Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes

A growing number of tet(X)-type tigecycline resistance determinants [tet(X1) to tet(X5)] constitutes an expanding family of tetracycline-inactivating enzymes, posing a potential risk to global public health. Here, we report the development of an efficient multiplex PCR method to detect the family of...

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Main Authors: Kai Ji, Yongchang Xu, Jian Sun, Man Huang, Xu Jia, Chengjian Jiang, Youjun Feng
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Virulence
Subjects:
Online Access:http://dx.doi.org/10.1080/21505594.2019.1706913
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spelling doaj-db9e4eb765a54fa6bb02b807dff7a7472021-01-15T13:32:57ZengTaylor & Francis GroupVirulence2150-55942150-56082020-01-01111495610.1080/21505594.2019.17069131706913Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genesKai Ji0Yongchang Xu1Jian Sun2Man Huang3Xu Jia4Chengjian Jiang5Youjun Feng6College of Life Science and Technology, Guangxi UniversityZhejiang University School of MedicineSouth China Agricultural UniversityZhejiang University School of MedicineNon-coding RNA and Drug Discovery Key Laboratory of Sichuan Province, Chengdu Medical CollegeCollege of Life Science and Technology, Guangxi UniversityCollege of Life Science and Technology, Guangxi UniversityA growing number of tet(X)-type tigecycline resistance determinants [tet(X1) to tet(X5)] constitutes an expanding family of tetracycline-inactivating enzymes, posing a potential risk to global public health. Here, we report the development of an efficient multiplex PCR method to detect the family of tet(X) variants. This method is successfully applied in the screen and validation of tet(X) genes in the field and clinic bacterial samples. In addition, we found that the formerly proposed tet(X1) is a premature truncated version by the inappropriate annotation, and fixed this error. Overall, it might be the first genetic tool for the detection of different Tet(X) members.http://dx.doi.org/10.1080/21505594.2019.1706913multiplex pcrantimicrobial resistancetigecycline resistancetet(x)tet(x1)tet(x2)tet(x3)tet(x4)tet(x5)
collection DOAJ
language English
format Article
sources DOAJ
author Kai Ji
Yongchang Xu
Jian Sun
Man Huang
Xu Jia
Chengjian Jiang
Youjun Feng
spellingShingle Kai Ji
Yongchang Xu
Jian Sun
Man Huang
Xu Jia
Chengjian Jiang
Youjun Feng
Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
Virulence
multiplex pcr
antimicrobial resistance
tigecycline resistance
tet(x)
tet(x1)
tet(x2)
tet(x3)
tet(x4)
tet(x5)
author_facet Kai Ji
Yongchang Xu
Jian Sun
Man Huang
Xu Jia
Chengjian Jiang
Youjun Feng
author_sort Kai Ji
title Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
title_short Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
title_full Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
title_fullStr Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
title_full_unstemmed Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes
title_sort harnessing efficient multiplex pcr methods to detect the expanding tet(x) family of tigecycline resistance genes
publisher Taylor & Francis Group
series Virulence
issn 2150-5594
2150-5608
publishDate 2020-01-01
description A growing number of tet(X)-type tigecycline resistance determinants [tet(X1) to tet(X5)] constitutes an expanding family of tetracycline-inactivating enzymes, posing a potential risk to global public health. Here, we report the development of an efficient multiplex PCR method to detect the family of tet(X) variants. This method is successfully applied in the screen and validation of tet(X) genes in the field and clinic bacterial samples. In addition, we found that the formerly proposed tet(X1) is a premature truncated version by the inappropriate annotation, and fixed this error. Overall, it might be the first genetic tool for the detection of different Tet(X) members.
topic multiplex pcr
antimicrobial resistance
tigecycline resistance
tet(x)
tet(x1)
tet(x2)
tet(x3)
tet(x4)
tet(x5)
url http://dx.doi.org/10.1080/21505594.2019.1706913
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