Loading…
Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I
Metschnikowia bicuspidata causes a “milky disease” in Chinese mitten crab, Eriocheir sinensis, which inflicts significant damage on the breeding industry, but there are no effective drugs for this disease. Precise detection technologies and clarification of transmission routes are now essential to p...
Saved in:
Published in: | Journal of fungi (Basel) 2023-07, Vol.9 (8) |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 8 |
container_start_page | |
container_title | Journal of fungi (Basel) |
container_volume | 9 |
creator | Xing, Yuenan Chen, Ye Feng, Chengcheng Bao, Jie Li, Xiaodong Jiang, Hongbo |
description | Metschnikowia bicuspidata causes a “milky disease” in Chinese mitten crab, Eriocheir sinensis, which inflicts significant damage on the breeding industry, but there are no effective drugs for this disease. Precise detection technologies and clarification of transmission routes are now essential to prevent its occurrence. A real-time fluorescent quantitative PCR (qPCR) detection method targeting the mitochondrial cytochrome c oxidase subunit VIA (COX6A) of M. bicuspidata was developed and its sensitivity, specificity, repeatability, and application effectiveness evaluated. There was a robust linear relationship between the qPCR threshold cycle value (Ct) and copy number of the standard with a wide dynamic range. The standard curve had a correlation coefficient (R[sup.2]) of 0.996, amplification efficiency of 103.092%, and a lower limit of detection sensitivity of 7.6 × 10[sup.1] copies/µL. The COX6A-qPCR method exhibited high specificity for the detection of M. bicuspidata, with no cross-reactivity. The intra- and inter-group variation coefficients were |
doi_str_mv | 10.3390/jof9080791 |
format | article |
fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracacademiconefile_A762478822</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A762478822</galeid><sourcerecordid>A762478822</sourcerecordid><originalsourceid>FETCH-gale_infotracacademiconefile_A7624788223</originalsourceid><addsrcrecordid>eNqVi81Kw0AUhQdRsGg3PsF9gTSTRPOzLG2KWRS0ZOFOppOb5tbJTMidKD6Nr2oQF27lLM7h43xC3EVylSSFDM-uLWQusyK6EIs4kUWQyvzl8s--Fkvms5QyesjTokgW4qtkr46GuOvRelC2gfUwGNLKk7PgWjigMkFNPcLOTG5E1mg1wvOkrCc_394RnjYH2KJH_SPVqDvrjDt9QutGqPboeSb05j5IwZH0xAM1yquwgi0xKkYgC1U5ktMd0ghMFi0Th9WtuGqVYVz-9o1Y7cp68xiclMFXsq3zo9JzGuxJO4stzXydpfF9ludxnPxb-AY6_GsZ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Xing, Yuenan ; Chen, Ye ; Feng, Chengcheng ; Bao, Jie ; Li, Xiaodong ; Jiang, Hongbo</creator><creatorcontrib>Xing, Yuenan ; Chen, Ye ; Feng, Chengcheng ; Bao, Jie ; Li, Xiaodong ; Jiang, Hongbo</creatorcontrib><description>Metschnikowia bicuspidata causes a “milky disease” in Chinese mitten crab, Eriocheir sinensis, which inflicts significant damage on the breeding industry, but there are no effective drugs for this disease. Precise detection technologies and clarification of transmission routes are now essential to prevent its occurrence. A real-time fluorescent quantitative PCR (qPCR) detection method targeting the mitochondrial cytochrome c oxidase subunit VIA (COX6A) of M. bicuspidata was developed and its sensitivity, specificity, repeatability, and application effectiveness evaluated. There was a robust linear relationship between the qPCR threshold cycle value (Ct) and copy number of the standard with a wide dynamic range. The standard curve had a correlation coefficient (R[sup.2]) of 0.996, amplification efficiency of 103.092%, and a lower limit of detection sensitivity of 7.6 × 10[sup.1] copies/µL. The COX6A-qPCR method exhibited high specificity for the detection of M. bicuspidata, with no cross-reactivity. The intra- and inter-group variation coefficients were <1% and 2%, respectively. The qPCR exhibited superior sensitivity compared to existing detection methods, with a positivity rate of 76.67%. The M. bicuspidata content ranged from 1.0 × 10[sup.1]–2.7 × 10[sup.6] copies/µL. The COX6A-qPCR detection technology exhibited high sensitivity, strong specificity, and excellent repeatability, enabling the accurate quantification of M. bicuspidata.</description><identifier>ISSN: 2309-608X</identifier><identifier>EISSN: 2309-608X</identifier><identifier>DOI: 10.3390/jof9080791</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Aquaculture industry ; Fluorescence ; Polymerase chain reaction</subject><ispartof>Journal of fungi (Basel), 2023-07, Vol.9 (8)</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Xing, Yuenan</creatorcontrib><creatorcontrib>Chen, Ye</creatorcontrib><creatorcontrib>Feng, Chengcheng</creatorcontrib><creatorcontrib>Bao, Jie</creatorcontrib><creatorcontrib>Li, Xiaodong</creatorcontrib><creatorcontrib>Jiang, Hongbo</creatorcontrib><title>Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I</title><title>Journal of fungi (Basel)</title><description>Metschnikowia bicuspidata causes a “milky disease” in Chinese mitten crab, Eriocheir sinensis, which inflicts significant damage on the breeding industry, but there are no effective drugs for this disease. Precise detection technologies and clarification of transmission routes are now essential to prevent its occurrence. A real-time fluorescent quantitative PCR (qPCR) detection method targeting the mitochondrial cytochrome c oxidase subunit VIA (COX6A) of M. bicuspidata was developed and its sensitivity, specificity, repeatability, and application effectiveness evaluated. There was a robust linear relationship between the qPCR threshold cycle value (Ct) and copy number of the standard with a wide dynamic range. The standard curve had a correlation coefficient (R[sup.2]) of 0.996, amplification efficiency of 103.092%, and a lower limit of detection sensitivity of 7.6 × 10[sup.1] copies/µL. The COX6A-qPCR method exhibited high specificity for the detection of M. bicuspidata, with no cross-reactivity. The intra- and inter-group variation coefficients were <1% and 2%, respectively. The qPCR exhibited superior sensitivity compared to existing detection methods, with a positivity rate of 76.67%. The M. bicuspidata content ranged from 1.0 × 10[sup.1]–2.7 × 10[sup.6] copies/µL. The COX6A-qPCR detection technology exhibited high sensitivity, strong specificity, and excellent repeatability, enabling the accurate quantification of M. bicuspidata.</description><subject>Aquaculture industry</subject><subject>Fluorescence</subject><subject>Polymerase chain reaction</subject><issn>2309-608X</issn><issn>2309-608X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqVi81Kw0AUhQdRsGg3PsF9gTSTRPOzLG2KWRS0ZOFOppOb5tbJTMidKD6Nr2oQF27lLM7h43xC3EVylSSFDM-uLWQusyK6EIs4kUWQyvzl8s--Fkvms5QyesjTokgW4qtkr46GuOvRelC2gfUwGNLKk7PgWjigMkFNPcLOTG5E1mg1wvOkrCc_394RnjYH2KJH_SPVqDvrjDt9QutGqPboeSb05j5IwZH0xAM1yquwgi0xKkYgC1U5ktMd0ghMFi0Th9WtuGqVYVz-9o1Y7cp68xiclMFXsq3zo9JzGuxJO4stzXydpfF9ludxnPxb-AY6_GsZ</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Xing, Yuenan</creator><creator>Chen, Ye</creator><creator>Feng, Chengcheng</creator><creator>Bao, Jie</creator><creator>Li, Xiaodong</creator><creator>Jiang, Hongbo</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20230701</creationdate><title>Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I</title><author>Xing, Yuenan ; Chen, Ye ; Feng, Chengcheng ; Bao, Jie ; Li, Xiaodong ; Jiang, Hongbo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_infotracacademiconefile_A7624788223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aquaculture industry</topic><topic>Fluorescence</topic><topic>Polymerase chain reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xing, Yuenan</creatorcontrib><creatorcontrib>Chen, Ye</creatorcontrib><creatorcontrib>Feng, Chengcheng</creatorcontrib><creatorcontrib>Bao, Jie</creatorcontrib><creatorcontrib>Li, Xiaodong</creatorcontrib><creatorcontrib>Jiang, Hongbo</creatorcontrib><jtitle>Journal of fungi (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xing, Yuenan</au><au>Chen, Ye</au><au>Feng, Chengcheng</au><au>Bao, Jie</au><au>Li, Xiaodong</au><au>Jiang, Hongbo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I</atitle><jtitle>Journal of fungi (Basel)</jtitle><date>2023-07-01</date><risdate>2023</risdate><volume>9</volume><issue>8</issue><issn>2309-608X</issn><eissn>2309-608X</eissn><abstract>Metschnikowia bicuspidata causes a “milky disease” in Chinese mitten crab, Eriocheir sinensis, which inflicts significant damage on the breeding industry, but there are no effective drugs for this disease. Precise detection technologies and clarification of transmission routes are now essential to prevent its occurrence. A real-time fluorescent quantitative PCR (qPCR) detection method targeting the mitochondrial cytochrome c oxidase subunit VIA (COX6A) of M. bicuspidata was developed and its sensitivity, specificity, repeatability, and application effectiveness evaluated. There was a robust linear relationship between the qPCR threshold cycle value (Ct) and copy number of the standard with a wide dynamic range. The standard curve had a correlation coefficient (R[sup.2]) of 0.996, amplification efficiency of 103.092%, and a lower limit of detection sensitivity of 7.6 × 10[sup.1] copies/µL. The COX6A-qPCR method exhibited high specificity for the detection of M. bicuspidata, with no cross-reactivity. The intra- and inter-group variation coefficients were <1% and 2%, respectively. The qPCR exhibited superior sensitivity compared to existing detection methods, with a positivity rate of 76.67%. The M. bicuspidata content ranged from 1.0 × 10[sup.1]–2.7 × 10[sup.6] copies/µL. The COX6A-qPCR detection technology exhibited high sensitivity, strong specificity, and excellent repeatability, enabling the accurate quantification of M. bicuspidata.</abstract><pub>MDPI AG</pub><doi>10.3390/jof9080791</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2309-608X |
ispartof | Journal of fungi (Basel), 2023-07, Vol.9 (8) |
issn | 2309-608X 2309-608X |
language | eng |
recordid | cdi_gale_infotracacademiconefile_A762478822 |
source | Publicly Available Content Database; PubMed Central |
subjects | Aquaculture industry Fluorescence Polymerase chain reaction |
title | Establishment and Application of Real-Time Fluorescence Quantitative PCR Detection Technology for IMetschnikowia bicuspidata/I Disease in IEriocheir sinensis/I |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T21%3A16%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Establishment%20and%20Application%20of%20Real-Time%20Fluorescence%20Quantitative%20PCR%20Detection%20Technology%20for%20IMetschnikowia%20bicuspidata/I%20Disease%20in%20IEriocheir%20sinensis/I&rft.jtitle=Journal%20of%20fungi%20(Basel)&rft.au=Xing,%20Yuenan&rft.date=2023-07-01&rft.volume=9&rft.issue=8&rft.issn=2309-608X&rft.eissn=2309-608X&rft_id=info:doi/10.3390/jof9080791&rft_dat=%3Cgale%3EA762478822%3C/gale%3E%3Cgrp_id%3Ecdi_FETCH-gale_infotracacademiconefile_A7624788223%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A762478822&rfr_iscdi=true |