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Multiplex PCR and Nanopore Sequencing of Genes Associated with Antimicrobial Resistance in Neisseria gonorrhoeae Directly from Clinical Samples
by
Li, Yizhun
, Li, Yamei
, Xiu, Leshan
, Zhang, Chi
, Peng, Junping
, Sun, Liying
, Zeng, Yaling
, Wang, Feng
in
Accuracy
/ Anti-Bacterial Agents - pharmacology
/ Antimicrobial agents
/ Antimicrobial resistance
/ Cross-reactivity
/ DNA sequencing
/ Drug resistance
/ Drug Resistance, Bacterial - genetics
/ Gene sequencing
/ Genes
/ Genetic aspects
/ Gonorrhea
/ Gonorrhea - diagnosis
/ Humans
/ Methods
/ Microbial Sensitivity Tests
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Nanopore Sequencing
/ Neisseria gonorrhoeae
/ Neisseria gonorrhoeae - drug effects
/ Neisseria gonorrhoeae - genetics
/ Nucleotide sequencing
/ Observations
/ Polymerase chain reaction
/ Sensitivity
2021
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Multiplex PCR and Nanopore Sequencing of Genes Associated with Antimicrobial Resistance in Neisseria gonorrhoeae Directly from Clinical Samples
by
Li, Yizhun
, Li, Yamei
, Xiu, Leshan
, Zhang, Chi
, Peng, Junping
, Sun, Liying
, Zeng, Yaling
, Wang, Feng
in
Accuracy
/ Anti-Bacterial Agents - pharmacology
/ Antimicrobial agents
/ Antimicrobial resistance
/ Cross-reactivity
/ DNA sequencing
/ Drug resistance
/ Drug Resistance, Bacterial - genetics
/ Gene sequencing
/ Genes
/ Genetic aspects
/ Gonorrhea
/ Gonorrhea - diagnosis
/ Humans
/ Methods
/ Microbial Sensitivity Tests
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Nanopore Sequencing
/ Neisseria gonorrhoeae
/ Neisseria gonorrhoeae - drug effects
/ Neisseria gonorrhoeae - genetics
/ Nucleotide sequencing
/ Observations
/ Polymerase chain reaction
/ Sensitivity
2021
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Multiplex PCR and Nanopore Sequencing of Genes Associated with Antimicrobial Resistance in Neisseria gonorrhoeae Directly from Clinical Samples
by
Li, Yizhun
, Li, Yamei
, Xiu, Leshan
, Zhang, Chi
, Peng, Junping
, Sun, Liying
, Zeng, Yaling
, Wang, Feng
in
Accuracy
/ Anti-Bacterial Agents - pharmacology
/ Antimicrobial agents
/ Antimicrobial resistance
/ Cross-reactivity
/ DNA sequencing
/ Drug resistance
/ Drug Resistance, Bacterial - genetics
/ Gene sequencing
/ Genes
/ Genetic aspects
/ Gonorrhea
/ Gonorrhea - diagnosis
/ Humans
/ Methods
/ Microbial Sensitivity Tests
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Nanopore Sequencing
/ Neisseria gonorrhoeae
/ Neisseria gonorrhoeae - drug effects
/ Neisseria gonorrhoeae - genetics
/ Nucleotide sequencing
/ Observations
/ Polymerase chain reaction
/ Sensitivity
2021
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Multiplex PCR and Nanopore Sequencing of Genes Associated with Antimicrobial Resistance in Neisseria gonorrhoeae Directly from Clinical Samples
Journal Article
Multiplex PCR and Nanopore Sequencing of Genes Associated with Antimicrobial Resistance in Neisseria gonorrhoeae Directly from Clinical Samples
2021
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Overview
Abstract
Background
Antimicrobial resistance (AMR) of Neisseria gonorrhoeae has spread worldwide. Rapid and comprehensive methods are needed to describe N. gonorrhoeae AMR profiles accurately. A method based on multiplex amplicon sequencing was developed to simultaneously sequence 13 genes related to AMR in N. gonorrhoeae directly from clinical samples.
Methods
Nine N. gonorrhoeae strains were used for the establishment and validation of the method. Eleven urethral swabs and their corresponding cultured isolates were matched as pairs to determine the accuracy of the method. Mock samples with different dilutions were prepared to determine the sensitivity of the method. Five nongonococcal Neisseria strains and 24 N. gonorrhoeae negative clinical samples were used to evaluate the cross-reactivity. Finally, the method was applied to 64 clinical samples to assess its performance.
Results
Using Sanger sequencing as a reference method, sequences recovered from amplicon sequencing had a base accuracy of over 99.5% and the AMR sites were correctly identified. The limit of detection (LOD) was lower than 31 copies/reaction. No significant cross-reactivity was observed. Furthermore, target genes were successfully recovered from 64 clinical samples including 9 urines, demonstrating this method could be used in different types of samples. For clinical samples, the results can be obtained within a time frame of 7 h 40 min to 10 h 40 min, while for isolates, the turnaround time was approximately 2 h shorter.
Conclusions
This method can serve as a versatile and convenient culture-free diagnostic method with the advantages of high sensitivity and accuracy.
Publisher
Oxford University Press
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