<?xml version="1.0" encoding="utf8"?>
 <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd"> <article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="research-article" dtd-version="1.0" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JFD</journal-id>
      <journal-title-group>
        <journal-title>Journal of Fungal Diversity</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2766-869X</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.2766-869X.jfd-20-3193</article-id>
      <article-id pub-id-type="publisher-id">JFD-20-3193</article-id>
      <article-categories>
        <subj-group>
          <subject>research-article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Influence of Carbon - Nitrogen Supplements and pH on Growth of Sugarcane Stem rot Pathogen <italic>Fusarium </italic><italic>S</italic><italic>olani</italic> NVS671</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Prittesh</surname>
            <given-names>Patel</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843064828">1</xref>
          <xref ref-type="aff" rid="idm1843064324">*</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843064828">
        <label>1</label>
        <addr-line>C. G. Bhakta Institute of Biotechnology, Uka Tarsadia University, Bardoli, Gujarat - 394350, India</addr-line>
      </aff>
      <aff id="idm1843064324">
        <label>*</label>
        <addr-line>Corresponding Author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Samantha</surname>
            <given-names>Chandranath Karunarathna</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843203604">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843203604">
        <label>1</label>
        <addr-line>Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China</addr-line>
      </aff>
      <author-notes>
        <corresp>Corresponding author: Prittesh Patel, Assistant Professor, C.G. Bhakta Institute of Biotechnology, Uka Tarsadia University, Maliba Campus, Bardoli, Surat, Gujarat 394350, India. Tel: <phone>+91 9913668812</phone> Email: <email>prittespatel@gmail.com</email></corresp>
        <fn fn-type="conflict" id="idm1850523076">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2020-03-13">
        <day>13</day>
        <month>03</month>
        <year>2020</year>
      </pub-date>
      <volume>1</volume>
      <issue>1</issue>
      <fpage>27</fpage>
      <lpage>32</lpage>
      <history>
        <date date-type="received">
          <day>29</day>
          <month>01</month>
          <year>2020</year>
        </date>
        <date date-type="accepted">
          <day>07</day>
          <month>03</month>
          <year>2020</year>
        </date>
        <date date-type="online">
          <day>13</day>
          <month>03</month>
          <year>2020</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2020</copyright-year>
        <copyright-holder>Prittesh Patel</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/jfd/article/1280">This article is available from http://openaccesspub.org/jfd/article/1280</self-uri>
      <abstract>
        <p><italic>Fusarium </italic><italic>solani</italic> NVS671 identified from infected sugarcane stem of Co 671 as a new pathogen was subjected to various cultural conditions to understand its physiological profile. In continuation with our previous work, cultural analysis was carried out under <italic>in vitro</italic> condition by supplementing various carbon and nitrogen sources in Czapek-Dox agar (CDA). Under different hydrogen ion concentrations, it was found that the growth of <italic>Fusarium </italic><italic>solani</italic>NVS671 was less at pH 4 and pH 10 and could reach up to 5 cm after 7 days of incubation on Potato Dextrose Agar (PDA). It is observed that the pH around 7 to 8 was optimum for the growth of <italic>F. </italic><italic>solani</italic>. Ten different nitrogenous (N) sources and nine different carbon sources were tested on CDA medium to know their effect on the mycelial growth rate and characteristics of the fungus. Among the N sources evaluated, ammonium chloride (7.96±0.11 cm) was found to be most efficient for mycelial growth promotion followed by ammonium nitrate (7.7±0.1 cm) and ammonium sulphate (7.3±0.1 cm). The most preferred carbon source recorded to promote best radial mycelial growth was starch (7.96±0.05 cm) and sucrose (7.93±0.05 cm). Capabilities of using different carbon and nitrogen sources and ability to grow at different pH levels may allow species to adapt to specific soil conditions.This study is important to understand the physiology and metabolite preference of <italic>F. </italic><italic>solani</italic>.</p>
      </abstract>
      <kwd-group>
        <kwd>Carbon</kwd>
        <kwd>Disease</kwd>
        <kwd>Fusarium solani</kwd>
        <kwd>Nitrogen</kwd>
        <kwd>Pathogen</kwd>
        <kwd>Sugarcane</kwd>
      </kwd-group>
      <counts>
        <fig-count count="1"/>
        <table-count count="2"/>
        <page-count count="6"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1842913316" sec-type="intro">
      <title>Introduction</title>
      <p><italic>Fusarium </italic><italic>solani</italic> (Teleomorph: <italic>Haematonectria</italic><italic>haematococca</italic>) is a widely distributed fungal plant pathogen that infects many different genera of                plants <xref ref-type="bibr" rid="ridm1843161996">1</xref><xref ref-type="bibr" rid="ridm1843165092">2</xref>. In nature, <italic>Fusarium </italic><italic>solani</italic> exist as different strains that exhibit variation in their morphological and cultural characters, pathogenicity and virulence. Due to <italic>F. </italic><italic>solani</italic>distribution across the environments is varied, it is essential to know which isolate is most virulent within a given species. <italic>F. </italic><italic>solani</italic> is pathogenic to at least 111 plant species spanning 87 genera <xref ref-type="bibr" rid="ridm1843178316">3</xref>. Recently El Haddadi Errifi et al. reported that <italic>Fusarium </italic><italic>solani</italic> had significantly affected preemergence, post emergence mortality rate and growth parameters in <italic>Tetraclinis articulate </italic><xref ref-type="bibr" rid="ridm1843263612">4</xref>. Present investigation was under taken to study the variability in growth requirement and morphological characters of <italic>F. </italic><italic>Solani</italic>.</p>
      <p><italic>F. </italic><italic>solani</italic> and <italic>R. </italic><italic>solani</italic> are the most important saprophytic pathogens, which develop in both cultured and non-cultured soils, causing the symptoms of damping off and root rot diseases to wide range of vegetable and crop plants including tomato <xref ref-type="bibr" rid="ridm1843021004">5</xref>. It causes wilt and rot diseases on a wide variety of crops including <italic>Cucurbita </italic><italic>spp</italic><italic>.,Pisum</italic><italic> sativum</italic> and <italic>Phaseolus vulgaris </italic><xref ref-type="bibr" rid="ridm1843027340">6</xref><xref ref-type="bibr" rid="ridm1843014276">7</xref><xref ref-type="bibr" rid="ridm1843011684">8</xref>. Environmental factors such as    temperature, and pH have a large influence on fungal growth <xref ref-type="bibr" rid="ridm1843016148">9</xref>. Study of effect of hydrogen ion               concentration on phytopathogen is important to understand their metabolism and probable correlation with soil pH. If the soil pH is favourable for the growth of phytopathogen, the severity of disease can be high. Similarly variation in carbon and nitrogen sources provided may also influence the growth of fungal phytopathogen. Despite the immense agronomic importance of this fungus, change in pH and the pattern of utilization of the substrate have not been worked upon. In present study, we analysed effect of different pH, carbon and nitrogen substrates in PDA and CDA medium on the growth of <italic>F.solani</italic> NVS671. </p>
    </sec>
    <sec id="idm1842907916" sec-type="materials">
      <title>Material and Methodology</title>
      <p><italic>Fusarium </italic><italic>solani</italic> NVS671 was identified as a pathogen causing stem rot in sugarcane. In our previous study we have reported that <italic>F.solani</italic> NVS671 is a new pathogen found to causing stem rot in sugarcane <xref ref-type="bibr" rid="ridm1842999484">10</xref>. Seven-day-old active culture of <italic>F.solani</italic> NVS671was used for this study.</p>
      <sec id="idm1842896804">
        <title>Effect of pH (Hydrogen ion Concentration) on Fusarium Solani </title>
        <p>Effect of pH on mycelial growth was studied by growing <italic>F.solani</italic>NVS671 on PDA mixed with an appropriate volume of the buffer to give desired pH in medium. The pH was obtained over the ranges 4-10 with citric acid or NaOH. The PDB medium and the buffers were autoclaved separately and aseptically mixed during cooling. Then medium was sterilized in autoclave at 120°C for 15 min. A five mm mycelial disc was transferred from the margin of the 7-day-old growing colony, to the PDA plates. After inoculation, Petri dishes were incubated at 28±2°C. The diameter was recorded in Centimetres in two directions at right angles to each other, and then average colony diameter in was calculated and recorded. Measurement of growth was made at 3<sup>rd</sup>, 5<sup>th</sup> and 7<sup>th</sup> day after incubation (DAI). The experimental design was a random complete block (RCB) with three replicate plates of each isolate for each pH treatment. </p>
      </sec>
      <sec id="idm1842897740">
        <title>Effect of Nitrogen Source on Fusarium Solani </title>
        <p>To scrutinize the effect of different carbon and inorganic nitrogen sources on growth and cultural characteristics of fungal pathogen Czapek Dox agar (CDA) media were used. All the ingredients with required quantity needed to prepare final amount were weighed and added. Nitrogen sources were added in equal amount to all the individual media. Czapek media without nitrogen source were served as control. Various nitrogen sources such as Potassium Nitrate, Sodium Nitrate, Ammonium Metavanadate, Calcium Nitrate, Cobalt Nitrate, Ammonium Fluoride, Ammonium Chloride, Ammonium Nitrate, Ammonium Oxalate, and Ammonium Sulphate were used at 0.2% concentration. </p>
      </sec>
      <sec id="idm1842897596">
        <title>Effect of Carbon Source on Fusarium Solani</title>
        <p>Various carbon sources were weighed and added to the basal medium. A 20 mL of sterilized medium was poured into sterilized Petri plates (90 mm diameter). Inoculations were made with cultural discs (5mm) from seven days old active culture of <italic>F. </italic><italic>solani</italic>NVS671. Inoculated Petri plates were incubated at room temperature and average colony diameter was recorded after 3, 5 and 7 days. Three replications of each nitrogen and carbon source were maintained. </p>
      </sec>
      <sec id="idm1842894212">
        <title>Statistical Analysis</title>
        <p>The experiment was carried out following RCB with three replicates of each treatment. All experimental data of C and N source were subjected to statistical analysis by standard deviation. In case of pH analysis the significance of differences between the treatments was evaluated by one way analysis of variance (ANOVA) at the significance level of 95 %. </p>
      </sec>
    </sec>
    <sec id="idm1842896156" sec-type="results">
      <title>Result &amp; Discussion</title>
      <p>A total of seven different pH values were evaluated for studying the growth of <italic>Fusarium </italic><italic>solani</italic>NVS671. Mycelia can grow only within a definite                    pH range and metabolism is often affected by                         pH <xref ref-type="bibr" rid="ridm1843006540">11</xref>.  Under acidic condition <italic>F. </italic><italic>solani</italic> growth was very slow and could reach up to 5 cm after 7 days of incubation. It is observed that the optimum pH for the growth of <italic>F. </italic><italic>solani</italic> was 7 to 8 (<xref ref-type="fig" rid="idm1842496676">Figure 1</xref>). Further increase in pH had shown reduced growth of phytopathogen. Our data are in accordance with Arunakumara et al., (2017) who reported significant differences in the growth of <italic>Fusarium </italic><italic>solani</italic> at different pH levels <xref ref-type="bibr" rid="ridm1843001212">12</xref>. Khan et al., (2011) reported that maximum growth of <italic>Fusarium </italic><italic>oxysporumf</italic><italic>. sp. </italic><italic>ciceri</italic> mycelial mat was observed at                 pH 7.0 <xref ref-type="bibr" rid="ridm1842963532">13</xref>. </p>
      <fig id="idm1842496676">
        <label>Figure 1.</label>
        <caption>
          <title> Growth of F. solani NVS671 at different pH.  Values are given as Mean growth in Cm ±SEM (n= 3) and considered to be significantly different at P&lt; 0.05.</title>
        </caption>
        <graphic xlink:href="images/image1.jpeg" mime-subtype="jpeg"/>
      </fig>
      <p>It is well known that supplementation of different nitrogen sources in media affect the                  micro-organism growth. In present study, ten different nitrogenous sources were tested on CDA medium to know their effect on the mycelial growth rate and characteristics of the fungus. All the nitrogen sources had support good mycelial growth at 1.5gm/L concentration except Ammonium Metavanadate and cobalt nitrate. By measuring the radial mycelial growth on CDA, ammonium chloride (7.96±0.11 cm) was found to be most efficient for growth promotion followed by ammonium nitrate (7.7±0.1 cm) and ammonium sulphate (7.3±0.1 cm). <xref ref-type="table" rid="idm1842493724">Table 1</xref>. There was no significant difference among potassium nitrate sodium nitrate and calcium nitrate in efficiency to promote the mycelial growth. Although there was good mycelial growth on ammonium and nitrate, their ability to use different forms of nitrogen are varies. Kamble (2011) reported the best nitrogen source for the growth of <italic>Fusarium </italic><italic>solani</italic> causing rhizome rot of Ginger was Calcium nitrate <xref ref-type="bibr" rid="ridm1842959788">14</xref>. Ammonium Metavanadate was less efficient as compare to other nitrogen sources and there was negligible growth on CDA media supplemented with it. There was no growth on cobalt nitrate, which indicates that fungus could not able to utilize it. It is possible that cobalt might have toxic effect on <italic>F. </italic><italic>Solani</italic><italic>.</italic></p>
      <table-wrap id="idm1842493724">
        <label>Table 1.</label>
        <caption>
          <title> Growth of F. solani NVS671 on different nitrogen source (Values represent Mean ± Standard   Deviation) (n= 3)</title>
        </caption>
        <table rules="all" frame="box">
          <tbody>
            <tr>
              <th>
                <bold>Nitrogen Source</bold>
              </th>
              <td colspan="3">
                <bold>Radial Growth in Centimetre</bold>
              </td>
              <td>
                <bold>Mycelial Morphology</bold>
              </td>
            </tr>
            <tr>
              <td/>
              <td>
                <bold>3 DAI</bold>
              </td>
              <td>
                <bold>5 DAI</bold>
              </td>
              <td>
                <bold>7 DAI</bold>
              </td>
              <td/>
            </tr>
            <tr>
              <td>Potassium Nitrate</td>
              <td>3.0±0.1</td>
              <td>5.03±0.05</td>
              <td>6.5±0.1</td>
              <td>White, Uneven, Thin, Sparse growth</td>
            </tr>
            <tr>
              <td>Sodium Nitrate</td>
              <td>2.93±0.15</td>
              <td>4.7±0.1</td>
              <td>6.26±0.11</td>
              <td>Dull White, Uneven, Thin, Sparse growth</td>
            </tr>
            <tr>
              <td>Ammonium Metavanadate</td>
              <td>0.13±0.05</td>
              <td>0.23±0.05</td>
              <td>0.36±0.05</td>
              <td>Dark Grey, Dense growth at centre</td>
            </tr>
            <tr>
              <td>Calcium Nitrate</td>
              <td>2.26±0.25</td>
              <td>4.2±0.1</td>
              <td>5.93±0.15</td>
              <td>White, Uneven, Thin, Scanty growth</td>
            </tr>
            <tr>
              <td>Cobalt Nitrate</td>
              <td>0</td>
              <td>0</td>
              <td>0</td>
              <td>-</td>
            </tr>
            <tr>
              <td>Ammonium Fluoride</td>
              <td>0.16±0.05</td>
              <td>0.33±0.05</td>
              <td>0.5±0.1</td>
              <td>Dark Grey, Dense growth at centre</td>
            </tr>
            <tr>
              <td>Ammonium Chloride</td>
              <td>3.3±0.2</td>
              <td>5.6±0.1</td>
              <td>7.96±0.11</td>
              <td>Dull White, Even, Thin, fluffy growth</td>
            </tr>
            <tr>
              <td>Ammonium Nitrate</td>
              <td>3.03±0.05</td>
              <td>5.4±0.1</td>
              <td>7.7±0.1</td>
              <td>White, Uneven, fluffy growth</td>
            </tr>
            <tr>
              <td>Ammonium Oxalate</td>
              <td>1.26±0.15</td>
              <td>2.63±0.15</td>
              <td>3.7±0.1</td>
              <td>Light Grey, Even, Scanty growth</td>
            </tr>
            <tr>
              <td>Ammonium Sulphate</td>
              <td>2.96±0.20</td>
              <td>5.56±0.15</td>
              <td>7.3±0.1</td>
              <td>White, Uneven, Dense growth at centre</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>Carbon is one of the most important nutrients required by living organisms for its growth. In present study, total nine different carbon sources were tested on CDA medium to observe their effect on the mycelial growth rate and characteristics of the fungus. All the nine kinds of carbon sources tested were found suitable for fungus growth. The efficiency of individual carbon sources could be divided into three categories. The first category which recorded to promote best radial mycelial growth included was starch (7.96±0.05 cm) and sucrose (7.93±0.05 cm). The capability of the fungus to utilized sucrose and starch was due to the possession of relevant enzymes to hydrolyze them into their component sugars <xref ref-type="bibr" rid="ridm1842956116">15</xref>. The second category included maltose lactose dextrose and mannitol which showed to efficiently supported growth between 6.9 cm and 7.7 cm on the 7<sup>th</sup> day. Cellulose was in the third category which was the least satisfactory. The growth of the pathogen in different carbon sources exhibited significant differences among the treatments. Several researchers reported Dextrose as best carbon source for growth of <italic>F. </italic><italic>oxysporum</italic><xref ref-type="bibr" rid="ridm1842968284">16</xref><xref ref-type="bibr" rid="ridm1842966124">17</xref>. (<xref ref-type="table" rid="idm1842420020">Table 2</xref>)</p>
      <table-wrap id="idm1842420020">
        <label>Table 2.</label>
        <caption>
          <title> Growth of F. solani NVS671 on different Carbon source (Values represent Mean ± Standard              Deviation) (n= 3)</title>
        </caption>
        <table rules="all" frame="box">
          <tbody>
            <tr>
              <td>
                <bold>Carbon Source</bold>
              </td>
              <td colspan="3">
                <bold>Radial Growth </bold>
                <bold>In</bold>
                <bold> Centimetre</bold>
              </td>
              <td>
                <bold>Mycelial Morphology</bold>
              </td>
            </tr>
            <tr>
              <td/>
              <td>
                <bold>3 DAI</bold>
              </td>
              <td>
                <bold>5 DAI</bold>
              </td>
              <td>
                <bold>7 DAI</bold>
              </td>
              <td/>
            </tr>
            <tr>
              <td>Mannitol</td>
              <td>3.13±0.05</td>
              <td>5.76±0.20</td>
              <td>7.23±0.11</td>
              <td>White, Uneven, Scanty growth</td>
            </tr>
            <tr>
              <td>Starch</td>
              <td>3.3±0.1</td>
              <td>6.33±0.05</td>
              <td>7.96±0.05</td>
              <td>Dull white, Uneven, Thick fluffy growth</td>
            </tr>
            <tr>
              <td>Cellulose</td>
              <td>2.13±0.05</td>
              <td>3.03±0.15</td>
              <td>4.83±0.05</td>
              <td>Light white, Even, Dense mycelia at centre</td>
            </tr>
            <tr>
              <td>Sucrose</td>
              <td>3.86±0.05</td>
              <td>6.53±0.35</td>
              <td>7.93±0.05</td>
              <td>Dull white, Even, Thin growth</td>
            </tr>
            <tr>
              <td>Maltose</td>
              <td>3.73±0.05</td>
              <td>6.83±0.05</td>
              <td>7.7±0.2</td>
              <td>Light grey, Uneven, Sparse growth</td>
            </tr>
            <tr>
              <td>Dextrose</td>
              <td>3.8±0.1</td>
              <td>6.33±0.11</td>
              <td>7.5±0.2</td>
              <td>White, Even, Scanty growth</td>
            </tr>
            <tr>
              <td>Fructose</td>
              <td>3.03±0.05</td>
              <td>5.13±0.05</td>
              <td>6.96±0.11</td>
              <td>White, Uneven, Thick fluffy at centre</td>
            </tr>
            <tr>
              <td>Lactose</td>
              <td>3.46±0.05</td>
              <td>6.26±0.25</td>
              <td>7.7±0.1</td>
              <td>Dull white, Even, Fluffy growth</td>
            </tr>
            <tr>
              <td>Xylose</td>
              <td>3.03±0.05</td>
              <td>5.53±0.05</td>
              <td>6.9±0.2</td>
              <td>White, Uneven, Thin growth</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec id="idm1842801572" sec-type="conclusions">
      <title>Conclusion</title>
      <p>This study is essential to recognize the physiology and metabolite preference of <italic>Fusarium </italic><italic>solani</italic>. Capabilities of using different N and C sources and ability to grow at different pH levels may allow species to adapt to specific soil conditions. Future research should be directed toward the study of the enzymatic activity of <italic>Fusarium </italic><italic>solani</italic>. In this way, it will be possible to obtain a more complete picture of the characteristics of <italic>Fusarium </italic><italic>solani</italic><italic>.</italic></p>
    </sec>
  </body>
  <back>
    <ref-list>
      <ref id="ridm1843161996">
        <label>1.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Bogale</surname>
            <given-names>M</given-names>
          </name>
          <article-title>DiverseFusariumsolaniisolates colonize agricultural environments in Ethiopia. European journal of plant pathology</article-title>
          <date>
            <year>2009</year>
          </date>
          <volume>124</volume>
          <issue>3</issue>
          <fpage>369</fpage>
          <lpage>378</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843165092">
        <label>2.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>A</surname>
            <given-names>Y Rossman</given-names>
          </name>
          <article-title>Genera in Bionectriaceae, Hypocreaceae, and Nectriaceae (Hypocreales) proposed for acceptance or rejection</article-title>
          <date>
            <year>2013</year>
          </date>
          <source>IMA fungus</source>
          <volume>4</volume>
          <issue>1</issue>
          <fpage>41</fpage>
          <lpage>51</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843178316">
        <label>3.</label>
        <mixed-citation xlink:type="simple" publication-type="book">
          <name>
            <surname>Singh</surname>
            <given-names>R</given-names>
          </name>
          <name>
            <surname>Singh</surname>
            <given-names>U</given-names>
          </name>
          <name>
            <surname>Kohmoto</surname>
            <given-names>K</given-names>
          </name>
          <article-title>Pathogenesis and host specificity in plant diseases</article-title>
          <date>
            <year>1995</year>
          </date>
          <chapter-title>Vol. III. Viruses &amp;viroids, Elsevier Science</chapter-title>
          <publisher-loc>Oxford, UK</publisher-loc>
        </mixed-citation>
      </ref>
      <ref id="ridm1843263612">
        <label>4.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>R</surname>
            <given-names>El Haddadi</given-names>
          </name>
          <article-title>First report of Fusariumsolani causing damping-off disease on Tetraclinisarticulata seedlings</article-title>
          <date>
            <year>2019</year>
          </date>
          <source>Plant Cell Biotechnology and Molecular Biology</source>
          <volume>20</volume>
          <issue>23</issue>
          <fpage>1106</fpage>
          <lpage>1114</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843021004">
        <label>5.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Amira</surname>
            <given-names>M</given-names>
          </name>
          <article-title>Assessment of antifungal activity ofRumexvesicariusL. andZiziphusspina-christi(L.) Willd Extracts against two phytopathogenic fungi</article-title>
          <date>
            <year>2011</year>
          </date>
          <source>African Journal of Microbiology Research</source>
          <volume>5</volume>
          <fpage>1001</fpage>
          <lpage>11</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843027340">
        <label>6.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Hawthorne</surname>
            <given-names>B</given-names>
          </name>
          <name>
            <surname>Rees-George</surname>
            <given-names>J</given-names>
          </name>
          <name>
            <surname>Broadhurst</surname>
            <given-names>P</given-names>
          </name>
          <article-title>Mating behaviour and pathogenicity of New Zealand isolates ofNectriahaematococca(Fusariumsolani)</article-title>
          <date>
            <year>1992</year>
          </date>
          <source>New Zealand Journal of Crop and Horticultural Science</source>
          <volume>20</volume>
          <issue>1</issue>
          <fpage>51</fpage>
          <lpage>57</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843014276">
        <label>7.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>H</surname>
            <given-names>D VanEtten</given-names>
          </name>
          <article-title>Identification of additional habitats of Nectriahaematococca mating population VI</article-title>
          <date>
            <year>1978</year>
          </date>
          <source>Phytopathology</source>
          <volume>68</volume>
          <fpage>1552</fpage>
          <lpage>1556</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843011684">
        <label>8.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Li</surname>
            <given-names>D</given-names>
          </name>
          <article-title>TheFusariumsolanigene encoding kievitone hydratase, a secreted enzyme that catalyzes detoxification of a bean phytoalexin. Molecular Plant Microbe Interactions</article-title>
          <date>
            <year>1995</year>
          </date>
          <volume>8</volume>
          <issue>3</issue>
          <fpage>388</fpage>
          <lpage>397</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843016148">
        <label>9.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>R</surname>
            <given-names>S Yadav</given-names>
          </name>
          <article-title>Effect of different cultural condition on the growth ofFusariummoniliformecausing bakanae disease</article-title>
          <date>
            <year>2014</year>
          </date>
          <source>European Journal of Molecular Biotechnology</source>
          <volume>2</volume>
          <fpage>95</fpage>
          <lpage>100</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842999484">
        <label>10.</label>
        <mixed-citation xlink:type="simple" publication-type="book">
          <name>
            <surname>Patel</surname>
            <given-names>P</given-names>
          </name>
          <chapter-title>(2019)FusariumsolaniA New Pathogen that Causes Stem Rot of Sugarcane in South Gujarat, India. National Academy Science Letters:</chapter-title>
          <fpage>1</fpage>
          <lpage>4</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843006540">
        <label>11.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>S</surname>
            <given-names>W Kim</given-names>
          </name>
          <article-title>Optimization of submerged culture process for the production of mycelial biomass and exo‐polysaccharides byCordycepsmilitarisC738</article-title>
          <date>
            <year>2003</year>
          </date>
          <source>Journal of applied microbiology</source>
          <volume>94</volume>
          <issue>1</issue>
          <fpage>120</fpage>
          <lpage>126</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843001212">
        <label>12.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Arunakumara</surname>
            <given-names>K</given-names>
          </name>
          <name>
            <surname>Satyanarayana</surname>
            <given-names>C</given-names>
          </name>
          <article-title>Impact of abiotic and nutritional factors on growth ofFusariumsolanicausing root rot of okra</article-title>
          <date>
            <year>2017</year>
          </date>
          <source>The Journal of Rural and Agricultural Research</source>
          <volume>17</volume>
          <issue>2</issue>
          <fpage>74</fpage>
          <lpage>77</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842963532">
        <label>13.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Khan</surname>
            <given-names>I</given-names>
          </name>
          <article-title>Effect of different media and environmental conditions on the growth ofFusariumoxysporumf. sp. ciceri causingFusariumwilt of chickpea</article-title>
          <date>
            <year>2011</year>
          </date>
          <source>Int. J. Sci. Nature</source>
          <volume>2</volume>
          <issue>2</issue>
          <fpage>402</fpage>
          <lpage>404</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842959788">
        <label>14.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Ramteke</surname>
            <given-names>P</given-names>
          </name>
          <name>
            <surname>Kamble</surname>
            <given-names>S</given-names>
          </name>
          <article-title>Physiological studies inFusariumsolanicausing rhizome rot of ginger (ZingiberofficinaleRosc.)</article-title>
          <date>
            <year>2011</year>
          </date>
          <source>The Bioscan</source>
          <volume>6</volume>
          <issue>2</issue>
          <fpage>195</fpage>
          <lpage>197</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842956116">
        <label>15.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>V</surname>
            <given-names>K Ravat</given-names>
          </name>
          <name>
            <surname>Basu</surname>
            <given-names>A</given-names>
          </name>
          <article-title>Supplement of carbon and nitrogen nutrition towards assessment of biomass and virulence of rice fungal pathogen and endophytes</article-title>
          <date>
            <year>2019</year>
          </date>
          <source>Journal of Pharmacognosy and Phytochemistry</source>
          <volume>8</volume>
          <issue>2</issue>
          <fpage>285</fpage>
          <lpage>295</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842968284">
        <label>16.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Irzykowska</surname>
            <given-names>L</given-names>
          </name>
          <article-title>Genetic variation ofFusariumoxysporumisolates forming fumonisin B 1 and moniliformin</article-title>
          <date>
            <year>2012</year>
          </date>
          <source>Journal of applied genetics</source>
          <volume>53</volume>
          <issue>2</issue>
          <fpage>237</fpage>
          <lpage>247</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842966124">
        <label>17.</label>
        <mixed-citation xlink:type="simple" publication-type="book">
          <name>
            <surname>Benaouali</surname>
            <given-names>H</given-names>
          </name>
          <article-title>Isolation, pathogenicity test and physicochemical studies ofFusariumoxysporumf</article-title>
          <date>
            <year>2014</year>
          </date>
          <chapter-title>spradicislycopersici. Advances in Environmental Biology</chapter-title>
          <volume>8</volume>
          <issue>10</issue>
          <fpage>36</fpage>
          <lpage>49</lpage>
        </mixed-citation>
      </ref>
    </ref-list>
  </back>
</article>
