<?xml version="1.0" encoding="UTF-8"?><article>
  <article-id pub-id-type="internal">13982</article-id>
  <article-id pub-id-type="doi">10.30848/PJB2026-7(19)</article-id>
  <article-title>&lt;p&gt;
	Biocontrol efficacy of &lt;em&gt;Bacillus marisflavi&lt;/em&gt; XJ-04 against watermelon sclerotiniose caused by &lt;em&gt;Sclerotinia sclerotiorum&lt;/em&gt;&lt;/p&gt;
</article-title>
  <contrib-group><contrib><name><string>Lingyue Zhu and Xiaomei Wang</string></name></contrib></contrib-group>
  <abstract>&lt;p style=&quot;text-align: justify;&quot;&gt;
	Watermelon sclerotiniose has become increasingly severe under conditions of expanded cultivation and continuous cropping. This study aimed to isolate the causal pathogen and evaluate a rhizosphere-derived bacterial antagonist for biological control. Strain LY24, isolated from diseased watermelon stems and vines, was identified as &lt;em&gt;S. sclerotiorum&lt;/em&gt; (Lib.) de Bary, through morphological and molecular analyses. Strain LY24 exhibited optimal growth under the following conditions: mannitol as the carbon source, tryptone as the nitrogen source, supplementation of NaCl, pH 9, a temperature of 25&amp;deg;C, and complete darkness. Forty rhizosphere soil samples were collected from watermelon-growing areas in Changchun (including Jiutai District), yielding 300 bacterial isolates. These isolates were screened using a dual-culture (plate confrontation) assay. Strain XJ-04 exhibited strong antagonism against &lt;em&gt;S. sclerotiorum,&lt;/em&gt; with a 5.21 mm inhibition zone and a 70.12% inhibition rate. Based on morphological and molecular evidence, combined with Gram staining and standard biochemical tests, strain XJ-04 was identified as &lt;em&gt;B. marisflavi&lt;/em&gt;. The fermentation medium was optimized using an orthogonal design combined with response surface methodology. The optimal formulation (sucrose 21.08 g/L, fine bran 9.17 g/L, K₂HPO₄&amp;middot;3H₂O 9.77 g/L, pH 9) increased the inhibition rate to 77.78%, compared to 71.75% before optimization. The optimal fermentation conditions were 100 mL working volume, 30&amp;deg;C, and a 3-day incubation period. The fermentation broth demonstrated stable antifungal activity after treatments involving temperature, pH, storage time, and light conditions. These results indicated that &lt;em&gt;B. marisflavi&lt;/em&gt; XJ-04 may be a promising biocontrol candidate for watermelon sclerotiniose&lt;/p&gt;
</abstract>
  <publication-status>Published</publication-status>
  <year>2026</year>
  <volume>58</volume>
  <issue>7</issue>
  <pages-from>1539</pages-from>
  <pages-to>1556</pages-to>
</article>
