Article(id=1277254380155966233, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277254112370623080, articleNumber=null, orderNo=null, doi=10.3969/j.issn.1000-2561.2026.02.019, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1759334400000, receivedDateStr=2025-10-02, revisedDate=null, revisedDateStr=null, acceptedDate=1763568000000, acceptedDateStr=2025-11-20, onlineDate=1782450774467, onlineDateStr=2026-06-26, pubDate=1771948800000, pubDateStr=2026-02-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782450774467, onlineIssueDateStr=2026-06-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782450774467, creator=13701087609, updateTime=1782450774467, updator=13701087609, issue=Issue{id=1277254112370623080, tenantId=1146029695717560320, journalId=1235980609244409860, year='2026', volume='47', issue='2', pageStart='281', pageEnd='551', issueExtLink='null', onlineDate='null', pubDate='1771948800000', pubDateStr='2026-02-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1782450710622, creator='13701087609', updateTime=1782451594955, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1277257821632729830, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277254112370623080, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1277257821632729831, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277254112370623080, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=489, endPage=497, ext={EN=ArticleExt(id=1277254382659965724, articleId=1277254380155966233, tenantId=1146029695717560320, journalId=1235980609244409860, language=EN, title=Effects of Mite-resistant and Mite Susceptible Cassava Cultivars on the Development, Reproduction, and Detoxification System of Abamectin-resistant and Susceptible Tetranychus urticae, columnId=1236292524264968282, journalTitle=Chinese Journal of Tropical Crops, columnName=Plant Protection & Bio-safety, runingTitle=null, highlight=null, articleAbstract=

Tetranychus urticae is a significant pest on cassava. Long-term use of abamectin has led to prominent resistance issues. Selecting mite-resistant cassava varieties represents a green, effective and straightforward approach to pest control. However, the effectiveness of resistant cassava varieties against resistant mite strains remains unclear, limiting its utility in supporting resistance management decisions. Accordingly, this study used mite-resistant cassava cultivar C1115, mite-susceptible cassava cultivar SC205 and the preferred host plant cowpea as test materials to investigate the effects on the development, reproduction and detoxification metabolism capabilities of abamectin-resistant (AB-R) and abamectin-sensitive (AB-S) strains. Results showed that compared to feeding on cowpea, feeding on SC205 did not significantly alter the developmental duration or population growth parameters [net reproductive rate (R₀), intrinsic rate of increase (r_m), mean generation time (T), population doubling time (DT)] of either AB-R or AB-S strains. In contrast, feeding on C1115 significantly prolonged the developmental duration and inhibited population growth (significantly decreased R₀ and r_m, significantly increased T and DT) of both strains. Furthermore, on C1115, the T and DT of the AB-R strain were also significantly lower than those of the AB-S strain. Regarding detoxification enzyme activities, compared to feeding on cowpea, feeding on both SC205 and C1115 significantly increased the activities of three detoxification enzymes-cytochrome P450 monooxygenases (P450s), glutathione S-transferases (GSTs) and uridine diphosphate-glycosyltransferases (UGTs) - in both mite strains. Enzyme activities were significantly higher in mites feeding on C1115 compared to those on SC205. Additionally, on all three host plants, the enzyme activities of the AB-R strain were consistently significantly higher than those of the AB-S strain. Detoxification genes associated with abamectin resistance exhibited different expression patterns. Although feeding on both C1115 and SC205 significantly upregulated the expression of six tested genes in both mite strains compared to feeding on cowpea, differences emerged when comparing strains on the same cassava variety. When AB-R and AB-S fed on the same cassava cultivar (C1115 or SC205), the expression levels of CYP389C10, UGT201D3 and UGT11 showed no significant difference. However, the expression of CYP392A16, GSTd01 and GSTm09 was significantly higher in the AB-R strain than in the AB-S strain. The results indicate that the AB-R strain of T. urticae, likely due to its enhanced detoxification capacity, might possess an advantage in neutralizing toxic secondary metabolites from the mite-resistant cassava, potentially compromising the pest control efficacy of this resistant cultivar. This hypothesis, however, requires further validation through subsequent field experiments. This study provides a preliminary theoretical basis for evaluating the application potential of mite-resistant cassava in the management of mite resistance to acaricides.

, authors=null, authorsList=Oluwole Gregory IJITI, Xiao LIANG, Ying LIU, Chunling WU, Xingkui AN, Changying NIU, Qing CHEN, authorCompany=null, correspAuthors=Changying NIU, Qing CHEN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1277254386917184288, articleId=1277254380155966233, tenantId=1146029695717560320, journalId=1235980609244409860, language=CN, title=抗、感螨木薯品种对阿维菌素抗性和敏感二斑叶螨发育繁殖及解毒代谢的影响, columnId=1236292524520820846, journalTitle=热带作物学报, columnName=植物保护与生物安全, runingTitle=null, highlight=null, articleAbstract=

二斑叶螨是木薯上的重要害虫，长期使用阿维菌素使其抗药性问题突出，选用抗螨木薯品种是绿色、有效、简便的虫害防治途径，当前，抗螨木薯品种对抗性二斑叶螨的控制效果尚不明确，难以为害螨的抗药性治理提供决策支持。据此，本研究以抗螨木薯品种C1115、感螨木薯品种SC205及二斑叶螨适宜的繁育寄主豇豆为参试材料，探究其对阿维菌素抗性（AB-R）和敏感（AB-S）品系发育繁殖和解毒代谢能力的影响。结果表明：与取食豇豆相比，取食SC205的AB-R、AB-S的发育历期、种群增长［净增殖率（R₀）、内禀增长率（r_m）、平均世代周期（T）］和种群加倍时间（DT）无显著差异，而取食C1115显著延长了AB-R、AB-S的发育历期，显著抑制种群增长（R₀、r_m显著降低，T和DT显著延长），且AB-R在C1115上的T和DT也显著低于B-S。在解毒酶活性方面，与取食豇豆相比，2种害螨品系取食SC205和C1115后，细胞色素P450酶（CYP450s）、谷胱甘肽S-转移酶（GSTs）、尿苷二磷酸糖基转移酶（UGTs）3种解毒酶活性均显著提高，并且取食C1115的酶活显著高于取食SC205，此外，取食3种寄主后，AB-R的酶活也均显著高于AB-S。阿维菌素抗性相关的解毒基因表现出不同的表达特性，与取食豇豆相比，虽然2种害螨品系取食C1115和SC205后，体内6个基因的表达量均显著提高，但是当AB-R和AB-S取食相同木薯品种时，CYP389C10、UGT201D3和UGT11的表达量无显著差异，而AB-R中的CYP392A16、GSTd01和GSTm09表达量显著高于AB-S。上述结果表明，二斑叶螨AB-R品系因其解毒代谢能力更强，可能在解毒抗螨木薯品种的有毒次生物质时更具优势，从而削弱抗螨木薯对二斑叶螨的控害效果，但该假设需通过后续的田间试验进一步证实。本研究结果为评估抗螨木薯在害螨抗药性治理中的应用潜力提供前期理论基础。

, authors=, authorsList=Oluwole Gregory IJITI, 梁晓, 刘迎, 伍春玲, 安兴奎, 牛长缨, 陈青, authorCompany=null, correspAuthors=牛长缨, 陈青, authorNote=null, correspAuthorsNote=, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=SJvosPhj1CC4uh9tq8yh0g==, magXml=YMsSSHNRF3uG8eNy24IyMg==, pdfUrl=null, pdf=IQgv3U71hRV/2YSJGZeNyg==, pdfFileSize=1556452, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=pH35Y3uNPCPYAJPk4Fn76g==, mapNumber=null, fund=null)}, authors=[Author(id=1277254392260727597, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1277254380155966233, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1277254394840224564, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1277254380155966233, authorId=1277254392260727597, language=EN, stringName=Oluwole Gregory IJITI, firstName=Oluwole Gregory, middleName=null, lastName=IJITI, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=^{1, 2, 3}, address=^1.College of Plant Science & Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, China
^2.Environment and Plant Protection Institute, China Academy of Tropical Agricultural Sciences/Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs/Hainan Engineering Research Center for Biological Control of Tropical Crops Diseases and Insect Pests, Haikou, Hainan 571101, China
^3.Sanya Research Academy, Chinese Academy of Tropical Agricultural Sciences/Hainan Key Laboratory for Biosafety Monitoring and Molecular Breeding in Off-Season Reproduction Regions, Sanya, Hainan 572000, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1277254395259654965, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1277254380155966233, authorId=1277254392260727597, language=CN, stringName=Oluwole Gregory IJITI, firstName=Oluwole Gregory, middleName=null, lastName=IJITI, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=^{1, 2, 3}, address=^1．华中农业大学植物科学技术学院，湖北武汉　430070
^2．中国热带农业科学院环境与植物保护研究所/农业农村部热带作物有害生物综合治理重点实验室/海南省热带作物病虫害生物防治工程技术研究中心，海南海口　571101
^3．中国热带农业科学院三亚研究院/海南省南繁生物安全与分子育种重点实验室，海南三亚　572000, bio={"content":"

IJITI Oluwole Gregory（1994—），男，硕士研究生，研究方向：虫害绿色防控。

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IJITI Oluwole Gregory（1994—），男，硕士研究生，研究方向：虫害绿色防控。

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