.S.C., del C. Orozco, M.M., Martinez-Pacheco, M.M., Farias-Rodriguez, R., Govindappa, M. and Santoyo, G. (2012) Isolation and Molecular Characterization of a Novel Strain of Bacillus with Antifungal Activity from the Sorghum Rhizosphere. Genetics and Molecular Research, 11, 2665-2673.  
https://doi.org/10.4238/2012.July.10.15</mixed-citation></ref><ref id="scirp.80419-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Delgado, J.J., Sousa, S., Gonzalez, F., Rey, M. and Llobell, A. (2006) ThHog1 Controls the Hyperosmotic Stress Response in Trichoderma harzianum. Microbiology, 152, 1687-700. https://doi.org/10.1099/mic.0.28729-0</mixed-citation></ref><ref id="scirp.80419-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Mercado, J.A., Barcelo, M. P.C., Rey, M.C.J.L., Munoz, B.J., RuanoRosa, D., Lopez, H.C., de los Santos, B., Romero, M.F., et al. (2015) Expression of the β-1,3-glucanase Gene bgn13.1 from Trichoderma harzianum in Strawberry Increases Tolerance to Crown Rot Diseases but Interferes with Plant Growth. Transgenic Research, 24, 979-989. https://doi.org/10.1007/s11248-015-9895-3</mixed-citation></ref><ref id="scirp.80419-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Fernando, T.H.P.S., Jayasinghe, C.K. and Wijesundera, R.L.C. (2000) Factors Affecting Spore Production, Germination and Viability of Colletotrichum acutatum Isolates from Hevea brasiliensis. Mycological Research, 104, 681-685.  
https://doi.org/10.1017/S0953756200002483</mixed-citation></ref><ref id="scirp.80419-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Grahovac, M., Indic, D., Vukovic, S., Hrustc, J., Gvozdenac, S., Mihajlovic, M. and Tanovic, B. (2012) Morphological and Ecological Features as Differentiation Criteria for Colletotrichum Species. Zemdirbyste (Agriculture), 99, 189-195.</mixed-citation></ref><ref id="scirp.80419-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Miles, T.D., Gillett, J.M., Jarosz, A.M. and Schilder, A.M.C. (2013) The Effect of Environmental Factors on Infection of Blueberry Fruit by Colletotrichum acutatum. Plant Pathology, 62, 1238-1247. https://doi.org/10.1111/ppa.12061</mixed-citation></ref><ref id="scirp.80419-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Mukherjee, P.K. and Raghu, K. (1997) Effect of Temperature on Antagonistic and Biocontrol Potential of Trichoderma sp. on Sclerotium rolfsii. Mycopathologia, 139, 151-155. https://doi.org/10.1023/A:1006868009184</mixed-citation></ref><ref id="scirp.80419-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">Elad, Y., Zimand, G., Zaqs, Y., Zuriel, S. and Chet, I. (1993) Use of Trichoderma harzianum in Combination or Alternation with Fungicides to Control Cucumber Gray Mould (Botrytis cinerea) under Commercial Greenhouse Conditions. Plant Pathology, 42, 324-332. https://doi.org/10.1111/j.1365-3059.1993.tb01508.x</mixed-citation></ref><ref id="scirp.80419-ref40"><label>40</label><mixed-citation publication-type="other" xlink:type="simple">Hjeljord, L.G., Stensvand, A. and Tronsmo, A. (2001) Antagonism of Nutrient-Activated Conidia of Trichoderma harzianum (Atroviride) P1 against Botrytis cinerea. Phytopathology, 91, 1172-1180.  
https://doi.org/10.1094/PHYTO.2001.91.12.1172</mixed-citation></ref><ref id="scirp.80419-ref41"><label>41</label><mixed-citation publication-type="other" xlink:type="simple">Naar, Z. and Kecskes, M. (1995) A Method for Selecting Trichoderma Strains Antagonistic against Sclerotinia minor. Microbiological Research, 150, 239-246.</mixed-citation></ref><ref id="scirp.80419-ref42"><label>42</label><mixed-citation publication-type="other" xlink:type="simple">Santamarina, M.P. and Roselló, J. (2006) Influence of Temperature and Water Activity on the Antagonism of Trichoderma harzianum to Verticillium and Rhizoctonia. Crop Protection, 25, 1130-1134.</mixed-citation></ref><ref id="scirp.80419-ref43"><label>43</label><mixed-citation publication-type="other" xlink:type="simple">Gotor-Vila, A., Teixido, N., Sisquella, M., Torres, R. and Usall, J. (2017) Biological Characterization of the Biocontrol Agent Bacillus amyloliquefaciens CPA-8: The Effect of Temperature, pH and Water Activity on Growth, Susceptibility to Antibiotics and Detection of Enterotoxic Genes. Current Microbiology, 74, 1089-1099. https://doi.org/10.1007/s00284-017-1289-8</mixed-citation></ref><ref id="scirp.80419-ref44"><label>44</label><mixed-citation publication-type="other" xlink:type="simple">Mossel, D.A.A., Corry, J.E.L., Struijk, C.B. and Baird, R.M. (1995) Essentials of the Microbiology of Foods: A Textbook for Advanced Studies. Wiley, New York.</mixed-citation></ref><ref id="scirp.80419-ref45"><label>45</label><mixed-citation publication-type="other" xlink:type="simple">Etcheverry, M.G., Scandolara, A., Nesci, A., Vilas Boas Ribeiro, M.S., Pereira, P., Battilani and Paola (2009) Biological Interactions to Select Biocontrol Agents against Toxigenic Strains of Aspergillus flavus and Fusarium verticillioides from Maize. Mycopathologia, 167, 287-295. https://doi.org/10.1007/s11046-008-9177-1</mixed-citation></ref><ref id="scirp.80419-ref46"><label>46</label><mixed-citation publication-type="other" xlink:type="simple">Bluma, R.V. and Etcheverry, M.G. (2006) Influence of Bacillus spp. Isolated from Maize Agroecosystem on Growth and Aflatoxin B1 Production by Aspergillus Section Flavi. Pest Management Science, 62, 242-251.  
https://doi.org/10.1002/ps.1154</mixed-citation></ref><ref id="scirp.80419-ref47"><label>47</label><mixed-citation publication-type="other" xlink:type="simple">Valero, A., Sanchis, V., Ramos, A.J. and Marin, S. (2007) Studies on the Interaction between Grape-Associated Filamentous Fungi on a Synthetic Medium. International Journal of Food Microbiology, 113, 271-276.</mixed-citation></ref><ref id="scirp.80419-ref48"><label>48</label><mixed-citation publication-type="other" xlink:type="simple">Kredics, L., Antal, Z. and Manczinger, L. (2000) Influence of Water Potential on Growth, Enzyme Secretion and in Vitro Enzyme Activities of Trichoderma harzianum at Different Temperatures. Current Microbiology, 40, 310-314.  
https://doi.org/10.1007/s002849910062</mixed-citation></ref><ref id="scirp.80419-ref49"><label>49</label><mixed-citation publication-type="other" xlink:type="simple">De Costa, D.M. and Chandima, A.A.G. (2014) Effect of Exogenous pH on Development and Growth of Colletotrichum musae and Development of Anthracnose in Different Banana Cultivars in Sri Lanka. Journal of the National Science Foundation of Sri Lanka, 42, 229-240.  
https://doi.org/10.4038/jnsfsr.v42i3.7396</mixed-citation></ref><ref id="scirp.80419-ref50"><label>50</label><mixed-citation publication-type="other" xlink:type="simple">Padan, E., Bibi, E., Ito, M. and Krulwich, T.A. (2005) Alkaline pH Homeostasis in Bacteria: New Insights. Biochimica Et Biophysica Acta-Biomembranes, 1717, 67-88.</mixed-citation></ref><ref id="scirp.80419-ref51"><label>51</label><mixed-citation publication-type="other" xlink:type="simple">Hyunsu, S. and Kim, M.-D. (2016) Antipathogenic Activity of Bacillus amyloliquefaciens Isolated from Korean Traditional Rice Wine. Han’guk Misaengmul-Saengmyongkong Hakhoechi, 44, 98-105.</mixed-citation></ref><ref id="scirp.80419-ref52"><label>52</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, S.M., Wang, X.M., Meng, L.Q., Li, J., Zhao, X.Y., Cao, X., Chen, X.L., Wang, A.X. and Li, J.F. (2012) Isolation and Characterization of Antifungal Lipopeptides Produced by Endophytic Bacillus amyloliquefaciens TF28. African Journal of Microbiology Research, 6, 1747-1755.</mixed-citation></ref><ref id="scirp.80419-ref53"><label>53</label><mixed-citation publication-type="other" xlink:type="simple">Zouari, I., Jlaiel, L., Tounsi, S. and Trigui, M. (2016) Biocontrol Activity of the Endophytic Bacillus amyloliquefaciens Strain CEIZ-11 against Pythium aphanidermatum and Purification of Its Bioactive Compounds. Biological Control, 100, 54-62.</mixed-citation></ref><ref id="scirp.80419-ref54"><label>54</label><mixed-citation publication-type="other" xlink:type="simple">Jackson, A.M., Whipps, J.M. and Lynch, J.M. (1991) Effects of Temperature, pH and Water Potential on Growth of Four Fungi with Disease Biocontrol Potential. World Journal of Microbiology and Biotechnology, 7, 494-501.  
https://doi.org/10.1007/BF00303376</mixed-citation></ref></ref-list></back></article>