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Autori principali: Huang, Yumei, Lau, Cia-Hin, Cai, Wenjie, Chen, Xiaoqing, Li, Jiahui, Xia, Qiyuan, Huang, Tingting, Xiao, Bing, Zhu, Haibao
Natura: Artículo científico
Lingua:en
Pubblicazione: Diagnostic microbiology and infectious disease 2026
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Accesso online:https://pubmed.ncbi.nlm.nih.gov/42143943/
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author Huang, Yumei
Lau, Cia-Hin
Cai, Wenjie
Chen, Xiaoqing
Li, Jiahui
Xia, Qiyuan
Huang, Tingting
Xiao, Bing
Zhu, Haibao
author_facet Huang, Yumei
Lau, Cia-Hin
Cai, Wenjie
Chen, Xiaoqing
Li, Jiahui
Xia, Qiyuan
Huang, Tingting
Xiao, Bing
Zhu, Haibao
Huang, Yumei
Lau, Cia-Hin
Cai, Wenjie
Chen, Xiaoqing
Li, Jiahui
Xia, Qiyuan
Huang, Tingting
Xiao, Bing
Zhu, Haibao
collection PubMed - marine biology
contents Rapid, portable, one-pot CRISPR/Dx system for multiplex detection of human rhinovirus, adenovirus, and Mycoplasma pneumoniae. Huang, Yumei Lau, Cia-Hin Cai, Wenjie Chen, Xiaoqing Li, Jiahui Xia, Qiyuan Huang, Tingting Xiao, Bing Zhu, Haibao Humans Adenovirus Infections, Human Adenoviruses, Human CRISPR-Cas Systems Molecular Diagnostic Techniques Mycoplasma pneumoniae Picornaviridae Infections Pneumonia, Mycoplasma Rapid Diagnostic Tests Rhinovirus Sensitivity and Specificity Human rhinovirus (HRV), human adenovirus (HAdV), and Mycoplasma pneumoniae (Mp) are the primary pathogens responsible for childhood pneumonia cases. These pathogens often co-infect the respiratory system, and their infections exhibit highly similar symptoms, making a differential diagnosis challenging. The inability to identify the specific causative pathogen often results in the administration of empirical antibiotics. Empirical antibiotic treatment may not be effective and can cause adverse patient outcomes and drive antibiotic resistance. We developed a rapid and one-pot RPA-CRISPR/Cas12a system (CRISPR/Dx) for multiplex detection of HRV, HAdV, and Mp. It is also equipped with our customized miniature device to enable portable diagnostics and visible signal readout. Our CRISPR/Dx system is able to detect 5 copies/μL of these respiratory pathogens, with a detection limit of 0.57 copies/μL for HRV, 0.18 copies/μL for HAdV, and 2.6 copies/μL for Mp. It completes the reaction and detection within 35 minutes, excluding sample preparation time or pretreatment steps. It has high detection specificity and no cross-reactivity between these respiratory pathogens. This CRISPR/Dx system could be integrated with a portable fluorescent detector to realize point-of-care testing of these pathogens. Our CRISPR/Dx system allows multiplex detection, intuitive results readout, and obviates the necessity for large instruments, thereby making it well-suited for field-deployable and point-of-care diagnostics of infectious diseases.
format Artículo científico
id pubmed_42143943
institution PubMed
language en
publishDate 2026
publisher Diagnostic microbiology and infectious disease
record_format pubmed
spellingShingle Rapid, portable, one-pot CRISPR/Dx system for multiplex detection of human rhinovirus, adenovirus, and Mycoplasma pneumoniae.
Huang, Yumei
Lau, Cia-Hin
Cai, Wenjie
Chen, Xiaoqing
Li, Jiahui
Xia, Qiyuan
Huang, Tingting
Xiao, Bing
Zhu, Haibao
Humans
Adenovirus Infections, Human
Adenoviruses, Human
CRISPR-Cas Systems
Molecular Diagnostic Techniques
Mycoplasma pneumoniae
Picornaviridae Infections
Pneumonia, Mycoplasma
Rapid Diagnostic Tests
Rhinovirus
Sensitivity and Specificity
Rapid, portable, one-pot CRISPR/Dx system for multiplex detection of human rhinovirus, adenovirus, and Mycoplasma pneumoniae. Huang, Yumei Lau, Cia-Hin Cai, Wenjie Chen, Xiaoqing Li, Jiahui Xia, Qiyuan Huang, Tingting Xiao, Bing Zhu, Haibao Humans Adenovirus Infections, Human Adenoviruses, Human CRISPR-Cas Systems Molecular Diagnostic Techniques Mycoplasma pneumoniae Picornaviridae Infections Pneumonia, Mycoplasma Rapid Diagnostic Tests Rhinovirus Sensitivity and Specificity Human rhinovirus (HRV), human adenovirus (HAdV), and Mycoplasma pneumoniae (Mp) are the primary pathogens responsible for childhood pneumonia cases. These pathogens often co-infect the respiratory system, and their infections exhibit highly similar symptoms, making a differential diagnosis challenging. The inability to identify the specific causative pathogen often results in the administration of empirical antibiotics. Empirical antibiotic treatment may not be effective and can cause adverse patient outcomes and drive antibiotic resistance. We developed a rapid and one-pot RPA-CRISPR/Cas12a system (CRISPR/Dx) for multiplex detection of HRV, HAdV, and Mp. It is also equipped with our customized miniature device to enable portable diagnostics and visible signal readout. Our CRISPR/Dx system is able to detect 5 copies/μL of these respiratory pathogens, with a detection limit of 0.57 copies/μL for HRV, 0.18 copies/μL for HAdV, and 2.6 copies/μL for Mp. It completes the reaction and detection within 35 minutes, excluding sample preparation time or pretreatment steps. It has high detection specificity and no cross-reactivity between these respiratory pathogens. This CRISPR/Dx system could be integrated with a portable fluorescent detector to realize point-of-care testing of these pathogens. Our CRISPR/Dx system allows multiplex detection, intuitive results readout, and obviates the necessity for large instruments, thereby making it well-suited for field-deployable and point-of-care diagnostics of infectious diseases.
title Rapid, portable, one-pot CRISPR/Dx system for multiplex detection of human rhinovirus, adenovirus, and Mycoplasma pneumoniae.
topic Humans
Adenovirus Infections, Human
Adenoviruses, Human
CRISPR-Cas Systems
Molecular Diagnostic Techniques
Mycoplasma pneumoniae
Picornaviridae Infections
Pneumonia, Mycoplasma
Rapid Diagnostic Tests
Rhinovirus
Sensitivity and Specificity
url https://pubmed.ncbi.nlm.nih.gov/42143943/