Highly Specific and Rapid Detection of Hepatitis C Virus Using RT-LAMP-Coupled CRISPR–Cas12 Assay DOI Creative Commons
Nang Kham-Kjing, Nicole Ngo‐Giang‐Huong, Khajornsak Tragoolpua

и другие.

Diagnostics, Год журнала: 2022, Номер 12(7), С. 1524 - 1524

Опубликована: Июнь 23, 2022

Hepatitis C virus (HCV) infection can be cured with pan-genotypic direct-acting antiviral agents. However, identifying individuals current hepatitis remains a major challenge, especially in resource-limited settings where access to or availability of molecular tests is still limited. The goal this study was develop and validate assay for the rapid detection HCV RNA settings. It based on combination reverse transcription loop-mediated isothermal amplification (RT-LAMP) clustered regularly interspaced short palindromic repeats–CRISPR-associated protein 12a (CRISPR–Cas12a) cleavage that allows recognition specific nucleic acid sequences. Amplified products after reactions visualized lateral flow strips measured fluorescence detector. When tested clinical samples from infected HCV, HIV, HBV, healthy donors, RT-LAMP-coupled CRISPR–Cas12 yielded 96% sensitivity, 100% specificity, 97% agreement as compared reference method (Roche COBAS AmpliPrep/COBAS TaqMan Test). This could detect concentrations low 10 ng/µL (an estimated 2.38 Log10 IU/mL). Therefore, sensitive may represent an affordable reliable point-of-care test identification active low-resource

Язык: Английский

Nucleic Acid Therapeutics DOI

Deo Prakash Chaturvedi,

Rajesh Ghangal,

Neha Bansal

и другие.

Resonance, Год журнала: 2025, Номер 30(2), С. 209 - 228

Опубликована: Март 3, 2025

Язык: Английский

Процитировано

1

Climate change and n-3 LC-PUFA availability DOI
Karsoon Tan, Hongkuan Zhang, Huaiping Zheng

и другие.

Progress in Lipid Research, Год журнала: 2022, Номер 86, С. 101161 - 101161

Опубликована: Март 14, 2022

Язык: Английский

Процитировано

36

Cytokinins: A Genetic Target for Increasing Yield Potential in the CRISPR Era DOI Creative Commons
Sayanti Mandal,

Mimosa Ghorai,

Uttpal Anand

и другие.

Frontiers in Genetics, Год журнала: 2022, Номер 13

Опубликована: Апрель 26, 2022

Over the last decade, remarkable progress has been made in our understanding phytohormones, cytokinin’s (CKs) biosynthesis, perception, and signalling pathways. Additionally, it became apparent that interfering with any of these steps a significant effect on all stages plant growth development. As result their complex regulatory cross-talk interactions other hormones networks, they influence control wide range biological activities, from cellular to organismal levels. In agriculture, CKs are extensively used for yield improvement management because wide-ranging effects growth, development physiology. One primary targets this regard is cytokinin oxidase/dehydrogenase (CKO/CKX), which encoded by CKX gene, catalyses irreversible degradation cytokinin. The previous studies various agronomically important crops indicated breeders have targeted directly. recent years, prokaryotic clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system increasingly editing CKO/CKX gene phenomenal results achieved. This review provides an updated information applications CRISPR-based gene-editing tools manipulating metabolism at genetic level improvement. Furthermore, we summarized current developments RNP-mediated DNA/transgene-free genomic plants would broaden application technology. will advance cytokinins role sustainably increase crop production through CRISPR/Cas genome tool.

Язык: Английский

Процитировано

35

Mitochondrial genome engineering coming-of-age DOI Creative Commons
Jose Domingo Barrera-Paez, Carlos T. Moraes

Trends in Genetics, Год журнала: 2022, Номер 38(8), С. 869 - 880

Опубликована: Май 19, 2022

Язык: Английский

Процитировано

34

Highly Specific and Rapid Detection of Hepatitis C Virus Using RT-LAMP-Coupled CRISPR–Cas12 Assay DOI Creative Commons
Nang Kham-Kjing, Nicole Ngo‐Giang‐Huong, Khajornsak Tragoolpua

и другие.

Diagnostics, Год журнала: 2022, Номер 12(7), С. 1524 - 1524

Опубликована: Июнь 23, 2022

Hepatitis C virus (HCV) infection can be cured with pan-genotypic direct-acting antiviral agents. However, identifying individuals current hepatitis remains a major challenge, especially in resource-limited settings where access to or availability of molecular tests is still limited. The goal this study was develop and validate assay for the rapid detection HCV RNA settings. It based on combination reverse transcription loop-mediated isothermal amplification (RT-LAMP) clustered regularly interspaced short palindromic repeats–CRISPR-associated protein 12a (CRISPR–Cas12a) cleavage that allows recognition specific nucleic acid sequences. Amplified products after reactions visualized lateral flow strips measured fluorescence detector. When tested clinical samples from infected HCV, HIV, HBV, healthy donors, RT-LAMP-coupled CRISPR–Cas12 yielded 96% sensitivity, 100% specificity, 97% agreement as compared reference method (Roche COBAS AmpliPrep/COBAS TaqMan Test). This could detect concentrations low 10 ng/µL (an estimated 2.38 Log10 IU/mL). Therefore, sensitive may represent an affordable reliable point-of-care test identification active low-resource

Язык: Английский

Процитировано

34