Evidence map›Paper›PMID 35135469›Full record

ArticleBMC bioinformatics2022

Primary case inference in viral outbreaks through analysis of intra-host variant population.

J Walker Gussler, David S Campo, Zoya Dimitrova, Pavel Skums, Yury Khudyakov

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

J Walker GusslerCenters for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA, 30333, USA.
David S CampoCenters for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA, 30333, USA. fyv6@cdc.gov.ORCID http://orcid.org/0000-0002-8970-3436
Zoya DimitrovaCenters for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA, 30333, USA.
Pavel SkumsDepartment of Computer Science, Georgia State University, 1 Park Place NE, Atlanta, GA, 30303, USA.
Yury KhudyakovCenters for Disease Control and Prevention, 1600 Clifton Rd, Atlanta, GA, 30333, USA.
Centers for Disease Control and Prevention · USGeorgia State University · US

Funding

QUBBD: VIRAL EVOLUTION AND SPREAD OF INFECTIOUS DISEASE IN COMPLEX NETWORK: BIG DATA ANALYSIS AND MODELINGR01EB025022 · NIBIB · GEORGIA STATE UNIVERSITY · PI SKUMS, PAVEL, VANNBERG, FREDRIK · 2017 to 2019
$891k
Foundation for the National Institutes of Health (US) 1R01EB025022-01NIBIB NIH HHS R01 EB025022
6 · The paper itself

Abstract

backgroundInvestigation of outbreaks to identify the primary case is crucial for the interruption and prevention of transmission of infectious diseases. These individuals may have a higher risk of participating in near future transmission events when compared to the other patients in the outbreak, so directing more transmission prevention resources towards these individuals is a priority. Although the genetic characterization of intra-host viral populations can aid the identification of transmission clusters, it is not trivial to determine the directionality of transmissions during outbreaks, owing to complexity of viral evolution. Here, we present a new computational framework, PYCIVO: primary case inference in viral outbreaks. This framework expands upon our earlier work in development of QUENTIN, which builds a probabilistic disease transmission tree based on simulation of evolution of intra-host hepatitis C virus (HCV) variants between cases involved in direct transmission during an outbreak. PYCIVO improves upon QUENTIN by also adding a custom heterogeneity index and identifying the scenario when the primary case may have not been sampled.

resultsThese approaches were validated using a set of 105 sequence samples from 11 distinct HCV transmission clusters identified during outbreak investigations, in which the primary case was epidemiologically verified. Both models can detect the correct primary case in 9 out of 11 transmission clusters (81.8%). However, while QUENTIN issues erroneous predictions on the remaining 2 transmission clusters, PYCIVO issues a null output for these clusters, giving it an effective prediction accuracy of 100%. To further evaluate accuracy of the inference, we created 10 modified transmission clusters in which the primary case had been removed. In this scenario, PYCIVO was able to correctly identify that there was no primary case in 8/10 (80%) of these modified clusters. This model was validated with HCV; however, this approach may be applicable to other microbial pathogens.

conclusionsPYCIVO improves upon QUENTIN by also implementing a custom heterogeneity index which empowers PYCIVO to make the important 'No primary case' prediction. One or more samples, possibly including the primary case, may have not been sampled, and this designation is meant to account for these scenarios.

Indexed as

Communicable DiseasesHepatitis CComputational BiologyDisease OutbreaksHepacivirusHumansPhylogeny

Identifiers

PMID35135469
PMCPMC8822801
OpenAlexW4226095671

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.