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other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. 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Recent molecular studies on endophytic bacterial diversity have revealed a large richness of species. Endophytes promote plant growth and yield, suppress pathogens, may help to remove contaminants, solubilize phosphate, or contribute assimilable nitrogen to plants. Some endophytes are seed-borne, but others have mechanisms to colonize the plants that are being studied. Bacterial mutants unable to produce secreted proteins are impaired in the colonization process. Plant genes expressed in the presence of endophytes provide clues as to the effects of endophytes in plants. Molecular analysis showed that plant defense responses limit bacterial populations inside plants. Some human pathogens, such as Salmonella spp., have been found as endophytes, and these bacteria are not removed by disinfection procedures that eliminate superficially occurring bacteria. Delivery of endo-phytes to the environment or agricultural fields should be carefully evaluated to avoid introducing pathogens. \u003C\u002Fjats:p>","\u003Cjats:p> Các nghiên cứu phân tử gần đây về sự đa dạng của vi khuẩn nội sinh đã tiết lộ sự phong phú lớn về các loài. Vi khuẩn nội sinh thúc đẩy tăng trưởng và năng suất thực vật, ức chế mầm bệnh, có thể giúp loại bỏ chất ô nhiễm, hòa tan photphat, hoặc cung cấp nitơ có thể hấp thụ cho thực vật. Một số vi khuẩn nội sinh được mang từ hạt giống, nhưng một số khác có cơ chế để định cư trong các loại thực vật đang được nghiên cứu. Các đột biến vi khuẩn không có khả năng sản xuất protein tiết ra bị hạn chế trong quá trình định cư. Các gen thực vật được biểu hiện trong sự hiện diện của vi khuẩn nội sinh cung cấp manh mối về ảnh hưởng của vi khuẩn nội sinh đối với thực vật. Phân tích phân tử cho thấy rằng các phản ứng phòng thủ của thực vật giới hạn quần thể vi khuẩn bên trong thực vật. Một số mầm bệnh của người, như Salmonella spp., đã được phát hiện là vi khuẩn nội sinh, và những vi khuẩn này không bị loại bỏ bởi các quy trình khử trùng loại bỏ vi khuẩn bề mặt. Việc đưa vi khuẩn nội sinh vào môi trường hoặc các cánh đồng nông nghiệp cần được đánh giá cẩn thận để tránh việc giới thiệu mầm bệnh.",{"EN":786,"VI":787},"Bacterial Endophytes and Their Interactions with Hosts","Vi khuẩn nội sinh và tương tác của chúng với vật chủ",{"VOID":789},"16903349",{"VOID":791},"10.1094\u002Fmpmi-19-0827","PUBLICATION","2024-10-11T02:42:52.472+00:00","Auto Verify",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI-19-0827",[799,821],{"id":800,"sortIndex":115,"researcher":26,"roles":801,"affiliations":802,"properties":814},"47f34ec3-804e-4c38-8ed8-62370ccd56c8",[],[803],{"id":804,"sortIndex":36,"affiliation":805,"properties":26},"f62477c3-828b-4e5f-aadc-81e1576d91a3",{"id":806,"createTime":807,"updateTime":808,"relativeEntities":809,"slug":810,"properties":811,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"0ce62f1f-01f6-4164-9892-4f8c6cee6d4e","2024-09-28T22:32:33.004+00:00","2024-10-11T02:42:52.499+00:00",[],"Microbiolog%C3%ADa-SNI-3-",{"title":812},{"EN":813},"Microbiología (SNI 3)",{"openalex":815,"orcid":817,"title":819},{"VOID":816},"A5083583173",{"VOID":818},"https:\u002F\u002Forcid.org\u002F0000-0002-2295-2606",{"EN":820},"Esperanza Martínez‐Romero",{"id":822,"sortIndex":36,"researcher":26,"roles":823,"affiliations":824,"properties":835},"8af1f311-4abf-48bb-94ca-24c6d7ad6bad",[],[825],{"id":826,"sortIndex":36,"affiliation":827,"properties":26},"a928bdc9-f738-4a6c-8455-6caad95f161d",{"id":828,"createTime":829,"updateTime":829,"relativeEntities":830,"slug":831,"properties":832,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"ceb5a0e8-c3f3-4c85-8ac9-fe1fd129ed05","2024-10-11T02:42:52.488+00:00",[],"Centro-de-Ciencias-Gen%C3%B3micas-Universidad-Nacional-Aut%C3%B3ma-de-M%C3%A9xico-Apdo-Postal-565-A-Cuernavaca-M%C3%A9xico-",{"title":833},{"EN":834},"Centro de Ciencias Genómicas, Universidad Nacional Autóma de México, Apdo. Postal 565-A, Cuernavaca, México.",{"openalex":836,"title":838},{"VOID":837},"A5074887878",{"EN":839},"Mónica Rosenblueth","ARTICLE",{"url":26,"publisher":842,"properties":867},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":843,"slug":663,"properties":844,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":850,"manageAffiliations":851,"indexDatabases":852,"url":764,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":845,"issn":846,"introduce":847,"eissn":848,"title":849},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[853,860],{"id":744,"indexDatabase":854,"url":759,"indexYears":26,"academicFieldIds":859,"indexDatabaseRanking":26},{"id":746,"createTime":747,"updateTime":748,"relativeEntities":855,"label":856,"description":857,"key":755,"publicationTags":858,"standard":26},[],{"EN":751,"VI":751},{"VI":753,"EN":754},[757,758],[761,762,763],{"id":723,"indexDatabase":861,"url":736,"indexYears":737,"academicFieldIds":866,"indexDatabaseRanking":742},{"id":725,"createTime":726,"updateTime":727,"relativeEntities":862,"label":863,"description":864,"key":733,"publicationTags":865,"standard":26},[],{"EN":730,"VI":730},{"EN":730,"VI":732},[735],[739,740,741],{"volume":868,"pages":870,"issue":872},{"VOID":869},"19",{"VOID":871},"827-837",{"VOID":873},"8",1379,{"total":874,"publishYear":26,"statisticByYear":876},{"2012":47,"2013":347,"2014":117,"2015":568,"2016":367,"2017":533,"2018":877,"2019":878,"2020":166,"2021":277,"2022":346,"2023":879,"2024":539},100,99,98,"2006-08-01",2006,[883,886,889,892,895,898,901,904,907,910,913,916,919,922,925,928,931,934,937,940,943,946,949,952,955,958,961,964,967,970,973,976,979,982,985,988,991,994,997,1000,1003,1006,1009,1013,1016,1019,1022,1025,1028,1031,1034,1037,1040,1043,1046,1049,1052,1055,1058,1061,1064,1067,1070,1073,1076,1079,1082,1085,1088,1091,1094,1097,1100,1103,1106,1109,1112,1115,1119,1122,1125,1128,1131,1134,1137,1140,1144,1147,1150,1153,1156,1160,1163,1166,1169,1172,1175,1178,1181,1184,1187,1190,1193,1196,1199,1202,1205,1208,1211,1214,1217,1220,1223,1226,1229,1232,1235,1238,1241,1244,1247,1250,1253,1256,1259,1262,1265,1268,1271,1274,1277,1280,1283,1286,1289,1292,1295,1298,1301,1304,1307,1310,1313,1317,1320,1323,1326,1329,1332,1335,1338,1341,1344,1347,1350,1353,1357,1361,1364,1368,1371,1374,1378,1381,1384,1387,1390,1393,1396],{"id":26,"text":884,"url":26,"identifiers":885},"α Proteobacteria Azorhizobium caulinodans Rice Engelhard et al. 2000 Azospirillum brasilense Banana Weber et al. 1999 Azospirillum amazonense Banana, pineapple Weber et al. 1999 Bradyrhizobium japonicum Rice Chantreuil et al. 2000 Gluconacetobacter diazotrophicus Sugarcane, coffee Cavalcante and Döbereiner 1988; Jiménez-Salgado et al. 1997 Methylobacterium mesophilicumaCitrus plants Araujo et al. 2002 Methylobacterium extorquens Scots pine, citrus plants Araujo et al. 2002; Pirttilä et al. 2004 Rhizobium leguminosarum Rice Yanni et al. 1997 Rhizobium (Agrobacterium) radiobacter Carrot, rice Surette et al. 2003 Sinorhizobium meliloti Sweet potato Reiter et al. 2003 Sphingomonas paucimobilisaRice Engelhard et al. 2000",{},{"id":26,"text":887,"url":26,"identifiers":888},"β Proteobacteria Azoarcus sp. Kallar grass, rice Engelhard et al. 2000; Reinhold-Hurek et al. 1993 Burkholderia pickettiiaMaize McInroy and Kloepper 1995 Burkholderia cepaciabYellow Iupine, citrus plants Araujo et al. 2001; Barac et al. 2004 Burkholderia sp. Banana, pineapple, rice Weber et al. 1999; Engelhard et al. 2000 Chromobacterium violaceumaRice Phillips et al. 2000 Herbaspirillum seropedicae Sugarcane, rice, maize, sorghum, banana Olivares et al. 1996; Weber et al. 1999 Herbaspirillum rubrisulbalbicans Sugarcane Olivares et al. 1996",{},{"id":26,"text":890,"url":26,"identifiers":891},"γ Proteobacteria Citrobacter sp. Banana Martínez et al. 2003 Enterobacter spp. Maize McInroy and Kloepper 1995 Enterobacter sakazakiiaSoybean Kuklinsky-Sobral et al. 2004 Enterobacter cloacaeaCitrus plants, maize Araujo et al. 2002; Hinton et al. 1995 Enterobacter agglomeransaSoybean Kuklinsky-Sobral et al. 2004 Enterobacter asburiae Sweet potato Asis and Adachi 2003 Erwinia sp. Soybean Kuklinsky-Sobral et al. 2004 Escherichia colibLettuce Ingham et al. 2005 Klebsiella sp. Wheat, sweet potato, rice Engelhard et al. 2000; Iniguez et al. 2004; Reiter et al. 2003 Klebsiella pneumoniaebSoybean Kuklinsky-Sobral et al. 2004 Klebsiella variicolabBanana, rice, maize, sugarcane Rosenblueth et al. 2004. Klebsiella terrigenaaCarrot Surette et al. 2003 Klebsiella oxytocabSoybean Kuklinsky-Sobral et al. 2004 Pantoea sp. Rice, soybean Kuklinsky-Sobral et al. 2004; Verma et al. 2004 Pantoea agglomerans Citrus plants, sweet potato Araujo et al. 2001, 2002; Asis and Adachi 2003 Pseudomonas chlororaphis Marigold (Tagetes spp.), carrot Sturz and Kimpinski 2004; Surette et al. 2003 Pseudomonas putidaaCarrot Surette et al. 2003 Pseudomonas fluorescens Carrot Surette et al. 2003 Pseudomonas citronellolis Soybean Kuklinsky-Sobral et al. 2004 Pseudomonas synxantha Scots pine Prittilä et al. 2004 Salmonella entericabAlfalfa, carrot, radish, tomato Cooley et al. 2003; Guo et al. 2002; Islam et al. 2004 Serratia sp. Rice Sandhiya et al. 2005 Serratia marcescensaRice Gyaneshwar et al. 2001 StenotrophomonasaDune grasses (Ammophila arenaria and",{},{"id":26,"text":893,"url":26,"identifiers":894},"Andreote F. D., 2004, J. 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K., and Triplett, E. W. 2000a. Diazotrophic endophytes associated with maize. Pages 779-791 in: Prokaryotic Nitrogen Fixation; A Model System for Analysis of a Biological Process. 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P., 1992, J. Biol. Chem., 267, 18814, 10.1016\u002FS0021-9258(19)37034-6",{"doi":1012},"10.1016\u002FS0021-9258(19)37034-6",{"id":26,"text":1014,"url":26,"identifiers":1015},"10.1094\u002FMPMI.1999.12.9.813",{"doi":1014},{"id":26,"text":1017,"url":26,"identifiers":1018},"10.1046\u002Fj.1462-2920.2000.00078.x",{"doi":1017},{"id":26,"text":1020,"url":26,"identifiers":1021},"10.1046\u002Fj.1365-313X.1999.00265.x",{"doi":1020},{"id":26,"text":1023,"url":26,"identifiers":1024},"10.1099\u002F00221287-142-9-2333",{"doi":1023},{"id":26,"text":1026,"url":26,"identifiers":1027},"10.1016\u002FS0168-6496(98)00125-1",{"doi":1026},{"id":26,"text":1029,"url":26,"identifiers":1030},"10.1016\u002Fj.femsec.2003.12.009",{"doi":1029},{"id":26,"text":1032,"url":26,"identifiers":1033},"10.1111\u002Fj.1574-6941.1998.tb01560.x",{"doi":1032},{"id":26,"text":1035,"url":26,"identifiers":1036},"Giller K. 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This regulatory mechanism, called autoinduction or quorumsensing, is based on the production by the bacteria of a small, diffusible signal molecule called the autoinducer. In the most well-studied systems the autoinducers are N-acylated derivatives of l-homoserine lactone (acyl-HSL). Signal specificity is conferred by the length, and the nature of the substitution at C-3, of the acyl side-chain. We evaluated four acyl-HSL bioreporters, based on tra of Agrobacterium tumefaciens, lux of Vibrio fischeri, las of Pseudomonas aeruginosa, and pigment production by Chromobacterium violaceum, for their ability to detect sets of 3-oxo acyl-HSLs, 3-hydroxy acyl-HSLs, and alkanoyl-HSLs with chain lengths ranging from C\u003Cjats:sub>4\u003C\u002Fjats:sub> to C\u003Cjats:sub>12\u003C\u002Fjats:sub>. The traG::lacZ fusion reporter from the A. tumefaciens Ti plasmid was the single most sensitive and versatile detector of the four. Using this reporter, we screened 106 isolates representing seven genera of bacteria that associate with plants. Most of the Agrobacterium, Rhizobium, and Pantoea isolates and about half of the Erwinia and Pseudomonas isolates gave positive reactions. Only a few isolates of Xanthomonas produced a detectable signal. We characterized the acyl-HSLs produced by a subset of the isolates by thin-layer chromatography. Among the pseudomonads and erwinias, most produced a single dominant activity chromatographing with the properties of N-(3-oxo-hexanoyl)-l-HSL. However, a few of the erwinias, and the P. fluorescens and Ralstonia solanacearum isolates, produced quite different signals, including 3-hydroxy forms, as well as active compounds that chromatographed with properties unlike any of our standards. The few positive xanthomonads, and almost all of the agrobacteria, produced small amounts of a compound with the chromatographic properties of N-(3-oxo-octanoyl)-l-HSL. Members of the genus Rhizobium showed the greatest diversity, with some producing as few as one and others producing as many as seven detectable signals. Several isolates produced extremely nonpolar compounds indicative of very long acyl side-chains. Production of these compounds suggests that quorum-sensing is common as a gene regulatory mechanism among gram-negative plant-associated bacteria. \u003C\u002Fjats:p>","\u003Cjats:p> Nhiều vi khuẩn Gram âm điều chỉnh sự biểu hiện của các tập hợp gen chuyên biệt khi đáp ứng với mật độ quần thể. Cơ chế điều chỉnh này, được gọi là tự định hình (autoinduction) hoặc cảm nhận mật độ quần thể (quorum sensing), dựa trên việc sản xuất bởi vi khuẩn một phân tử tín hiệu nhỏ, dễ khuếch tán gọi là autoinducer. Trong các hệ thống được nghiên cứu kỹ lưỡng nhất, các autoinducer là các dẫn xuất N-acyl hóa của l-homoserine lactone (acyl-HSL). Đặc tính tín hiệu được quy định bởi độ dài và bản chất của sự thay thế tại C-3 của chuỗi bên acyl. Chúng tôi đã đánh giá bốn báo cáo sinh học acyl-HSL, dựa trên tra của Agrobacterium tumefaciens, lux của Vibrio fischeri, las của Pseudomonas aeruginosa, và sản xuất sắc tố của Chromobacterium violaceum, về khả năng phát hiện các tập hợp 3-oxo acyl-HSLs, 3-hydroxy acyl-HSLs, và alkanoyl-HSLs với độ dài chuỗi từ C\u003Cjats:sub>4\u003C\u002Fjats:sub> đến C\u003Cjats:sub>12\u003C\u002Fjats:sub>. Báo cáo fusion traG::lacZ từ plasmid Ti của A. tumefaciens là thiết bị cảm biến nhạy cảm và linh hoạt nhất trong bốn loại. Sử dụng thiết bị báo cáo này, chúng tôi đã sàng lọc 106 chủng đại diện cho bảy giống vi khuẩn liên kết với thực vật. Phần lớn các chủng Agrobacterium, Rhizobium, và Pantoea cùng khoảng một nửa các chủng Erwinia và Pseudomonas đã cho phản ứng dương tính. Chỉ một vài chủng Xanthomonas tạo ra tín hiệu có thể phát hiện. Chúng tôi đã xác định các acyl-HSLs được sản xuất bởi một phần nhỏ các chủng thông qua sắc ký lớp mỏng. Trong số các pseudomonads và erwinias, phần lớn sản xuất một hoạt động chiếm ưu thế duy nhất phản ánh tính chất của N-(3-oxo-hexanoyl)-l-HSL. Tuy nhiên, một số ít erwinias, cùng với các chủng P. fluorescens và Ralstonia solanacearum, đã sản xuất tín hiệu hoàn toàn khác biệt, bao gồm các dạng 3-hydroxy, cũng như các hợp chất hoạt động đã sắc ký với các tính chất không giống bất cứ tiêu chuẩn nào của chúng tôi. Một vài xanthomonads dương tính, và gần như tất cả các vi khuẩn Agrobacterium, sản xuất một lượng nhỏ hợp chất với các tính chất sắc ký của N-(3-oxo-octanoyl)-l-HSL. Các chi Rhizobium cho thấy sự đa dạng lớn nhất, với một số sản xuất chỉ một tín hiệu và số khác sản xuất đến bảy tín hiệu có thể phát hiện. Một số chủng sản xuất các hợp chất cực kỳ không phân cực cho thấy chuỗi bên acyl rất dài. Việc sản xuất các hợp chất này gợi ý rằng cảm nhận mật độ quần thể là điều phổ biến như một cơ chế điều chỉnh gen giữa các vi khuẩn liên kết với thực vật thuộc nhóm Gram âm.",{"EN":1417,"VI":1418},"Production of Acyl-Homoserine Lactone Quorum-Sensing Signals by Gram-Negative Plant-Associated Bacteria","Sản xuất tín hiệu Quorum-Sensing Acyl-Homoserine Lactone bởi các vi khuẩn liên kết với thực vật thuộc nhóm Gram âm",{"VOID":1420},"9805399",{"VOID":1422},"10.1094\u002Fmpmi.1998.11.11.1119",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI.1998.11.11.1119",[1427,1458,1475,1490,1505],{"id":1428,"sortIndex":111,"researcher":26,"roles":1429,"affiliations":1430,"properties":1451},"2531ea6b-efff-48dd-98da-12cae48f2dbc",[],[1431,1441],{"id":1432,"sortIndex":36,"affiliation":1433,"properties":26},"526ce8b4-6c7e-4340-997b-c2bd4d05cdab",{"id":1434,"createTime":1435,"updateTime":1435,"relativeEntities":1436,"slug":1437,"properties":1438,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"9e840189-7ae6-49bb-a9f1-1e6d02786a5e","2024-09-24T21:13:52.999+00:00",[],"Department-of-Crop-Sciences-University-of-Illinois-at-Urbana-Champaign-Urbana-61801-U-S-A-",{"title":1439},{"EN":1440},"Department of Crop Sciences, University of Illinois at Urbana-Champaign, Urbana 61801, U.S.A.",{"id":1442,"sortIndex":115,"affiliation":1443,"properties":26},"d74eb2cd-d630-4971-913f-b73b77b4cff6",{"id":1444,"createTime":1445,"updateTime":1445,"relativeEntities":1446,"slug":1447,"properties":1448,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"5ee36b7e-66a3-42a6-9ae6-02daee2ede02","2024-09-24T21:13:53.038+00:00",[],"Department-of-Microbiology-University-of-Illinois-at-Urbana-Champaign-Urbana-61801-U-S-A-",{"title":1449},{"EN":1450},"Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana 61801, U.S.A.",{"openalex":1452,"orcid":1454,"title":1456},{"VOID":1453},"A5061349867",{"VOID":1455},"https:\u002F\u002Forcid.org\u002F0000-0002-2489-7161",{"EN":1457},"Stephen K. Farrand",{"id":1459,"sortIndex":114,"researcher":26,"roles":1460,"affiliations":1461,"properties":1468},"0a158f56-3993-4e25-9901-4e2585ab8405",[],[1462],{"id":1463,"sortIndex":36,"affiliation":1464,"properties":26},"717f8297-bd9a-48a0-8a95-dd269253d86e",{"id":1434,"createTime":1435,"updateTime":1435,"relativeEntities":1465,"slug":1437,"properties":1466,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":1467},{"EN":1440},{"openalex":1469,"orcid":1471,"title":1473},{"VOID":1470},"A5031964929",{"VOID":1472},"https:\u002F\u002Forcid.org\u002F0000-0002-9932-1298",{"EN":1474},"Yu-Ching Chen",{"id":1476,"sortIndex":36,"researcher":26,"roles":1477,"affiliations":1478,"properties":1485},"f9416593-c0e3-403e-8d2a-2757c26ff4db",[],[1479],{"id":1480,"sortIndex":36,"affiliation":1481,"properties":26},"71d714e1-8037-4fc9-aa90-afc03b2ae245",{"id":1434,"createTime":1435,"updateTime":1435,"relativeEntities":1482,"slug":1437,"properties":1483,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":1484},{"EN":1440},{"openalex":1486,"title":1488},{"VOID":1487},"A5052207533",{"EN":1489},"Chung Cha",{"id":1491,"sortIndex":59,"researcher":26,"roles":1492,"affiliations":1493,"properties":1500},"09f27f25-4792-48b8-b1b6-b4bef69deea5",[],[1494],{"id":1495,"sortIndex":36,"affiliation":1496,"properties":26},"a94b0fe8-4e8c-42ed-9156-2e4a1d835cf6",{"id":1434,"createTime":1435,"updateTime":1435,"relativeEntities":1497,"slug":1437,"properties":1498,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":1499},{"EN":1440},{"openalex":1501,"title":1503},{"VOID":1502},"A5103416025",{"EN":1504},"Paul D. 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Bacteriol., 104, 313, 10.1128\u002Fjb.104.1.313-322.1970",{"doi":1643},"10.1128\u002Fjb.104.1.313-322.1970",{"id":26,"text":1645,"url":26,"identifiers":1646},"10.1073\u002Fpnas.92.14.6424",{"doi":1645},{"id":26,"text":1648,"url":26,"identifiers":1649},"10.1126\u002Fscience.8493556",{"doi":1648},{"id":26,"text":1651,"url":26,"identifiers":1652},"10.1073\u002Fpnas.91.1.197",{"doi":1651},{"id":26,"text":1654,"url":26,"identifiers":1655},"10.1128\u002Fjb.179.18.5756-5767.1997",{"doi":1654},{"id":26,"text":1657,"url":26,"identifiers":1658},"10.1128\u002Fjb.176.13.3966-3974.1994",{"doi":1657},{"id":26,"text":1660,"url":26,"identifiers":1661},"10.1038\u002F362448a0",{"doi":1660},{"id":26,"text":1663,"url":26,"identifiers":1664},"10.1002\u002Fj.1460-2075.1993.tb05901.x",{"doi":1663},{"id":26,"text":1666,"url":26,"identifiers":1667},"10.1128\u002FJB.179.2.439-444.1997",{"doi":1666},{"id":26,"text":1669,"url":26,"identifiers":1670},"10.1094\u002FMPMI.1998.11.1.68",{"doi":1669},{"id":26,"text":1672,"url":26,"identifiers":1673},"10.1128\u002Fjb.179.23.7530-7537.1997",{"doi":1672},{"id":26,"text":1675,"url":26,"identifiers":1676},"Rosemeyer V., 1998, J. Bacteriol., 180, 815, 10.1128\u002FJB.180.4.815-821.1998",{"doi":1677},"10.1128\u002FJB.180.4.815-821.1998",{"id":26,"text":1679,"url":26,"identifiers":1680},"Sambrook, J., Fritsch, E. F., and Maniatis, T. A. 1989. Molecular Cloning: A Laboratory Manual. 2nd ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.",{},{"id":26,"text":1682,"url":26,"identifiers":1683},"10.1128\u002Fjb.178.2.366-371.1996",{"doi":1682},{"id":26,"text":1685,"url":26,"identifiers":1686},"10.1073\u002Fpnas.94.12.6036",{"doi":1685},{"id":26,"text":1688,"url":26,"identifiers":1689},"Somasegaran, P., and Hoben, H. J. 1985. Page 273 in: Methods in Legume-Rhizobium Technology. NiftTAL, University of Hawaii Press, Honolulu.",{},{"id":26,"text":1691,"url":26,"identifiers":1692},"10.1128\u002Fjb.179.17.5271-5281.1997",{"doi":1691},{"id":26,"text":1694,"url":26,"identifiers":1695},"10.1128\u002FJB.170.8.3499-3508.1988",{"doi":1694},{"id":26,"text":1697,"url":26,"identifiers":1698},"10.1111\u002Fj.1365-2958.1995.mmi_17020345.x",{"doi":1697},{"id":26,"text":1700,"url":26,"identifiers":1701},"Vogel H. J., 1956, J. Biol. Chem., 218, 97, 10.1016\u002FS0021-9258(18)65874-0",{"doi":1702},"10.1016\u002FS0021-9258(18)65874-0",{"id":26,"text":1704,"url":26,"identifiers":1705},"Watson B, 1975, J. Bacteriol., 123, 255, 10.1128\u002Fjb.123.1.255-264.1975",{"doi":1706},"10.1128\u002Fjb.123.1.255-264.1975",{"id":26,"text":1708,"url":26,"identifiers":1709},"10.1073\u002Fpnas.92.20.9427",{"doi":1708},{"id":26,"text":1711,"url":26,"identifiers":1712},"10.1038\u002F362446a0",{"doi":1711},{"id":1714,"createTime":1715,"updateTime":1716,"relativeEntities":1717,"slug":1718,"properties":1719,"entityType":792,"verifyStatus":28,"verifyTime":1736,"verifyNote":1737,"syncStatus":28,"languages":1738,"translateLanguages":1739,"viewCount":36,"primaryUrl":1740,"fullTextUrl":26,"authors":1741,"publicationType":840,"publisherRelationship":1849,"citationCount":1882,"citationInfo":1883,"publishDate":1885,"publishYear":1886,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":1887,"isForceReanalyzing":1399},"50d9b130-4a35-4ab9-8e51-64afe5bbbd27","2024-09-20T19:04:20.142+00:00","2025-02-22T18:43:06.269+00:00",[],"OsWRKY13-Mediates-Rice-Disease-Resistance-by-Regulating-Defense-Related-Genes-in-Salicylate-and-Jasmonate-Dependent-Signaling",{"mag":1720,"keywords":1722,"openalex":1724,"abstract":1726,"title":1729,"pm":1732,"doi":1734},{"VOID":1721},"2148962030",{"VI":1723},"WRKY genes, rice disease resistance, OsWRKY13, salicylic acid, jasmonic acid, transgenic tool",{"VOID":1725},"W2148962030",{"EN":1727,"VI":1728},"\u003Cjats:p> Although 109 WRKY genes have been identified in the rice genome, the functions of most are unknown. Here, we show that OsWRKY13 plays a pivotal role in rice disease resistance. Overexpression of OsWRKY13 can enhance rice resistance to bacterial blight and fungal blast, two of the most devastating diseases of rice worldwide, at both the seedling and adult stages, and shows no influence on the fertility. This overexpression was accompanied by the activation of salicylic acid (SA) synthesis-related genes and SA-responsive genes and the suppression of jasmonic acid (JA) synthesis-related genes and JA-responsive genes. OsWRKY13 bound to the promoters of its own and at least three other genes in SA- and JA-dependent signaling pathways. Its DNA-binding activity was influenced by pathogen infection. These results suggest that OsWRKY13, as an activator of the SA-dependent pathway and a suppressor of JA-dependent pathways, mediates rice resistance by directly or indirectly regulating the expression of a subset of genes acting both upstream and downstream of SA and JA. Furthermore, OsWRKY13 will provide a transgenic tool for engineering wider-spectrum and whole-growth-stage resistance rice in breeding programs. \u003C\u002Fjats:p>","\u003Cjats:p> Mặc dù đã xác định được 109 gen WRKY trong bộ gen lúa, chức năng của hầu hết chúng vẫn chưa được biết đến. Trong nghiên cứu này, chúng tôi chỉ ra rằng OsWRKY13 đóng vai trò quan trọng trong khả năng chống bệnh của lúa. Việc overexpression OsWRKY13 có thể tăng cường khả năng kháng bệnh của lúa đối với bệnh cháy bacterial và bệnh nấm blast, hai trong số những bệnh tồi tệ nhất đối với lúa trên toàn cầu, ở cả giai đoạn cây giống và cây trưởng thành, và không ảnh hưởng đến độ phì nhiêu. Việc overexpression này đi kèm với sự kích hoạt của các gen liên quan đến tổng hợp axit salicylic (SA) và các gen phản ứng với SA cũng như sự подавление của các gen liên quan đến tổng hợp axit jasmonic (JA) và các gen phản ứng với JA. OsWRKY13 đã liên kết với các promoter của chính nó và ít nhất ba gen khác trong các đường tín hiệu phụ thuộc vào SA và JA. Hoạt động liên kết DNA của nó bị ảnh hưởng bởi sự nhiễm khuẩn. Các kết quả này gợi ý rằng OsWRKY13, với tư cách là một chất kích hoạt của đường dẫn phụ thuộc vào SA và chất ức chế các đường dẫn phụ thuộc vào JA, làm trung gian cho khả năng chống bệnh của lúa bằng cách điều chỉnh trực tiếp hoặc gián tiếp việc biểu hiện của một tập hợp các gen hoạt động ở cả phía thượng và hạ nguồn của SA và JA. Hơn nữa, OsWRKY13 sẽ cung cấp một công cụ biến đổi gen để kỹ thuật lúa có khả năng kháng rộng hơn và ở tất cả các giai đoạn phát triển trong các chương trình nhân giống.\u003C\u002Fjats:p>",{"EN":1730,"VI":1731},"OsWRKY13 Mediates Rice Disease Resistance by Regulating Defense-Related Genes in Salicylate- and Jasmonate-Dependent Signaling","OsWRKY13 Điều Hòa Khả Năng Chống Chọi Bệnh Ở Lúa Bằng Cách Điều Chỉnh Các Gen Liên Quan Đến Phòng Thủ Trong Các Đường Tín Hiệu Phụ Thuộc Vào Axit Salicylic và Axit Jasmonic",{"VOID":1733},"17506327",{"VOID":1735},"10.1094\u002Fmpmi-20-5-0492","2024-09-20T19:04:20.141+00:00","Author affiliation is 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China.",{"openalex":1779,"orcid":1781,"title":1783},{"VOID":1780},"A5102853070",{"VOID":1782},"https:\u002F\u002Forcid.org\u002F0000-0002-7297-8660",{"EN":1784},"Deyun Qiu",{"id":1786,"sortIndex":59,"researcher":26,"roles":1787,"affiliations":1788,"properties":1789},"e9df674a-7a4b-48a1-bc32-8b18dd2d12c4",[],[],{"openalex":1790,"orcid":1792,"title":1794},{"VOID":1791},"A5075391403",{"VOID":1793},"https:\u002F\u002Forcid.org\u002F0000-0001-9926-3836",{"EN":1795},"Min Xiong",{"id":1797,"sortIndex":114,"researcher":26,"roles":1798,"affiliations":1799,"properties":1800},"01d026f4-c955-4318-a0cb-8cd95d86e82f",[],[],{"openalex":1801,"orcid":1803,"title":1805},{"VOID":1802},"A5082057029",{"VOID":1804},"https:\u002F\u002Forcid.org\u002F0000-0002-6510-5992",{"EN":1806},"Xinhua 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N., Somssich, I. E., Roby, D., and Kroj, T. 2006. The transcription factors WRKY11 and WRKY17 act as negative regulators of basal resistance in Arabidopsis thaliana. Plant Cell (in press).",{"doi":1948},"10.1105\u002Ftpc.106.044149",{"id":26,"text":1950,"url":26,"identifiers":1951},"Kauffman H. E., 1973, Plant Dis. 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Here, we present a historical overview of the progress that has been made to date in elucidating the role of SA in signaling plant immune responses. The ability of plants to develop acquired immunity after pathogen infection was first proposed in 1933. However, most of our knowledge about plant immune signaling was generated over the last three decades, following the discovery that SA is an endogenous defense signal. During this timeframe, researchers have identified i) two pathways through which SA can be synthesized, ii) numerous proteins that regulate SA synthesis and metabolism, and iii) some of the signaling components that function downstream of SA, including a large number of SA targets or receptors. In addition, it has become increasingly evident that SA does not signal immune responses by itself but, rather, as part of an intricate network that involves many other plant hormones. Future efforts to develop a comprehensive understanding of SA-mediated immune signaling will therefore need to close knowledge gaps that exist within the SA pathway itself as well as clarify how crosstalk among the different hormone signaling pathways leads to an immune response that is both robust and optimized for maximal efficacy, depending on the identity of the attacking pathogen. \u003C\u002Fjats:p>","\u003Cjats:p> Bài báo này là một phần trong loạt bài đánh giá nổi bật về những đột phá khái niệm và phương pháp trong tương tác giữa thực vật và vi sinh vật. \u003C\u002Fjats:p>\u003Cjats:p> Axit Salicylic (SA) là một hormone thực vật quan trọng điều chỉnh nhiều khía cạnh của sự phát triển và sinh trưởng của thực vật cũng như việc kích hoạt các cơ chế phòng vệ chống lại căng thẳng sinh học và phi sinh học. Ở đây, chúng tôi trình bày một cái nhìn tổng quan lịch sử về tiến trình mà chúng tôi đã đạt được đến nay trong việc làm sáng tỏ vai trò của SA trong việc thông hiệu ứng miễn dịch của thực vật. Khả năng của thực vật có thể phát triển miễn dịch thu được sau khi bị nhiễm bệnh được đề xuất lần đầu tiên vào năm 1933. Tuy nhiên, hầu hết những kiến thức của chúng ta về thông hiệu miễn dịch thực vật được hình thành trong ba thập kỷ qua, sau khi phát hiện ra rằng SA là một tín hiệu phòng vệ nội sinh. Trong khoảng thời gian này, các nhà nghiên cứu đã xác định i) hai con đường mà qua đó SA có thể được tổng hợp, ii) nhiều protein điều chỉnh sự tổng hợp và chuyển hóa của SA, và iii) một số thành phần thông hiệu hoạt động dưới tác động của SA, bao gồm một số lượng lớn các đích hoặc thụ thể của SA. Ngoài ra, ngày càng rõ ràng rằng SA không thông hiệu kích ứng miễn dịch một mình mà, thay vào đó, là một phần của một mạng lưới phức tạp có liên quan đến nhiều hormone thực vật khác. 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Arabidopsis NPR1\u002FNIM1 is a key regulator of systemic acquired resistance (SAR), which confers lasting broad-spectrum resistance. Previous reports indicate that rice has a disease-resistance pathway similar to the Arabidopsis SAR pathway. Here we report the isolation and characterization of a rice NPR1 homologue (NH1). Transgenic rice plants overexpressing NH1 (NH1ox) acquire high levels of resistance to Xanthomonas oryzae pv. oryzae. The resistance phenotype is heritable and correlates with the presence of the transgene and reduced bacterial growth. Northern analysis shows that NH1ox rice spontaneously activates defense genes, contrasting with NPR1-overexpressing Arabidopsis, where defense genes are not activated until induction. Wild-type NH1, but not a point mutant corresponding to npr1-1, interacts strongly with the rice transcription factor rTGA2.2 in yeast two-hybrid. Greenhouse-grown NH1ox plants develop lesion-mimic spots on leaves at preflowering stage although no other developmental effects are observed. However, when grown in growth chambers (GCs) under low light, NH1ox plants are dwarfed, indicating elevated sensitivity to light. The GC-grown NH1ox plants show much higher salicylic acid (SA) levels than the wild type, whereas greenhouse-grown NH1ox plants contain lower SA. These results indicate that NH1 may be involved in the regulation of SA in response to environmental changes. \u003C\u002Fjats:p>","\u003Cjats:p> NPR1\u002FNIM1 của Arabidopsis là một yếu tố điều tiết chính trong khả năng kháng bệnh thu được theo hệ thống (SAR), mang lại khả năng kháng bền vững rộng rãi. Các báo cáo trước đây cho thấy lúa có một con đường kháng bệnh tương tự như con đường SAR của Arabidopsis. Ở đây, chúng tôi báo cáo việc phân lập và đặc tính hóa một đồng hình NPR1 ở lúa (NH1). Các cây lúa chuyển gen biểu hiện quá mức NH1 (NH1ox) đạt được mức độ kháng cao đối với Xanthomonas oryzae pv. oryzae. Biểu hiện kháng này có thể di truyền và tương quan với sự hiện diện của gen chuyển và sự giảm tăng trưởng của vi khuẩn. Phân tích Northern cho thấy rằng cây lúa NH1ox tự phát kích hoạt các gen phòng thủ, trái ngược với ngô Arabidopsis biểu hiện quá mức NPR1, nơi mà các gen phòng thủ không được kích hoạt cho đến khi có sự khởi động. NH1 kiểu hoang dã, nhưng không phải là một đột biến điểm tương ứng với npr1-1, tương tác mạnh mẽ với yếu tố phiên mã rTGA2.2 của lúa trong thí nghiệm lai hai thủy tinh. Các cây NH1ox trồng trong nhà kính phát triển các đốm giống như tổn thương trên lá ở giai đoạn trước ra hoa mặc dù không quan sát thấy các hiệu ứng phát triển khác. Tuy nhiên, khi được trồng trong các buồng tăng trưởng (GCs) dưới ánh sáng yếu, các cây NH1ox bị lùn lại, cho thấy có độ nhạy cảm cao hơn với ánh sáng. Các cây NH1ox trồng trong GC cho thấy mức axit salicylic (SA) cao hơn nhiều so với kiểu hoang dã, trong khi các cây NH1ox trồng trong nhà kính chứa ít SA hơn. Những kết quả này chỉ ra rằng NH1 có thể tham gia vào việc điều tiết SA phản ứng với thay đổi môi trường.",{"EN":2919,"VI":2920},"Overexpression of a Rice NPR1 Homolog Leads to Constitutive Activation of Defense Response and Hypersensitivity to Light","Sự biểu hiện quá mức của đồng hình NPR1 ở lúa dẫn đến việc kích hoạt liên tục phản ứng phòng thủ và nhạy cảm với ánh sáng",{"VOID":2922},"15986920",{"VOID":2924},"10.1094\u002Fmpmi-18-0511",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI-18-0511",[2929,2938,2971,2982,3004],{"id":2930,"sortIndex":115,"researcher":26,"roles":2931,"affiliations":2932,"properties":2933},"a9b30d0a-521d-46a7-9411-74f8fe0d96c9",[],[],{"openalex":2934,"title":2936},{"VOID":2935},"A5069154529",{"EN":2937},"Heather A. 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Ronald",{"id":2972,"sortIndex":59,"researcher":26,"roles":2973,"affiliations":2974,"properties":2975},"26acb2f3-20c6-4234-bd97-57fb2512675f",[],[],{"openalex":2976,"orcid":2978,"title":2980},{"VOID":2977},"A5046120926",{"VOID":2979},"https:\u002F\u002Forcid.org\u002F0000-0002-7763-2108",{"EN":2981},"Duroy A. 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L., Wood, J., and Hicks, J. B. 1984. Pages 36-37 in: Molecular Biology of Plants. A Laboratory Course Manual. M. Russell, ed. 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Differential expression of rice PR-1 and PR-10 genes induced by blast fungus, elicitor, and chemical treatments. (Abstr.) Phytopathology 89:S62",{},{"id":26,"text":3136,"url":26,"identifiers":3137},"Rohilla R., 2002, Sci., 58, 63",{},{"id":26,"text":3139,"url":26,"identifiers":3140},"10.2307\u002F3870231",{"doi":3139},{"id":26,"text":2562,"url":26,"identifiers":3142},{"doi":2562},{"id":26,"text":3144,"url":26,"identifiers":3145},"10.1023\u002FA:1008791223608",{"doi":3144},{"id":26,"text":2580,"url":26,"identifiers":3147},{"doi":2580},{"id":26,"text":3149,"url":26,"identifiers":3150},"10.1104\u002Fpp.108.2.633",{"doi":3149},{"id":26,"text":3152,"url":26,"identifiers":3153},"10.1016\u002F0885-5765(91)90011-6",{"doi":3152},{"id":26,"text":1998,"url":26,"identifiers":3155},{"doi":1998},{"id":26,"text":3157,"url":26,"identifiers":3158},"10.1105\u002Ftpc.000679",{"doi":3157},{"id":26,"text":3160,"url":26,"identifiers":3161},"10.1094\u002FMPMI.2000.13.8.869",{"doi":3160},{"id":26,"text":2028,"url":26,"identifiers":3163},{"doi":2028},{"id":26,"text":3165,"url":26,"identifiers":3166},"10.1105\u002Ftpc.014894",{"doi":3165},{"id":26,"text":3168,"url":26,"identifiers":3169},"10.1094\u002FMPMI.2000.13.2.191",{"doi":3168},{"id":3171,"createTime":3172,"updateTime":3173,"relativeEntities":3174,"slug":3175,"properties":3176,"entityType":792,"verifyStatus":28,"verifyTime":3193,"verifyNote":1737,"syncStatus":28,"languages":3194,"translateLanguages":3195,"viewCount":36,"primaryUrl":3196,"fullTextUrl":26,"authors":3197,"publicationType":840,"publisherRelationship":3293,"citationCount":3324,"citationInfo":3325,"publishDate":3327,"publishYear":881,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":3328,"isForceReanalyzing":1399},"eeb96a6f-9893-4690-814d-6cbeaaf48319","2024-08-31T00:04:07.497+00:00","2025-02-22T18:46:01.062+00:00",[],"The-Eight-Amino-Acid-Differences-Within-Three-Leucine-Rich-Repeats-Between-Pi2-and-Piz-t-Resistance-Proteins-Determine-the-Resistance-Specificity-to-i-Magnaporthe-grisea-i-",{"mag":3177,"keywords":3179,"openalex":3181,"abstract":3183,"title":3186,"pm":3189,"doi":3191},{"VOID":3178},"2015458952",{"VI":3180},"gene kháng, Pi2, Piz-t, Magnaporthe grisea, protein kháng, amino acid, leucine-rich repeat, mảng gen.",{"VOID":3182},"W2015458952",{"EN":3184,"VI":3185},"\u003Cjats:p> The rice blast resistance (R) genes Pi2 and Piz-t confer broad-spectrum resistance against different sets of Magnaporthe grisea isolates. We first identified the Pi2 gene using a map-based cloning strategy. The Pi2 gene is a member of a gene cluster comprising nine gene members (named Nbs1-Pi2 to Nbs9-Pi2) and encodes a protein with a nucleotide-binding site and leucine-rich repeat (LRR) domain. Fine genetic mapping, molecular characterization of the Pi2 susceptible mutants, and complementation tests indicated that Nbs4-Pi2 is the Pi2 gene. The Piz-t gene, a Pi2 allele in the rice cultivar Toride 1, was isolated based on the Pi2 sequence information. Complementation tests confirmed that the family member Nbs4-Piz-t is Piz-t. Sequence comparison revealed that only eight amino-acid changes, which are confined within three consecutive LRR, differentiate Piz-t from Pi2. Of the eight variants, only one locates within the xxLxLxx motif. A reciprocal exchange of the single amino acid between Pi2 and Piz-t did not convert the resistance specificity to each other but, rather, abolished the function of both resistance proteins. These results indicate that the single amino acid in the xxLxLxx motif may be critical for maintaining the recognition surface of Pi2 and Piz-t to their respective avirulence proteins. \u003C\u002Fjats:p>","\u003Cjats:p> Các gen kháng phấn hôi gạo (R) Pi2 và Piz-t mang lại khả năng kháng rộng rãi đối với các bộ tách khác nhau của các isolát Magnaporthe grisea. Chúng tôi đã xác định gen Pi2 đầu tiên bằng chiến lược nhân bản dựa trên bản đồ gen. Gen Pi2 là thành viên của một cụm gen bao gồm chín thành viên (được đặt tên là Nbs1-Pi2 đến Nbs9-Pi2) và mã hóa một protein có vị trí liên kết nucleotide và miền lặp lại giàu leucine (LRR). Việc lập bản đồ gen tinh vi, đặc trưng phân tử của các đột biến nhạy cảm với Pi2, và các thử nghiệm bổ sung chỉ ra rằng Nbs4-Pi2 là gen Pi2. Gen Piz-t, một alen của Pi2 trong giống lúa Toride 1, được tách biệt dựa trên thông tin trình tự của Pi2. Các thử nghiệm bổ sung xác nhận rằng thành viên trong gia đình Nbs4-Piz-t là Piz-t. So sánh trình tự cho thấy chỉ có tám thay đổi amino acid, mà chỉ nằm trong ba LRR liên tiếp, phân biệt Piz-t với Pi2. Trong số tám biến thể này, chỉ có một biến thể nằm trong motif xxLxLxx. Việc trao đổi tương hỗ một amino acid đơn giữa Pi2 và Piz-t không chuyển đổi tính đặc hiệu kháng của nhau mà ngược lại, đã làm mất chức năng của cả hai protein kháng. Những kết quả này cho thấy rằng một amino acid đơn trong motif xxLxLxx có thể là rất quan trọng để duy trì bề mặt nhận diện của Pi2 và Piz-t đối với các protein avirulence tương ứng của chúng.",{"EN":3187,"VI":3188},"The Eight Amino-Acid Differences Within Three Leucine-Rich Repeats Between Pi2 and Piz-t Resistance Proteins Determine the Resistance Specificity to \u003Ci>Magnaporthe grisea\u003C\u002Fi>","Tám sự khác biệt amino acid trong ba vòng lặp giàu leucine giữa các protein kháng Pi2 và Piz-t xác định tính đặc hiệu kháng với \u003Ci>Magnaporthe grisea\u003C\u002Fi>",{"VOID":3190},"17073304",{"VOID":3192},"10.1094\u002Fmpmi-19-1216","2024-08-31T00:04:07.496+00:00",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI-19-1216",[3198,3209,3220,3229,3240,3262,3273,3284],{"id":3199,"sortIndex":158,"researcher":26,"roles":3200,"affiliations":3201,"properties":3202},"c6cd3cae-0731-4adb-a7f3-307f034b8de6",[],[],{"openalex":3203,"orcid":3205,"title":3207},{"VOID":3204},"A5100621243",{"VOID":3206},"https:\u002F\u002Forcid.org\u002F0000-0001-8877-3064",{"EN":3208},"Guo‐Liang Wang",{"id":3210,"sortIndex":162,"researcher":26,"roles":3211,"affiliations":3212,"properties":3213},"dd2025ec-1236-4d93-99a5-9b0ccccf8612",[],[],{"openalex":3214,"orcid":3216,"title":3218},{"VOID":3215},"A5025742489",{"VOID":3217},"https:\u002F\u002Forcid.org\u002F0000-0001-6325-9165",{"EN":3219},"Guodong Lu",{"id":3221,"sortIndex":111,"researcher":26,"roles":3222,"affiliations":3223,"properties":3224},"97efd198-3788-477f-bf3d-08ac93fca987",[],[],{"openalex":3225,"title":3227},{"VOID":3226},"A5001474799",{"EN":3228},"Hajime Sakai",{"id":3230,"sortIndex":114,"researcher":26,"roles":3231,"affiliations":3232,"properties":3233},"9cd3cbd7-c844-4663-a354-076cb71b058a",[],[],{"openalex":3234,"orcid":3236,"title":3238},{"VOID":3235},"A5101837266",{"VOID":3237},"https:\u002F\u002Forcid.org\u002F0000-0001-8285-7160",{"EN":3239},"Guifu Liu",{"id":3241,"sortIndex":36,"researcher":26,"roles":3242,"affiliations":3243,"properties":3255},"93c1886e-0766-44cc-8ec2-d918a4850288",[],[3244],{"id":3245,"sortIndex":36,"affiliation":3246,"properties":26},"3b11292a-2abc-455d-899b-87031dd8666f",{"id":3247,"createTime":3248,"updateTime":3249,"relativeEntities":3250,"slug":3251,"properties":3252,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"aa488504-2d06-4ee1-b033-311e16f8cc4d","2023-12-02T01:02:28.063+00:00","2024-08-31T00:04:07.514+00:00",[],"Department-of-Plant-Pathology-Ohio-State-University-Columbus-OH-43210-USA",{"title":3253},{"VI":3254},"Department of Plant Pathology, Ohio State University, Columbus, OH 43210, USA",{"openalex":3256,"orcid":3258,"title":3260},{"VOID":3257},"A5075749676",{"VOID":3259},"https:\u002F\u002Forcid.org\u002F0000-0001-9631-954X",{"EN":3261},"Bo Zhou",{"id":3263,"sortIndex":135,"researcher":26,"roles":3264,"affiliations":3265,"properties":3266},"cfc36997-cc7a-4f1f-b5d9-891ce42ca092",[],[],{"openalex":3267,"orcid":3269,"title":3271},{"VOID":3268},"A5017537645",{"VOID":3270},"https:\u002F\u002Forcid.org\u002F0000-0003-1212-0723",{"EN":3272},"Maria Bellizzi",{"id":3274,"sortIndex":115,"researcher":26,"roles":3275,"affiliations":3276,"properties":3277},"40f1ffb3-2249-4079-8f7f-3be05259960a",[],[],{"openalex":3278,"orcid":3280,"title":3282},{"VOID":3279},"A5090021726",{"VOID":3281},"https:\u002F\u002Forcid.org\u002F0000-0003-2072-122X",{"EN":3283},"Shaohong Qu",{"id":3285,"sortIndex":59,"researcher":26,"roles":3286,"affiliations":3287,"properties":3288},"cd391965-18bf-499a-965b-6dfcbbb824e7",[],[],{"openalex":3289,"title":3291},{"VOID":3290},"A5066394265",{"EN":3292},"M. 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This inhibition appears to be reversible because removal of the NO donor led to a significant recovery of enzymatic activity. In contrast, APX and catalase were irreversibly inhibited by peroxynitrite. The ability of NO and peroxynitrite to inhibit the two major H\u003Cjats:sub>2\u003C\u002Fjats:sub>O\u003Cjats:sub>2\u003C\u002Fjats:sub>-scavenging enzymes in plant cells suggests that NO may participate in redox signaling during the activation of defense responses following pathogen attack. \u003C\u002Fjats:p>","\u003Cjats:p> Chúng tôi đã sử dụng nhiều loại tác nhân cho nitric oxide (NO) để chứng minh rằng NO ức chế các hoạt động của catalase thuốc lá và ascorbate peroxidase (APX). Sự ức chế này dường như là có thể đảo ngược vì việc loại bỏ tác nhân NO dẫn đến sự phục hồi đáng kể của hoạt động enzym. Ngược lại, APX và catalase bị ức chế không thể đảo ngược bởi peroxynitrite. Khả năng của NO và peroxynitrite trong việc ức chế hai enzym chính trong việc thu hồi H\u003Cjats:sub>2\u003C\u002Fjats:sub>O\u003Cjats:sub>2\u003C\u002Fjats:sub> trong các tế bào thực vật cho thấy rằng NO có thể tham gia vào tín hiệu redox trong quá trình kích hoạt các phản ứng phòng thủ sau khi bị tấn công bởi mầm bệnh. \u003C\u002Fjats:p>",{"EN":3535,"VI":3536},"Nitric Oxide Inhibition of Tobacco Catalase and Ascorbate Peroxidase","Sự ức chế của Nitric Oxide đối với Catalase và Ascorbate Peroxidase của thuốc lá",{"VOID":3538},"11106031",{"VOID":3540},"10.1094\u002Fmpmi.2000.13.12.1380",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI.2000.13.12.1380",[3545,3566,3574,3604],{"id":3546,"sortIndex":36,"researcher":26,"roles":3547,"affiliations":3548,"properties":3559},"696405ed-b157-4808-a2f9-6b78f9f5793b",[],[3549],{"id":3550,"sortIndex":36,"affiliation":3551,"properties":26},"847c3467-da2a-4ba1-b28d-c5b18ee43d3a",{"id":3552,"createTime":3553,"updateTime":3553,"relativeEntities":3554,"slug":3555,"properties":3556,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"77d24eb2-11c1-4826-8e67-b6477f769b66","2024-09-20T11:25:22.588+00:00",[],"Waksman-Institute-Rutgers-The-State-University-of-New-Jersey-Piscataway-08854-8020-USA-",{"title":3557},{"EN":3558},"Waksman Institute, Rutgers--The State University of New Jersey, Piscataway 08854-8020, USA.",{"openalex":3560,"orcid":3562,"title":3564},{"VOID":3561},"A5024266081",{"VOID":3563},"https:\u002F\u002Forcid.org\u002F0000-0001-5819-0132",{"EN":3565},"Daniel D. 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interference is of value in determining gene function in many organisms. Plant parasitic nematodes are refractory to microinjection as a means of introducing RNA and do not show any oral uptake until they are within plants. We have used octopamine to stimulate uptake by prepara-sitic second stage juveniles of two cyst nematodes, Heterodera glycines and Globodera pallida. This new technique was used to facilitate uptake of double stranded RNA (dsRNA) together with fluoroscein isothiocyanate as a visual marker. Targeting cysteine proteinases did not reduce the number of parasites but caused a shift from the normal female\u002Fmale ratio of 3:1 to 1:1 by 14 days postinfection (dpi). Exposure of H. glycines to dsRNA corresponding to a newly characterized protein with homology to C-type lectins did not affect sexual fate, but 41% fewer parasites were recovered from the plants. As expected, treatment with dsRNA corresponding to the major sperm protein (MSP) had no effect on either parasite development or sexual fate over 14 days. Northern analysis showed lower transcript abundance for the two targeted mRNAs that occur in J2, plus a later inhibition for MSP transcripts when males developed sperm at 15 dpi. These findings establish a procedure for RNAi of plant parasitic nematodes.\u003C\u002Fjats:p>","\u003Cjats:p>Can thiệp RNA có giá trị trong việc xác định chức năng gen ở nhiều sinh vật. Giun tròn ký sinh thực vật không thể tiếp nhận RNA thông qua tiêm vi, và không có sự hấp thụ qua đường miệng cho đến khi chúng ở trong cây. Chúng tôi đã sử dụng octopamine để kích thích sự hấp thụ từ những con giun tròn tiền ký sinh giai đoạn hai của hai loại giun tròn kén, Heterodera glycines và Globodera pallida. Kỹ thuật mới này đã được sử dụng để tạo điều kiện cho sự hấp thụ RNA hai sợi (dsRNA) cùng với isothiocyanate fluorescein như một dấu hiệu trực quan. Việc nhắm mục tiêu vào các proteinase cysteine không làm giảm số lượng ký sinh trùng, nhưng đã gây ra sự thay đổi từ tỷ lệ giới tính nữ\u002Fnam bình thường là 3:1 sang 1:1 sau 14 ngày bị nhiễm (dpi). Việc tiếp xúc H. glycines với dsRNA tương ứng với một protein mới được đặc trưng có tính đồng đoạn với lectin loại C không ảnh hưởng đến số phận giới tính, nhưng đã thu hồi ít hơn 41% ký sinh trùng từ cây trồng. Như mong đợi, việc điều trị bằng dsRNA tương ứng với protein tinh trùng chính (MSP) không có ảnh hưởng đến sự phát triển của ký sinh trùng hay số phận giới tính trong 14 ngày. Phân tích Northern cho thấy có sự giảm sự dồi dào của bản sao cho hai mRNA nhắm mục tiêu xuất hiện trong J2, cùng với một sự ức chế muộn hơn đối với bản sao MSP khi con đực phát triển tinh trùng ở 15 dpi. Những phát hiện này thiết lập một quy trình cho RNAi của giun tròn ký sinh thực vật.\u003C\u002Fjats:p>",{"EN":3750,"VI":3751},"Ingestion of Double-Stranded RNA by Preparasitic Juvenile Cyst Nematodes Leads to RNA Interference","Sự hấp thụ RNA hai chuỗi của giống giun tròn tiền ký sinh dẫn đến RNA can thiệp",{"VOID":3753},"12182331",{"VOID":3755},"10.1094\u002Fmpmi.2002.15.8.747",[102],[101],"https:\u002F\u002Fapsjournals.apsnet.org\u002Fdoi\u002F10.1094\u002FMPMI.2002.15.8.747",[3760,3771,3792],{"id":3761,"sortIndex":115,"researcher":26,"roles":3762,"affiliations":3763,"properties":3764},"f747eab8-4ffa-448f-b7aa-748a4a9fcb57",[],[],{"openalex":3765,"orcid":3767,"title":3769},{"VOID":3766},"A5033077423",{"VOID":3768},"https:\u002F\u002Forcid.org\u002F0000-0001-8958-0272",{"EN":3770},"Catherine J. 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