Evidence map›Paper›PMID 29381722›Full record

ArticlePLoS neglected tropical diseases2018

Mycobacterium leprae genomes from naturally infected nonhuman primates.

Tanvi P Honap, Luz-Andrea Pfister, Genevieve Housman, Sarah Mills, Ross P Tarara, Koichi Suzuki, Frank P Cuozzo, Michelle L Sauther, Michael S Rosenberg, Anne C Stone

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
6.1field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 3 syntheses or guidelines pooled it, 68 citations in OpenAlex.

  1. Silence on the plate: revisiting the enigma ofFrontiers in microbiology · 2025
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    Article
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  16. Human macrophage polarization in the response toCurrent research in microbial sciences · 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

10 authors at 4 institutions in 2 countries.

Tanvi P HonapSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States of America.ORCID 0000-0001-5271-9162
Luz-Andrea PfisterSchool of Human Evolution and Social Change, Arizona State University, Tempe, Arizona, United States of America.
Genevieve HousmanSchool of Human Evolution and Social Change, Arizona State University, Tempe, Arizona, United States of America.
Sarah MillsCalifornia National Primate Research Center, University of California, Davis, California, United States of America.
Ross P TararaCalifornia National Primate Research Center, University of California, Davis, California, United States of America.
Koichi SuzukiDepartment of Clinical Laboratory Science, Teikyo University, Tokyo, Japan.
Frank P CuozzoLajuma Research Centre, Louis Trichardt (Machado), South Africa.
Michelle L SautherDepartment of Anthropology, University of Colorado, Boulder, Colorado, United States of America.
Michael S RosenbergSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States of America.
Anne C StoneSchool of Human Evolution and Social Change, Arizona State University, Tempe, Arizona, United States of America.
Arizona State University · USUniversity of California, Davis · USTeikyo University · JPUniversity of Colorado Boulder · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leprosy is caused by the bacterial pathogens Mycobacterium leprae and Mycobacterium lepromatosis. Apart from humans, animals such as nine-banded armadillos in the Americas and red squirrels in the British Isles are naturally infected with M. leprae. Natural leprosy has also been reported in certain nonhuman primates, but it is not known whether these occurrences are due to incidental infections by human M. leprae strains or by M. leprae strains specific to nonhuman primates. In this study, complete M. leprae genomes from three naturally infected nonhuman primates (a chimpanzee from Sierra Leone, a sooty mangabey from West Africa, and a cynomolgus macaque from The Philippines) were sequenced. Phylogenetic analyses showed that the cynomolgus macaque M. leprae strain is most closely related to a human M. leprae strain from New Caledonia, whereas the chimpanzee and sooty mangabey M. leprae strains belong to a human M. leprae lineage commonly found in West Africa. Additionally, samples from ring-tailed lemurs from the Bezà Mahafaly Special Reserve, Madagascar, and chimpanzees from Ngogo, Kibale National Park, Uganda, were screened using quantitative PCR assays, to assess the prevalence of M. leprae in wild nonhuman primates. However, these samples did not show evidence of M. leprae infection. Overall, this study adds genomic data for nonhuman primate M. leprae strains to the existing M. leprae literature and finds that this pathogen can be transmitted from humans to nonhuman primates as well as between nonhuman primate species. While the prevalence of natural leprosy in nonhuman primates is likely low, nevertheless, future studies should continue to explore the prevalence of leprosy-causing pathogens in the wild.

Indexed as

Genome, BacterialAfrica, WesternAnimalsCercocebus atysGenetic VariationLemurLeprosyMacaca fascicularisMycobacterium lepraePan troglodytesPhilippinesPhylogenyPrimate Diseases

Identifiers

PMID29381722
PMCPMC5790234
OpenAlexW2787168150

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.