Jiajun Li , Haiqian Huang , Zerui Song , Shiying Chen , Jingsong Xu , Jun Yang , Chenyue Zheng , Yu Liu , Junheng Zhang , Li Cao , Qian Liu , Qiong Li , Min Li , Zhen Gu , Hua Wang
{"title":"手掌大小的CRISPR传感平台用于现场肺炎支原体检测","authors":"Jiajun Li , Haiqian Huang , Zerui Song , Shiying Chen , Jingsong Xu , Jun Yang , Chenyue Zheng , Yu Liu , Junheng Zhang , Li Cao , Qian Liu , Qiong Li , Min Li , Zhen Gu , Hua Wang","doi":"10.1016/j.bios.2025.117458","DOIUrl":null,"url":null,"abstract":"<div><div>Pneumonia remains a prevalent childhood illness and is the foremost cause of mortality due to infectious diseases among children under the age of five. <em>Mycoplasma pneumoniae</em> (<em>M. pneumoniae</em>) causes the most frequent type of atypical pneumonia in this age group, has raised global health concern. Therefore, there is a pressing need for a rapid, low cost, and user-friendly method for the early diagnosis of <em>M. pneumoniae</em> pneumonia. Herein, we develop a CRISPR sensing platform for on-site <em>M. pneumoniae</em> detection, termed CRAFT (<strong>C</strong>rispr-based rapid assay device for field testing). The CRAFT provides “sample in-result out” functionality. It completed sample processing and nucleic acid extraction within 5 min at room temperature, with efficiency comparable to commercial kits. RPA and CRISPR/Cas12a reagents were isolated in a closed tube using a movable magnetic bead valve, and the RPA product was then mixed with the CRISPR reagent. The limit of detection for <em>M. pneumoniae</em> using CRAFT was 100 copies/μL, and the method exhibited no cross-reactivity with other respiratory pathogens. CRAFT was utilized to validate 50 clinical samples, and the results demonstrated 100 % consistency with those obtained by qPCR. This versatile platform holds significant potential for point-of-care testing of <em>M. pneumoniae</em>, particularly in resource-limited settings.</div></div>","PeriodicalId":259,"journal":{"name":"Biosensors and Bioelectronics","volume":"281 ","pages":"Article 117458"},"PeriodicalIF":10.7000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palm-sized CRISPR sensing platform for on-site Mycoplasma pneumoniae detection\",\"authors\":\"Jiajun Li , Haiqian Huang , Zerui Song , Shiying Chen , Jingsong Xu , Jun Yang , Chenyue Zheng , Yu Liu , Junheng Zhang , Li Cao , Qian Liu , Qiong Li , Min Li , Zhen Gu , Hua Wang\",\"doi\":\"10.1016/j.bios.2025.117458\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Pneumonia remains a prevalent childhood illness and is the foremost cause of mortality due to infectious diseases among children under the age of five. <em>Mycoplasma pneumoniae</em> (<em>M. pneumoniae</em>) causes the most frequent type of atypical pneumonia in this age group, has raised global health concern. Therefore, there is a pressing need for a rapid, low cost, and user-friendly method for the early diagnosis of <em>M. pneumoniae</em> pneumonia. Herein, we develop a CRISPR sensing platform for on-site <em>M. pneumoniae</em> detection, termed CRAFT (<strong>C</strong>rispr-based rapid assay device for field testing). The CRAFT provides “sample in-result out” functionality. It completed sample processing and nucleic acid extraction within 5 min at room temperature, with efficiency comparable to commercial kits. RPA and CRISPR/Cas12a reagents were isolated in a closed tube using a movable magnetic bead valve, and the RPA product was then mixed with the CRISPR reagent. The limit of detection for <em>M. pneumoniae</em> using CRAFT was 100 copies/μL, and the method exhibited no cross-reactivity with other respiratory pathogens. CRAFT was utilized to validate 50 clinical samples, and the results demonstrated 100 % consistency with those obtained by qPCR. This versatile platform holds significant potential for point-of-care testing of <em>M. pneumoniae</em>, particularly in resource-limited settings.</div></div>\",\"PeriodicalId\":259,\"journal\":{\"name\":\"Biosensors and Bioelectronics\",\"volume\":\"281 \",\"pages\":\"Article 117458\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2025-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biosensors and Bioelectronics\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S095656632500332X\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosensors and Bioelectronics","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S095656632500332X","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
Palm-sized CRISPR sensing platform for on-site Mycoplasma pneumoniae detection
Pneumonia remains a prevalent childhood illness and is the foremost cause of mortality due to infectious diseases among children under the age of five. Mycoplasma pneumoniae (M. pneumoniae) causes the most frequent type of atypical pneumonia in this age group, has raised global health concern. Therefore, there is a pressing need for a rapid, low cost, and user-friendly method for the early diagnosis of M. pneumoniae pneumonia. Herein, we develop a CRISPR sensing platform for on-site M. pneumoniae detection, termed CRAFT (Crispr-based rapid assay device for field testing). The CRAFT provides “sample in-result out” functionality. It completed sample processing and nucleic acid extraction within 5 min at room temperature, with efficiency comparable to commercial kits. RPA and CRISPR/Cas12a reagents were isolated in a closed tube using a movable magnetic bead valve, and the RPA product was then mixed with the CRISPR reagent. The limit of detection for M. pneumoniae using CRAFT was 100 copies/μL, and the method exhibited no cross-reactivity with other respiratory pathogens. CRAFT was utilized to validate 50 clinical samples, and the results demonstrated 100 % consistency with those obtained by qPCR. This versatile platform holds significant potential for point-of-care testing of M. pneumoniae, particularly in resource-limited settings.
期刊介绍:
Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.