Evidence map›Paper›PMID 31780694›Full record

ArticleScientific reports2019

Development of a diagnostic compatible BCG vaccine against Bovine tuberculosis.

Aneesh Chandran, Kerstin Williams, Tom Mendum, Graham Stewart, Simon Clark, Sirine Zadi, Faye Lanni, Neil McLeod, Ann Williams, Bernardo Villarreal-Ramos and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. HarnessingVaccines · 2022
    Review
  8. Review
  9. Article
  10. Zoonotic Tuberculosis - The Changing Landscape.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 2 countries.

Aneesh ChandranSchool of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, UK.
Kerstin WilliamsSchool of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, UK.
Tom MendumSchool of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, UK.
Graham StewartSchool of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, UK.
Simon ClarkPublic Health England, Porton Down, Salisbury, UK.
Sirine ZadiPublic Health England, Porton Down, Salisbury, UK.
Faye LanniPublic Health England, Porton Down, Salisbury, UK.
Neil McLeodPublic Health England, Porton Down, Salisbury, UK.
Ann WilliamsPublic Health England, Porton Down, Salisbury, UK.
Bernardo Villarreal-RamosAnimal and Plant Health Agency, Addlestone, Surrey, UK.
Martin VordermeierAnimal and Plant Health Agency, Addlestone, Surrey, UK.
Veerasamy MaroudamTranslational Research Platform for Veterinary Biologicals, Chennai, India.
Aravind PrasadHPC-Medical and Bioinformatics Applications Group, Centre for Development of Advanced Computing, Innovation Park, Panchavati, Pashan, Pune, 411008, Maharashtra, India.
Neeraj BhartiHPC-Medical and Bioinformatics Applications Group, Centre for Development of Advanced Computing, Innovation Park, Panchavati, Pashan, Pune, 411008, Maharashtra, India.
Ruma BanerjeeHPC-Medical and Bioinformatics Applications Group, Centre for Development of Advanced Computing, Innovation Park, Panchavati, Pashan, Pune, 411008, Maharashtra, India.
Sunitha Manjari KasibhatlaHPC-Medical and Bioinformatics Applications Group, Centre for Development of Advanced Computing, Innovation Park, Panchavati, Pashan, Pune, 411008, Maharashtra, India.
Johnjoe McFaddenSchool of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, GU2 7XH, UK. j.mcfadden@surrey.ac.uk.
Public Health England · GBUniversity of Surrey · GBCentre for Development of Advanced Computing · INAnimal and Plant Health Agency · GBTranslational Research Platform for Veterinary Biologicals (India) · IN

Funding

Bill and Melinda Gates Foundation (Bill & Melinda Gates Foundation) BMGF:03011000075Biotechnology and Biological Sciences Research Council BB/L004569/1RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/L024209/1
6 · The paper itself

Abstract

Bovine tuberculosis (BTB) caused by Mycobacterium bovis remains a major problem in both the developed and developing countries. Control of BTB in the UK is carried out by test and slaughter of infected animals, based primarily on the tuberculin skin test (PPD). Vaccination with the attenuated strain of the M. bovis pathogen, BCG, is not used to control bovine tuberculosis in cattle at present, due to its variable efficacy and because it interferes with the PPD test. Diagnostic tests capable of Differentiating Infected from Vaccinated Animals (DIVA) have been developed that detect immune responses to M. bovis antigens absent in BCG; but these are too expensive and insufficiently sensitive to be used for BTB control worldwide. To address these problems we aimed to generate a synergistic vaccine and diagnostic approach that would permit the vaccination of cattle without interfering with the conventional PPD-based surveillance. The approach was to widen the pool of M. bovis antigens that could be used as DIVA targets, by identifying antigenic proteins that could be deleted from BCG without affecting the persistence and protective efficacy of the vaccine in cattle. Using transposon mutagenesis we identified genes that were essential and those that were non-essential for persistence in bovine lymph nodes. We then inactivated selected immunogenic, but non-essential genes in BCG Danish to create a diagnostic-compatible triple knock-out ΔBCG TK strain. The protective efficacy of the ΔBCG TK was tested in guinea pigs experimentally infected with M. bovis by aerosol and found to be equivalent to wild-type BCG. A complementary diagnostic skin test was developed with the antigenic proteins encoded by the deleted genes which did not cross-react in vaccinated or in uninfected guinea pigs. This study demonstrates the functionality of a new and improved BCG strain which retains its protective efficacy but is diagnostically compatible with a novel DIVA skin test that could be implemented in control programmes.

Indexed as

AnimalsBCG VaccineCattleCross ReactionsGene Knockout TechniquesGuinea PigsMacrophagesMycobacterium bovisTransduction, GeneticTuberculinTuberculin TestTuberculosisTuberculosis, BovineVaccinationVaccines, AttenuatedBCG VaccineTuberculinVaccines, Attenuated

Identifiers

PMID31780694
PMCPMC6882907
OpenAlexW2980585189

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.