Spatiotemporal distribution of <i>Mycobacterium ulcerans</i> and other Mycolactone Producing Mycobacteria in Southeastern United States
2025
Dogbe, Magdalene | Roberts, Cody | Fast, Kayla, M | Rakestraw, Alex, W | Yoskowitz, Katherine | Pechal, Jennifer, L | Sandel, Michael, W | Chevillon, Christine | Guégan, Jean-François | Benbow, Mark, E | Jordan, Heather, R | Mississippi State University [Mississippi] | Michigan State University [East Lansing] ; Michigan State University System | Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC) ; Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [Occitanie])-Université de Montpellier (UM) | Unité Mixte de Recherche d'Épidémiologie des maladies Animales et zoonotiques (UMR EPIA) ; VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE) | joint NSF-NIH-NIFA Ecology and Evolution of Infectious Disease program (grant number DEB 1911457)
International audience
显示更多 [+] 显示较少 [-]英语. <div><p>Buruli ulcer (BU) is a chronic and debilitating skin disease caused by the environmental pathogen, Mycobacterium ulcerans (MU). The primary virulence determinant is mycolactone, a cytotoxic lipid compound unique to MU and its other mycolactone producing mycobacteria (MPM) ecological variants. Although BU prevalence is highest in West Africa and Australia, little is known about MU and other MPM distribution in non-endemic regions such as the Southeastern United States (US). In this study, environmental samples (water filtrand, plant biofilm, soil, aquatic invertebrates) were collected from nine freshwater sites across Louisiana, Mississippi and Alabama over three sampling periods (August 2020, November 2020, March 2021). Samples were screened for MU and MPM presence and abundance by PCR and genotyped using variable number tandem repeat (VNTR) profiling. All nine sites were positive for MU or other MPM DNA in at least one substrate, except invertebrates. Overall, mean concentrations were 4.3 × 10 4 genome units (GU)/sample in August 2020, 1.26 GU/sample in November 2020, and 55.5 GU/sample in March 2021. Profiling by VNTR identified four MU (designated A-D) and one M. liflandii genotype(s), among environmental samples, with genotype frequencies varying by site and sampling time. Detection of MU and M. liflandii genotypes in Southeastern US aquatic environments, matching those from BU endemic regions, provides rationale for ongoing surveillance. Our findings broaden the known geographic range of MU and MPMs and offer baseline data to help predict and prevent and predict the possibility of zoonotic transmission in Southeastern US.</p></div>
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