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Infection and Immunity, January 2008, p. 380-390, Vol. 76, No. 1
0019-9567/08/$08.00+0     doi:10.1128/IAI.01043-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Surfactant-Associated Protein A Provides Critical Immunoprotection in Neonatal Mice{triangledown}

Caroline L. S. George,1* Kelli L. Goss,2 David K. Meyerholz,3 Fred S. Lamb,1 and Jeanne M. Snyder1,2

Departments of Pediatrics,1 Anatomy and Cell Biology,2 Pathology, University of Iowa, Carver College of Medicine, Iowa City, Iowa 522423

Received 27 July 2007/ Returned for modification 4 September 2007/ Accepted 19 October 2007

The collectins surfactant-associated protein A (SP-A) and SP-D are components of innate immunity that are present before birth. Both proteins bind pathogens and assist in clearing infection. The significance of SP-A and SP-D as components of the neonatal immune system has not been investigated. To determine the role of SP-A and SP-D in neonatal immunity, wild-type, SP-A null, and SP-D null mice were bred in a bacterium-laden environment (corn dust bedding) or in a semisterile environment (cellulose fiber bedding). When reared in the corn dust bedding, SP-A null pups had significant mortality (P < 0.001) compared to both wild-type and SP-D null pups exposed to the same environment. The mortality of the SP-A null pups was associated with significant gastrointestinal tract pathology but little lung pathology. Moribund SP-A null newborn mice exhibited Bacillus sp. and Enterococcus sp. peritonitis. When the mother or newborn produced SP-A, newborn survival was significantly improved (P < 0.05) compared to the results when there was a complete absence of SP-A in both the mother and the pup. Significant sources of SP-A likely to protect a newborn include the neonatal lung and gastrointestinal tract but not the lactating mammary tissue of the mother. Furthermore, exogenous SP-A delivered by mouth to newborn SP-A null pups with SP-A null mothers improved newborn survival in the corn dust environment. Therefore, a lack of SP-D did not affect newborn survival, while SP-A produced by either the mother or the pup or oral exogenous SP-A significantly reduced newborn mortality associated with environmentally induced infection in SP-A null newborns.


* Corresponding author. Present address: University of Minnesota, Department of Pediatrics, 420 Delaware Street SE, MMC 742, Minneapolis, MN 55455. Phone: (612) 626-2963. Fax: (612) 626-0413. E-mail: cgeorge{at}umn.edu

{triangledown} Published ahead of print on 29 October 2007.

Editor: A. J. Bäumler


Infection and Immunity, January 2008, p. 380-390, Vol. 76, No. 1
0019-9567/08/$08.00+0     doi:10.1128/IAI.01043-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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