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Infection and Immunity, January 2005, p. 599-608, Vol. 73, No. 1
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.1.599-608.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

A Mutation in the sap Operon Attenuates Survival of Nontypeable Haemophilus influenzae in a Chinchilla Model of Otitis Media

Kevin M. Mason, Robert S. Munson Jr., and Lauren O. Bakaletz*

Department of Pediatrics, Columbus Children's Research Institute, The Ohio State University College of Medicine and Public Health, Columbus, Ohio

Received 23 June 2004/ Returned for modification 30 July 2004/ Accepted 20 September 2004

Bacteria have evolved strategies to resist killing by antimicrobial peptides (APs), important effectors of innate immunity. The sap (sensitivity to antimicrobial peptides) operon confers resistance to AP-mediated killing of Salmonella. We have recently shown that sapA gene expression is upregulated in the middle ear in a chinchilla model of nontypeable Haemophilus influenzae (NTHI)-induced otitis media. Based on these findings, we constructed an NTHI strain containing a Lux reporter plasmid driven by the sapA promoter and demonstrated early yet transient expression of the sap operon within sites of the chinchilla upper airway upon infection. We hypothesized that the sap operon products mediate NTHI resistance to APs. In order to test this hypothesis, we constructed a nonpolar mutation in the sapA gene of NTHI strain 86-028NP, a low-passage-number clinical isolate. The sapA mutant was approximately eightfold more sensitive than the parent strain to killing by recombinant chinchilla ß-defensin 1. We then assessed the ability of this mutant to both colonize and cause otitis media in chinchillas. The sapA mutant was significantly attenuated compared to the parent strain in its ability to survive in both the nasopharynx and the middle ear of the chinchilla. In addition, the mutant was impaired in its ability to compete with the parent strain in a dual-strain challenge model of infection. Our results indicate that the products of the sap operon are important for resisting the activity of APs and may regulate, in part, the balance between normal carriage and disease caused by NTHI.


* Corresponding author. Mailing address: Department of Pediatrics, Center for Microbial Pathogenesis, Columbus Children's Research Institute, The Ohio State University College of Medicine and Public Health, 700 Children's Dr., Rm. W591, Columbus, OH 43205-2696. Phone: (614) 722-2915. Fax: (614) 722-2818. E-mail: BakaletL{at}pediatrics.ohio-state.edu.

Editor: D. L. Burns


Infection and Immunity, January 2005, p. 599-608, Vol. 73, No. 1
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.1.599-608.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




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