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Author

Maryza Graham

Bio: Maryza Graham is an academic researcher from University of Melbourne. The author has contributed to research in topics: Coronavirus. The author has an hindex of 2, co-authored 6 publications receiving 11 citations.
Topics: Coronavirus

Papers
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Journal ArticleDOI
TL;DR: Evaluating the performance of Cepheid Xpert® Xpress SARS-CoV-2 RT-PCR assay for testing samples in pools of four and six finds pooling of four or six samples may be an effective strategy to increase testing capacity.

12 citations

Journal ArticleDOI
TL;DR: In this paper, the authors present a review of emerging testing technologies for detection of SARS-CoV-2, including those that are rapid and can be used at point-of-care (POC), and those facilitating high throughput laboratory-based testing.

11 citations

Journal ArticleDOI
TL;DR: In this paper, the authors evaluated the performance of three serology assays for SARS-CoV-2 infection, including Abbott, DiaSorin, and Roche, using 217 serum samples from 131 participants up to 7 months following COVID-19 infection.

6 citations

Journal ArticleDOI
TL;DR: Two instances of healthcare workers contracting SARS-CoV-2 despite no known breach of personal protective equipment were reported, and viral genomic sequencing supported this transmission hypothesis and the subsequent response.
Abstract: Healthcare workers are at increased risk of occupational transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We report 2 instances of healthcare workers contracting SARS-CoV-2 despite no known breach of personal protective equipment. Additional specific equipment cleaning was initiated. Viral genomic sequencing supported this transmission hypothesis and our subsequent response.

2 citations


Cited by
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Journal ArticleDOI
TL;DR: In this article, a large number of alternative test methods based on SARS-CoV-2 RNA or proteins or host factors associated with SARS CoV2 infection have been developed and evaluated.
Abstract: Coronavirus disease 2019 (COVID-19) pandemic triggered an unprecedented global effort in developing rapid and inexpensive diagnostic and prognostic tools. Since the genome of SARS-CoV-2 was uncovered, detection of viral RNA by RT-qPCR has played the most significant role in preventing the spread of the virus through early detection and tracing of suspected COVID-19 cases and through screening of at-risk population. However, a large number of alternative test methods based on SARS-CoV-2 RNA or proteins or host factors associated with SARS-CoV-2 infection have been developed and evaluated. The application of metabolomics in infectious disease diagnostics is an evolving area of science that was boosted by the urgency of COVID-19 pandemic. Metabolomics approaches that rely on the analysis of volatile organic compounds exhaled by COVID-19 patients hold promise for applications in a large-scale screening of population in point-of-care (POC) setting. On the other hand, successful application of mass-spectrometry to detect specific spectral signatures associated with COVID-19 in nasopharyngeal swab specimens may significantly save the cost and turnaround time of COVID-19 testing in the diagnostic microbiology and virology laboratories. Active research is also ongoing on the discovery of potential metabolomics-based prognostic markers for the disease that can be applied to serum or plasma specimens. Several metabolic pathways related to amino acid, lipid and energy metabolism were found to be affected by severe disease with COVID-19. In particular, tryptophan metabolism via the kynurenine pathway were persistently dysregulated in several independent studies, suggesting the roles of several metabolites of this pathway such as tryptophan, kynurenine and 3-hydroxykynurenine as potential prognostic markers of the disease. However, standardization of the test methods and large-scale clinical validation are necessary before these tests can be applied in a clinical setting. With rapidly expanding data on the metabolic profiles of COVID-19 patients with varying degrees of severity, it is likely that metabolomics will play an important role in near future in predicting the outcome of the disease with a greater degree of certainty.

35 citations

Posted ContentDOI
26 Oct 2021-medRxiv
TL;DR: In this article, the authors presented two flexible RT-qPCR platforms for small-and large-scale screening to detect these mutations, and schemes for adapting the platforms for future mutations.
Abstract: Multiple mutations in SARS-CoV-2 variants of concern (VOCs) may increase, transmission, disease severity, immune evasion and facilitate zoonotic or anthoprozoonotic infections. Four such mutations, {Delta}H69/V70, L452R, E484K and N501Y, occur in the SARS-CoV-2 spike glycoprotein in combinations that allow detection of the most important VOCs. Here we present two flexible RT-qPCR platforms for small-and large-scale screening to detect these mutations, and schemes for adapting the platforms for future mutations. The large-scale RT-qPCR platform, was validated by pair-wise matching of RT-qPCR results with WGS consensus genomes, showing high specificity and sensitivity. Detection of mutations using this platform served as an important interventive measure for the Danish public health system to delay the emergence of VOCs and to gain time for vaccine administration. Both platforms are valuable tools for WGS-lean laboratories, as well for complementing WGS to support rapid control of local transmission chains worldwide.

14 citations

Journal ArticleDOI
TL;DR: In this paper, the authors reviewed various theoretically simulated and clinically validated pooled testing models and proposed practical guidelines on applying this strategy for large scale screening for SARS-CoV-2.

14 citations

Journal ArticleDOI
TL;DR: Here, localities that have demonstrated success with saliva-based SARS-CoV-2 testing approaches are reviewed and can serve as models for transforming concepts into globally-implemented best practices.
Abstract: ABSTRACT Introduction Symptomatic testing and asymptomatic screening for SARS-CoV-2 continue to be essential tools for mitigating virus transmission. Though COVID-19 diagnostics initially defaulted to oropharyngeal or nasopharyngeal sampling, the worldwide urgency to expand testing efforts spurred innovative approaches and increased diversity of detection methods. Strengthening innovation and facilitating widespread testing remains critical for global health, especially as additional variants emerge and other mitigation strategies are recalibrated. Areas covered A growing body of evidence reflects the need to expand testing efforts and further investigate the efficiency, sensitivity, and acceptability of saliva samples for SARS-CoV-2 detection. Countries have made pandemic response decisions based on resources, costs, procedures, and regional acceptability – the adoption and integration of saliva-based testing among them. Saliva has demonstrated high sensitivity and specificity while being less invasive relative to nasopharyngeal swabs, securing saliva’s position as a more acceptable sample type. Expert opinion Despite the accessibility and utility of saliva sampling, global implementation remains low compared to swab-based approaches. In some cases, countries have validated saliva-based methods but face challenges with testing implementation or expansion. Here, we review the localities that have demonstrated success with saliva-based SARS-CoV-2 testing approaches and can serve as models for transforming concepts into globally-implemented best practices.

11 citations

Journal ArticleDOI
TL;DR: In this article, two recombinase-based isothermal techniques, reverse transcription recombinases polymerase amplification (RT-RPA) and reverse transcription aided amplification (RAA), were evaluated for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in clinical samples.

9 citations