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<article xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="1.3" article-type="research-article" xml:lang="en"><front><journal-meta><journal-id journal-id-type="issn">1907-770X</journal-id><journal-title-group><journal-title> BIOTROPIA</journal-title><abbrev-journal-title>BIOTROPIA</abbrev-journal-title></journal-title-group><issn pub-type="epub">1907-770X</issn><issn pub-type="ppub">0215-6334</issn><publisher><publisher-name>SEAMEO BIOTROP</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.11598/btb.2025.32.2.2448</article-id><article-categories/><title-group><article-title>THE EFFICACY OF BACTERIAL AND FUNGAL ANTAGONIST SUSPENSIONS IN CONTROLLING FOLIAR MILDEW DISEASE IN ZUCCHINI PLANTS</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ramona</surname><given-names>Yan</given-names></name><address><country>Indonesia</country><email>yanramonaunud@gmail.com</email></address><xref ref-type="aff" rid="AFF-1"/><xref ref-type="corresp" rid="cor-0"/></contrib><contrib contrib-type="author"><name><surname>Line</surname><given-names>Martin A.</given-names></name><address><country>Australia</country></address><xref ref-type="aff" rid="AFF-2"/></contrib><contrib contrib-type="author"><name><surname>Septiari</surname><given-names>I Gusti Ayu Agung</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Darmayasa</surname><given-names>Ida Bagus Gede</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Dwipayana</surname><given-names>I Dewa Agung Panji</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-1"/></contrib><contrib contrib-type="author"><name><surname>Shetty</surname><given-names>Kalidas</given-names></name><address><country>United States</country></address><xref ref-type="aff" rid="AFF-3"/></contrib></contrib-group><contrib-group><contrib contrib-type="editor"><name><surname>Cahya</surname><given-names>Haritz</given-names></name></contrib><contrib contrib-type="editor"><name><surname>Soerianegara</surname><given-names>Ms. Sri I.</given-names></name><address><country>Indonesia</country></address></contrib><contrib contrib-type="editor"><name><surname>Rosita</surname><given-names>Risa</given-names></name><address><country>Indonesia</country></address></contrib></contrib-group><aff id="AFF-1"><institution content-type="dept">Department of Biology, Faculty of Mathematics and Natural Sciences</institution><institution-wrap><institution>Udayana University</institution><institution-id institution-id-type="ror">https://ror.org/035qsg823</institution-id></institution-wrap><addr-line>Badung 80361, Bali</addr-line><country country="ID">Indonesia</country></aff><aff id="AFF-2">School of Agricultural Sciences, Faculty of Sciences and Engineering, Tasmania University, Dynnyrne TAS 7005, Australia</aff><aff id="AFF-3"><institution content-type="dept">Department of Microbiology</institution><institution-wrap><institution>North Dakota State University</institution><institution-id institution-id-type="ror">https://ror.org/05h1bnb22</institution-id></institution-wrap><addr-line>Fargo, ND 58105</addr-line><country>USA</country></aff><author-notes><corresp id="cor-0"><bold>Corresponding author: Yan Ramona</bold>, Department of Biology, Faculty of Mathematics and Natural Sciences, Udayana University, Badung 80361, Bali, Indonesia .Email:<email>yanramonaunud@gmail.com</email></corresp></author-notes><pub-date date-type="pub" iso-8601-date="2025-8-28" publication-format="electronic"><day>28</day><month>8</month><year>2025</year></pub-date><pub-date date-type="collection" iso-8601-date="2025-8-28" publication-format="electronic"><day>28</day><month>8</month><year>2025</year></pub-date><volume>32</volume><issue>2</issue><fpage>162</fpage><lpage>170</lpage><history><date date-type="received" iso-8601-date="2025-2-6"><day>6</day><month>2</month><year>2025</year></date><date date-type="rev-recd" iso-8601-date="2025-5-20"><day>20</day><month>5</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-8-1"><day>1</day><month>8</month><year>2025</year></date></history><permissions><copyright-statement>Copyright (c) 2025 Yan Ramona, Martin, I Gusti Ayu Agung, Ida Bagus Gede Darmayasa, Kalidas Shetty</copyright-statement><copyright-year>2025</copyright-year><copyright-holder>Yan Ramona, Martin, I Gusti Ayu Agung, Ida Bagus Gede Darmayasa, Kalidas Shetty</copyright-holder><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by-nc-nd/4.0/"><ali:license_ref 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In this study, the efficacy of selected bacterial (<italic>Lysobacter antibioticus Bali G, Pseudomonas corrugata</italic> SAJ6) and fungal (<italic>Trichoderma</italic> sp. Td22) antagonists was evaluated for the management of this foliar disease on zucchini plants as an alternative to chemical fungicides. The efficacy of these bacterial and fungal antagonists against a suspected downy mildew pathogen was assessed on zucchini leaves in a glasshouse. It was found that the antagonists provided 22 - 83% protection (P &lt; 0.05) against the pathogen two weeks after application. However, the level of protection declined over time, with 46 - 60% of leaves infected five weeks after pathogen exposure, regardless of treatment. The combination of <italic>Trichoderma</italic> sp. Td22, the most effective agent, with either <italic>Lysobacter antibioticus</italic> Bali <italic>G, Pseudomonas corrugata</italic> SAJ6, or both, was observed to reduce its overall effectiveness. Survival of the biological agents on leaf surfaces was low, although prior research has indicated that survival may not be essential for sustained disease control. Further investigation is required to determine the potential role of these agents in inducing systemic acquired resistance in crops such as grapes and poppies. For commercial application, repeated treatments may be necessary to maintain disease management. Notably, the protection provided by <italic>Trichoderma</italic> sp. Td<sub>22</sub> was found to be comparable to that of chemical treatments, representing a promising step toward more sustainable agricultural practices.</p><sec><title>ARTICLE HIGLIGHTS</title><p><list list-type="bullet"><list-item><p>Diverse microbial antagonists can be used as alternatives to control foliar disease</p></list-item><list-item><p>Microbial agents offer zucchini protection against downy mildew causing microbes</p></list-item><list-item><p>Biocontrol agents effectively control mildew infection in zucchini plants</p></list-item><list-item><p>Diverse microbial antagonists have potential to control foliar disease in zucchini</p></list-item><list-item><p>New bio-based strategy supports sustainable crop disease management</p></list-item><list-item><p>Diverse microbial antagonists are promising for controlling mildew in zucchini</p></list-item></list></p></sec></abstract><kwd-group><kwd>bacterial  antagonists</kwd><kwd>biocontrol</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>File created by JATS Editor</meta-name><meta-value><ext-link ext-link-type="uri" xlink:href="https://jatseditor.com" xlink:title="JATS Editor">JATS Editor</ext-link></meta-value></custom-meta><custom-meta><meta-name>issue-created-year</meta-name><meta-value>2025</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec><title>INTRODUCTION</title><p>Downy mildew is a widespread and economically impactful plant disease that affects various crops, including cucumbers, grapes, cantaloupes, and other cucurbits, across different agricultural regions globally. This disease is caused by obligate fungal-like pathogens, such as <italic>Plasmopara viticola</italic><xref ref-type="bibr" rid="BIBR-16">(Heger et al., 2022)</xref>; <xref ref-type="bibr" rid="BIBR-7">(Clippinger et al., 2024)</xref> and <italic>Pseudoperonospora</italic> <italic>cubensis</italic> <xref ref-type="bibr" rid="BIBR-40">(Wallace et al., 2020)</xref>; <xref ref-type="bibr" rid="BIBR-37">(Sun et al., 2022)</xref>, which predominantly infect green plant tissues, especially the leaves. Typical symptoms include irregular spots on the leaves, which can range from pale green to yellow or brown in color <xref ref-type="bibr" rid="BIBR-23">(Unknown Author, 2019)</xref> <xref ref-type="bibr" rid="BIBR-28">(Purayannur et al., 2021)</xref>. Favorable conditions, including high humidity and moderate temperatures, facilitate rapid disease spread through wind-borne spores or rain splashes, often resulting in large-scale outbreaks.</p><p>In severe cases, downy mildew can lead to defoliation, stunted growth, poor fruit quality, and even total crop failure, making it a critical challenge for growers <xref ref-type="bibr" rid="BIBR-28">(Purayannur et al., 2021)</xref>; <xref ref-type="bibr" rid="BIBR-21">(E et al., 2022)</xref>. As global temperatures and weather patterns shift, the range and frequency of downy mildew outbreaks are projected to increase, emphasizing the need for integrated disease management strategies that combine resistant crop varieties, cultural practices, and sustainable control measures <xref ref-type="bibr" rid="BIBR-34">(Singh et al., 2023)</xref>.</p><p>Globally, downy mildew significantly impacts food security and agricultural output, particularly in areas where susceptible crops are grown extensively. <italic>Plasmopara viticola</italic> for example, continues to challenge grape production in Europe, North America, and Australia, leading to reduced harvests and increased dependency on fungicides <xref ref-type="bibr" rid="BIBR-19">(Koledenkova et al., 2022)</xref>. Similarly, <italic>P. cubensis</italic> is a key limitation for cucurbit farming in Asia, the Americas, and parts of Africa, where recurrent outbreaks cause severe losses to commercial yields <xref ref-type="bibr" rid="BIBR-32">(Salcedo et al., 2020)</xref>.</p><p>Downy mildew, a destructive disease affecting the foliage of many crops, has traditionally been managed using several strategies. These include crop rotation, which interrupts the pathogen’s lifecycle by alternating host availability, and the deployment of resistant plant varieties that utilize genetic traits to fend off infections <xref ref-type="bibr" rid="BIBR-39">(Tör et al., 2023)</xref> <xref ref-type="bibr" rid="BIBR-7">(Clippinger et al., 2024)</xref>. Efficient irrigation practices, such as drip systems and proper drainage, reduce moisture levels conducive to the disease’s growth <xref ref-type="bibr" rid="BIBR-39">(Tör et al., 2023)</xref>; <xref ref-type="bibr" rid="BIBR-7">(Clippinger et al., 2024)</xref>. Chemical fungicides remain a common solution, offering rapid disease suppression during critical periods <xref ref-type="bibr" rid="BIBR-38">(Unknown Author, 2024)</xref>; <xref ref-type="bibr" rid="BIBR-7">(Clippinger et al., 2024)</xref>. However, their frequent use has raised concerns over environmental pollution, public health, and the evolution of fungicide-resistant pathogens <xref ref-type="bibr" rid="BIBR-25">(Ons et al., 2020)</xref>; <xref ref-type="bibr" rid="BIBR-17">(Islam et al., 2024)</xref>.</p><p>Current research underscores the value of integrated disease management (IDM) approaches that combine various practices to achieve effective and sustainable disease control. Studies by <xref ref-type="bibr" rid="BIBR-9">(Corkley et al., 2022)</xref> and <xref ref-type="bibr" rid="BIBR-41">(Wang et al., 2022)</xref> demonstrated the advantages of integrating resistant crop varieties with targeted fungicide applications to manage disease outbreaks. This dual approach, leveraging genetic resistance to reduce pathogen pressure and applying fungicides strategically to mitigate severe infections, minimizes reliance on chemicals while sustaining crop yields. Such strategies align with contemporary goals of reducing the environmental impact of agriculture.</p><p>In growing concerns about fungicide overuse, biological control options are becoming increasingly popular within IDM frameworks <xref ref-type="bibr" rid="BIBR-25">(Ons et al., 2020)</xref>. Compost teas, liquid extracts produced through compost fermentation, represent one promising strategy <xref ref-type="bibr" rid="BIBR-8">(Coker &amp; Ozores-Hampton, 2021)</xref>. These solutions are rich in beneficial microorganisms and bioactive compounds that combat pathogens and enhance plant immunity <xref ref-type="bibr" rid="BIBR-29">(Ramírez-Gottfried et al., 2023)</xref>. They offer a natural and sustainable alternative or complement to synthetic chemicals, integrating seamlessly into environmentally conscious agricultural practices.</p><p>Recent research also highlights the role of specific biocontrol agents, such as <italic>L. antibioticus, P. corrugata,</italic> and <italic>Trichoderma</italic> spp. in managing zucchini diseases such as downy mildew <xref ref-type="bibr" rid="BIBR-3">(Unknown Author, 2023)</xref>. <italic>L. antibioticus</italic> produces antibiotics that suppress <italic>Pseudoperonospora cubensis</italic> <xref ref-type="bibr" rid="BIBR-12">(Unknown Author, 2023)</xref>, the pathogen responsible for downy mildew, while <italic>P. corrugata</italic> inhibits spore germination and disease spread through antagonistic interactions <xref ref-type="bibr" rid="BIBR-30">(Ramona et al., 2020)</xref>. Meanwhile, <italic>Trichoderma</italic> sp. not only protect plants by colonizing root systems but also enhance systemic resistance, making plants more resilient to infections <xref ref-type="bibr" rid="BIBR-6">(Chakraborty et al., 2020)</xref>.</p><p>Combining traditional practices with these innovative biological tools provides a balanced way forward <xref ref-type="bibr" rid="BIBR-7">(Clippinger et al., 2024)</xref>. This integrated approach reduces harmful inputs while addressing key challenges in plant health management, promoting sustainable and resilient agricultural systems.</p><p>The effectiveness of compost teas in managing plant diseases arises primarily from the diversity of their microbial communities, which actively suppress pathogens while supporting plant health <xref ref-type="bibr" rid="BIBR-4">(Barghouth et al., 2023)</xref>. Beneficial microbes, such as <italic>Bacillus</italic> and <italic>Pseudomonas</italic> produce antimicrobial compounds that inhibit pathogen growth, while fungi like <italic>Trichoderma</italic> outcompete pathogens for space and nutrients and form protective root barriers <xref ref-type="bibr" rid="BIBR-36">(Martin CCG et al., 2020)</xref>. Some microorganisms in compost teas also trigger systemic resistance, equipping plants with enhanced defense mechanisms against diverse pathogens <xref ref-type="bibr" rid="BIBR-14">(M et al., 2024)</xref>.</p><p><xref ref-type="bibr" rid="BIBR-33">(Sarmah et al., 2020)</xref> emphasized that enriching compost teas with targeted strains, including <italic>Trichoderma</italic> spp. and <italic>Bacillus</italic> spp., boosts their efficacy against a broader spectrum of diseases. This approach addresses common challenges like variability in compost tea effectiveness, which often results from differences in compost quality and brewing conditions. Introducing well-characterized microbial strains ensures consistency and reliability, enhancing the utility of compost teas in agriculture.</p><p>Beyond their role in disease management, compost teas promote healthier plants by improving soil quality and nutrient availability <xref ref-type="bibr" rid="BIBR-10">(Corato U, 2020)</xref>;<xref ref-type="bibr" rid="BIBR-29">(Ramírez-Gottfried et al., 2023)</xref>. Their microorganisms facilitate the release of essential nutrients like nitrogen and phosphorus, boosting plant growth and vitality <xref ref-type="bibr" rid="BIBR-35">(Singh et al., 2022)</xref>. By combining disease suppression with nutrient enhancement, compost teas serve as a multifunctional tool that aligns with the goals of sustainable agriculture. Leveraging these biological solutions offers a scalable and eco-friendly way to address modern agricultural challenges.</p><p>Based on the above rationale, this research focused on assessing the effectiveness of bacterial suspensions of <italic>Lysobacter antibioticus</italic> Bali G and <italic>Pseudomonas corrugata</italic> SAJ 6 in TSB, as well as a fungal spore suspension of Td<sub>22</sub> in saline, for controlling downy mildew in zucchini plants. The study aimed to offer alternatives to conventional “compost teas” by using selective microbial antagonists as active agents for disease management in important crops, including, zucchini, grapes, and poppies.</p></sec><sec><title>MATERIALS AND METHODS</title><sec><title>Bacterial and Fungal Antagonist Isolates</title><p>Three antagonistic microorganisms, including <italic>Lysobacter antibioticus</italic> Bali G, <italic>Pseudomonas corrugata</italic> SAJ6, and <italic>Trichoderma</italic> sp. Td<sub>22</sub> that effective against Sclerotinia minor in lettuce plants <xref ref-type="bibr" rid="BIBR-31">(Ramona et al., 2022)</xref>, were evaluated in the current study for their potential to manage a foliar mildew disease, downy mildew, in zucchini. The <italic>L. antibioticus</italic> Bali G and <italic>P. corrugata</italic> SAJ6 were obtained from lettuce farms in Bedugul, Bali, Indonesia, whereas the <italic>Trichoderma</italic> sp. Td<sub>22 </sub>was obtained from Dr Dean Metcalf, a senior researcher at Department of Primary Industries, Parks, Water, and Environment (DPIWE) in Tasmania, Australia</p></sec><sec><title>Downy Mildew Isolate</title><p>The pathogen analyzed in this research was obtained from diseased grape leaves sourced from the Horticultural Research Centre (HRC) at the University of Tasmania, Australia. The characteristic leaf damage initially suggested identification as downy mildew. As obligate parasites, downy mildew pathogens necessitate the need for living tissue; therefore, the infected leaves were collected just prior to preparing the pathogen suspension in saline solution.</p></sec><sec><title>Preparation of Antagonist Suspensions</title><p>The bacterial antagonists were grown in a medium containing 0.5% (w/v) trypticase soya broth (OXOID) at 25 °C for 48 hours without agitation, achieving a final concentration of roughly 10⁸ cells/mL. The <italic>Trichoderma</italic> sp. Td<sub>22</sub> spores were obtained from wood fiber waste (WFW) compost, which had previously supported Td<sub>22</sub> cultivation during our previous lettuce or pyrethrum experiments. To extract the spores, the Td<sub>22</sub>-grown WFW compost was agitated to release most spores in a saline solution at a 1 : 10 (w/v) ratio for around 10 minutes before being utilized. The <italic>Trichoderma</italic> sp. Td<sub>22 </sub>spore density obtained was 8.42 ± 0.01 log10 cfu/mL (average of triplicates measurements with an Improved New Bauer Hemacytometer).</p></sec><sec><title>Preparation of the Pathogen Suspension</title><p>Approximately 10 g of infected grape leaves were placed in 200 mL of sterile saline solution (0.85% NaCl) and shaken thoroughly to release the pathogen from the leaves. The mixture was then sieved with a piece of sterile cloth to remove the leaf debris, before being used in the trials. A density of 2.7 x 10<sup>7</sup> propagules/mL were obtained following determination with an Improved New Bauer Hemacytometer.</p></sec><sec><title>Glasshouse Scale Experiments</title><p>Zucchini seeds (‘Blackjack’ Yates<sup>®</sup>) were sown in 1.5 L pots containing a steam-sterilized standard potting mix. After 14 days, the seedlings’ leaves were sprayed with 2 mL of antagonist suspensions. The study included various combinations of antagonists, such as <italic>L. antibioticus</italic> + <italic>P. corrugata, L. antibioticus</italic> + <italic>Trichoderma</italic> sp. Td<sub>22</sub>, <italic>P. corrugata</italic> + <italic>Trichoderma</italic> sp. Td<sub>22</sub>, and a mixture of all three (<italic>L. antibioticus</italic> + <italic>P. corrugata</italic> + <italic>Trichoderma</italic> sp. Td<sub>22</sub>) in equal proportions (v/v). Three days following the antagonist application, a 2 mL suspension of the pathogen was sprayed onto the leaves. Each treatment consisted of five replicate pots, with each pot holding a single 3 weeks old plant or approximately 10 cm in height. Control groups were either sprayed with only the pathogen or with a saline solution lacking both pathogens and antagonists.</p><p>The pots were maintained in a shaded house for eight weeks, with infection levels evaluated at two and five weeks post-pathogen application. To avoid cross-contamination, control pots (A0B0) were positioned separately from those exposed to the pathogen. Infection severity on the leaves was assessed using a 0 - 5 scale, as described by <xref ref-type="bibr" rid="BIBR-22">(Nakasaki et al., 1998)</xref>, where 0 indicated no visible symptoms, 1 represented infection on ≤ 20% of the leaf area, 2 on 21 - 40%, 3 on 41 - 60%, 4 on 61 - 80%, and 5 on 81 - 100%.</p></sec><sec><title>Establishment of the Antagonists on the Zucchini Leaves</title><p>The experiment was completed six weeks after the pathogen inoculation, with efforts made to recover antagonists from randomly chosen healthy leaves. To assess the colonization of bacterial antagonists, 10 g of leaves from each pot were mixed with 90 mL of saline solution and homogenized for 3 - 5 minutes. Colony-forming units (cfu) were quantified using dilution plating on Trypticase Soya Agar (TSA), followed by incubation at 25 °C for 2 - 5 days. The identities of the bacteria were verified by comparing colony characteristics on TSA with those of the original strains</p><p>To evaluate the presence of <italic>Trichoderma</italic> sp.Td<sub>22</sub>, 20 leaf plugs (~3x3 mm) per treatment were aseptically collected and placed on pectin agar medium (MERCK) containing 60 μg/mL tetracycline. These samples were incubated at 25 °C for 4 - 7 days to allow fungal growth. Emerging fungal colonies were isolated and grown on the same medium to compare their morphology with a <italic>Trichoderma</italic> sp. Td<sub>22</sub> stock culture. Observations were extended for one week to monitor conidial development for accurate identification.</p></sec><sec><title>Data Analysis</title><p>The data obtained from this study were analyzed using analysis of variance (ANOVA), which was carried out with the help of Minitab software for Windows. ANOVA enabled the assessment of any significant variations between the treatment groups. To identify specific differences between group means, the least significant difference (LSD) test was employed following the ANOVA procedure. The LSD test is a post-hoc statistical test that compares means to detect significant differences. A significance threshold of P &lt; 0.05 was set to determine whether the differences observed were statistically meaningful, ensuring the results were valid and reliable.</p></sec></sec><sec><title>Results and discussion</title><p>The efficacy of the selected antagonistic fungus and bacteria in preventing zucchini leaves from downy mildew infection, as evaluated by the percentage of infected leaves and the disease severity index is presented in <xref ref-type="fig" rid="figure-1">Figure 1</xref>. The use of antagonists, excluding treatment A<sub>2</sub>B<sub>1</sub> (plants treated with <italic>L. antibioticus</italic> and the pathogen), significantly lowered disease incidence compared to the untreated-pathogen control (A0B<sub>1</sub>) two weeks post-infection (P &lt; 0.05) <xref ref-type="fig" rid="figure-1">Figure 1</xref>.</p><p>The most effective disease suppression was achieved with the fungal antagonist <italic>Trichoderma</italic> sp. Td<sub>22</sub> (A<sub>3</sub>B<sub>1</sub>), providing an 83% reduction in disease (calculated from disease incidence) compared to the control group at two-weeks post-inoculation. However, this effect declined and became statistically insignificant after five weeks. A non-significant synergistic effect (P &gt; 0.05) was noted when <italic>L. antibioticus</italic> and <italic>P. corrugata</italic> were applied in combination (treatment A<sub>4</sub>B<sub>1</sub>), resulting in 57% disease protection (calculated from disease incidence; <xref ref-type="fig" rid="figure-1">Figure 1</xref> A) relative to the untreated-pathogen control. This was higher (higher protection) than when each bacterial antagonist was applied individually (A<sub>1</sub>B<sub>1</sub> or A<sub>2</sub>B<sub>1</sub>; <xref ref-type="fig" rid="figure-1">Figure 1</xref>). When the <italic>Trichoderma</italic> sp. Td<sub>22</sub> was combined with the bacterial antagonists, its effectiveness diminished, possibly due to reduced levels of the primary biocidal compounds on leaf surfaces <xref ref-type="bibr" rid="BIBR-26">(Poromarto et al., 2021)</xref>. Additionally, the lack of synergy between the fungal and bacterial antagonists could be from antagonistic interactions, as dual-culture tests showed inhibition zones produced by both bacteria against <italic>Trichoderma</italic> sp. Td<sub>22</sub> <xref ref-type="fig" rid="figure-2">Figure 2</xref>. In contrast to our findings, <xref ref-type="bibr" rid="BIBR-27">(Poveda &amp; Eugui, 2022)</xref> suggested synergic effect when they were applied in combination in a sustainable agriculture system.</p><fig id="figure-1" ignoredToc=""><label>Figure 1</label><caption><p>The effectiveness of <italic>Lysobacter antibioticus</italic> Bali G, <italic>Pseudomonas corrugata</italic> SAJ6, and Trichoderma sp. Td<sub>22 </sub>to prevent zucchini plants from foliar downy mildew infection in a glasshouse scale experiment</p></caption><p>Notes: A = percentage of infected leaves; B = disease severity index; the assessments were conducted at 2 and 5 weeks after infection; treatments applied: A0B0 = control group (no antagonist or pathogen applied); A0B<sub>1</sub> = control treatment (pathogen only applied); A<sub>1</sub>B<sub>1</sub> = plants treated with <italic>P. corrugata</italic> and pathogen; A<sub>2</sub>B<sub>1</sub> = plants treated with <italic>L. antibioticus</italic> and pathogen; A<sub>3</sub>B<sub>1</sub> = plants treated with Td<sub>22</sub> and pathogen; A<sub>4</sub>B<sub>1</sub> = plants treated with a mixture of <italic>L. antibioticus</italic>, <italic>P. corrugata</italic>, and pathogen; A<sub>5</sub>B<sub>1</sub> = plants treated with a mixture of <italic>L. antibioticus</italic>, Td<sub>22</sub>, and pathogen; A<sub>6</sub>B<sub>1</sub> = plants treated with a mixture of <italic>P. corrugata</italic>, Td<sub>22</sub>, and pathogen; A<sub>7</sub>B<sub>1</sub> = plants treated with a mixture of all three antagonists and pathogen; Each bar represents the mean of disease ± standard error.</p><graphic xlink:href="https://journal.biotrop.org/index.php/biotropia/article/download/2448/version/2939/897/12979/BIOTROPIA-32-2-162-g1.png" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig><fig id="figure-2" ignoredToc=""><label>Figure 2</label><caption><p>In vitro dual culture assays between <italic>L. antibioticus</italic> Bali G and <italic>Trichoderma</italic> sp. Td<sub>22 </sub>(left) and between <italic>P. corrugata</italic> SAJ 6 and <italic>Trichoderma</italic> sp. Td<sub>22</sub> (right) on TSA plates after incubation at 25 °C for three days</p></caption><graphic xlink:href="https://journal.biotrop.org/index.php/biotropia/article/download/2448/version/2939/897/12980/BIOTROPIA-32-2-162-g2.png" mimetype="image" mime-subtype="png"><alt-text>Image</alt-text></graphic></fig><p>An interesting phenomenon was observed in this glasshouse trial where some plants in the control group (no antagonist or pathogen applied or A0B0) showed disease symptom <xref ref-type="fig" rid="figure-1">Figure 1</xref>. This could be due to cross contamination from the infected leaves nearby (plants in pots treated with pathogen). Water splash during irrigation or the blowing wind could be the main cause of this cross contamination.</p><p>The protection shown by the antagonists against downy mildew was no longer significant (P &gt; 0.05) after five weeks. At that time, 60% of the leaves in the untreated control group were infected. The survival rate of the applied antagonists on the leaf surfaces was observed to be low. For instance, <italic>Trichodermasp</italic>. Td<sub>22</sub> was recovered from only two out of 20 leaf samples taken from treatment A<sub>5</sub>B<sub>1</sub> (plants treated with <italic>L. antibioticus, Trichoderma</italic> sp. Td<sub>22</sub>, and the pathogen) five weeks post-application, and it was undetectable in samples from other treatments. Likewise, the bacterial antagonists applied to the leaves were not found (exist) from any treatments after the five-week exposure.</p><p>Applying fungal and bacterial antagonists, either individually or in combination, showed potential for managing foliar diseases, such as downy mildew in zucchini plants. Significant reductions in disease incidence (P &lt; 0.05) were observed two weeks after the pathogen was introduced <xref ref-type="fig" rid="figure-1">Figure 1</xref>. These findings indicate the possibility of modifying compost to develop specialized “compost teas” or cultivating specific biocontrol agents to manage foliar pathogens.</p><p>The application of <italic>Trichoderma</italic> sp. Td<sub>22</sub> yielded the most successful results in our study, particularly when the strain was cultivated in a mixture of wood fiber waste (WFW) compost and millet seed (80 : 20 w/w), as detailed in our previous research <xref ref-type="bibr" rid="BIBR-31">(Ramona et al., 2022)</xref>. The biocontrol agent was stored for approximately 10 months at around 20 °C before being applied in the current study. In efforts to further improve the effectiveness of both fungal and bacterial antagonists, recent research by <xref ref-type="bibr" rid="BIBR-5">(Brost, 2020)</xref> suggested that the addition of chelating agents and detergents may enhance the activity of these biocontrol agents. By incorporating such additives, it may be possible to increase the stability, viability, and overall efficacy of microbial antagonists under various application conditions.</p><p>Previous studies have pointed out the compatibility challenges between bacterial and fungal antagonists, which can significantly influence the success of biocontrol strategies. <xref ref-type="bibr" rid="BIBR-13">(El-Sharkawy et al., 2021)</xref> for example, reported that the combination of <italic>T. harzianum</italic> with <italic>P. fluorescensreduced</italic> the efficacy of the fungus in controlling Aphanomyces euteiches, a root rot pathogen in peas. This finding highlights the importance of understanding microbial interactions, as incompatibility can undermine the individual effectiveness of biocontrol agents. On the other hand, research by <xref ref-type="bibr" rid="BIBR-2">(Amirthalingam et al., 2020)</xref> and <xref ref-type="bibr" rid="BIBR-24">(Ntakirutimana et al., 2024)</xref> showed that using mixed cultures of antagonistic microorganisms often improved disease control. These contrasting outcomes emphasize the need for comprehensive evaluations of compatibility when developing microbial formulations for disease management.</p><p>The broad-spectrum potential of <italic>Trichodermastrains</italic>, such as Td<sub>22</sub>, is particularly significant in this regard. Its ability to combat various fungal pathogens has been consistently demonstrated in several studies, establishing it as a promising biocontrol agent <xref ref-type="bibr" rid="BIBR-1">(Ali et al., 2021)</xref>; <xref ref-type="bibr" rid="BIBR-20">(Kumar et al., 2023)</xref>. In our current study, <italic>Trichoderma</italic> sp. Td<sub>22</sub> achieved an 83% reduction in zucchini downy mildew during a two-week glasshouse trial, offering a level of protection comparable to chemical fungicides. Such results validate its potential as a sustainable alternative to synthetic treatments. However, achieving similar effectiveness in field conditions remains challenging, as environmental factors often necessitate frequent reapplication to maintain the agent’s activity and persistence.Reapplication intervals for biocontrol agents align closely with those recommended for chemical fungicides. <xref ref-type="bibr" rid="BIBR-18">(Jones et al., 2021)</xref> for example, suggested reapplying fungicides every 10 - 14 days to sustain protection against downy mildew. This similarity underscores the practical challenges of deploying biological control agents while highlighting their potential integration into established disease management practices. Optimizing formulations, improving the stability of biocontrol products, and addressing compatibility issues are essential for advancing the reliability and scalability of biological control solutions.Mildew symptoms observed in the nil-pathogen control group (A0B0) after five weeks <xref ref-type="fig" rid="figure-1">Figure 1</xref> were likely caused by natural infection from spores originating in a nearby vineyard with known disease presence or accidental transfer through human activity. Despite this unintended exposure, the infection levels remained minimal compared to those in inoculated plants, ensuring that the overall conclusions of the study were unaffected. This minimal infection demonstrates the robustness of the experimental setup in isolating key variables under investigation.</p><p>The limited persistence of biocontrol agents on leaf surfaces was expected due to several environmental challenges. Factors such as low moisture levels, ultraviolet (UV) radiation from sunlight, and the washing effect of overhead irrigation contributed to the reduced survival of these agents <xref ref-type="bibr" rid="BIBR-11">(Devi, 2024)</xref>. These environmental conditions are well-known to limit the effectiveness of biocontrol organisms in outdoor applications. A thorough review by <xref ref-type="bibr" rid="BIBR-15">(Fedele et al., 2020)</xref> discussed the impacts of environmental stressors, including humidity, temperature variations, and irrigation practices, on the survival and performance of biocontrol agents in field environments. These findings emphasize the need for improved application techniques and protective formulations to enhance the stability and efficacy of biocontrol agents under field conditions.</p></sec><sec><title>Conclusion</title><p>The biological control agents evaluated in this study, with the exception of <italic>L. antibioticus</italic> Bali G, demonstrated significant effectiveness (P &lt; 0.05) in protecting zucchini leaves from downy mildew during the first two weeks of the glasshouse trial. These findings highlighted their potential for managing foliar diseases. It is necessary to maintain protection beyond 14 days by reapplying the biocontrol agents.</p><p>The fungal antagonist <italic>Trichoderma</italic> sp. Td<sub>22</sub> was found to be incompatible with both <italic>L. antibioticus</italic> Bali G and <italic>P. corrugata</italic> SAJ6. In contrast, the combination of <italic>L. antibioticus</italic> Bali G and <italic>P. corrugata</italic> SAJ6 appeared to be compatible but did not significantly enhanced disease control when compared to <italic>P. corrugata</italic> SAJ6 alone. The survival of all three antagonists on zucchini leaf surfaces was notably very low.</p></sec></body><back><ack><title>Acknowledgments</title><p>The   authors   express   their   gratitude   to   the   Ministry   of   Higher   Education,   Research,   and   Technology   of   the   Republic   of   Indonesia   for   partially  funding  this  research.  Appreciation  is  also  extended  to  Dr.  Dean  Metcalf,  the  head  of   Integrated   Laboratory   for   Biosciences   and   Biotechnology, Udayana University, and the School of  Agricultural  Sciences,  Faculty  of  Sciences  and  Engineering,  Tasmania  University  for  providing  the <italic>Trichoderma</italic> isolate,  necessary  consumables,  and  equipment,  respectively,  used  in  this  study.  Our  acknowledgment  should  also  go  to  Prof.  John  Bowman  for  his  assistance  in  the  molecular  identification of our bacterial isolates.</p></ack><ref-list><title>References</title><ref id="BIBR-1"><element-citation publication-type="article-journal"><article-title>A comprehensive note on Trichoderma as a potential biocontrol agent against soil borne fungal pathogens: A review</article-title><source>Plant Prot</source><volume>5</volume><issue>3</issue><person-group person-group-type="author"><name><surname>Ali</surname><given-names>A.</given-names></name><name><surname>Zeshan</surname><given-names>M.A.</given-names></name><name><surname>Mehtab</surname><given-names>M.</given-names></name><name><surname>Khursheed</surname><given-names>S.</given-names></name><name><surname>Mudasir</surname><given-names>M.</given-names></name><name><surname>Abid</surname><given-names>M.</given-names></name><name><surname>Mahdi</surname><given-names>M.</given-names></name><name><surname>Rauf</surname><given-names>H.A.</given-names></name><name><surname>Ameer</surname><given-names>S.</given-names></name><name><surname>Younis</surname><given-names>M.</given-names></name><etal/></person-group><year>2021</year><fpage>171</fpage><lpage>96</lpage><page-range>171-96</page-range><pub-id pub-id-type="doi">10.33804/pp.005.03.3934</pub-id></element-citation></ref><ref id="BIBR-2"><element-citation publication-type="article-journal"><article-title>Evaluation of bioagents for their compatibility in the development of consortium for enhanced efficacy</article-title><source>J Biol Control</source><volume>34</volume><issue>2</issue><person-group person-group-type="author"><name><surname>Amirthalingam</surname><given-names>V.K.</given-names></name><name><surname>Tewari</surname><given-names>A.</given-names></name><name><surname>Sharma</surname><given-names>M.</given-names></name><name><surname>Sharma</surname><given-names>R.</given-names></name><name><surname>J</surname><given-names>Kumar R.</given-names></name></person-group><year>2020</year><fpage>164</fpage><lpage>67</lpage><page-range>164-67</page-range><pub-id pub-id-type="doi">10.18311/jbc/2020/23179</pub-id></element-citation></ref><ref id="BIBR-3"><element-citation publication-type="article-journal"><article-title>Bacterial and fungal biocontrol agents for plant disease protection: journey from lab to field, current status, challenges, and global perspectives</article-title><source>Molecules</source><volume>28</volume><issue>18</issue><year>2023</year><pub-id pub-id-type="doi">10.3390/molecules28186735</pub-id></element-citation></ref><ref id="BIBR-4"><element-citation publication-type="article-journal"><article-title>Microbial compost tea properties affect suppression of strawberry grey mould (Botrytis cinerea Pers</article-title><source>Biocontrol Sci Technol</source><volume>33</volume><issue>1</issue><person-group person-group-type="author"><name><surname>Barghouth</surname><given-names>Z.</given-names></name><name><surname>Khazzam</surname><given-names>E.</given-names></name><name><surname>Ramlawi</surname><given-names>S.</given-names></name><name><surname>Wong</surname><given-names>A.</given-names></name><name><surname>Smith</surname><given-names>M.L.</given-names></name><name><surname>Avis</surname><given-names>T.J.</given-names></name></person-group><year>2023</year><fpage>1</fpage><lpage>18</lpage><page-range>1-18</page-range><pub-id pub-id-type="doi">10.1080/09583157.2022.2141688</pub-id></element-citation></ref><ref id="BIBR-5"><element-citation publication-type="thesis"><article-title>Chelation-based enhancement of novel and commercially available antimicrobials against foodborne pathogens</article-title><person-group person-group-type="author"><name><surname>Brost</surname><given-names>A.</given-names></name></person-group><year>2020</year><publisher-name>Iowa State University</publisher-name><publisher-loc>Ames (US</publisher-loc></element-citation></ref><ref id="BIBR-6"><element-citation publication-type="chapter"><article-title>Induced immunity developed by Trichoderma species in plants</article-title><source>Trichoderma: Host Pathogen Interactions and Applications</source><person-group person-group-type="author"><name><surname>Chakraborty</surname><given-names>B.N.</given-names></name><name><surname>Chakraborty</surname><given-names>U.</given-names></name><name><surname>Sunar</surname><given-names>K.</given-names></name></person-group><year>2020</year><fpage>125</fpage><lpage>47</lpage><page-range>125-47</page-range><publisher-name>Springer</publisher-name><publisher-loc>Singapore (SG</publisher-loc><pub-id pub-id-type="doi">10.1007/978-981-15-3321-1_7</pub-id></element-citation></ref><ref id="BIBR-7"><element-citation publication-type="article-journal"><article-title>Traditional and emerging approaches for disease management of Plasmopara viticola, causal agent of downy mildew of grape</article-title><source>Agriculture</source><volume>14</volume><issue>3</issue><person-group person-group-type="author"><name><surname>Clippinger</surname><given-names>J.I.</given-names></name><name><surname>Dobry</surname><given-names>E.P.</given-names></name><name><surname>Laffan</surname><given-names>I.</given-names></name><name><surname>Zorbas</surname><given-names>N.</given-names></name><name><surname>Hed</surname><given-names>B.</given-names></name><name><surname>Campbell</surname><given-names>M.A.</given-names></name></person-group><year>2024</year><pub-id pub-id-type="doi">10.3390/agriculture14030406</pub-id></element-citation></ref><ref id="BIBR-8"><element-citation publication-type="chapter"><article-title>Compost tea foliar disease suppression in horticulture crops</article-title><source>Compost Utilization in Production of Horticultural Crops</source><person-group person-group-type="author"><name><surname>Coker</surname><given-names>C.S.</given-names></name><name><surname>Ozores-Hampton</surname><given-names>M.</given-names></name></person-group><year>2021</year><fpage>123</fpage><lpage>34</lpage><page-range>123-34</page-range><publisher-name>CRC Press</publisher-name><publisher-loc>Boca Raton (US</publisher-loc><pub-id pub-id-type="doi">10.1201/9781003140412-11</pub-id></element-citation></ref><ref id="BIBR-9"><element-citation publication-type="article-journal"><article-title>Fungicide resistance management: Maximizing the effective life of plant protection products</article-title><source>Plant Pathol</source><volume>71</volume><issue>1</issue><person-group person-group-type="author"><name><surname>Corkley</surname><given-names>I.</given-names></name><name><surname>Fraaije</surname><given-names>B.</given-names></name><name><surname>Hawkins</surname><given-names>N.</given-names></name></person-group><year>2022</year><fpage>150</fpage><lpage>69</lpage><page-range>150-69</page-range><pub-id pub-id-type="doi">10.1111/ppa.13467</pub-id></element-citation></ref><ref id="BIBR-10"><element-citation publication-type="article-journal"><article-title>Agricultural waste recycling in horticultural intensive farming systems by on-farm composting and compost-based tea application improves soil quality and plant health: A review under the perspective of a circular economy</article-title><source>Science of the Total Environment</source><volume>738</volume><issue>139840</issue><person-group person-group-type="author"><name><surname>Corato U</surname></name></person-group><year>2020</year><pub-id pub-id-type="doi">10.1016/j.scitotenv.2020.139840</pub-id></element-citation></ref><ref id="BIBR-11"><element-citation publication-type="article-journal"><article-title>Influence of abiotic factors on efficacy of entomopathogenic nematodes</article-title><source>Int J Plant Soil Sci</source><volume>36</volume><issue>3</issue><person-group person-group-type="author"><name><surname>Devi</surname><given-names>G.</given-names></name></person-group><year>2024</year><fpage>283</fpage><lpage>90</lpage><page-range>283-90</page-range><pub-id pub-id-type="doi">10.9734/ijpss/2024/v36i34425</pub-id></element-citation></ref><ref id="BIBR-12"><element-citation publication-type="article-journal"><article-title>Characterization of a disease-suppressive isolate of Lysobacter enzymogenes with broad antagonistic activity against bacterial, oomycetal and fungal pathogens in different crops</article-title><source>Plants</source><volume>12</volume><issue>3</issue><year>2023</year><pub-id pub-id-type="doi">10.3390/plants12030682</pub-id></element-citation></ref><ref id="BIBR-13"><element-citation publication-type="chapter"><article-title>Synergistic effect of growth-promoting microorganisms on bio-control of Fusarium oxysporum f</article-title><source>sp. pisi, growth, yield, physiological and anatomical characteristics of pea plants. Pestic Biochem Physiol 178:104939</source><person-group person-group-type="author"><name><surname>El-Sharkawy</surname><given-names>H.H.A.</given-names></name><name><surname>Abbas</surname><given-names>M.S.</given-names></name><name><surname>Soliman</surname><given-names>A.S.</given-names></name><name><surname>Ibrahim</surname><given-names>S.A.</given-names></name><name><surname>El-Nady</surname><given-names>I.A.I.</given-names></name></person-group><year>2021</year><pub-id pub-id-type="doi">10.1016/j.pestbp.2021.104939</pub-id></element-citation></ref><ref id="BIBR-14"><element-citation publication-type="article-journal"><article-title>Unlocking plant defenses: Harnessing the power of beneficial microorganisms for induced systemic resistance in vegetables – A systematic review</article-title><source>Biol Control</source><volume>188</volume><issue>105428</issue><person-group person-group-type="author"><name><surname>M</surname><given-names>Emannuel Oliveira Vieira</given-names></name><name><surname>V</surname><given-names>Vieira Nunes</given-names></name><name><surname>C</surname><given-names>Costa Calazans</given-names></name><name><surname>R</surname><given-names>Silva-Mann</given-names></name></person-group><year>2024</year><pub-id pub-id-type="doi">10.1016/j.biocontrol.2023.105428</pub-id></element-citation></ref><ref id="BIBR-15"><element-citation publication-type="chapter"><article-title>Influence of environment on the biocontrol of Botrytis cinerea: A systematic literature review</article-title><source>How Research Can Stimulate the Development of Commercial Biological Control Against Plant Diseases</source><person-group person-group-type="author"><name><surname>Fedele</surname><given-names>G.</given-names></name><name><surname>González-Domínguez</surname><given-names>E.</given-names></name><name><surname>Rossi</surname><given-names>V.</given-names></name></person-group><year>2020</year><fpage>61</fpage><lpage>82</lpage><page-range>61-82</page-range><publisher-name>Springer Cham</publisher-name><publisher-loc>Cham (CH</publisher-loc><pub-id pub-id-type="doi">10.1007/978-3-030-53238-3_5</pub-id></element-citation></ref><ref id="BIBR-16"><element-citation publication-type="article-journal"><article-title>Advances in molecular and optical detection strategies for grape downy mildew</article-title><source>BIO Web Conf</source><volume>50</volume><issue>01005</issue><person-group person-group-type="author"><name><surname>Heger</surname><given-names>L.</given-names></name><name><surname>Martin</surname><given-names>F.</given-names></name><name><surname>Sharma</surname><given-names>N.</given-names></name><name><surname>Miles</surname><given-names>T.D.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.1051/bioconf/20225001005</pub-id></element-citation></ref><ref id="BIBR-17"><element-citation publication-type="article-journal"><article-title>Resistance mechanisms of plant pathogenic fungi to fungicide, environmental impacts of fungicides, and sustainable solutions</article-title><source>Plants</source><volume>13</volume><issue>19</issue><person-group person-group-type="author"><name><surname>Islam</surname><given-names>T.</given-names></name><name><surname>Danishuddin</surname><given-names>Tamanna</given-names></name><name><surname>NT</surname><given-names>Matin</given-names></name><name><surname>MN</surname><given-names>Barai</given-names></name><name><surname>HR</surname><given-names>Haque</given-names></name><name name-style="given-only"><given-names>M.A.</given-names></name></person-group><year>2024</year><pub-id pub-id-type="doi">10.3390/plants13192737</pub-id></element-citation></ref><ref id="BIBR-18"><element-citation publication-type="article-journal"><article-title>Efficacy of fungicides for Pseudoperonospora cubensis determined using bioassays over multiple years in the Mid-Atlantic and Northeastern United States</article-title><source>Plant Health Prog</source><volume>22</volume><issue>3</issue><person-group person-group-type="author"><name><surname>Jones</surname><given-names>J.G.</given-names></name><name><surname>Everts</surname><given-names>K.L.</given-names></name><name><surname>McGrath</surname><given-names>M.T.</given-names></name><name><surname>Gugino</surname><given-names>B.K.</given-names></name></person-group><year>2021</year><fpage>355</fpage><lpage>61</lpage><page-range>355-61</page-range><pub-id pub-id-type="doi">10.1094/PHP-10-20-0086-FI</pub-id></element-citation></ref><ref id="BIBR-19"><element-citation publication-type="chapter"><article-title>Plasmopara viticola the causal agent of downy mildew of grapevine: From its taxonomy to disease management</article-title><source>Front Microbiol 13</source><person-group person-group-type="author"><name><surname>Koledenkova</surname><given-names>K.</given-names></name><name><surname>Esmaeel</surname><given-names>Q.</given-names></name><name><surname>Jacquard</surname><given-names>C.</given-names></name><name><surname>Nowak</surname><given-names>J.</given-names></name><name><surname>Clément</surname><given-names>C.</given-names></name><name><surname>Ait Barka</surname><given-names>E.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.3389/fmicb.2022.889472</pub-id></element-citation></ref><ref id="BIBR-20"><element-citation publication-type="article-journal"><article-title>Journey of Trichoderma from pilot scale to mass production: A review</article-title><source>Agriculture</source><volume>13</volume><issue>10</issue><person-group person-group-type="author"><name><surname>Kumar</surname><given-names>V.</given-names></name><name><surname>Koul</surname><given-names>B.</given-names></name><name><surname>Taak</surname><given-names>P.</given-names></name><name><surname>Yadav</surname><given-names>D.</given-names></name><name><surname>Song</surname><given-names>M.</given-names></name></person-group><year>2023</year><pub-id pub-id-type="doi">10.3390/agriculture13102022</pub-id></element-citation></ref><ref id="BIBR-21"><element-citation publication-type="article-journal"><article-title>Screening for adaptation to resistant grapevine accessions in Plasmopara viticola population of north-eastern Italy</article-title><source>BIO Web Conf</source><volume>50</volume><issue>02007</issue><person-group person-group-type="author"><name><surname>E</surname><given-names>Marone Fassolo</given-names></name><name><surname>G</surname><given-names>Maddalena</given-names></name><name><surname>SL</surname><given-names>Toffolatti</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.1051/bioconf/20225002007</pub-id></element-citation></ref><ref id="BIBR-22"><element-citation publication-type="article-journal"><article-title>A new operation for producing disease-suppressive compost from grass clippings</article-title><source>Appl Environ Microbiol</source><volume>64</volume><issue>10</issue><person-group person-group-type="author"><name><surname>Nakasaki</surname><given-names>K.</given-names></name><name><surname>Hiraoka</surname><given-names>S.</given-names></name><name><surname>Nagata</surname><given-names>H.</given-names></name></person-group><year>1998</year><fpage>4015</fpage><lpage>20</lpage><page-range>4015-20</page-range><pub-id pub-id-type="doi">10.1128/AEM.64.10.4015-4020.1998</pub-id></element-citation></ref><ref id="BIBR-23"><element-citation publication-type="article-journal"><article-title>Management of cucurbit downy mildew in Florida</article-title><source>EDIS</source><volume>2019</volume><issue>4</issue><year>2019</year><pub-id pub-id-type="doi">10.32473/edis-pp325-2019</pub-id></element-citation></ref><ref id="BIBR-24"><element-citation publication-type="article-journal"><article-title>Multiple-strain biological control agents and their impact on soil borne plant diseases</article-title><source>Int J Res Agron</source><volume>7</volume><issue>4</issue><person-group person-group-type="author"><name><surname>Ntakirutimana</surname><given-names>R.</given-names></name><name><surname>Ishimwe</surname><given-names>J.</given-names></name><name><surname>Ukobukeye</surname><given-names>J.</given-names></name></person-group><year>2024</year><fpage>577</fpage><lpage>83</lpage><page-range>577-83</page-range><pub-id pub-id-type="doi">10.33545/2618060X.2024.v7.i4h.607</pub-id></element-citation></ref><ref id="BIBR-25"><element-citation publication-type="article-journal"><article-title>Combining biocontrol agents with chemical fungicides for integrated plant fungal disease control</article-title><source>Microorganisms</source><volume>8</volume><issue>12</issue><person-group person-group-type="author"><name><surname>Ons</surname><given-names>L.</given-names></name><name><surname>Bylemans</surname><given-names>D.</given-names></name><name><surname>Thevissen</surname><given-names>K.</given-names></name><name><surname>Cammue</surname><given-names>B.P.A.</given-names></name></person-group><year>2020</year><pub-id pub-id-type="doi">10.3390/microorganisms8121930</pub-id></element-citation></ref><ref id="BIBR-26"><element-citation publication-type="paper-conference"><article-title>Trichoderma and Bacillus as combined biocontrol agent of moler disease on shallots</article-title><source>Proceedings of the International Seminar on Promoting Local Resources for Sustainable Agriculture and Development (ISPLRSAD 2020</source><volume>13</volume><person-group person-group-type="author"><name><surname>Poromarto</surname><given-names>S.H.</given-names></name><name><surname>Supyani</surname><given-names>Supriyadi</given-names></name><name><surname>Indriani</surname><given-names>S.A.</given-names></name><name name-style="given-only"><given-names>Hadiwiyono</given-names></name></person-group><year>2021</year><pub-id pub-id-type="doi">10.2991/absr.k.210609.016</pub-id></element-citation></ref><ref id="BIBR-27"><element-citation publication-type="article-journal"><article-title>Combined use of Trichoderma and beneficial bacteria (mainly Bacillus and Pseudomonas): Development of microbial synergistic bio-inoculants in sustainable agriculture</article-title><source>Biol Control</source><volume>176</volume><issue>105100</issue><person-group person-group-type="author"><name><surname>Poveda</surname><given-names>J.</given-names></name><name><surname>Eugui</surname><given-names>D.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.1016/j.biocontrol.2022.105100</pub-id></element-citation></ref><ref id="BIBR-28"><element-citation publication-type="article-journal"><article-title>The hop downy mildew pathogen Pseudoperonospora humuli</article-title><source>Mol Plant Pathol</source><volume>22</volume><issue>7</issue><person-group person-group-type="author"><name><surname>Purayannur</surname><given-names>S.</given-names></name><name><surname>Gent</surname><given-names>D.H.</given-names></name><name><surname>Miles</surname><given-names>T.D.</given-names></name><name><surname>Radišek</surname><given-names>S.</given-names></name><name><surname>Quesada‐Ocampo</surname><given-names>L.M.</given-names></name></person-group><year>2021</year><fpage>755</fpage><lpage>68</lpage><page-range>755-68</page-range><pub-id pub-id-type="doi">10.1111/mpp.13063</pub-id></element-citation></ref><ref id="BIBR-29"><element-citation publication-type="article-journal"><article-title>Compost tea as organic fertilizer and plant disease control: Bibliometric analysis</article-title><source>Agronomy</source><volume>13</volume><issue>9</issue><person-group person-group-type="author"><name><surname>Ramírez-Gottfried</surname><given-names>R.I.</given-names></name><name><surname>Preciado-Rangel</surname><given-names>P.</given-names></name><name><surname>Carrillo</surname><given-names>M.G.</given-names></name><name><surname>García</surname><given-names>A.B.</given-names></name><name><surname>González-Rodríguez</surname><given-names>G.</given-names></name><name><surname>Espinosa-Palomeque</surname><given-names>B.</given-names></name></person-group><year>2023</year><pub-id pub-id-type="doi">10.3390/agronomy13092340</pub-id></element-citation></ref><ref id="BIBR-30"><element-citation publication-type="article-journal"><article-title>Diversity of biocontrol agents, isolated from several sources, inhibitory to several fungal plant pathogens</article-title><source>Biodiversitas</source><volume>22</volume><issue>1</issue><person-group person-group-type="author"><name><surname>Ramona</surname><given-names>Y.</given-names></name><name><surname>Darmayasa</surname><given-names>I.B.G.</given-names></name><name><surname>Kusuma</surname><given-names>A.A.N.N.</given-names></name><name><surname>Line</surname><given-names>M.</given-names></name></person-group><year>2020</year><fpage>298</fpage><lpage>303</lpage><page-range>298-303</page-range><pub-id pub-id-type="doi">10.13057/biodiv/d220136</pub-id></element-citation></ref><ref id="BIBR-31"><element-citation publication-type="article-journal"><article-title>Biological control of Sclerotinia minor attack on pyrethrum plants by Trichoderma harzianum in glasshouse experiment</article-title><source>Biodiversitas</source><volume>23</volume><issue>6</issue><person-group person-group-type="author"><name><surname>Ramona</surname><given-names>Y.</given-names></name><name><surname>Darmayasa</surname><given-names>I.B.G.</given-names></name><name><surname>Line</surname><given-names>M.A.</given-names></name></person-group><year>2022</year><fpage>3264</fpage><lpage>69</lpage><page-range>3264-69</page-range><pub-id pub-id-type="doi">10.13057/biodiv/d230655</pub-id></element-citation></ref><ref id="BIBR-32"><element-citation publication-type="article-journal"><article-title>Diagnostic guide for cucurbit downy mildew</article-title><source>Plant Health Prog</source><volume>21</volume><issue>3</issue><person-group person-group-type="author"><name><surname>Salcedo</surname><given-names>A.</given-names></name><name><surname>Hausbeck</surname><given-names>M.</given-names></name><name><surname>Pigg</surname><given-names>S.</given-names></name><name><surname>Quesada-Ocampo</surname><given-names>L.M.</given-names></name></person-group><year>2020</year><fpage>166</fpage><lpage>72</lpage><page-range>166-72</page-range><pub-id pub-id-type="doi">10.1094/PHP-12-19-0095-DG</pub-id></element-citation></ref><ref id="BIBR-33"><element-citation publication-type="article-journal"><article-title>Microbial biocides - Viable alternatives to chemicals for tea disease management</article-title><source>J Biol Control</source><volume>34</volume><issue>2</issue><person-group person-group-type="author"><name><surname>Sarmah</surname><given-names>S.</given-names></name><name><surname>Bhattacharyya</surname><given-names>P.</given-names></name><name><surname>Barooah</surname><given-names>A.</given-names></name></person-group><year>2020</year><fpage>144</fpage><lpage>52</lpage><page-range>144-52</page-range><pub-id pub-id-type="doi">10.18311/jbc/2020/22689</pub-id></element-citation></ref><ref id="BIBR-34"><element-citation publication-type="article-journal"><article-title>Climate change impacts on plant pathogens, food security and paths forward</article-title><source>Nat Rev Microbiol</source><volume>21</volume><issue>10</issue><person-group person-group-type="author"><name><surname>Singh</surname><given-names>B.K.</given-names></name><name><surname>Delgado-Baquerizo</surname><given-names>M.</given-names></name><name><surname>Egidi</surname><given-names>E.</given-names></name><name><surname>Guirado</surname><given-names>E.</given-names></name><name><surname>Leach</surname><given-names>J.E.</given-names></name><name><surname>Liu</surname><given-names>H.</given-names></name><name><surname>Trivedi</surname><given-names>P.</given-names></name></person-group><year>2023</year><fpage>640</fpage><lpage>56</lpage><page-range>640-56</page-range><pub-id pub-id-type="doi">10.1038/s41579-023-00900-7</pub-id></element-citation></ref><ref id="BIBR-35"><element-citation publication-type="article-journal"><article-title>Microbial enhancement of plant nutrient acquisition</article-title><source>Stress Biology</source><volume>2</volume><issue>1</issue><person-group person-group-type="author"><name><surname>Singh</surname><given-names>S.K.</given-names></name><name><surname>Wu</surname><given-names>X.</given-names></name><name><surname>Shao</surname><given-names>C.</given-names></name><name><surname>Zhang</surname><given-names>H.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.1007/s44154-021-00027-w</pub-id></element-citation></ref><ref id="BIBR-36"><element-citation publication-type="chapter"><article-title>Compost and compost tea microbiology: the “-omics” era</article-title><source>Biology of Composts: Soil biology</source><volume>58</volume><person-group person-group-type="author"><name><surname>Martin CCG</surname></name><name><surname>J</surname><given-names>Rouse-Miller</given-names></name><name><surname>GT</surname><given-names>Barry</given-names></name><name><surname>P</surname><given-names>Vilpigue</given-names></name></person-group><year>2020</year><fpage>3</fpage><lpage>30</lpage><page-range>3-30</page-range><publisher-name>Springer Cham</publisher-name><publisher-loc>Cham (CH</publisher-loc><pub-id pub-id-type="doi">10.1007/978-3-030-39173-7_1</pub-id></element-citation></ref><ref id="BIBR-37"><element-citation publication-type="article-journal"><article-title>Biological control of the cucumber downy mildew pathogen Pseudoperonospora cubensis</article-title><source>Horticulturae</source><volume>8</volume><issue>5</issue><person-group person-group-type="author"><name><surname>Sun</surname><given-names>Z.</given-names></name><name><surname>Yu</surname><given-names>S.</given-names></name><name><surname>Hu</surname><given-names>Y.</given-names></name><name><surname>Wen</surname><given-names>Y.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.3390/horticulturae8050410</pub-id></element-citation></ref><ref id="BIBR-38"><element-citation publication-type="article-journal"><article-title>The management of grapevine downy mildew: From anti-resistance strategies to innovative approaches for fungicide resistance monitoring</article-title><source>J Plant Dis Prot</source><volume>131</volume><issue>4</issue><year>2024</year><fpage>1225</fpage><lpage>32</lpage><page-range>1225-32</page-range><pub-id pub-id-type="doi">10.1007/s41348-024-00867-4</pub-id></element-citation></ref><ref id="BIBR-39"><element-citation publication-type="article-journal"><article-title>Recent developments in plant-downy mildew interactions</article-title><source>Semin Cell Dev Biol</source><volume>149</volume><person-group person-group-type="author"><name><surname>Tör</surname><given-names>M.</given-names></name><name><surname>Wood</surname><given-names>T.</given-names></name><name><surname>Webb</surname><given-names>A.</given-names></name><name><surname>Göl</surname><given-names>D.</given-names></name><name><surname>McDowell</surname><given-names>J.M.</given-names></name></person-group><year>2023</year><fpage>42</fpage><lpage>50</lpage><page-range>42-50</page-range><pub-id pub-id-type="doi">10.1016/j.semcdb.2023.01.010</pub-id></element-citation></ref><ref id="BIBR-40"><element-citation publication-type="article-journal"><article-title>Population analyses reveal two host-adapted clades of Pseudoperonospora cubensis, the causal agent of cucurbit downy mildew, on commercial and wild cucurbits</article-title><source>Phytopathology</source><volume>110</volume><issue>9</issue><person-group person-group-type="author"><name><surname>Wallace</surname><given-names>E.C.</given-names></name><name><surname>D’Arcangelo</surname><given-names>K.N.</given-names></name><name><surname>Quesada-Ocampo</surname><given-names>L.M.</given-names></name></person-group><year>2020</year><fpage>1578</fpage><lpage>87</lpage><page-range>1578-87</page-range><pub-id pub-id-type="doi">10.1094/PHYTO-01-20-0009-R</pub-id></element-citation></ref><ref id="BIBR-41"><element-citation publication-type="chapter"><article-title>The quantitative analyses for the effects of two wheat varieties with different resistance levels on the fungicide control efficacies to powdery mildew</article-title><source>Front Plant Sci 13</source><person-group person-group-type="author"><name><surname>Wang</surname><given-names>A.</given-names></name><name><surname>Zhao</surname><given-names>Y.</given-names></name><name><surname>Zhang</surname><given-names>M.</given-names></name><name><surname>Yuan</surname><given-names>J.</given-names></name><name><surname>Liu</surname><given-names>W.</given-names></name><name><surname>Fan</surname><given-names>J.</given-names></name><name><surname>Hu</surname><given-names>X.</given-names></name><name><surname>Zhou</surname><given-names>Y.</given-names></name></person-group><year>2022</year><pub-id pub-id-type="doi">10.3389/fpls.2022.864192</pub-id></element-citation></ref></ref-list></back></article>
