Evidence map›Paper›PMID 27165798›Full record

ArticlemBio2016

Emerging Tuberculosis Pathogen Hijacks Social Communication Behavior in the Group-Living Banded Mongoose (Mungos mungo).

Kathleen A Alexander, Claire E Sanderson, Michelle H Larsen, Suelee Robbe-Austerman, Mark C Williams, Mitchell V Palmer

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in mBio, 2016. 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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Complete genome and transcriptome ofMicrobiology resource announcements · 2025
    Article
  7. Variation between species, populations, groups and individuals in the fitness consequences of out-group conflict.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  8. Application of metagenomic next-generation sequencing in cutaneous tuberculosis.Frontiers in cellular and infection microbiology · 2022
    Article
  9. Article
  10. Pathogenomic analyses ofMicrobial genomics · 2021
    Article
  11. Pathogens, odors, and disgust in rodents.Neuroscience and biobehavioral reviews · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Silver Nanoparticles for the Therapy of Tuberculosis.International journal of nanomedicine · 2020
    Review
  16. Mongoose (Veterinary sciences · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Kathleen A AlexanderDepartment of Fish and Wildlife Conservation, Virginia Tech, Blacksburg, Virginia, USA CARACAL, Centre for Conservation of African Resources: Animals, Communities, and Land Use, Kasane, Botswana kathyalx@vt.edu.
Claire E SandersonDepartment of Fish and Wildlife Conservation, Virginia Tech, Blacksburg, Virginia, USA CARACAL, Centre for Conservation of African Resources: Animals, Communities, and Land Use, Kasane, Botswana.
Michelle H LarsenDepartment of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA.
Suelee Robbe-AustermanDiagnostic Bacteriology Laboratory, National Veterinary Services Laboratories, Ames, Iowa, USA.
Mark C WilliamsUniversity of Pretoria, Onderstepoort, South Africa.
Mitchell V PalmerBacterial Diseases of Livestock Research Unit, National Animal Disease Center, Ames, Iowa, USA.
National Animal Disease Center · USVirginia Tech · USAlbert Einstein College of Medicine · USOnderstepoort Veterinary Academic Hospital · ZA

Funding

Development and Dissemination of Operational Real-Time Respiratory Virus ForecastU01GM110748 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHAMAN, JEFFREY L · 2014 to 2018
$2.6M
NIGMS NIH HHS U01 GM110748
6 · The paper itself

Abstract

unlabelledAn emerging Mycobacterium tuberculosis complex (MTC) pathogen, M. mungi, infects wild banded mongooses (Mungos mungo) in Northern Botswana, causing significant mortality. This MTC pathogen did not appear to be transmitted through a primary aerosol or oral route. We utilized histopathology, spoligotyping, mycobacterial interspersed repetitive units-variable number of tandem repeats (MIRU-VNTR), quantitative PCR (qPCR), and molecular markers (regions of difference [RDs] from various MTC members, including region of difference 1 [RD1] from M. bovis BCG [RD1(BCG)], M. microti [RD1(mic)], and M. pinnipedii [RD1(seal)], genes Rv1510 [RD4], Rv1970 [RD7], Rv3877/8 [RD1], and Rv3120 [RD12], insertion element IS1561, the 16S RNA gene, and gene Rv0577 [cfp32]), including the newly characterized mongoose-specific deletion in RD1 (RD1(mon)), in order to demonstrate the presence of M. mungi DNA in infected mongooses and investigate pathogen invasion and exposure mechanisms. M. mungi DNA was identified in 29% of nasal planum samples (n = 52), 56% of nasal rinses and swabs (n = 9), 53% of oral swabs (n = 19), 22% of urine samples (n = 23), 33% of anal gland tissue (n = 18), and 39% of anal gland secretions (n = 44). The occurrence of extremely low cycle threshold values obtained with qPCR in anal gland and nasal planum samples indicates that high levels of M. mungi can be found in these tissue types. Histological data were consistent with these results, suggesting that pathogen invasion occurs through breaks in the nasal planum and/or skin of the mongoose host, which are in frequent contact with anal gland secretions and urine during olfactory communication behavior. Lesions in the lung, when present, occurred only with disseminated disease. No environmental sources of M. mungi DNA could be found. We report primary environmental transmission of an MTC pathogen that occurs in association with social communication behavior. IMPORTANCE: Organisms causing infectious disease evolve modes of transmission that exploit environmental and host conditions favoring pathogen spread and persistence. We report a novel mode of environmental infectious disease transmission that occurs in association with olfactory secretions (e.g., urine and anal gland secretions), allowing pathogen exposure to occur within and between social groups through intricate social communication behaviors of the banded mongoose host. The presence of M. mungi in these environmentally deposited secretions would effectively circumvent natural social barriers (e.g., territoriality), facilitating between-group pathogen transmission in the absence of direct physical contact, a rare occurrence in this highly territorial species. This work identifies an important potential mechanism of pathogen transmission of epidemiological significance in social species. We also provide evidence of a novel mechanism of pathogen transmission for the MTC complex, where pathogen movement in the environment and host exposure dynamics are driven by social behavior.

Indexed as

Animal CommunicationAnal CanalAnimalsBacterial ProteinsBotswanaDNA, BacterialDNA Transposable ElementsHerpestidaeLungMycobacterium tuberculosisNoseReal-Time Polymerase Chain ReactionSequence Analysis, DNATuberculosisBacterial ProteinsDNA, BacterialDNA Transposable Elements

Identifiers

PMID27165798
PMCPMC4895101
OpenAlexW2379769283

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.