Evidence map›Paper›PMID 25521850›Full record

ArticlePLoS neglected tropical diseases2014

Long-term survival and virulence of Mycobacterium leprae in amoebal cysts.

William H Wheat, Amy L Casali, Vincent Thomas, John S Spencer, Ramanuj Lahiri, Diana L Williams, Gerald E McDonnell, Mercedes Gonzalez-Juarrero, Patrick J Brennan, Mary Jackson

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Leprosy.Nature reviews. Disease primers · 2024
    Review
  7. Article
  8. Human Skin as an Ex Vivo Model for MaintainingTropical medicine and infectious disease · 2024
    Article
  9. International journal of molecular sciences · 2023
    Article
  10. CanMicroorganisms · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Microbial warfare in the wild-the impact of protists on the evolution and virulence of bacterial pathogens.International microbiology : the official journal of the Spanish Society for Microbiology · 2021
    Review
  15. Pathogens (Basel, Switzerland) · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Frontiers in microbiology · 2021
    Article
  20. One Health Approaches to TraceFrontiers in microbiology · 2021
    Review
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

10 authors at 3 institutions in 1 country.

William H WheatMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Amy L CasaliMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Vincent ThomasSTERIS SA R&D, Fontenay-aux-Roses, France.
John S SpencerMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Ramanuj LahiriDepartment of Health & Human Services, HRSA, HSB, National Hansen's Disease Programs, Laboratory Research Branch, Baton Rouge, Louisiana, United States of America; School of Veterinary Medicine, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Diana L WilliamsDepartment of Health & Human Services, HRSA, HSB, National Hansen's Disease Programs, Laboratory Research Branch, Baton Rouge, Louisiana, United States of America; School of Veterinary Medicine, Louisiana State University, Baton Rouge, Louisiana, United States of America.
Gerald E McDonnellDepartment of Research and Development, STERIS Corporation, Mentor, Ohio, United States of America.
Mercedes Gonzalez-JuarreroMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Patrick J BrennanMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Mary JacksonMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Colorado State University · USNational Hansen's Disease Program · USSteris (United States) · US

Funding

Disinfectant-resistant mycobacteriaR01AI089718 · NIAID · COLORADO STATE UNIVERSITY · PI JACKSON, MARY · 2011 to 2015
$1.8M
NIAID NIH HHS AI089718NIAID NIH HHS R01 AI089718
6 · The paper itself

Abstract

Leprosy is a curable neglected disease of humans caused by Mycobacterium leprae that affects the skin and peripheral nerves and manifests clinically in various forms ranging from self-resolving, tuberculoid leprosy to lepromatous leprosy having significant pathology with ensuing disfiguration disability and social stigma. Despite the global success of multi-drug therapy (MDT), incidences of clinical leprosy have been observed in individuals with no apparent exposure to other cases, suggestive of possible non-human sources of the bacteria. In this study we show that common free-living amoebae (FLA) can phagocytose M. leprae, and allow the bacillus to remain viable for up to 8 months within amoebic cysts. Viable bacilli were extracted from separate encysted cocultures comprising three common Acanthamoeba spp.: A. lenticulata, A. castellanii, and A. polyphaga and two strains of Hartmannella vermiformis. Trophozoites of these common FLA take up M. leprae by phagocytosis. M. leprae from infected trophozoites induced to encyst for long-term storage of the bacilli emerged viable by assessment of membrane integrity. The majority (80%) of mice that were injected with bacilli extracted from 35 day cocultures of encysted/excysted A. castellanii and A. polyphaga showed lesion development that was similar to mice challenged with fresh M. leprae from passage mice albeit at a slower initial rate. Mice challenged with coculture-extracted bacilli showed evidence of acid-fast bacteria and positive PCR signal for M. leprae. These data support the conclusion that M. leprae can remain viable long-term in environmentally ubiquitous FLA and retain virulence as assessed in the nu/nu mouse model. Additionally, this work supports the idea that M. leprae might be sustained in the environment between hosts in FLA and such residence in FLA may provide a macrophage-like niche contributing to the higher-than-expected rate of leprosy transmission despite a significant decrease in human reservoirs due to MDT.

Indexed as

AmoebaAnimalsCoculture TechniquesHumansMacrophagesMiceMice, NudeMycobacterium lepraePhagocytosisVirulence

Identifiers

PMID25521850
PMCPMC4270725
OpenAlexW1983608278

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.