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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Sustain. Food Syst.</journal-id>
<journal-title>Frontiers in Sustainable Food Systems</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Sustain. Food Syst.</abbrev-journal-title>
<issn pub-type="epub">2571-581X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-meta>
<article-id pub-id-type="doi">10.3389/fsufs.2025.1597039</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Sustainable Food Systems</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Artificial intelligence tool for cassava viral diseases diagnosis using participatory surveillance in Burkina Faso</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Sawadogo</surname>
<given-names>Seydou</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Tiendrebeogo</surname>
<given-names>Fid&#x00E8;le</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Tibiri</surname>
<given-names>Ezechiel B.</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Name</surname>
<given-names>Pakyendou E.</given-names>
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<contrib contrib-type="author">
<name>
<surname>Djigma</surname>
<given-names>Florencia</given-names>
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<surname>Traor&#x00E9;</surname>
<given-names>Lassina</given-names>
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<surname>Pita</surname>
<given-names>Justin S.</given-names>
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<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author">
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<surname>Eni</surname>
<given-names>Angela O.</given-names>
</name>
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<aff id="aff1"><sup>1</sup><institution>Laboratoire de Virologie et de Biotechnologies V&#x00E9;g&#x00E9;tales, Institut de l&#x2019;Environnement et de Recherches Agricoles (INERA)</institution>, <addr-line>Ouagadougou</addr-line>, <country>Burkina Faso</country></aff>
<aff id="aff2"><sup>2</sup><institution>Laboratoire de Biologie Mol&#x00E9;culaire et de G&#x00E9;n&#x00E9;tique (LABIOGENE), Universit&#x00E9; Joseph Ki-Zerbo</institution>, <addr-line>Ouagadougou</addr-line>, <country>Burkina Faso</country></aff>
<aff id="aff3"><sup>3</sup><institution>Central and West African Virus Epidemiology (WAVE), P&#x00F4;le Scientifique et d&#x2019;Innovation de Bingerville, Universit&#x00E9; F&#x00E9;lix Houphou&#x00EB;t-Boigny (UFHB)</institution>, <addr-line>Bingerville</addr-line>, <country>C&#x00F4;te d'Ivoire</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/517618/overview">Duraisamy Saravanakumar</ext-link>, The University of the West Indies St. Augustine, Trinidad and Tobago</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1598332/overview">Mir Muhammad Nizamani</ext-link>, Shantou University, China</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1872069/overview">Sibghat Ullah Bazai</ext-link>, Balochistan University of Information Technology, Engineering and Management Sciences, Pakistan</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Fid&#x00E8;le Tiendrebeogo, <email>fidele.tiendrebeogo@wave-center.org</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>02</day>
<month>09</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>9</volume>
<elocation-id>1597039</elocation-id>
<history>
<date date-type="received">
<day>20</day>
<month>03</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>08</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Sawadogo, Tiendrebeogo, Tibiri, Name, Djigma, Traor&#x00E9;, Pita and Eni.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Sawadogo, Tiendrebeogo, Tibiri, Name, Djigma, Traor&#x00E9;, Pita and Eni</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>In the area of plant health, there has been little work using participatory approaches to control emerging infectious diseases such as cassava mosaic disease (CMD) and cassava brown streak disease (CBSD). These diseases cause significant yield losses in Sub-Saharan Africa. The current study provided low cost and early detection method of cassava viral diseases surveillance, based on participatory approaches using an AI tool (Plantvillage nuru app). The study involved farmers, agricultural extension agents (AEA), and cassava diseases diagnosis experts. Farmers were made aware of CMD and CBSD damage through a national campaign, while AEA received training to identify CMD, CBSD, and cassava green mite (CGM) symptoms using an AI-based diagnostic tool. Sixty trained AEA, equipped with smartphones running the AI tool, conducted fields surveillance either through visual inspection or with AI tool. The participation rate of the AEA and the diagnostic accuracy of the AI tool and visual assessments were evaluated and compared to experts perception validated by molecular analysis. Workshops and smartphones allocation enhanced AEA participation rate to 60%, and increased surveyed fields number to 132. CMD detection revealed no significant difference between users of AI tool (<italic>p</italic>-value&#x202F;=&#x202F;0.709) and visual inspection (<italic>p</italic>-value&#x202F;=&#x202F;0.997). The mean scores of CMD detection were 29.83&#x202F;&#x00B1;&#x202F;12.99% for AI tool, 37.12&#x202F;&#x00B1;&#x202F;12.78% for experts, and 36.10&#x202F;&#x00B1;&#x202F;12.74% for molecular analysis among AI tool users. With visual inspection users, the mean scores detection were 46.07&#x202F;&#x00B1;&#x202F;13.00% for AEA and experts perception, and 43.87&#x202F;&#x00B1;&#x202F;12.07% for molecular analysis. The AI tool misdiagnosed 5% of CMD as CBSD, but molecular analysis confirmed it as CMD. The CMD infected fields was 31.06%, with a predominantly <italic>African Cassava Mosaic Virus</italic> (93.33%) detected. The results demonstrated that participatory approaches could be effective in the plant pathogens early management.</p>
</abstract>
<kwd-group>
<kwd>participatory surveillance</kwd>
<kwd>artificial intelligence</kwd>
<kwd>cassava virus diagnosis</kwd>
<kwd>smartphone</kwd>
<kwd>Burkina Faso</kwd>
</kwd-group>
<counts>
<fig-count count="5"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="52"/>
<page-count count="10"/>
<word-count count="7695"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Crop Biology and Sustainability</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>Cassava (<italic>Manihot esculenta</italic> Crantz) is a staple food for approximately 800 million people worldwide, including 500 million in Africa (<xref ref-type="bibr" rid="ref21">Howeler et al., 2013</xref>). Africa accounts for more than half of the global production (<xref ref-type="bibr" rid="ref13">FAOSTAT, 2021</xref>). However, this production faces several diseases, with cassava mosaic disease (CMD) and cassava brown streak disease (CBSD) being the major biotic threats affecting cassava production in Africa (<xref ref-type="bibr" rid="ref28">Legg et al., 2011</xref>). The genus Begomovirus and ipomovirus are reported to be the major viruses responsible for CMD and CBSD in Africa (<xref ref-type="bibr" rid="ref29">Legg et al., 2014</xref>). Yield losses associated with CMD damage reach up to US$ 2 billion annually in Africa (<xref ref-type="bibr" rid="ref36">Patil and Fauquet, 2009</xref>). CMD is therefore a real threat to cassava production and food security. Epidemiological studies have shown that its widespread is due to the ignorance of smallholder farmers, who constantly re-use infected cuttings as planting material (<xref ref-type="bibr" rid="ref46">Soro et al., 2021</xref>), the porosity of borders (<xref ref-type="bibr" rid="ref10">Del&#x00EA;tre et al., 2021</xref>), and the lack of phytosanitary facilities. The lack of diagnostic tools to detect plant viruses at phytosanitary inspection posts has been cited as a reason for cross-border exchange of CMD (<xref ref-type="bibr" rid="ref51">Whattam et al., 2021</xref>). In Burkina Faso and several African countries where CMD is widespread, disease management is based on classical epidemiology with field surveillance and disease diagnosis. These epidemiological efforts are aimed at promoting virus-free cuttings and resistant varieties, and at sensitizing farmers to adopt good agricultural practices through the efforts of the CENTRAL AND WEST AFRICAN VIRUS EPIDEMIOLOGY (WAVE; <ext-link xlink:href="https://wave-center.org/" ext-link-type="uri">https://wave-center.org/</ext-link>) program against transboundary plant pathogens (<xref ref-type="bibr" rid="ref12">Eni et al., 2021</xref>; <xref ref-type="bibr" rid="ref46">Soro et al., 2021</xref>; <xref ref-type="bibr" rid="ref20">Houngue et al., 2022</xref>; <xref ref-type="bibr" rid="ref33">Mouketou et al., 2022</xref>; <xref ref-type="bibr" rid="ref4">Amoakon et al., 2023</xref>). However, classical epidemiological studies are subject to high financial costs, require expertise and considerable time to cover large areas and obtain diagnostic results (<xref ref-type="bibr" rid="ref8">Calba et al., 2015</xref>; <xref ref-type="bibr" rid="ref50">Vluggen et al., 2017</xref>; <xref ref-type="bibr" rid="ref23">Jafar et al., 2024</xref>). Therefore, participatory surveillance approaches have been developed to overcome these constraints in the application of classical epidemiology and formal studies (<xref ref-type="bibr" rid="ref44">Smolinski et al., 2017</xref>).</p>
<p>Participatory surveillance is the use of the bi-directional process of receiving and transmitting of health-related data through community engagement (<xref ref-type="bibr" rid="ref32">McNeil et al., 2022</xref>). Participatory surveillance takes into account the knowledge of local communities and their involvement in disease control efforts (<xref ref-type="bibr" rid="ref9">Catley et al., 2012</xref>). This approach has achieved considerable success in animal and human health through the development of Information and Communication Technology (ICT) tools combined with artificial intelligence applications for disease diagnosis and surveillance (<xref ref-type="bibr" rid="ref26">Karimuribo et al., 2017</xref>; <xref ref-type="bibr" rid="ref15">Fornace et al., 2018</xref>; <xref ref-type="bibr" rid="ref18">Genevi&#x00E8;ve et al., 2019</xref>; <xref ref-type="bibr" rid="ref22">Huang and Loschen, 2019</xref>; <xref ref-type="bibr" rid="ref31">McNeil et al., 2025</xref>). Several AI mobile application such as, AgroScout, CropsAI, Crop Doctor, and Plantix were developed based on convolutional neural networks model for plant diseases symptoms recognition (<xref ref-type="bibr" rid="ref52">Yadav and Yadav, 2025</xref>). In addition to their portability and accessibility on smartphones and ICT tools without the need for an internet connection, they offer the advantages of low-cost and real-time disease diagnosis and monitoring, allowing for the anticipation of alerts and the reduction of the time of the disease spread (<xref ref-type="bibr" rid="ref27">Kizito et al., 2013</xref>; <xref ref-type="bibr" rid="ref17">Gadicherla et al., 2020</xref>; <xref ref-type="bibr" rid="ref19">Hasan and Haque, 2023</xref>). However, in plant health, participatory approaches for monitoring and management of plant pathogens and pests remain underutilized. Nevertheless, several IA-based applications have been designed for the diagnosis, monitoring, and management of plant diseases, with the particularity of being easily usable by farmers and agricultural extension agents (<xref ref-type="bibr" rid="ref16">Fuentes et al., 2017</xref>; <xref ref-type="bibr" rid="ref24">Johannes et al., 2017</xref>; <xref ref-type="bibr" rid="ref41">Ramcharan et al., 2019</xref>). Among these tools, PlantVillage Nuru is one that has been successfully tested in Sub-Saharan Africa (<xref ref-type="bibr" rid="ref34">Mrisho et al., 2020</xref>).</p>
<p>Nuru is a mobile application that can be free downloaded for free from Play Store and operates in real-time without internet (<xref ref-type="bibr" rid="ref34">Mrisho et al., 2020</xref>). The working principle of the AI tool is based on an image recognition system and has been trained to recognize and detect healthy cassava leaves as well as leaves showing typical symptoms of cassava mosaic disease (CMD), cassava brown streak disease (CBSD), damage caused by cassava mites and brown leaf spot (<xref ref-type="bibr" rid="ref40">Ramcharan et al., 2017</xref>, <xref ref-type="bibr" rid="ref41">2019</xref>). WAVE program contributed to Nuru integration as first line diagnosis tool in Central and West Africa. Since this, the tool help farmers and extension agents in CMD early detection in Benin (<xref ref-type="bibr" rid="ref2">Ahoya et al., 2024</xref>), C&#x00F4;te d&#x2019;Ivoire (<xref ref-type="bibr" rid="ref1">Adj&#x00E9;i et al., 2024</xref>) and Sierra Leone (<xref ref-type="bibr" rid="ref42">Saffa et al., 2025</xref>). In East Africa, Nuru using for diseases detection allowed farmers to mitigate crop losses (<xref ref-type="bibr" rid="ref52">Yadav and Yadav, 2025</xref>). In Burkina Faso, cassava viruses diseases management longtime focused on traditional methods engaging only limited personal of researchers for nationals surveillance. Unfortunately, these methods are costly and time consuming, which do not allow early management. Due to financial resources limitations, research personnel and laboratory infrastructures in developing countries, awareness campaigns and trainings with mobile tools engaging farmer and extension agents through participatory epidemiology could enabled early detection and rapid response to disease management (<xref ref-type="bibr" rid="ref11">Dhavale et al., 2025</xref>).</p>
<p>In view of the above and the vegetative propagation nature of cassava, it seems imperative to involve communities at the grassroots level for awareness of viral diseases and also for participatory surveillance and early warning. The era of ICTs is well suited to support the plant health sector by developing the concept of participatory surveillance. ICTs tools such as AI are positioned as tools that can contribute to improve knowledge of viral diseases and reconnect farmers, breeders, phytosanitary offices, extension agents, researchers and political leaders. In this study, participatory approaches were applied to CMD and CBSD surveillance in Burkina Faso. The participation rate of extension agents was assessed. The diagnostic results of the AI tool, visual diagnosis based on extension agents&#x2019; perceptions and experts&#x2019; perception of cassava viral diseases diagnosis in agreement with molecular laboratory analysis were also compared.</p>
</sec>
<sec sec-type="material|methods" id="sec2">
<label>2</label>
<title>Material and methods</title>
<sec id="sec3">
<label>2.1</label>
<title>Participatory surveillance approach implementation</title>
<p>This study involved cassava farmers, extension agents from the Plant Protection Department of the Ministry of Agriculture, Burkina Faso, and cassava viral diseases experts from WAVE program. The stakeholders were structured to three level following a hierarchical flowchart (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The farmers were responsible for recognizing cassava disease symptoms and to reporting fields status to the extension agents. The extension agents were involved in field surveys and collection of cassava leaf samples using the AI tool (Group 1) and visual observations (Group 2). These two groups were established at the beginning of the study after training. The role of the experts was to validate symptoms status of the collected leaves, before running molecular analysis using polymerase chain reaction (PCR). The accuracy of AI diagnosis and visual assessments performed by extension agents were evaluated and compared with experts visual assessments, which were validated by PCR results as a reference.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Stakeholders flowchart for the surveillance.</p>
</caption>
<graphic xlink:href="fsufs-09-1597039-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Flowchart depicting the communication process for cassava disease diagnosis. Level 1: Farmers conduct field diagnosis, data, and samples collection, and provide alerts. Level 2: Agricultural Extension Agents receive data and samples, conduct symptoms validation, lab analysis by PCR, and communicate results. Level 3: Cassava Diseases Diagnosis Experts are involved in data and samples transmission. Arrows indicate the flow of information between levels.</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec4">
<label>2.2</label>
<title>Raising awareness among farmers</title>
<p>Cassava farmers were made aware of the damage caused by CMD and CBSD during a national campaign in April 2022 called &#x201C;Together, Let us save our cassava.&#x201D; The main cassava producing areas were visited and farmers were trained to recognize symptomatic leaves. Flyers with typical CMD and CBSD damage and cassava disease management practices were distributed to farmers. During the campaign, audio and visual spots on CMD and CBSD damage and management advice were recorded and airedon national and private TV and radio stations.</p>
</sec>
<sec id="sec5">
<label>2.3</label>
<title>Training of extension agents</title>
<p>In July 2022, the participatory surveillance started with the training of agricultural extension agents (AEA). Sixty AEA were trained. They were came from the following regions of Burkina Faso: Boucle du Mouhoun (<italic>n</italic>&#x202F;=&#x202F;8), Cascades (<italic>n</italic>&#x202F;=&#x202F;8), Center (<italic>n</italic>&#x202F;=&#x202F;2), Center-Est (<italic>n</italic>&#x202F;=&#x202F;8), Center-Ouest (<italic>n</italic>&#x202F;=&#x202F;6), Center-Sud (<italic>n</italic>&#x202F;=&#x202F;6), Est (<italic>n</italic>&#x202F;=&#x202F;6), Hauts-Bassins (<italic>n</italic>&#x202F;=&#x202F;8) and Sud-Ouest (<italic>n</italic>&#x202F;=&#x202F;8). Apart from the Center region, all the others are known to be cassava producing areas. The training consisted of the recognition of the typical symptoms CMD and CBSD, the use of the AI tool for plant diagnosis and the management of any disease if fields are infected. The use of the AI tool for real-time diagnosis of CMD and CBSD in cassava fields was also described. A practical test was carried out in a cassava field infected with CMD. At the end of the training, a WhatsApp platform was created to support participants and keep them in touch. In July 2023, a monitoring and evaluation workshop was organized to equip the sixty extension agents with smartphones (iTel P17 Pro, camera 5 MP Back).</p>
</sec>
<sec id="sec6">
<label>2.4</label>
<title>Sample collection</title>
<p>The two groups of trained AEA conducted cassava fields surveillance and collected leaf samples. The first group used the AI tool as described previously (<xref ref-type="bibr" rid="ref34">Mrisho et al., 2020</xref>). The second group used visual observation according to their knowledge of the symptoms of CMD, CBSD and CGM. Each group collected leaf samples in paper envelopes and dried them briefly before sending them to the experts. The samples collected were either healthy or suspected to be infected by CMD, CBSD, and CGM symptoms. Information on the region, district, village, collector, sample identity, date of collection and disease were recorded on each envelope. A georeferenced map (<xref ref-type="fig" rid="fig2">Figure 2</xref>), showing the sampling locations was generated using QGIS v 3.6.3-Noosa software. The quality and status of the leaf samples received were checked by experts. The leaf samples were then oven dried at 37 &#x00B0;C for dehydration for 72&#x202F;h and stored at room temperature until nucleic acid extraction.</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>Map of Burkina Faso showing the area of sampling across the regions of the study.</p>
</caption>
<graphic xlink:href="fsufs-09-1597039-g002.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Map of Burkina Faso showing sampling areas, regions, and climatic zones. Yellow highlights indicate sampling areas, while shades of green distinguish Sahelian, Soudanian, and Sudano-Sahelian zones. The map includes a scale and compass. Neighboring countries are labeled.</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec7">
<label>2.5</label>
<title>Molecular detection of casava mosaic begomoviruses and cassava brown streak ipomoviruses</title>
<p>Total DNA and RNA were extracted from cassava dried leaves following the CTAB method (<xref ref-type="bibr" rid="ref37">Permingeat et al., 1998</xref>). The extracted DNA and RNA were eluted in 200&#x202F;&#x03BC;L nuclease-free water and their quality checked using a spectrophotometer (NanoDrop 2000, Thermo Fisher Scientific). All DNA and RNA were stored at &#x2212;20 &#x00B0;C until further use.</p>
<p>Casava mosaic begomoviruses (CMB) detection was performed in 20&#x202F;&#x03BC;L of reaction mixture containing 4&#x202F;&#x03BC;L of 1 FIREPol Blend Master Mix (Solis BioDyne, Tartu, Estonia), 0.5&#x202F;&#x03BC;L of 10&#x202F;&#x03BC;M each forward and reverse primers, nuclease-free water, and 100&#x202F;ng/&#x03BC;l of DNA. The reaction was performed in the Veriti Thermal Cycler (Thermo Fisher Scientific 2017, US) using specific primers (<xref ref-type="table" rid="tab1">Table 1</xref>). The PCR program consisted of an initial denaturation at 94 &#x00B0;C for 15&#x202F;min, followed by 35&#x202F;cycles of denaturation at 94 &#x00B0;C for 45&#x202F;s, hybridization for 45&#x202F;s, from 55 &#x00B0;C to 70 &#x00B0;C according to the primer, extension at 72 &#x00B0;C for 60&#x202F;s, and a final extension at 72 &#x00B0;C for 10&#x202F;min. PCR products were separated by electrophoresis on a 1% agarose gel stained with ethidium bromide (10&#x202F;mg/mL) in 1X TAE buffer using 100 base pair DNA ladder (Solis Biodyne, Estonia). The gels were visualized under UV light using a Gel DocTM XR&#x202F;+&#x202F;Molecular Imager from Bio-Rad (ibec&#x00AE;, Institut de bioenginyeria de Catalunya).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Primers used for CMB and CBSI detection.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Viruses</th>
<th align="left" valign="top">Primer name</th>
<th align="left" valign="top">Primer sequences (5&#x2032; to 3&#x2032;)</th>
<th align="left" valign="top">Target region</th>
<th align="left" valign="top">Size</th>
<th align="left" valign="top">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="12">CMB</td>
<td align="left" valign="top">JSP 001</td>
<td align="left" valign="top">ATGTCGAAGCGACCAGGAGAT</td>
<td align="left" valign="top" rowspan="2">ACMV DNA-A (CP)</td>
<td align="left" valign="top" rowspan="2">783&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref38">Pita et al. (2001)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">JSP 002</td>
<td align="left" valign="top">TGTTTATTAATTGCCAATACT</td>
</tr>
<tr>
<td align="left" valign="top">ACMVBF</td>
<td align="left" valign="top">TCGGGAGTGATACATGCGAAGGC</td>
<td align="left" valign="top" rowspan="2">ACMV DNA-B (BV1/BC1)</td>
<td align="left" valign="top" rowspan="2">628&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref30">Matic et al. (2012)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">ACMVBR</td>
<td align="left" valign="top">GGCTACACCAGCTACCTGAAGCT</td>
</tr>
<tr>
<td align="left" valign="top">ACMV21for</td>
<td align="left" valign="top">GCAGTGATGAGTTCCCCGGTGCG</td>
<td align="left" valign="top" rowspan="2">DNA-A (AC3-AC2-AC1)</td>
<td align="left" valign="top" rowspan="2">552&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref30">Matic et al. (2012)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">ACMV21rev</td>
<td align="left" valign="top">ATTCCGCTGCGCGGCCATGGAGACC</td>
</tr>
<tr>
<td align="left" valign="top">JSP 001</td>
<td align="left" valign="top">ATGTCGAAGCGACCAGGAGAT</td>
<td align="left" valign="top" rowspan="2">EACMV DNA-A (CP)</td>
<td align="left" valign="top" rowspan="2">780&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref38">Pita et al. (2001)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">JSP 003</td>
<td align="left" valign="top">CCTTTATTAATTTGTCACTGC</td>
</tr>
<tr>
<td align="left" valign="top">CMBRepF</td>
<td align="left" valign="top">CRTCAATGACGTTGTACCA</td>
<td align="left" valign="top" rowspan="2">EACMV DNA-A (AC1)</td>
<td align="left" valign="top" rowspan="2">650&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref3">Alabi et al. (2008)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">EACMVRepR</td>
<td align="left" valign="top">GGTTTGCAGAGAACTACATC</td>
</tr>
<tr>
<td align="left" valign="top">VNF031/F</td>
<td align="left" valign="top">GGATACAGATAGGGTTCCCAC</td>
<td align="left" valign="top" rowspan="2">EACMV-CM DNA-A (AC2/AC3)</td>
<td align="left" valign="top" rowspan="2">&#x2248; 560&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref14">Fondong et al. (2000)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">VNF032/R</td>
<td align="left" valign="top">GACGAGGACAAGAATTCCAAT</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">CBSI</td>
<td align="left" valign="top">Pri277</td>
<td align="left" valign="top">GGRCCATACATYAARTGGTT</td>
<td align="left" valign="top" rowspan="2">CBSVs universal</td>
<td align="left" valign="top" rowspan="2">1,670&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref5">Apio et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">CBSVDR</td>
<td align="left" valign="top">GGATATGGAGAAAGRKCTCC</td>
</tr>
<tr>
<td align="left" valign="top">CBSVDF2</td>
<td align="left" valign="top">GCTMGAAATGCYGGRTAYACAA</td>
<td align="left" valign="top">UCBSV</td>
<td align="left" valign="top" rowspan="2">437&#x202F;bp and 343&#x202F;bp</td>
<td align="left" valign="top" rowspan="2">
<xref ref-type="bibr" rid="ref5">Apio et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">CBSVDR</td>
<td align="left" valign="top">GGATATGGAGAAAGRKCTCC</td>
<td align="left" valign="top">CBSV</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>For cassava brown streak ipomoviruses (CBSI) detection, cDNAs were prepared using the Revert-Aid cDNA synthesis kit (Thermo Fisher Scientific) according to the manufacturer&#x2019;s instruction. Briefly, first strand cDNA was synthesized using 5&#x202F;&#x03BC;g of total RNA, 1&#x202F;&#x03BC;L of Oligo (dT)<sub>18</sub> primer (10&#x202F;&#x03BC;M) and nuclease-free water (11&#x202F;&#x03BC;L). The mixture was incubated at 65 &#x00B0;C for 5&#x202F;min. To the above mixture, 5X Reaction Buffer, RiboLock RNase Inhibitor (20&#x202F;U/&#x03BC;l), 10&#x202F;mM dNTP Mix, RevertAid M-MuLV RT (200&#x202F;U/&#x03BC;l) were added. The reaction was incubated at 42 &#x00B0;C For 60&#x202F;min and terminated at 70 &#x00B0;C for 5&#x202F;min. The resulting cDNAs were used as templates for PCR amplification. The PCR was performed using the universal primer Pri277/CBSVDR to amplify target product of 1,670&#x202F;bp and the specific primer CBSVDF2/CBSVDR (<xref ref-type="bibr" rid="ref5">Apio et al., 2021</xref>) toamplify products of 437&#x202F;bp (UCBSV) and 343&#x202F;bp (CBSV). The reaction mixture consisted of 20&#x202F;&#x03BC;L, containing OneTaq Quick-Load 2X Master Mix with Standard Buffer, 20 pmole of each primer at 10&#x202F;mM, nuclease-free water and 500&#x202F;ng of cDNA. Amplification conditions were initial denaturation at 94 &#x00B0;C for 30&#x202F;s, followed by 30&#x202F;cycles at 94 &#x00B0;C for 30&#x202F;s, 51 &#x00B0;C for 30&#x202F;s, 72 &#x00B0;C for 30&#x202F;s and final extension at 70 &#x00B0;C for 10&#x202F;min. PCR products were separated by electrophoresis on a 1.2% agarose gel stained with ethidium bromide (10&#x202F;mg/mL) in 1X TAE buffer. The gel was visualized under UV light.</p>
</sec>
<sec id="sec8">
<label>2.6</label>
<title>Statistical analysis</title>
<p>Data were analyzed using R software v 4.3.1 (<xref ref-type="bibr" rid="ref39">R Core Team, 2022</xref>). CMD, CBSD, and CGM scores detection distribution across groups were first checked for normality and homogeneity, using Shapiro&#x2013;Wilk and Bartlett tests, respectively. When the data meet normality and homogeneity assumptions (<italic>p</italic>-value &#x003E; 0.05), a one-way analysis of variance (ANOVA) was performed, and means compared using Tukey&#x2019;s HSD <italic>post hoc</italic> test. In contrast, Kruskal-Wallis non parametric test followed by Dunn&#x2019;s test with Bonferroni correction were applied. Differences between groups were considered significant at <italic>p</italic>-value &#x003C; 0.05. The boxplots of the scores recorded by each diagnostic method were also drawn.</p>
</sec>
</sec>
<sec sec-type="results" id="sec9">
<label>3</label>
<title>Results</title>
<sec id="sec10">
<label>3.1</label>
<title>Extension agents&#x2019; participation to surveillance</title>
<p>The participation rate of extension agents in this study was assessed by the percentage of participants who surveyed cassava fields, collected samples and sent to the laboratory, in relation to the total number of participants. The overall participation rate of extension agents in cassava field sampling during one year of surveillance (from July, 2022 to June, 2023 without a phone allocated) was 21.67% (13/60). The highest participation rate was recorded in the Cascades region (62.50%, 5/8). In the other regions, the participation rate varied between 12.5 and 25.0% (<xref ref-type="table" rid="tab2">Table 2</xref>). During this period, only 31 cassava fields were surveyed. After the allocation of phones during the second workshop, the number of cassava fields surveyed increased to 132 from July to September 2023. The overall participation rate reached 60% (36/60). Group 1 using the AI tool recorded a participation rate of 36.67% (22/60) and t Group 2 using visual observation 23.33% (14/60). With the Exception of the Boucle du Mouhoun and Est regions, where the participation rate remained unchanged at 12.5% (1/8) and 16.67% (1/6) respectively, a significant increase was observed in the other regions (<xref ref-type="table" rid="tab2">Table 2</xref>). The highest rates of 100% were recorded in the regions of Cascades (8/8), Center-Ouest (6/6) and Sud-Ouest (8/8). In the regions of Hauts-Bassins, Center-Est and Center-Sud, the participation rate was 87.5% (7/8), 37.5% (3/8) and 33.33% (2/6), respectively.</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Extension agents participation rate across all surveyed regions in 2022 and 2023.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Regions</th>
<th align="center" valign="top">Participation rate after the first workshop without smartphones in 2022</th>
<th align="center" valign="top">Participation rate after the second workshop with smartphones allocation in 2023</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Boucle du Mouhoun</td>
<td align="center" valign="top">12.50%</td>
<td align="center" valign="top">12.50%</td>
</tr>
<tr>
<td align="left" valign="top">Cascades</td>
<td align="center" valign="top">62.50%</td>
<td align="center" valign="top">100.00%</td>
</tr>
<tr>
<td align="left" valign="top">Center-Est</td>
<td align="center" valign="top">25.00%</td>
<td align="center" valign="top">37.50%</td>
</tr>
<tr>
<td align="left" valign="top">Center-Ouest</td>
<td align="center" valign="top">16.67%</td>
<td align="center" valign="top">100.00%</td>
</tr>
<tr>
<td align="left" valign="top">Center-Sud</td>
<td align="center" valign="top">16.67%</td>
<td align="center" valign="top">33.33%</td>
</tr>
<tr>
<td align="left" valign="top">Est</td>
<td align="center" valign="top">16.67%</td>
<td align="center" valign="top">16.67%</td>
</tr>
<tr>
<td align="left" valign="top">Hauts-Bassins</td>
<td align="center" valign="top">12.50%</td>
<td align="center" valign="top">87.50%</td>
</tr>
<tr>
<td align="left" valign="top">Sud-Ouest</td>
<td align="center" valign="top">12.50%</td>
<td align="center" valign="top">100.00%</td>
</tr>
<tr>
<td align="left" valign="top">Total</td>
<td align="center" valign="top">21.67%</td>
<td align="center" valign="top">60.00%</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec11">
<label>3.2</label>
<title>CMB and CBSI status in collected leaf samples by the group 1 using AI tool</title>
<p>In this group, a total of 65 cassava fields was surveyed to collect 142 leaf samples. Forty (40) leaf samples were recognized as infected with CMD and 102 as apparently healthy according to the perception of Cassava Disease Diagnosis Experts (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Molecular analyses by PCR confirmed CMB viruses in 95% (38/40) of symptomatic CMD leaves and 100% (102/102) of apparently healthy were identified as free of CMB virus. Comparing the previous results with the AI tool diagnosis, it was observed that 80% (32/40) of CMD symptomatic leaf samples were diagnosed as CMD by AI tool (<xref ref-type="fig" rid="fig2">Figure 2</xref>). However, the AI tool misdiagnosed 15% (6/40) of CMD symptomatic leaves as healthy and 5% (2/40) as CBSD. Nevertheless, the observed symptoms were clearly consistent with CMD. Overall, the AI tool diagnosis was reasonably close to the expert perception of Cassava Disease Diagnosis supported by molecular analysis (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Furthermore, all leaf samples subjected to molecular analysis by RT-PCR were negative for CBSI.</p>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p>CMB and CBSI detection within collected leaf samples.</p>
</caption>
<graphic xlink:href="fsufs-09-1597039-g003.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Bar chart comparing the number of leaf samples diagnosed as healthy, CMD_CMB, and CBSD_CBSI using CDDEP plus molecular analyses and AI tool diagnosis. Healthy samples: 102 (CDDEP) and 108 (AI); CMD_CMB: 40 (CDDEP) and 32 (AI); CBSD_CBSI: 0 (CDDEP) and 2 (AI).</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec12">
<label>3.3</label>
<title>CMB status in leaf samples collected by group 2 by visual observation</title>
<p>In this group, 234 leaf samples were collected from 67 cassava surveyed fields. Sixty-five leaf samples were recognized as infected by CMD and 169 as apparently healthy according to the perception of Cassava Disease Diagnosis Experts. Molecular analysis by PCR confirmed the presence of CMB viruses in 92.31% (60/65) of symptomatic CMD leaves and 100% (169/169) of apparently healthy leaves were found to be free of CMB viruses. Compared to visual observation carried out by Group 2, the latter also recorded 65 leaf samples as CMD infected and 169 as apparently healthy. In summary, the diagnosis based on visual observation was reasonably similar to those observed by Cassava Disease Diagnosis Experts&#x2019; Perception supported by molecular analysis.</p>
</sec>
<sec id="sec13">
<label>3.4</label>
<title>Accuracy of AI tool, AEAP, and CDDEP to detect cassava diseases</title>
<p>The diagnostic results of the AI tool, the Agricultural Extension Agents&#x2019; Perception (AEAP) of CMD, CBSD and CGM symptoms recognition compared to Cassava Disease Diagnostic Experts&#x2019; Perception (CDDEP) and molecular diagnosis were evaluated. For Group 1 AI tool users, AI diagnosis showed no significant difference (<italic>p</italic>-value&#x202F;=&#x202F;0.709) in CMD symptoms recognition compared to CDDEP and molecular detection by PCR (<xref ref-type="fig" rid="fig4">Figure 4A</xref>). The mean scores (<xref ref-type="table" rid="tab3">Table 3</xref>) for CMD detection were 29.83&#x202F;&#x00B1;&#x202F;12.99% for AI tool diagnosis, 37.12&#x202F;&#x00B1;&#x202F;12.78% for expert perception of cassava disease diagnosis and 36.10&#x202F;&#x00B1;&#x202F;12.74% for molecular detection. In addition, there was no significant difference (<italic>p</italic>-value&#x202F;=&#x202F;0.551) in CGM detection between AI diagnosis and CDDEP (<xref ref-type="fig" rid="fig4">Figure 4B</xref>). The mean scores for CGM symptom recognition were 6.936&#x202F;&#x00B1;&#x202F;3.62% for AI diagnosis and 3.746&#x202F;&#x00B1;&#x202F;3.13% for Cassava Disease Diagnostic Expert Perception (<xref ref-type="table" rid="tab3">Table 3</xref>). Following CBSD symptoms recognition, only AI diagnosis revealed its presence with a mean score of 0.866&#x202F;&#x00B1;&#x202F;0.866% (<xref ref-type="table" rid="tab3">Table 3</xref>). However, according Experts&#x2019; Perception of Cassava Diseases Diagnosis supported by RT-PCR testing, no CBSD was present in the collected cassava samples.</p>
<fig position="float" id="fig4">
<label>Figure 4</label>
<caption>
<p><bold>(A)</bold> Comparison of the ability of AI diagnosis (AI) and cassava disease diagnosis experts&#x2019; perception (CDDEP) to cassava mosaic disease (CMD) symptoms recognition and confirmed by molecular analysis. The black line within the boxes represents the median, the top and bottom of the box represent the 75th and the 25th percentiles, the whiskers represent the maximum and minimum and the symbol (&#x00B0;) represent the outlier. <bold>(B)</bold> Comparison of the ability of AI diagnosis (AI) and cassava disease diagnosis experts&#x2019; perception (CDDEP) to cassava green mite (CGM) symptoms recognition. The black line within the boxes represents the median, the top and bottom of the box represent the 75th and the 25th percentiles, the whiskers represent the maximum and minimum and the symbol (&#x00B0;) represent the outlier.</p>
</caption>
<graphic xlink:href="fsufs-09-1597039-g004.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two box plots labeled A and B compare diagnosis methods. In plot A, CMD scores for AI show lower values than CDDEP and Molecular, which are similar. Plot B shows CGM scores, with AI having higher values than CDDEP. AI is represented in gray, and CDDEP and Molecular in cyan.</alt-text>
</graphic>
</fig>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>Mean scores of AI diagnosis, CDDEP, AEAP about diseases symptoms recognition and molecular analysis.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="top">CMD (%)</th>
<th align="center" valign="top">CBSD (%)</th>
<th align="center" valign="top">CGM (%)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" colspan="4">Mean scores of diagnosis based on AI tool</td>
</tr>
<tr>
<td align="left" valign="top">AI</td>
<td align="center" valign="top">29.830&#x202F;&#x00B1;&#x202F;12.99</td>
<td align="center" valign="top">0.866 &#x00B1; 0.866</td>
<td align="center" valign="top">6.936&#x202F;&#x00B1;&#x202F;3.62</td>
</tr>
<tr>
<td align="left" valign="top">CDDEP</td>
<td align="center" valign="top">37.124&#x202F;&#x00B1;&#x202F;12.78</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">3.746&#x202F;&#x00B1;&#x202F;3.13</td>
</tr>
<tr>
<td align="left" valign="top">Molecular analyses</td>
<td align="center" valign="top">36.097&#x202F;&#x00B1;&#x202F;12.74</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">nd</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.709</td>
<td align="center" valign="top">0.368</td>
<td align="center" valign="top">0.551</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Mean scores of diagnosis based on perception</td>
</tr>
<tr>
<td align="left" valign="top">AEAP</td>
<td align="center" valign="top">46.07&#x202F;&#x00B1;&#x202F;13.00</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">22.29 &#x00B1; 9.03</td>
</tr>
<tr>
<td align="left" valign="top">CDDEP</td>
<td align="center" valign="top">46.07&#x202F;&#x00B1;&#x202F;13.00</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">22.29 &#x00B1; 9.03</td>
</tr>
<tr>
<td align="left" valign="top">Molecular analyses</td>
<td align="center" valign="top">43.87&#x202F;&#x00B1;&#x202F;12.07</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">nd</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.997</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">1</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>In Group 2, which used visual observation based on perception, no CBSD was detected in the fields surveyed. RT-PCR results confirmed these observations. However, no significant difference (<italic>p</italic>-value&#x202F;=&#x202F;0.997) was observed for CMD detection. The mean scores of CMD symptoms detection between the extension agents&#x2019; perception and cassava disease diagnosis experts&#x2019; perception (46.07&#x202F;&#x00B1;&#x202F;13.00%) were similar (<xref ref-type="table" rid="tab3">Table 3</xref>), but higher than the molecular analysis results, which were 43.87&#x202F;&#x00B1;&#x202F;12.07% (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). The CGM symptoms were detected with a mean score of 22.29&#x202F;&#x00B1;&#x202F;9.03% for extension agents&#x2019; perception and 22.29&#x202F;&#x00B1;&#x202F;9.03% for cassava disease diagnosis experts&#x2019; perception (<xref ref-type="fig" rid="fig5">Figure 5B</xref>).</p>
<fig position="float" id="fig5">
<label>Figure 5</label>
<caption>
<p><bold>(A)</bold> Comparison of the agricultural extension agents&#x2019; perception (AEAP) and cassava disease diagnosis experts&#x2019; perception (CDDEP) to cassava mosaic disease (CMD) symptoms recognition and confirmed by molecular analysis. The black line within the boxes represents the median, the top and bottom of the box represent the 75th and the 25th percentiles, the whiskers represent the maximum and minimum. <bold>(B)</bold> Comparison of the ability of agricultural extension agents&#x2019; perception (AEAP) and cassava disease diagnosis experts&#x2019; perception (CDDEP) to cassava green mite (CGM) symptoms recognition. The black line within the boxes represents the median, the top and bottom of the box represent the 75th and the 25th percentiles, the whiskers represent the maximum and minimum and the symbols (&#x00B0;) represent the outlier.</p>
</caption>
<graphic xlink:href="fsufs-09-1597039-g005.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two box plots labeled A and B compare diagnosis methods for CMD and CGM score detection. Plot A shows AEAP, CDDEP, and Molecular methods, with detection percentages ranging up to 100. Plot B includes AEAP and CDDEP methods, with detection percentages up to 70. Both plots use different colors for each method.</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec14">
<label>3.5</label>
<title>ACMV prevalence in CMD-infected leaf samples</title>
<p>In the current study, a total of 41 CMD-infected fields were recorded, giving an overall prevalence of 31.06% (41/132). The CMB detected in CMD-infected leaves was <italic>African Cassava Mosaic Virus</italic> (ACMV) in single infections. The prevalence of ACMV in CMD symptomatic leaf samples collected from Group 1 was 95% (38/40) and 92.31% (60/65) for Group 2. The total prevalence was 93.33% (98/105). <italic>East African Cassava Mosaic Virus</italic> (EACMV) was not detected.</p>
</sec>
</sec>
<sec sec-type="discussion" id="sec15">
<label>4</label>
<title>Discussion</title>
<p>Viruses are a major threat to cassava production in sub-Saharan Africa. Attempts to control these pathogens rely mainly on field inspections and the promotion of good management practices through the use of heathy cuttings. Classical epidemiology, which has been the most widely used strategy to date, is expensive and time-consuming. However, in the field of human and animal health, participatory surveillance is increasingly applied (<xref ref-type="bibr" rid="ref32">McNeil et al., 2022</xref>), and offers the advantage of warm anticipation and rapid response (<xref ref-type="bibr" rid="ref43">Smolinski, 2016</xref>).</p>
<p>Recent innovations in ICT have also provided tools, termed &#x201C;AI tools,&#x201D; that have contributed significantly to the management of emerging infectious diseases (<xref ref-type="bibr" rid="ref7">Brownstein et al., 2023</xref>; <xref ref-type="bibr" rid="ref45">Sood et al., 2023</xref>). Unfortunately, the field of plant health has benefited little from work using participatory approaches and AI tools for the control of plant viral diseases. The present study, based on participatory approaches combined with the use of an AI tool (Nuru), was implemented as an alternative to the classical surveillance and epidemiology of cassava viral diseases in Burkina Faso. The accuracy of the agricultural extension agents and AI tool to detect CMD and CBSD are discussed.</p>
<p>The overall participation rate of agricultural extension agents has been improved after the workshops and mobile phone equipment for data collection. Previous studies have reported that workshops are a key factor in the success of applying participatory surveillance (<xref ref-type="bibr" rid="ref6">Bordier et al., 2021</xref>). In fact, the workshop is known to correct any eventual limitations related to the surveillance. It also helps to build confidence among stakeholders, particularly agricultural extension agents. Here, the number of cassava fields monitored increased gradually from 31 to 132 after the workshop. Actually, participants provision with smartphones improves significantly their involvement in diseases surveillance (<xref ref-type="bibr" rid="ref35">Orozco et al., 2020</xref>). As reported by <xref ref-type="bibr" rid="ref11">Dhavale et al. (2025)</xref>, awareness campaigns and trainings with mobile tools engaging farmer and extension agents through participatory epidemiology enables early detection and rapid response to disease management. Nevertheless, the participation rate remained low in two regions such us Boucle du Mouhoun and Est. The security crisis which affected these regions would have negatively affected the ability of agricultural extension agents to survey fields and collect data. Despite this fact, cassava samples have been collected and sent to the experts of cassava disease diagnosis for laboratory analysis.</p>
<p>Molecular analysis confirmed the presence of CMB within CMD symptomatic leaf samples both samples collected by visual perception and AI tool (<xref ref-type="fig" rid="fig3">Figure 3</xref>). AI tool detected accurately symptoms of CMD as well as CGM damages (<xref ref-type="fig" rid="fig4">Figure 4</xref>), as reported previously (<xref ref-type="bibr" rid="ref34">Mrisho et al., 2020</xref>). Although, the accuracy of AI to recognize CMD and CGM symptoms was similar to that of the visual perception of agricultural extension agents, AI tool showed slight precision (80%). These findings agree with <xref ref-type="bibr" rid="ref42">Saffa et al. (2025)</xref>, who reported that AI tool is efficient for the CMD detection like molecular analysis. The current study found that AI tool accurately recognized asymptomatic leaf, which was supported by experts perception and molecular analysis. A similar result was observed by <xref ref-type="bibr" rid="ref1">Adj&#x00E9;i et al. (2024)</xref>, supported that AI tool helped farmers in selecting cassava virus-free cutting in C&#x00F4;te d&#x2019;Ivoire. Obviously, AI tool misdiagnosed some cassava leaf samples. The CBSD symptoms and healthy leave recorded with AI tool were clearly matched with CMD and molecular analysis confirmed the presence of CMB in these samples. Low accuracy of CBSD symptoms recognition by AI diagnosis was reported during AI tool development (<xref ref-type="bibr" rid="ref41">Ramcharan et al., 2019</xref>; <xref ref-type="bibr" rid="ref34">Mrisho et al., 2020</xref>). On the other hand, it was reported that CBSD is localized only in East and Southern Africa (<xref ref-type="bibr" rid="ref49">Tumwegamire et al., 2018</xref>), with a high risk of its spreading to West Africa (<xref ref-type="bibr" rid="ref28">Legg et al., 2011</xref>). CBSD and healthy leave misdiagnose could also be attributed to the low resolution of the camera (5 MP Back) implemented in the smartphones used in the current study as reported by <xref ref-type="bibr" rid="ref34">Mrisho et al. (2020)</xref>. So, AI tool for cassava symptoms diagnosis need to be further improved in CBSD symptoms recognition by providing more similar symptoms to Nuru databases, which could contributed to the tool accuracy. But in the meantime, molecular diagnosis remains the better suited to detecting CBSD.</p>
<p>In the group of visual observation based on perception, each stakeholder (AEAP and CDDEP) was able to identify clearly CMD and CGM symptoms as reported in <xref ref-type="fig" rid="fig5">Figure 5</xref>. Agricultural extension agents have a good perception on cassava symptoms recognition. The training organized during the workshop would have strengthened the ability of the extension agents of agriculture to accurately identify the main diseases of cassava. As reported by <xref ref-type="bibr" rid="ref34">Mrisho et al. (2020)</xref>, rigorous training of agricultural extension workers about diseases symptom recognition contributes effectively to improve their perception.</p>
<p>This study revealed that the prevalence of CMD was relatively moderate in the cassava producing regions 31.06% (41/132), showing that CMD is regressing in Burkina Faso comparatively to prevalences observed in 2016 (84.0%) and 2017 (65.9%) (<xref ref-type="bibr" rid="ref46">Soro et al., 2021</xref>). This regression of CMD prevalence could be to the results of an awareness about CMD damages as well as adoption of good agricultural practices by farmers. However, ACMV in single infection showed high abundance across all surveyed regions 93.33% (98/105). Many reports support that ACMV are the most widespread cassava virus in West Africa (<xref ref-type="bibr" rid="ref38">Pita et al., 2001</xref>; <xref ref-type="bibr" rid="ref47">Tiendr&#x00E9;b&#x00E9;ogo et al., 2012</xref>; <xref ref-type="bibr" rid="ref48">Torkpo et al., 2018</xref>; <xref ref-type="bibr" rid="ref12">Eni et al., 2021</xref>; <xref ref-type="bibr" rid="ref46">Soro et al., 2021</xref>; <xref ref-type="bibr" rid="ref20">Houngue et al., 2022</xref>; <xref ref-type="bibr" rid="ref4">Amoakon et al., 2023</xref>).</p>
<p>The transfer of ICTs to the agricultural sector is increasingly encouraged in order to relieve the efforts of extension agents and farmers (<xref ref-type="bibr" rid="ref25">Kalaitzandonakes et al., 2018</xref>). When these innovations are suitable for non-specialists such as extension&#x2019; agents and farmers, they improve not only their knowledge, but also help to increase agricultural yields. However, some of these innovations are subjected to easy applicability because of the complexity of their use by extension agents and farmers. Finding in the current study, which involved the use of Nuru through participatory surveillance approaches, are proof of a model of technological innovation that is easily transferable to non-specialists. It will be certainly a powerful tool to maintain the dialog between extensions agents, model farmers and seed multipliers with researchers to monitor the cassava disease and prevent any incursion of CBSD in West Africa.</p>
</sec>
<sec sec-type="conclusions" id="sec16">
<label>5</label>
<title>Conclusion</title>
<p>Finding in this study revealed that participatory approaches can be effective for the control of cassava viral diseases. The success of participatory approaches is founded on the training and equipping of grassroots stakeholders such as extension agents and farmers with adapted tools. AI tool diagnosis and visual inspection about CMD detection, performed by extension agents revealed similar results to experts perception supported by molecular analysis. The epidemiological data of this study revealed that CMD is declining in Burkina. However, considering the low ability of AI tool to accurately detect symptoms of the CBSD, an improvement of AI this tool would be essential for cassava&#x2019;s fields diagnosis. AI tool could play a first-line diagnostic role if users are properly trained. AI tool could support agricultural extension agents&#x2019; perception about symptom recognition and help to bridge knowledge gap between agricultural extension agents and cassava diagnostics experts for a better management of cassava viral diseases. So, the surveillance and skills of agricultural extension agents must be regularly strengthened by continuous trainings, combined with awareness.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec17">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec sec-type="author-contributions" id="sec18">
<title>Author contributions</title>
<p>SS: Data curation, Investigation, Methodology, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. FT: Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Validation, Writing &#x2013; review &#x0026; editing, Writing &#x2013; original draft. ET: Data curation, Investigation, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. PN: Data curation, Investigation, Methodology, Writing &#x2013; review &#x0026; editing, Writing &#x2013; original draft. FD: Supervision, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. LT: Supervision, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. JP: Funding acquisition, Resources, Supervision, Validation, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. AE: Funding acquisition, Project administration, Resources, Supervision, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<sec sec-type="funding-information" id="sec19">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the Central and West African Virus Epidemiology (WAVE) Program for root and tuber crops with the Grant Number INV-002969 (OPP1212988) from the Bill and Melinda Gates Foundation (BMGF) and the UK Foreign, Commonwealth, and Development Office (FCDO).</p>
</sec>
<ack>
<p>The authors thank cassava farmers and Ministry of Agriculture in Burkina Faso for their collaboration and participation to this study.</p>
</ack>
<sec sec-type="COI-statement" id="sec20">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec21">
<title>Generative AI statement</title>
<p>The authors declare that no Gen AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="sec22">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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