Evidence map›Paper›PMID 37986859›Full record

ArticlebioRxiv : the preprint server for biology2023

Universal Digital High Resolution Melt for the detection of pulmonary mold infections.

Tyler Goshia, April Aralar, Nathan Wiederhold, Jeffrey D Jenks, Sanjay R Mehta, Mridu Sinha, Aprajita Karmakar, Ankit Sharma, Rachit Shrivastava, Haoxiang Sun and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 3 countries.

Tyler GoshiaDepartment of Bioengineering, University of California San Diego, San Diego, CA, USA.
April AralarDepartment of Bioengineering, University of California San Diego, San Diego, CA, USA.
Nathan WiederholdDepartment of Pathology, University of Texas Health Science Center, San Antonio, TX, USA.ORCID 0000-0002-2225-5122
Jeffrey D JenksDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Sanjay R MehtaDepartment of Medicine, University of California San Diego, San Diego, CA, USA.
Mridu SinhaMelioLabs, Inc., Santa Clara, CA, USA.
Aprajita KarmakarMelioLabs, Inc., Santa Clara, CA, USA.
Ankit SharmaMelioLabs, Inc., Santa Clara, CA, USA.
Rachit ShrivastavaMelioLabs, Inc., Santa Clara, CA, USA.
Haoxiang SunDepartment of Bioengineering, University of California San Diego, San Diego, CA, USA.
P Lewis WhitePublic Health Wales Microbiology Cardiff, and Cardiff University Centre for Trials Research/Division of Infection/Immunity, University Hospital of Wales, Cardiff, United Kingdom.ORCID 0000-0003-3056-4205
Martin HoeniglDepartment of Medicine, Medical University of Graz, Graz, Austria.
Stephanie I FraleyDepartment of Bioengineering, University of California San Diego, San Diego, CA, USA.ORCID 0000-0003-1548-4442
University of California San Diego · USDuke University · USMedical University of Graz · ATThe University of Texas Health Science Center at San Antonio · USUniversity Hospital of Wales · GB

Funding

Digital High Resolution Melt and Machine Learning for Rapid and Specific Diagnosis in Neonatal SepsisR01AI134982 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FRALEY, STEPHANIE IRENE · 2018 to 2022
$2.3M
NIAID NIH HHS R01 AI134982
6 · The paper itself

Abstract

Background: Invasive mold infections (IMIs) such as aspergillosis, mucormycosis, fusariosis, and lomentosporiosis are associated with high morbidity and mortality, particularly in immunocompromised patients, with mortality rates as high as 40% to 80%. Outcomes could be substantially improved with early initiation of appropriate antifungal therapy, yet early diagnosis remains difficult to establish and often requires multidisciplinary teams evaluating clinical and radiological findings plus supportive mycological findings. Universal digital high resolution melting analysis (U-dHRM) may enable rapid and robust diagnosis of IMI. This technology aims to accomplish timely pathogen detection at the single genome level by conducting broad-based amplification of microbial barcoding genes in a digital polymerase chain reaction (dPCR) format, followed by high-resolution melting of the DNA amplicons in each digital reaction to generate organism-specific melt curve signatures that are identified by machine learning. Methods: A universal fungal assay was developed for U-dHRM and used to generate a database of melt curve signatures for 19 clinically relevant fungal pathogens. A machine learning algorithm (ML) was trained to automatically classify these 19 fungal melt curves and detect novel melt curves. Performance was assessed on 73 clinical bronchoalveolar lavage (BAL) samples from patients suspected of IMI. Novel curves were identified by micropipetting U-dHRM reactions and Sanger sequencing amplicons. Results: U-dHRM achieved an average of 97% fungal organism identification accuracy and a turn-around-time of 4hrs. Pathogenic molds ( Conclusions: U-dHRM showed promising performance as a separate or combination diagnostic approach to standard mycological tests. The speed of U-dHRM and its ability to simultaneously identify and quantify clinically relevant mold pathogens in polymicrobial samples as well as detect emerging opportunistic pathogens may provide information that could aid in treatment decisions and improve patient outcomes.

Indexed as

dPCRHRMIMImachine learning

Identifiers

PMID37986859
PMCPMC10659414
OpenAlexW4388570106

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.