Evidence map›Paper›PMID 27852224›Full record

ArticleBMC genomics2016

Novel approach for identification of influenza virus host range and zoonotic transmissible sequences by determination of host-related associative positions in viral genome segments.

Fatemeh Kargarfard, Ashkan Sami, Manijeh Mohammadi-Dehcheshmeh, Esmaeil Ebrahimie

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Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

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18citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Fatemeh KargarfardDepartment of Computer Science and Engineering, School of Electrical and Computer Engineering, Shiraz University, Shiraz, Iran.
Ashkan SamiDepartment of Computer Science and Engineering, School of Electrical and Computer Engineering, Shiraz University, Shiraz, Iran. asami@cse.shirazu.ac.ir.
Manijeh Mohammadi-DehcheshmehSchool of Animal and Veterinary Sciences, The University of Adelaide, Adelaide, Australia.
Esmaeil EbrahimieSchool of Animal and Veterinary Sciences, The University of Adelaide, Adelaide, Australia. esmaeil.ebrahimie@adelaide.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent (2013 and 2009) zoonotic transmission of avian or porcine influenza to humans highlights an increase in host range by evading species barriers. Gene reassortment or antigenic shift between viruses from two or more hosts can generate a new life-threatening virus when the new shuffled virus is no longer recognized by antibodies existing within human populations. There is no large scale study to help understand the underlying mechanisms of host transmission. Furthermore, there is no clear understanding of how different segments of the influenza genome contribute in the final determination of host range.

methodsTo obtain insight into the rules underpinning host range determination, various supervised machine learning algorithms were employed to mine reassortment changes in different viral segments in a range of hosts. Our multi-host dataset contained whole segments of 674 influenza strains organized into three host categories: avian, human, and swine. Some of the sequences were assigned to multiple hosts. In point of fact, the datasets are a form of multi-labeled dataset and we utilized a multi-label learning method to identify discriminative sequence sites. Then algorithms such as CBA, Ripper, and decision tree were applied to extract informative and descriptive association rules for each viral protein segment.

resultWe found informative rules in all segments that are common within the same host class but varied between different hosts. For example, for infection of an avian host, HA14V and NS1230S were the most important discriminative and combinatorial positions.

conclusionHost range identification is facilitated by high support combined rules in this study. Our major goal was to detect discriminative genomic positions that were able to identify multi host viruses, because such viruses are likely to cause pandemic or disastrous epidemics.

Indexed as

Genome, ViralAlgorithmsAnimalsBirdsHemagglutinin Glycoproteins, Influenza VirusHost SpecificityHumansInfluenza A virusInfluenza in BirdsOrthomyxoviridae InfectionsSwineViral ProteinsVirus InternalizationZoonosesHemagglutinin Glycoproteins, Influenza VirusViral ProteinsAssociation rule miningDetecting hot spotsHost range of influenza

Identifiers

PMID27852224
PMCPMC5112743

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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.