Evidence map›Paper›PMID 26121128›Full record

ArticlePloS one2015

Full-Genome Sequencing as a Basis for Molecular Epidemiology Studies of Bluetongue Virus in India.

Sushila Maan, Narender S Maan, Manjunatha N Belaganahalli, Pavuluri Panduranga Rao, Karam Pal Singh, Divakar Hemadri, Kalyani Putty, Aman Kumar, Kanisht Batra, Yadlapati Krishnajyothi and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
21.9field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 61 citations in OpenAlex.

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  6. Development of a multiplexed Luminex assay for simultaneous detection of enteric viruses in cattle.Veterinary research forum : an international quarterly journal · 2024
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  8. Co-infection of bluetongue virus serotypes 12 and 16 in sheep from Haryana, India.Veterinary research forum : an international quarterly journal · 2023
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  11. Exposure ofViruses · 2021
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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

17 authors at 7 institutions in 2 countries.

Sushila MaanVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom; College of Veterinary Sciences, LLR University of Veterinary and Animal Sciences, Hisar, 125 004, Haryana, India.
Narender S MaanVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom; College of Veterinary Sciences, LLR University of Veterinary and Animal Sciences, Hisar, 125 004, Haryana, India.
Manjunatha N BelaganahalliVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom.
Pavuluri Panduranga RaoElla Foundation, Genome Valley Hyderabad, 500 078, T.S, India.
Karam Pal SinghPathology Laboratory, Centre for Animal Disease Research and Diagnosis, Indian Veterinary Research Institute, Izatnagar, 243122, U.P, India.
Divakar HemadriNational Institute of Veterinary Epidemiology and Disease Informatics (NIVEDI), Hebbal, Bengaluru, 560024, K.A, India.
Kalyani PuttyCollege of Veterinary Science, Acharya N.G. Ranga Agricultural University, Rajendra Nagar, Hyderabad, 500 030, T.S, India.
Aman KumarCollege of Veterinary Sciences, LLR University of Veterinary and Animal Sciences, Hisar, 125 004, Haryana, India.
Kanisht BatraCollege of Veterinary Sciences, LLR University of Veterinary and Animal Sciences, Hisar, 125 004, Haryana, India.
Yadlapati KrishnajyothiVeterinary Biological & Research Institute, Govt. of Andhra Pradesh, Hyderabad, 500028, T.S, India.
Bharat S ChandelCollege of Veterinary Science and AH, S.D. Agricultural University, Sardarkrushinagar-385 506, B.K., Gujarat, India.
G Hanmanth ReddyVeterinary Biological & Research Institute, Govt. of Andhra Pradesh, Hyderabad, 500028, T.S, India.
Kyriaki NomikouVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom.
Yella Narasimha ReddyCollege of Veterinary Science, Acharya N.G. Ranga Agricultural University, Rajendra Nagar, Hyderabad, 500 030, T.S, India.
Houssam AttouiVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom.
Nagendra R HegdeElla Foundation, Genome Valley Hyderabad, 500 078, T.S, India.
Peter P C MertensVector-borne Viral Diseases Programme, The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, United Kingdom.
Kerala Veterinary and Animal Sciences University · INThe Pirbright Institute · GBVeterinary Biological and Research Institute · INAcharya N. G. Ranga Agricultural University · INIndian Veterinary Research Institute · INNational Institute Of Veterinary Epidemiology And Disease Informatics · INSardarkrushinagar Dantiwada Agricultural University · IN

Funding

Biotechnology and Biological Sciences Research Council BB/H531478/1Biotechnology and Biological Sciences Research Council BB/L004690/1Biotechnology and Biological Sciences Research Council BBS/E/I/00001144
6 · The paper itself

Abstract

Since 1998 there have been significant changes in the global distribution of bluetongue virus (BTV). Ten previously exotic BTV serotypes have been detected in Europe, causing severe disease outbreaks in naïve ruminant populations. Previously exotic BTV serotypes were also identified in the USA, Israel, Australia and India. BTV is transmitted by biting midges (Culicoides spp.) and changes in the distribution of vector species, climate change, increased international travel and trade are thought to have contributed to these events. Thirteen BTV serotypes have been isolated in India since first reports of the disease in the country during 1964. Efficient methods for preparation of viral dsRNA and cDNA synthesis, have facilitated full-genome sequencing of BTV strains from the region. These studies introduce a new approach for BTV characterization, based on full-genome sequencing and phylogenetic analyses, facilitating the identification of BTV serotype, topotype and reassortant strains. Phylogenetic analyses show that most of the equivalent genome-segments of Indian BTV strains are closely related, clustering within a major eastern BTV 'topotype'. However, genome-segment 5 (Seg-5) encoding NS1, from multiple post 1982 Indian isolates, originated from a western BTV topotype. All ten genome-segments of BTV-2 isolates (IND2003/01, IND2003/02 and IND2003/03) are closely related (>99% identity) to a South African BTV-2 vaccine-strain (western topotype). Similarly BTV-10 isolates (IND2003/06; IND2005/04) show >99% identity in all genome segments, to the prototype BTV-10 (CA-8) strain from the USA. These data suggest repeated introductions of western BTV field and/or vaccine-strains into India, potentially linked to animal or vector-insect movements, or unauthorised use of 'live' South African or American BTV-vaccines in the country. The data presented will help improve nucleic acid based diagnostics for Indian serotypes/topotypes, as part of control strategies.

Indexed as

Sequence Analysis, DNAAnimalsBluetongueBluetongue virusCell LineGenes, ViralIndiaMolecular EpidemiologyPhylogenyViral ProteinsViral Proteins

Identifiers

PMID26121128
PMCPMC4488075
OpenAlexW801672335

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.