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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; 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. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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Chúng tôi phát hiện rằng cặp mồi phổ biến \u003Cjats:styled-content style=\"fixed-case\">515F\u003C\u002Fjats:styled-content> (\u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content>) và \u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> đã đánh giá thấp (ví dụ \u003Cjats:styled-content style=\"fixed-case\">SAR\u003C\u002Fjats:styled-content>11) hoặc đánh giá quá cao (ví dụ Gammaproteobacteria) các taxa biển phổ biến. Chúng tôi đã đánh giá các mẫu biển và cộng đồng giả (chứa 11 hoặc 27 clone 16S biển), cho thấy mồi thay thế 515F‐\u003Cjats:styled-content style=\"fixed-case\">Y\u003C\u002Fjats:styled-content> (5′‐\u003Cjats:styled-content style=\"fixed-case\">GTG\u003Cjats:bold>Y\u003C\u002Fjats:bold>CAGCMGCCGCGGTAA\u003C\u002Fjats:styled-content>) và \u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> (5′‐\u003Cjats:styled-content style=\"fixed-case\">CCGYCAATTYMTTTRAGTTT\u003C\u002Fjats:styled-content>) cho kết quả ước lượng chính xác hơn về độ dày quần thể cộng đồng giả, tạo ra các amplicon dài hơn có thể phân biệt được các taxa không thể phân giải được bằng \u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content>, và khuếch đại \u003Cjats:styled-content style=\"fixed-case\">18S rRNA\u003C\u002Fjats:styled-content> eukaryotic. Các cộng đồng giả được khuếch đại bằng \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> cho thấy sự tương đồng cao hơn giữa thành phần cộng đồng quan sát được so với mong đợi (r\u003Cjats:sup>2\u003C\u002Fjats:sup> = 0.95) so với \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> (r\u003Cjats:sup>2\u003C\u002Fjats:sup> ∼ 0.5). Một cách bất ngờ, sự thiên lệch với \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> chống lại \u003Cjats:styled-content style=\"fixed-case\">SAR11\u003C\u002Fjats:styled-content> trong các mẫu hiện trường (∼4–10 lần) mạnh hơn so với trong các cộng đồng giả (∼2 lần). Sửa một sai lệch với \u003Cjats:styled-content style=\"fixed-case\">T\u003C\u002Fjats:styled-content>haumarchaea trong \u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content> đã làm tăng độ dày rõ ràng của chúng trong các mẫu hiện trường, nhưng không nhiều bằng việc sử dụng \u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> thay vì \u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content>. Với các mẫu fitoplankton phong phú DNA \u003Cjats:styled-content style=\"fixed-case\">eukaryotic\u003C\u002Fjats:styled-content> (&gt; 1 μm size fraction), các trình tự 18S chiếm trung bình ∼17% tổng số trình tự. Một sai sót đơn lẻ có thể làm thiên lệch mạnh việc khuếch đại, nhưng ngay cả các mồi hoàn hảo vẫn có thể thể hiện sự ưu tiên trong việc khuếch đại. Chúng tôi chứng minh rằng ngoài các dự đoán \u003Cjats:italic>in silico\u003C\u002Fjats:italic>, việc thử nghiệm với các cộng đồng giả và mẫu hiện trường là quan trọng trong việc lựa chọn mồi.","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>Microbial community analysis via high‐throughput sequencing of amplified \u003Cjats:styled-content style=\"fixed-case\">16S rRNA\u003C\u002Fjats:styled-content> genes is an essential microbiology tool. We found the popular primer pair \u003Cjats:styled-content style=\"fixed-case\">515F\u003C\u002Fjats:styled-content> (\u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content>) and \u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> greatly underestimated (e.g. \u003Cjats:styled-content style=\"fixed-case\">SAR\u003C\u002Fjats:styled-content>11) or overestimated (e.g. Gammaproteobacteria) common marine taxa. We evaluated marine samples and mock communities (containing 11 or 27 marine 16S clones), showing alternative primers 515F‐\u003Cjats:styled-content style=\"fixed-case\">Y\u003C\u002Fjats:styled-content> (5′‐\u003Cjats:styled-content style=\"fixed-case\">GTG\u003Cjats:bold>Y\u003C\u002Fjats:bold>CAGCMGCCGCGGTAA\u003C\u002Fjats:styled-content>) and \u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> (5′‐\u003Cjats:styled-content style=\"fixed-case\">CCGYCAATTYMTTTRAGTTT\u003C\u002Fjats:styled-content>) yield more accurate estimates of mock community abundances, produce longer amplicons that can differentiate taxa unresolvable with \u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content>, and amplify eukaryotic \u003Cjats:styled-content style=\"fixed-case\">18S rRNA\u003C\u002Fjats:styled-content>. Mock communities amplified with \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> yielded closer observed community composition versus expected (r\u003Cjats:sup>2\u003C\u002Fjats:sup> = 0.95) compared with \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> (r\u003Cjats:sup>2\u003C\u002Fjats:sup> ∼ 0.5). Unexpectedly, biases with \u003Cjats:styled-content style=\"fixed-case\">515F‐Y\u003C\u002Fjats:styled-content>\u002F\u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content> against \u003Cjats:styled-content style=\"fixed-case\">SAR11\u003C\u002Fjats:styled-content> in field samples (∼4–10‐fold) were stronger than in mock communities (∼2‐fold). Correcting a mismatch to \u003Cjats:styled-content style=\"fixed-case\">T\u003C\u002Fjats:styled-content>haumarchaea in the \u003Cjats:styled-content style=\"fixed-case\">515F‐C\u003C\u002Fjats:styled-content> increased their apparent abundance in field samples, but not as much as using \u003Cjats:styled-content style=\"fixed-case\">926R\u003C\u002Fjats:styled-content> rather than \u003Cjats:styled-content style=\"fixed-case\">806R\u003C\u002Fjats:styled-content>. With plankton samples rich in eukaryotic \u003Cjats:styled-content style=\"fixed-case\">DNA\u003C\u002Fjats:styled-content> (&gt; 1 μm size fraction), 18S sequences averaged ∼17% of all sequences. A single mismatch can strongly bias amplification, but even perfectly matched primers can exhibit preferential amplification. 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Điều này được minh chứng bởi việc sử dụng kháng sinh dự phòng một cách phổ biến và không bị kiểm soát trong ngành công nghiệp này, đặc biệt là ở các nước đang phát triển, nhằm ngăn chặn các bệnh nhiễm trùng do vệ sinh kém trong quá trình nuôi cá. Việc sử dụng nhiều loại kháng sinh với khối lượng lớn, bao gồm cả kháng sinh không phân hủy sinh học có ích cho y học con người, đảm bảo rằng chúng sẽ tồn tại trong môi trường nước, tạo áp lực chọn lọc trong thời gian dài. Quá trình này đã dẫn đến sự xuất hiện của các vi khuẩn kháng kháng sinh trong môi trường nuôi trồng thủy sản, gia tăng kháng thuốc kháng sinh trong các tác nhân gây bệnh ở cá, chuyển giao các yếu tố kháng này cho vi khuẩn của động vật trên cạn và các tác nhân gây bệnh ở con người, cũng như thay đổi quần thể vi khuẩn cả trong bùn và trong cột nước. Việc sử dụng lượng lớn kháng sinh cần phải trộn với thức ăn cho cá cũng gây ra vấn đề cho sức khỏe công nghiệp và tăng khả năng tồn tại của dư lượng kháng sinh trong thịt cá và các sản phẩm từ cá. Do đó, có vẻ như cần có những nỗ lực toàn cầu để thúc đẩy việc sử dụng kháng sinh dự phòng một cách hợp lý hơn trong nuôi trồng thủy sản, khi có bằng chứng ngày càng nhiều cho thấy việc sử dụng không kiểm soát là bất lợi cho cá, động vật trên cạn, sức khỏe con người và môi trường.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>The accelerated growth of finfish aquaculture has resulted in a series of developments detrimental to the environment and human health. The latter is illustrated by the widespread and unrestricted use of prophylactic antibiotics in this industry, especially in developing countries, to forestall bacterial infections resulting from sanitary shortcomings in fish rearing. The use of a wide variety of antibiotics in large amounts, including non‐biodegradable antibiotics useful in human medicine, ensures that they remain in the aquatic environment, exerting their selective pressure for long periods of time. This process has resulted in the emergence of antibiotic‐resistant bacteria in aquaculture environments, in the increase of antibiotic resistance in fish pathogens, in the transfer of these resistance determinants to bacteria of land animals and to human pathogens, and in alterations of the bacterial flora both in sediments and in the water column. The use of large amounts of antibiotics that have to be mixed with fish food also creates problems for industrial health and increases the opportunities for the presence of residual antibiotics in fish meat and fish products. 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tắt\u003C\u002Fjats:title>\u003Cjats:p>Vi sinh vật đường ruột của con người lên men các carbohydrate không thể tiêu hóa trong chế độ ăn thành axit béo chuỗi ngắn (SCFA). Các sản phẩm vi sinh này được cơ thể sử dụng, trong đó propionate và butyrate đặc biệt phát huy một loạt các chức năng có lợi cho sức khỏe. Bài viết này cung cấp một cái nhìn tổng quan về các con đường chuyển hóa mà vi sinh vật đường ruột sử dụng để sản xuất hai SCFA này từ carbohydrate trong chế độ ăn và từ amino acid do phân hủy protein tạo ra. Tổng quan này nhấn mạnh vai trò quan trọng của việc trao đổi các chất chuyển hóa trung gian (đặc biệt là lactate, succinate và 1,2-propanediol) giữa các vi khuẩn đường ruột khác nhau. Sinh lý sinh thái, bao gồm các yêu cầu về sự phát triển và phản ứng với các yếu tố môi trường, của các vi khuẩn sản xuất propionate và butyrate chính được thảo luận liên quan đến việc điều chỉnh chế độ ăn uống của các chất chuyển hóa này. Việc hiểu rõ về quá trình chuyển hóa SCFA bởi vi sinh vật đường ruột là rất cần thiết để xây dựng các chiến lược hiệu quả nhằm tối ưu hóa nguồn cung SCFA cho cơ thể.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>The human gut microbiota ferments dietary non‐digestible carbohydrates into short‐chain fatty acids (SCFA). These microbial products are utilized by the host and propionate and butyrate in particular exert a range of health‐promoting functions. Here an overview of the metabolic pathways utilized by gut microbes to produce these two SCFA from dietary carbohydrates and from amino acids resulting from protein breakdown is provided. This overview emphasizes the important role played by cross‐feeding of intermediary metabolites (in particular lactate, succinate and 1,2‐propanediol) between different gut bacteria. The ecophysiology, including growth requirements and responses to environmental factors, of major propionate and butyrate producing bacteria are discussed in relation to dietary modulation of these metabolites. A detailed understanding of SCFA metabolism by the gut microbiota is necessary to underpin effective strategies to optimize SCFA supply to the host.\u003C\u002Fjats:p>",{"EN":1691,"VI":1692},"Formation of propionate and butyrate by the human colonic microbiota","Hình thành propionate và butyrate bởi vi sinh vật đường ruột người",{"VOID":1694},"27928878",{"VOID":1696},"10.1111\u002F1462-2920.13589",[31],[30],"https:\u002F\u002Fsfamjournals.onlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002F1462-2920.13589",[1701,1720],{"id":1702,"sortIndex":32,"researcher":28,"roles":1703,"affiliations":1704,"properties":1713,"displayName":1717,"givenName":28,"familyName":28},"647de6c7-6b40-402d-a7c5-f6ea039ead51",[],[1705],{"id":1706,"sortIndex":32,"affiliation":1707,"properties":28},"ff015c83-879a-444b-98fd-ef431aff86dc",{"id":1706,"createTime":28,"updateTime":28,"relativeEntities":1708,"slug":28,"properties":1709,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1712,"statistic":28},[],{"title":1710},{"EN":1711},"Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, Foresterhill UK.",[],{"orcid":1714,"title":1716,"openalex":1718},{"VOID":1715},"https:\u002F\u002Forcid.org\u002F0000-0003-2115-2399",{"EN":1717},"Petra Louis",{"VOID":1719},"A5041649537",{"id":1721,"sortIndex":40,"researcher":28,"roles":1722,"affiliations":1723,"properties":1730,"displayName":1734,"givenName":28,"familyName":28},"6446abec-1a78-434c-895e-b44105c3921f",[],[1724],{"id":1706,"sortIndex":32,"affiliation":1725,"properties":28},{"id":1706,"createTime":28,"updateTime":28,"relativeEntities":1726,"slug":28,"properties":1727,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1729,"statistic":28},[],{"title":1728},{"EN":1711},[],{"orcid":1731,"title":1733,"openalex":1735},{"VOID":1732},"https:\u002F\u002Forcid.org\u002F0000-0003-2116-0188",{"EN":1734},"Harry J. 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tắt\u003C\u002Fjats:title>\u003Cjats:p> \u003Cjats:italic>Pseudomonas putida\u003C\u002Fjats:italic> là một loại vi khuẩn đất saprophytic có khả năng trao đổi chất đa dạng, đã được chứng nhận là vật chủ an toàn sinh học để cấy ghép các gen ngoại lai. Vi khuẩn này cũng có tiềm năng đáng kể cho các ứng dụng công nghệ sinh học. Phân tích trình tự của bộ gen 6,18 Mb của chủng KT2440 tiết lộ các hệ thống vận chuyển và trao đổi chất đa dạng. Mặc dù có mức độ bảo tồn genome cao với vi khuẩn gây bệnh Pseudomonad \u003Cjats:italic>Pseudomonas aeruginosa\u003C\u002Fjats:italic> (85% các vùng mã hóa dự đoán được chia sẻ), các yếu tố virulance chính như exotoxin A và hệ thống tiết loại III lại vắng mặt. Phân tích genome cung cấp cái nhìn sâu sắc về bản chất không gây bệnh của \u003Cjats:italic>P. putida\u003C\u002Fjats:italic> và chỉ ra những ứng dụng tiềm năng mới trong nông nghiệp, xúc tác sinh học, phục hồi sinh học và sản xuất nhựa sinh học.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p> \u003Cjats:italic>Pseudomonas putida\u003C\u002Fjats:italic> is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign genes. The bacterium also has considerable potential for biotechnological applications. Sequence analysis of the 6.18 Mb genome of strain KT2440 reveals diverse transport and metabolic systems. Although there is a high level of genome conservation with the pathogenic Pseudomonad \u003Cjats:italic>Pseudomonas aeruginosa\u003C\u002Fjats:italic> (85% of the predicted coding regions are shared), key virulence factors including exotoxin A and type III secretion systems are absent. 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Tuy nhiên, các quy luật chi phối sự hình thành những cộng đồng này vẫn chưa được hiểu rõ, và cần có một mô tả toán học có thể sử dụng cho quá trình này. Thông thường, cấu trúc cộng đồng vi sinh vật được cho là bị chi phối chủ yếu bởi các yếu tố xác định như cạnh tranh và phân hóa môi trường sinh thái. Ở đây, chúng tôi chỉ ra rằng, đối với một loạt các cộng đồng prokaryote, sự phong phú tương đối và tần suất mà các taxa khác nhau được quan sát trong các mẫu có thể được giải thích bằng một mô hình cộng đồng trung lập (NCM). NCM, là một quá trình ngẫu nhiên về sinh sản, chết và nhập cư, không thể hiện rõ các yếu tố xác định và do đó không thể là một mô tả hoàn chỉnh hoặc trung thành của việc lắp ráp cộng đồng. Tuy nhiên, sự thành công của nó cho thấy rằng sự ngẫu nhiên và nhập cư là những lực lượng quan trọng trong việc hình thành các mẫu thấy được trong các cộng đồng prokaryote.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>Naturally occurring populations of bacteria and archaea are vital to life on the earth and are of enormous practical significance in medicine, engineering and agriculture. However, the rules governing the formation of such communities are still poorly understood, and there is a need for a usable mathematical description of this process. Typically, microbial community structure is thought to be shaped mainly by deterministic factors such as competition and niche differentiation. Here we show, for a wide range of prokaryotic communities, that the relative abundance and frequency with which different taxa are observed in samples can be explained by a neutral community model (NCM). The NCM, which is a stochastic, birth–death immigration process, does not explicitly represent the deterministic factors and therefore cannot be a complete or literal description of community assembly. 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Newcastle upon Tyne: University of Newcastle upon Tyne Department of Civil Engineering and Geosciences.",{},{"id":28,"text":3224,"url":28,"identifiers":3225},"10.1111\u002Fj.0030-1299.2004.12685.x",{"doi":3224},{"id":28,"text":3227,"url":28,"identifiers":3228},"MacArthur R.H., 1967, The Theory of Island Biogeography",{},{"id":28,"text":3230,"url":28,"identifiers":3231},"10.1038\u002Fnature01583",{"doi":3230},{"id":28,"text":3233,"url":28,"identifiers":3234},"10.1016\u002Fj.tpb.2003.08.001",{"doi":3233},{"id":28,"text":3236,"url":28,"identifiers":3237},"10.1016\u002Fj.femsec.2004.05.005",{"doi":3236},{"id":28,"text":3239,"url":28,"identifiers":3240},"10.1128\u002FAEM.66.12.5368-5382.2000",{"doi":3239},{"id":28,"text":3242,"url":28,"identifiers":3243},"10.2307\u002F1939377",{"doi":3242},{"id":28,"text":3245,"url":28,"identifiers":3246},"10.1073\u002Fpnas.0403458101",{"doi":3245},{"id":28,"text":3248,"url":28,"identifiers":3249},"Tilman D., 1993, Species Diversity in Ecological Communities, 13",{},{"id":28,"text":3251,"url":28,"identifiers":3252},"10.1103\u002FPhysRevE.68.061902",{"doi":3251},{"id":28,"text":3254,"url":28,"identifiers":3255},"10.1038\u002Fnature01883",{"doi":3254},{"id":28,"text":3257,"url":28,"identifiers":3258},"10.1016\u002FS0958-1669(02)00315-4",{"doi":3257},{"id":28,"text":3260,"url":28,"identifiers":3261},"10.1073\u002Fpnas.95.12.6578",{"doi":3260},{"id":28,"text":3263,"url":28,"identifiers":3264},"10.1038\u002Fnature03211",{"doi":3263},{"id":28,"text":3266,"url":28,"identifiers":3267},"10.1006\u002Fjtbi.1997.0491",{"doi":3266},{"id":28,"text":3269,"url":28,"identifiers":3270},"10.1080\u002F089106001750462669",{"doi":3269},{"id":28,"text":3272,"url":28,"identifiers":3273},"Zwart G., 2002, Typical freshwater bacteria: an analysis of available 16S rRNA gene sequences from plankton of lakes and rivers, Aquat Microbial Ecol, 28, 141, 10.3354\u002Fame028141",{"doi":3274},"10.3354\u002Fame028141",{"id":28,"text":3276,"url":28,"identifiers":3277},"10.1128\u002FAEM.69.10.5875-5883.2003",{"doi":3276},{"id":3279,"createTime":3280,"updateTime":3281,"relativeEntities":3282,"slug":3283,"properties":3284,"entityType":1008,"verifyStatus":26,"verifyTime":3280,"verifyNote":1009,"languages":3300,"translateLanguages":3301,"viewCount":32,"primaryUrl":3302,"fullTextUrl":28,"authors":3303,"publicationType":1067,"publisherRelationship":3416,"citationCount":3470,"citationInfo":3471,"publishDate":3475,"publishYear":3472,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":3476,"openAccess":28,"references":3477,"isForceReanalyzing":1281},"e50f361e-92f6-455b-8a2e-1f94ef42372f","2024-10-07T07:21:14.408+00:00","2025-01-29T23:53:54.132+00:00",[],"The-bacterial-biogeography-of-British-soils",{"mag":3285,"keywords":3287,"openalex":3288,"abstract":3290,"title":3293,"pm":3296,"doi":3298},{"VOID":3286},"1920295170",{"VI":995},{"VOID":3289},"W1920295170",{"VI":3291,"EN":3292},"\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Mặc dù đã nhận thức được tầm quan trọng của vi khuẩn đất đối với chức năng của hệ sinh thái trên cạn, nhưng vẫn còn ít sự đồng thuận về các yếu tố điều chỉnh đa dạng sinh học dưới lòng đất. Ở đây, chúng tôi trình bày một đánh giá không gian đa quy mô về hồ sơ cộng đồng vi khuẩn đất trên toàn Vương quốc Anh (> 1000 lõi đất) và cho thấy bản đồ phân bố vi khuẩn trên quy mô cảnh quan đầu tiên ở cấp quốc gia. Độ đa dạng vi khuẩn và sự khác biệt cộng đồng, được đánh giá bằng phương pháp polime hóa chiều dài đoạn phân mảnh hạn chế, được liên kết chặt chẽ nhất với độ pH của đất, cung cấp một xác nhận quy mô lớn về vai trò của pH trong việc cấu trúc các ngành vi khuẩn. Tuy nhiên, trong khi đa dạng α có mối liên quan tích cực với pH, thì điều ngược lại với đa dạng β (biến thiên giữa các mẫu trong đa dạng α). Đa dạng β được tìm thấy là lớn nhất trong các loại đất axit, tương ứng với sự không đồng nhất môi trường lớn hơn. Phân tích các thư viện bản sao cho thấy các ảnh hưởng của pH chủ yếu thể hiện ở cấp độ các nhóm phân loại vi khuẩn rộng, với các loại đất axit được chi phối bởi một vài ngành (đặc biệt là nhóm 1 Acidobacteria và Alphaproteobacteria). Chúng tôi cũng ghi nhận sự tương quan đáng kể giữa các cộng đồng vi khuẩn và hầu hết các biến số môi trường khác được đo (hóa học đất, đặc điểm trên mặt đất và các biến khí hậu), cùng với sự tương quan không gian đáng kể ở khoảng cách gần. Cụ thể, các cộng đồng vi khuẩn và thực vật có mối liên hệ chặt chẽ với nhau, cho thấy không có bằng chứng mạnh mẽ rằng vi khuẩn đất bị thúc đẩy bởi các quy trình sinh thái khác với những quy định cho các sinh vật cao hơn. Chúng tôi kết luận rằng các khảo sát quy mô rộng hữu ích trong việc xác định các sinh quyển đất rõ rệt bao gồm các cộng đồng lặp lại của các ngành chiếm ưu thế. Tất cả những kết quả này cung cấp một khuôn khổ sinh thái cơ sở để theo đuổi nghiên cứu trong tương lai về chức năng vi sinh vật đất, cũng như các đánh giá dựa trên sinh quyển rõ ràng hơn về các yếu tố điều khiển sinh thái địa phương của đa dạng sinh học vi khuẩn.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>Despite recognition of the importance of soil bacteria to terrestrial ecosystem functioning there is little consensus on the factors regulating belowground biodiversity. Here we present a multi‐scale spatial assessment of soil bacterial community profiles across Great Britain (&gt; 1000 soil cores), and show the first landscape scale map of bacterial distributions across a nation. Bacterial diversity and community dissimilarities, assessed using terminal restriction fragment length polymorphism, were most strongly related to soil pH providing a large‐scale confirmation of the role of pH in structuring bacterial taxa. However, while α diversity was positively related to pH, the converse was true for β diversity (between sample variance in α diversity). β diversity was found to be greatest in acidic soils, corresponding with greater environmental heterogeneity. Analyses of clone libraries revealed the pH effects were predominantly manifest at the level of broad bacterial taxonomic groups, with acidic soils being dominated by few taxa (notably the group 1 Acidobacteria and Alphaproteobacteria). We also noted significant correlations between bacterial communities and most other measured environmental variables (soil chemistry, aboveground features and climatic variables), together with significant spatial correlations at close distances. In particular, bacterial and plant communities were closely related signifying no strong evidence that soil bacteria are driven by different ecological processes to those governing higher organisms. We conclude that broad scale surveys are useful in identifying distinct soil biomes comprising reproducible communities of dominant taxa. Together these results provide a baseline ecological framework with which to pursue future research on both soil microbial function, and more explicit biome based assessments of the local ecological drivers of bacterial biodiversity.\u003C\u002Fjats:p>",{"EN":3294,"VI":3295},"The bacterial biogeography of British soils","Địa lý vi sinh vật của đất Anh",{"VOID":3297},"21507180",{"VOID":3299},"10.1111\u002Fj.1462-2920.2011.02480.x",[31],[30],"https:\u002F\u002Fsfamjournals.onlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1462-2920.2011.02480.x",[3304,3323,3338,3363,3382,3399],{"id":3305,"sortIndex":32,"researcher":28,"roles":3306,"affiliations":3307,"properties":3316,"displayName":3320,"givenName":28,"familyName":28},"aab5452d-abd5-467a-9983-315749d972fb",[],[3308],{"id":3309,"sortIndex":32,"affiliation":3310,"properties":28},"e987ecac-71fd-4b52-85a1-064a89ee6173",{"id":3309,"createTime":28,"updateTime":28,"relativeEntities":3311,"slug":28,"properties":3312,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3315,"statistic":28},[],{"title":3313},{"VI":3314},"Centre for Ecology & Hydrology, Maclean Building, Benson Lane, Crowmarsh Gifford, Wallingford, Oxfordshire, OX10 8BB, UK",[],{"orcid":3317,"title":3319,"openalex":3321},{"VOID":3318},"https:\u002F\u002Forcid.org\u002F0000-0002-3341-4547",{"EN":3320},"Robert I. 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Những vi khuẩn này được khai thác để kiểm soát sinh học, phục hồi sinh thái và thúc đẩy sự phát triển của cây trồng, nhưng các vấn đề về an toàn liên quan đến nhiễm trùng ở người, đặc biệt là ở bệnh nhân xơ nang, vẫn chưa được giải quyết. Bài tổng quan ngắn này cung cấp cái nhìn tổng thể về sự đa dạng phân loại và sinh thái của chi này, đặc biệt nhấn mạnh vào các dòng thuộc phức hợp \u003Cjats:italic>Burkholderia cepacia\u003C\u002Fjats:italic>, và đề cập đến câu hỏi quan trọng liệu các dòng “tốt” và “xấu” thực sự có phải là cùng một loại không.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>Members of the genus \u003Cjats:italic>Burkholderia\u003C\u002Fjats:italic> are versatile organisms that occupy a surprisingly wide range of ecological niches. These bacteria are exploited for biocontrol, bioremediation and plant growth promotion purposes, but safety issues regarding human infections, especially in cystic fibrosis patients, have not been solved. 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Những tương tác này có thể rất quan trọng trong các hệ thống nông nghiệp bền vững, với sự đầu tư thấp, dựa vào các quá trình sinh học thay vì hóa chất nông nghiệp để duy trì độ phì nhiêu của đất và sức khỏe của cây trồng. Mặc dù có nhiều nghiên cứu về sự tương tác giữa nấm AM và vi khuẩn, nhưng các cơ chế cơ bản đứng sau những mối liên hệ này thường không được hiểu rõ, và các đặc tính chức năng của chúng vẫn cần được xác nhận thêm qua các thí nghiệm. Do đó, nghiên cứu mycorrhiza trong tương lai cần hướng tới việc cải thiện hiểu biết về các cơ chế chức năng đứng sau những tương tác vi sinh vật này, để các sự kết hợp vi sinh vật tối ưu có thể được sử dụng như các nguồn giống hiệu quả trong các hệ thống sản xuất cây trồng bền vững. Trong bối cảnh này, bài viết hiện tại nhằm xem xét và thảo luận các kiến thức hiện có về sự tương tác giữa nấm AM và vi khuẩn kích thích sự phát triển của rễ, các tương tác vật lý giữa nấm AM và vi khuẩn, sự gia tăng khả năng sinh khả dụng của photpho và nitơ qua những tương tác này, và cuối cùng là sự liên kết giữa nấm AM và các vi khuẩn nội cộng sinh của chúng. Tổng thể, bài đánh giá này tóm tắt những gì đã biết cho đến nay trong lĩnh vực này và cố gắng xác định những hướng nghiên cứu hứa hẹn trong tương lai.\u003C\u002Fjats:p>","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>Arbuscular mycorrhizal (AM) fungi and bacteria can interact synergistically to stimulate plant growth through a range of mechanisms that include improved nutrient acquisition and inhibition of fungal plant pathogens. These interactions may be of crucial importance within sustainable, low‐input agricultural cropping systems that rely on biological processes rather than agrochemicals to maintain soil fertility and plant health. Although there are many studies concerning interactions between AM fungi and bacteria, the underlying mechanisms behind these associations are in general not very well understood, and their functional properties still require further experimental confirmation. Future mycorrhizal research should therefore strive towards an improved understanding of the functional mechanisms behind such microbial interactions, so that optimized combinations of microorganisms can be applied as effective inoculants within sustainable crop production systems. In this context, the present article seeks to review and discuss the current knowledge concerning interactions between AM fungi and plant growth‐promoting rhizobacteria, the physical interactions between AM fungi and bacteria, enhancement of phosphorus and nitrogen bioavailability through such interactions, and finally the associations between AM fungi and their bacterial endosymbionts. 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Jansson J.K.(2005)Antifungal and root surface colonization properties of GFP‐taggedPaenibacillus brasilensisPB177.World J Microbiol Biotech(in press).",{"doi":4569},"10.1007\u002Fs11274-005-8123-3",{"id":28,"text":4571,"url":28,"identifiers":4572},"10.1146\u002Fannurev.py.26.090188.002115",{"doi":4571},{"id":28,"text":4574,"url":28,"identifiers":4575},"10.1016\u002FS0038-0717(03)00003-8",{"doi":4574},{"id":28,"text":4577,"url":28,"identifiers":4578},"10.1128\u002FAEM.66.10.4361-4365.2000",{"doi":4577},{"id":28,"text":4580,"url":28,"identifiers":4581},"10.1016\u002FS1360-1385(03)00184-5",{"doi":4580},{"id":4583,"createTime":4584,"updateTime":4585,"relativeEntities":4586,"slug":4587,"properties":4588,"entityType":1008,"verifyStatus":26,"verifyTime":4604,"verifyNote":1009,"languages":4605,"translateLanguages":4606,"viewCount":32,"primaryUrl":4607,"fullTextUrl":28,"authors":4608,"publicationType":1067,"publisherRelationship":4806,"citationCount":4859,"citationInfo":4860,"publishDate":4863,"publishYear":4861,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":4864,"openAccess":28,"references":4865,"isForceReanalyzing":1281},"66c5b5e5-3b19-4e48-83dc-85c2cd6099b0","2024-09-27T10:39:19.366+00:00","2025-01-29T23:56:46.525+00:00",[],"How-natural-infection-by-i-Nosema-ceranae-i-causes-honeybee-colony-collapse",{"mag":4589,"keywords":4591,"openalex":4592,"abstract":4594,"title":4597,"pm":4600,"doi":4602},{"VOID":4590},"2107810840",{"VI":995},{"VOID":4593},"W2107810840",{"VI":4595,"EN":4596},"\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Trong những năm gần đây, ong mật (\u003Cjats:italic>Apis mellifera\u003C\u002Fjats:italic>) đã biến mất một cách kỳ lạ khỏi tổ ong của chúng, và những đàn ong khỏe mạnh đột nhiên trở nên yếu và chết. Nguyên nhân chính xác dẫn đến sự biến mất của những con ong vẫn là điều bí ẩn. Tuy nhiên, trong cùng thời gian đó, \u003Cjats:italic>Nosema ceranae\u003C\u002Fjats:italic>, một loại vi sinh vật thuộc họ vi nấm châu Á của ong \u003Cjats:italic>Apis cerana\u003C\u002Fjats:italic>, dường như đã xâm chiếm \u003Cjats:italic>A. mellifera\u003C\u002Fjats:italic>, và giờ đây nó thường được phát hiện trên khắp thế giới ở cả đàn ong mật khỏe mạnh và yếu. Lần đầu tiên, chúng tôi cho thấy rằng nhiễm tự nhiên \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> có thể gây ra sự sụp đổ đột ngột của các đàn ong, xác lập mối tương quan trực tiếp giữa nhiễm \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> và cái chết của các đàn ong mật trong điều kiện thực địa. Các dấu hiệu của sự yếu kém của đàn không xuất hiện cho đến khi nữ hoàng không còn khả năng thay thế cho sự mất mát của những con ong bị nhiễm bệnh. Thời gian ủ bệnh dài không có triệu chứng có thể giải thích cho việc thiếu vắng các triệu chứng rõ ràng trước khi đàn ong sụp đổ. Hơn nữa, kết quả của chúng tôi cho thấy rằng các đàn ong khỏe mạnh gần với một đàn đã bị nhiễm cũng có thể bị nhiễm, và nhiễm \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> có thể được kiểm soát bằng một loại kháng sinh cụ thể, fumagillin. Hơn nữa, việc quản lý 120 mg fumagillin đã chứng minh là loại bỏ được nhiễm trùng, nhưng không thể tránh được nguy cơ tái nhiễm sau 6 tháng. Chúng tôi cung cấp các yếu tố hợp thành của Koch giữa nhiễm \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> và một hội chứng có thời gian ủ bệnh dài liên quan đến cái chết liên tục của ong trưởng thành, việc nuôi trứng không ngừng của những con ong và sự mất mát đàn vào mùa đông hoặc đầu mùa xuân mặc dù còn đủ phấn hoa và mật tồn tại.","\u003Cjats:title>Summary\u003C\u002Fjats:title>\u003Cjats:p>In recent years, honeybees (\u003Cjats:italic>Apis mellifera\u003C\u002Fjats:italic>) have been strangely disappearing from their hives, and strong colonies have suddenly become weak and died. The precise aetiology underlying the disappearance of the bees remains a mystery. However, during the same period, \u003Cjats:italic>Nosema ceranae\u003C\u002Fjats:italic>, a microsporidium of the Asian bee \u003Cjats:italic>Apis cerana\u003C\u002Fjats:italic>, seems to have colonized \u003Cjats:italic>A. mellifera\u003C\u002Fjats:italic>, and it's now frequently detected all over the world in both healthy and weak honeybee colonies. For first time, we show that natural \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> infection can cause the sudden collapse of bee colonies, establishing a direct correlation between \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> infection and the death of honeybee colonies under field conditions. Signs of colony weakness were not evident until the queen could no longer replace the loss of the infected bees. The long asymptomatic incubation period can explain the absence of evident symptoms prior to colony collapse. Furthermore, our results demonstrate that healthy colonies near to an infected one can also become infected, and that \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> infection can be controlled with a specific antibiotic, fumagillin. Moreover, the administration of 120 mg of fumagillin has proven to eliminate the infection, but it cannot avoid reinfection after 6 months. We provide Koch's postulates between \u003Cjats:italic>N. ceranae\u003C\u002Fjats:italic> infection and a syndrome with a long incubation period involving continuous death of adult bees, non‐stop brood rearing by the bees and colony loss in winter or early spring despite the presence of sufficient remaining pollen and honey.\u003C\u002Fjats:p>",{"EN":4598,"VI":4599},"How natural infection by \u003Ci>Nosema ceranae\u003C\u002Fi> causes honeybee colony collapse","Cách nhiễm tự nhiên bởi \u003Ci>Nosema ceranae\u003C\u002Fi> gây ra sự sụp đổ của đàn ong 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