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Record W2801352411 · doi:10.1097/olq.0000000000000860

Utilization of Nucleic Acid Amplification Testing Samples for Antimicrobial Resistance Surveillance in Remote Canadian Communities

2018· letter· en· W2801352411 on OpenAlexaffabout
Michael R. Mulvey, Irene Martín, Tom Wong

Bibliographic record

VenueSexually Transmitted Diseases · 2018
Typeletter
Languageen
FieldImmunology and Microbiology
TopicReproductive tract infections research
Canadian institutionsFirst Nations Health and Social Secretariat of ManitobaAssembly of First NationsPublic Health Agency of Canada
Fundersnot available
KeywordsNeisseria gonorrhoeaeMedicineTypingAntibiotic resistanceMicrobiologyNucleic Acid Amplification TestsPolymerase chain reactionVirologyDrug resistanceChlamydia trachomatisAntibioticsBiologyGeneticsGene

Abstract

fetched live from OpenAlex

Dear Editor: We have read the article by Thakur et al.1 with great interest. We agree with their general statement that Neisseria gonorrhoeae diagnosis continues to expand to non–culture-based methods directly from clinical specimens. There is a need to use remnants of existing nucleic acid amplification testing (NAAT) samples generated from frontline laboratories for N. gonorrhoeae to predict antimicrobial resistance and generate a molecular type to track the dissemination of strains for surveillance and public health response. To this end, the Public Health Agency of Canada has developed real-time polymerase chain reaction (RT-PCR) assays to predict the presence of antimicrobial resistance markers and PCR sequence analysis to generate an Neisseria gonorrhoeae multi-antigen sequence typing (NG-MAST) directly from NAAT specimens. Specifically, we have developed RT-PCR assays to detect mutations associated with ciprofloxacin and cephalosporin resistance directly from residual NAAT specimens with high degrees of sensitivity and specificity when compared with culture.2,3 In addition, we have adopted an existing RT-PCR protocol for the detection of azithromycin-resistant mutations.4 Finally, we have validated these methods along with the molecular typing of NG-MAST from NAAT specimens with matched clinical isolates using traditional antimicrobial resistance and NG-MAST testing of the clinical isolate.5 In remote northern parts of Canada, it is very difficult to obtain specimens that have viable N. gonorrhoeae due to cold temperatures and the time it takes to transport a specimen to a laboratory with the expertise to culture an isolate. We are using our RT-PCR assays and NG-MAST typing assay to establish molecular antimicrobial resistance surveillance in remote northern communities. We believe that this is the first step in using molecular methods to predict and type N. gonorrhoeae for antimicrobial resistance surveillance and public health interventions. The NG-MAST typing data will also aid in identifying transmission patterns, which will hopefully lead to interventions to limit the dissemination of N. gonorrhoeae in these remote communities. In conclusion, we believe that the molecular detection of antimicrobial resistance genes and the typing of N. gonorrhoeae directly from NAATs will expand the availability of the much-needed information to remote communities where culture is not possible. Finally, we continue to explore methods to generate whole-genome sequence data from either NAAT or urine specimens. We believe that this is the future of the technology as our recent collaborations have shown that the use of whole-genome sequence can accurately predict not only susceptible/intermediate/resistant interpretations but also minimum inhibitory concentrations for specific antimicrobials.6 Michael R. MulveyIrene Martin Public Health Agency of Canada Winnipeg, Manitoba Canada [email protected]Tom Wong First Nations and Inuit Health Branch Ottawa, Ontario Canada

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.219
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.069
GPT teacher head0.302
Teacher spread0.233 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designNot applicable
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2018
Admission routes2
Has abstractyes

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