Toxins
(Nov 2024)
Aerosolized Harmful Algal Bloom Toxin Microcystin-LR Induces Type 1/Type 17 Inflammation of Murine Airways
Joshua D. Breidenbach,
Benjamin W. French,
Lauren M. Stanoszek,
John-Paul Lavik,
Krishna Rao Maddipati,
Sanduni H. Premathilaka,
David Baliu-Rodriguez,
Bivek Timalsina,
Vaishnavi Aradhyula,
Shivani C. Patel,
Apurva Lad,
Irum Syed,
Andrew L. Kleinhenz,
Thomas M. Blomquist,
Amira Gohara,
Prabhatchandra Dube,
Shungang Zhang,
Dhilhani Faleel,
Fatimah K. Khalaf,
Dragan Isailovic,
R. Mark Wooten,
James C. Willey,
Jeffrey R. Hammersley,
Nikolai N. Modyanov,
Deepak Malhotra,
Lance D. Dworkin,
David J. Kennedy,
Steven T. Haller
Affiliations
Joshua D. Breidenbach
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Benjamin W. French
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Lauren M. Stanoszek
Department of Pathology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
John-Paul Lavik
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA
Krishna Rao Maddipati
Department of Pathology, Lipidomics Core Facility, Wayne State University, Detroit, MI 48202, USA
Sanduni H. Premathilaka
Department of Chemistry and Biochemistry, College of Natural Sciences and Mathematics, University of Toledo, Toledo, OH 43606, USA
David Baliu-Rodriguez
Department of Chemistry and Biochemistry, College of Natural Sciences and Mathematics, University of Toledo, Toledo, OH 43606, USA
Bivek Timalsina
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Vaishnavi Aradhyula
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Shivani C. Patel
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Apurva Lad
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Irum Syed
Department of Medical Microbiology and Immunology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
Andrew L. Kleinhenz
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Thomas M. Blomquist
Department of Pathology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
Amira Gohara
Department of Pathology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
Prabhatchandra Dube
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Shungang Zhang
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Dhilhani Faleel
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Fatimah K. Khalaf
Department of Medicine, College of Medicine, University of Alkafeel, Najaf 54001, Iraq
Dragan Isailovic
Department of Chemistry and Biochemistry, College of Natural Sciences and Mathematics, University of Toledo, Toledo, OH 43606, USA
R. Mark Wooten
Department of Medical Microbiology and Immunology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
James C. Willey
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Jeffrey R. Hammersley
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Nikolai N. Modyanov
Department of Physiology and Pharmacology, College of Medicine and Life Sciences, University of Toledo, Toledo, OH 43614, USA
Deepak Malhotra
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Lance D. Dworkin
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
David J. Kennedy
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
Steven T. Haller
Department of Medicine, College of Medicine and Life Sciences, University of Toledo, 2801 W. Bancroft, Toledo, OH 43614, USA
DOI
https://doi.org/10.3390/toxins16110470
Journal volume & issue
Vol. 16,
no. 11
p.
470
Abstract
Read online
Harmful algal blooms are increasing globally and pose serious health concerns releasing cyanotoxins. Microcystin-LR (MC-LR), one of the most frequently produced cyanotoxins, has recently been detected in aerosols generated by the normal motions of affected bodies of water. MC-LR aerosol exposure has been linked to a pro-inflammatory influence on the airways of mice; however, little is understood about the underlying mechanism or the potential consequences. This study aimed to investigate the pro-inflammatory effects of aerosolized MC-LR on murine airways. C57BL/6 and BALB/c mice were exposed to MC-LR aerosols, as these strains are predisposed to type 1/type 17 and type 2 immune responses, respectively. Exposure to MC-LR induced granulocytic inflammation in C57BL/6 but not BALB/c mice, as observed by increased expression of cytokines MIP-1α, CXCL1, CCL2, and GM-CSF compared with their respective vehicle controls. Furthermore, the upregulation of interleukins IL-17A and IL-12 is consistent with Th1- and Th17-driven type 1/type 17 inflammation. Histological analysis confirmed inflammation in the C57BL/6 lungs, with elevated neutrophils and macrophages in the bronchoalveolar lavage fluid and increased pro-inflammatory and pro-resolving oxidized lipids. In contrast, BALB/c mice showed no significant airway inflammation. These results highlight the ability of aerosolized MC-LR to trigger harmful airway inflammation, requiring further research, particularly into populations with predispositions to type 1/type 17 inflammation.
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