Evidence map›Paper›PMID 39464732›Full record

ArticleVirusdisease2024

A predictive approach for host-pathogen interactions using deep learning and protein sequences.

Taha Shakibania, Masoud Arabfard, Ali Najafi

Abstract read
In one paragraph

Article in Virusdisease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

3 authors.

Taha Shakibania *Molecular Biology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Masoud Arabfard *Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-3955-613X
Ali NajafiMolecular Biology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.ORCID 0000-0001-7700-2053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research on host-pathogen interactions (HPIs) has evolved rapidly during the past decades. The more humans discover new pathogens, the more challenging it gets to find a cure and prevent infections caused by those pathogens. Many experimental techniques have been proposed to predict the interactions but most of them are highly costly and time-consuming. Fortunately, computational methods have been proven to be efficient in overcoming such limitations. In this study, we propose utilizing Deep Learning methods to predict HPIs using protein sequences. We use the monoMonoKGap (mMKGap) algorithm with K = 2 to extract features from the sequences. We also used the Negatome Database to generate negative interactions. The proposed method was performed on three separate balanced human-pathogen datasets with 10-fold cross-validation. Our method yielded very high accuracies of 99.65%, 99.52%, and 99.66% (mean accuracy of 99.61%). To further evaluate the performance of the deep Network, we compared it with other classification methods, which were the Random Forest (RF) as multiple Decision Tree, the Support Vector Machine (SVM), and Convolutional Neural Network (CNN). We also tested the Dipeptide Composition algorithm as another feature extraction method to compare the results with the mMKGap method. The experimental results prove that the proposed method is very accurate, robust, and practical and could be used as a reliable framework in HPI research.

Indexed as

Convolutional neural networkDeep learningHost-pathogen protein-protein interactionmonoMonoKGapNegatome

Identifiers

PMID39464732
PMCPMC11502655

What OpenQuestion holds

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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.