University of Iowa Iowa Research Online Theses and Dissertations Summer 2010 The role of salivary antimicrobial peptides in shaping Streptococcus mutans ecology Ekarat Phattarataratip University of Iowa Copyright 2010 Ekarat Phattarataratip This dissertation is available at Iowa Research Online: https://ir.uiowa.edu/etd/724 Recommended Citation Phattarataratip, Ekarat. "The role of salivary antimicrobial peptides in shaping Streptococcus mutans ecology." PhD (Doctor of Philosophy) thesis, University of Iowa, 2010. https://doi.org/10.17077/etd.1pjhbf54. Follow this and additional works at:https://ir.uiowa.edu/etd Part of theOral Biology and Oral Pathology Commons THE ROLE OF SALIVARY ANTIMICROBIAL PEPTIDES IN SHAPING STREPTOCOCCUS MUTANS ECOLOGY by Ekarat Phattarataratip An Abstract Of a thesis submitted in partial fulfillment of the requirements for the Doctor of Philosophy degree in Oral Science in the Graduate College of The University of Iowa July 2010 Thesis Supervisor: Professor Jeffrey A. Banas 1 ABSTRACT Antimicrobial peptides are among the repertoire of host innate immune defenses. In mucosal immunity, the health-disease balance can be greatly modulated by the interplay between host immune factors and colonized microflora. Microbial ecology within dental plaque is constantly shaped by environmental factors present within the oral cavity. Several antimicrobial peptides are detected in saliva and their bactericidal activities against oral bacteria, including Streptococcus mutans, the primary etiologic agent of dental caries, have been clearly demonstrated. However, the role of these antimicrobial peptides in S .mutans ecology and host caries experience is not well- defined. We hypothesized that various strains of S. mutans possess different inherent susceptibility/resistance profiles to host salivary antimicrobial peptides and that host- specific quantities of these peptides may influence plaque colonization by particular S. mutans strains. S. mutans strains from subjects with variable caries experience were tested for susceptibility to a panel of antimicrobial peptides, including HNP-1-3, HBD-2-3 and LL- 37, revealing that the susceptibilities of S. mutans to these peptides were strain-specific. S. mutans strains from high caries subjects showed greater resistance to these peptides at varying concentrations than those from caries-free subjects. In addition, when combinations of these peptides were tested, they showed either additive or synergistic interaction against S. mutans. Determinations of the salivary levels of these peptides showed that their concentrations were highly variable among subjects with no correlation to host caries experience. However, positive relationships between the salivary concentrations of HNP- 2 1-3 and MS in dental plaque were found. Additionally, the levels of a number of these peptides in saliva appeared to be positively correlated within an individual. An analysis of the salivary peptide concentrations and the susceptibility profiles of S. mutans strains showed that S. mutans strains obtained from subjects with higher concentrations of HNP- 1-3 in saliva appeared to be more resistant to HNP-1. Collectively, our findings showed that salivary antimicrobial peptides affect S. mutans ecology by restricting the overall growth of this bacterium within the oral cavity and that their activity may help select resistant strains of S. mutans to colonize within dental plaque. The relative ability of S. mutans to resist host salivary antimicrobial peptides may be considered a potential virulence factor for this species. Abstract Approved: ____________________________________ Thesis Supervisor ____________________________________ Title and Department ____________________________________ Date THE ROLE OF SALIVARY ANTIMICROBIAL PEPTIDES IN SHAPING STREPTOCOCCUS MUTANS ECOLOGY by Ekarat Phattarataratip A thesis submitted in partial fulfillment of the requirements for the Doctor of Philosophy degree in Oral Science in the Graduate College of The University of Iowa July 2010 Thesis Supervisor: Professor Jeffrey A. Banas Graduate College The University of Iowa Iowa City, Iowa CERTIFICATE OF APPROVAL _______________________ PH.D. THESIS _______________ This is to certify that the Ph.D. thesis of Ekarat Phattarataratip has been approved by the Examining Committee for the thesis requirement for the Doctor of Philosophy degree in Oral Science at the July 2010 graduation. Thesis Committee: ___________________________________ Jeffrey A. Banas, Thesis Supervisor ___________________________________ Kim A. Brogden ___________________________________ David R. Drake ___________________________________ John W. Hellstein ___________________________________ Timothy D. Starner ___________________________________ Fang Qian To Mom and Dad ii ACKNOWLEDGMENTS This thesis would not have been completed without many people who have helped and supported me in every way over the years. I am grateful to have Dr. Jeff Banas as my thesis supervisor, for the opportunities he has given me, and for his guidance, support and understanding throughout my study. I would like to thank my thesis committee members, Drs. Kim Brogden, David Drake, John Hellstein, Fang Qian and Timothy Starner. Their questions, comments and suggestions are invaluable and greatly help my research progress forward in a timely manner. I would also like to thank Dr. Steven Levy for kindly allowing me to use the samples in this study, as well as Barbara Broffitt who promptly provided me the subject information and is always there to answer my questions. I am fortunate to have worked with many great people in Dows, including Min Zhu, David Lynch, Yuan Liu, Bonny Olson, and Deepa Gadre who have become good friends and are very helpful in discussing problems and ideas in my project. I also owe my deepest gratitude to former and current faculty and staff members of OPRM department, as well as my fellow residents, who always provide me great support throughout the course of five years in Iowa. Special thanks to Dr. Zoya Kurago, who has taught me from the very beginning and always believes in me. I also feel extremely lucky to know and share my time here in Iowa with a lot of good friends, Ohm, Dew, Oi, Kaew, Jib, Ore, Ron, Moovan, Ball, Fon, Ik, Bow, Todd, Kim-E, and many other Thai students in Iowa. I can’t thank them enough for their nicest companionships. Special thanks to Ohm who has been an incredible support and iii encouragement. I am also grateful for kind hospitality and generosity of Dr. Ronald Ettinger and his wife, Sonia, who always provide the warmest support for us, Thai students. Importantly, I would like to thank my mom, dad, sisters, brother and friends in Thailand, including Ann, Oat, Antt and Earth, who have been there for me throughout this long process. I could not have done this without them. Last but not least, I would like to thank the Royal Thai Government Scholarship for providing me the financial support for my graduate study and giving me the opportunity to study here in Iowa. iv ABSTRACT Antimicrobial peptides are among the repertoire of host innate immune defenses. In mucosal immunity, the health-disease balance can be greatly modulated by the interplay between host immune factors and colonized microflora. Microbial ecology within dental plaque is constantly shaped by environmental factors present within the oral cavity. Several antimicrobial peptides are detected in saliva and their bactericidal activities against oral bacteria, including Streptococcus mutans, the primary etiologic agent of dental caries, have been clearly demonstrated. However, the role of these antimicrobial peptides in S .mutans ecology and host caries experience is not well- defined. We hypothesized that various strains of S. mutans possess different inherent susceptibility/resistance profiles to host salivary antimicrobial peptides and that host- specific quantities of these peptides may influence plaque colonization by particular S. mutans strains. S. mutans strains from subjects with variable caries experience were tested for susceptibility to a panel of antimicrobial peptides, including HNP-1-3, HBD-2-3 and LL- 37, revealing that the susceptibilities of S. mutans to these peptides were strain-specific. S. mutans strains from high caries subjects showed greater resistance to these peptides at varying concentrations than those from caries-free subjects. In addition, when combinations of these peptides were tested, they showed either additive or synergistic interaction against S. mutans. Determinations of the salivary levels of these peptides showed that their concentrations were highly variable among subjects with no correlation to host caries experience. However, positive relationships between the salivary concentrations of HNP- v
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