Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces
Abstract Background Opisthorchis viverrini infection is traditionally diagnosed using the Kato–Katz method and formalin ethyl–acetate concentration technique. However, the limited sensitivity and specificity of these techniques have prompted the exploration of various molecular approaches, such as c...
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2024-02-01
|
| Series: | Parasites & Vectors |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13071-024-06134-7 |
| _version_ | 1797275715687677952 |
|---|---|
| author | Orawan Phuphisut Akkarin Poodeepiyasawat Tippayarat Yoonuan Dorn Watthanakulpanich Charin Thawornkuno Onrapak Reamtong Megumi Sato Poom Adisakwattana |
| author_facet | Orawan Phuphisut Akkarin Poodeepiyasawat Tippayarat Yoonuan Dorn Watthanakulpanich Charin Thawornkuno Onrapak Reamtong Megumi Sato Poom Adisakwattana |
| author_sort | Orawan Phuphisut |
| collection | DOAJ |
| description | Abstract Background Opisthorchis viverrini infection is traditionally diagnosed using the Kato–Katz method and formalin ethyl–acetate concentration technique. However, the limited sensitivity and specificity of these techniques have prompted the exploration of various molecular approaches, such as conventional polymerase chain reaction (PCR) and real-time PCR, to detect O. viverrini infection. Recently, a novel technique known as recombinase polymerase amplification (RPA)–clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) (RPA–CRISPR/Cas) assay was developed as a point-of-care tool for the detection of various pathogens, including viruses and bacteria such as severe acute respiratory syndrome coronavirus 2 and Mycobacterium tuberculosis. This technology has demonstrated high sensitivity and specificity. Therefore, we developed and used the RPA–CRISPR/Cas assay to detect O. viverrini infection in field-collected human feces. Methods To detect O. viverrini infection in fecal samples, we developed a CRISPR/Cas12a (RNA-guided endonuclease) system combined with RPA (Ov-RPA–CRISPR/Cas12a). Several fecal samples, both helminth-positive and helminth-negative, were used for the development and optimization of amplification conditions, CRISPR/Cas detection conditions, detection limits, and specificity of the RPA–CRISPR/Cas12a assay for detecting O. viverrini infection. The detection results were determined using a real-time PCR system based on fluorescence values. Additionally, as the reporter was labeled with fluorescein, the detection results were visually inspected using an ultraviolet (UV) transilluminator. A receiver operating characteristic curve (ROC) was used to determine the optimal cutoff value for fluorescence detection. The diagnostic performance, including sensitivity and specificity, of the Ov-RPA–CRISPR/Cas12a assay was evaluated on the basis of comparison with standard methods. Results The Ov-RPA–CRISPR/Cas12a assay exhibited high specificity for detecting O. viverrini DNA. On the basis of the detection limit, the assay could detect O. viverrini DNA at concentrations as low as 10−1 ng using the real-time PCR system. However, in this method, visual inspection under UV light required a minimum concentration of 1 ng. To validate the Ov-RPA–CRISPR/Cas12a assay, 121 field-collected fecal samples were analyzed. Microscopic examination revealed that 29 samples were positive for O. viverrini-like eggs. Of these, 18 were confirmed as true positives on the basis of the Ov-RPA–CRISPR/Cas12a assay and microscopic examination, whereas 11 samples were determined as positive solely via microscopic examination, indicating the possibility of other minute intestinal fluke infections. Conclusions The Ov-RPA–CRISPR/Cas12a assay developed in this study can successfully detect O. viverrini infection in field-collected feces. Due to the high specificity of the assay reported in this study, it can be used as an alternative approach to confirm O. viverrini infection, marking an initial step in the development of point-of-care diagnosis. Graphical abstract |
| first_indexed | 2024-03-07T15:17:29Z |
| format | Article |
| id | doaj.art-db7f38e93d174aaf8654fc8c60c7162e |
| institution | Directory Open Access Journal |
| issn | 1756-3305 |
| language | English |
| last_indexed | 2024-03-07T15:17:29Z |
| publishDate | 2024-02-01 |
| publisher | BMC |
| record_format | Article |
| series | Parasites & Vectors |
| spelling | doaj.art-db7f38e93d174aaf8654fc8c60c7162e2024-03-05T17:50:54ZengBMCParasites & Vectors1756-33052024-02-0117111510.1186/s13071-024-06134-7Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human fecesOrawan Phuphisut0Akkarin Poodeepiyasawat1Tippayarat Yoonuan2Dorn Watthanakulpanich3Charin Thawornkuno4Onrapak Reamtong5Megumi Sato6Poom Adisakwattana7Department of Helminthology, Faculty of Tropical Medicine, Mahidol UniversityDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol UniversityDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol UniversityDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol UniversityDepartment of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol UniversityDepartment of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol UniversityGraduate School of Health Sciences, Niigata UniversityDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol UniversityAbstract Background Opisthorchis viverrini infection is traditionally diagnosed using the Kato–Katz method and formalin ethyl–acetate concentration technique. However, the limited sensitivity and specificity of these techniques have prompted the exploration of various molecular approaches, such as conventional polymerase chain reaction (PCR) and real-time PCR, to detect O. viverrini infection. Recently, a novel technique known as recombinase polymerase amplification (RPA)–clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) (RPA–CRISPR/Cas) assay was developed as a point-of-care tool for the detection of various pathogens, including viruses and bacteria such as severe acute respiratory syndrome coronavirus 2 and Mycobacterium tuberculosis. This technology has demonstrated high sensitivity and specificity. Therefore, we developed and used the RPA–CRISPR/Cas assay to detect O. viverrini infection in field-collected human feces. Methods To detect O. viverrini infection in fecal samples, we developed a CRISPR/Cas12a (RNA-guided endonuclease) system combined with RPA (Ov-RPA–CRISPR/Cas12a). Several fecal samples, both helminth-positive and helminth-negative, were used for the development and optimization of amplification conditions, CRISPR/Cas detection conditions, detection limits, and specificity of the RPA–CRISPR/Cas12a assay for detecting O. viverrini infection. The detection results were determined using a real-time PCR system based on fluorescence values. Additionally, as the reporter was labeled with fluorescein, the detection results were visually inspected using an ultraviolet (UV) transilluminator. A receiver operating characteristic curve (ROC) was used to determine the optimal cutoff value for fluorescence detection. The diagnostic performance, including sensitivity and specificity, of the Ov-RPA–CRISPR/Cas12a assay was evaluated on the basis of comparison with standard methods. Results The Ov-RPA–CRISPR/Cas12a assay exhibited high specificity for detecting O. viverrini DNA. On the basis of the detection limit, the assay could detect O. viverrini DNA at concentrations as low as 10−1 ng using the real-time PCR system. However, in this method, visual inspection under UV light required a minimum concentration of 1 ng. To validate the Ov-RPA–CRISPR/Cas12a assay, 121 field-collected fecal samples were analyzed. Microscopic examination revealed that 29 samples were positive for O. viverrini-like eggs. Of these, 18 were confirmed as true positives on the basis of the Ov-RPA–CRISPR/Cas12a assay and microscopic examination, whereas 11 samples were determined as positive solely via microscopic examination, indicating the possibility of other minute intestinal fluke infections. Conclusions The Ov-RPA–CRISPR/Cas12a assay developed in this study can successfully detect O. viverrini infection in field-collected feces. Due to the high specificity of the assay reported in this study, it can be used as an alternative approach to confirm O. viverrini infection, marking an initial step in the development of point-of-care diagnosis. Graphical abstracthttps://doi.org/10.1186/s13071-024-06134-7Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 12a (CRISPR/Cas12a)Diagnostic methodFecal sampleOpisthorchiasisOpisthorchis viverriniRecombinase polymerase amplification |
| spellingShingle | Orawan Phuphisut Akkarin Poodeepiyasawat Tippayarat Yoonuan Dorn Watthanakulpanich Charin Thawornkuno Onrapak Reamtong Megumi Sato Poom Adisakwattana Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces Parasites & Vectors Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 12a (CRISPR/Cas12a) Diagnostic method Fecal sample Opisthorchiasis Opisthorchis viverrini Recombinase polymerase amplification |
| title | Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces |
| title_full | Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces |
| title_fullStr | Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces |
| title_full_unstemmed | Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces |
| title_short | Ov-RPA–CRISPR/Cas12a assay for the detection of Opisthorchis viverrini infection in field-collected human feces |
| title_sort | ov rpa crispr cas12a assay for the detection of opisthorchis viverrini infection in field collected human feces |
| topic | Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 12a (CRISPR/Cas12a) Diagnostic method Fecal sample Opisthorchiasis Opisthorchis viverrini Recombinase polymerase amplification |
| url | https://doi.org/10.1186/s13071-024-06134-7 |
| work_keys_str_mv | AT orawanphuphisut ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT akkarinpoodeepiyasawat ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT tippayaratyoonuan ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT dornwatthanakulpanich ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT charinthawornkuno ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT onrapakreamtong ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT megumisato ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces AT poomadisakwattana ovrpacrisprcas12aassayforthedetectionofopisthorchisviverriniinfectioninfieldcollectedhumanfeces |