TY - JOUR
T1 - Mycobacterium leprae genomes from naturally infected nonhuman primates
AU - Honap, Tanvi P.
AU - Pfister, Luz Andrea
AU - Housman, Genevieve
AU - Mills, Sarah
AU - Tarara, Ross P.
AU - Suzuki, Koichi
AU - Cuozzo, Frank P.
AU - Sauther, Michelle L.
AU - Rosenberg, Michael S.
AU - Stone, Anne
N1 - Funding Information:
This study was supported by a Dissertation Fieldwork Grant entitled "On the origins of Leprosy: the primate connection" from the Wenner Gren Foundation for Anthropological Research (www.wennergren.org) to LAP and a JumpStart Research Grant entitled "Of monkeys and mycobacteria" from the Graduate and Professional Students Association, Arizona State University, (www.gpsa.asu.edu) to TPH. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors thank Josephine E. Clark-Curtiss and David G. Smith for providing M. leprae DNA samples; Charlotte Payne, Gary Aronson, Brenda Bradley, and David Watts for providing the chimpanzee fruit wadge samples; Scott Larsen for veterinary assistance; Teague O’Mara and Stephanie Meredith for providing the ring-tailed lemur buccal swab samples; Nicholas Banovich and Danielle Johnson for help with DNA extractions and qPCR assays; and Crystal Hepp and Andrej Benjak for bioinformatics advice. Genomic DNA from M. leprae strains NHDP (NR-19350), Br4923 (NR-19351), and Thai-53 (NR-19352) was obtained through BEI Resources, NIAID, NIH. M. leprae whole-genome baits were provided by MYcroarray, Ann Arbor, MI. The raw sequence data generated by this study have been deposited in the Sequence Read Archive under study SRP112601.
Publisher Copyright:
© 2018 Honap et al.
PY - 2018/1
Y1 - 2018/1
N2 - 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.
AB - 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.
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U2 - 10.1371/journal.pntd.0006190
DO - 10.1371/journal.pntd.0006190
M3 - Article
C2 - 29381722
AN - SCOPUS:85041613364
SN - 1935-2727
VL - 12
JO - PLoS Neglected Tropical Diseases
JF - PLoS Neglected Tropical Diseases
IS - 1
M1 - e0006190
ER -