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Journal of Virology, August 2001, p. 6884-6893, Vol. 75, No. 15
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.15.6884-6893.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Adeno-Associated Virus Serotype 4 (AAV4) and AAV5 Both Require Sialic Acid Binding for Hemagglutination and Efficient Transduction but Differ in Sialic Acid Linkage Specificity

Nikola Kaludov,1 Kevin E. Brown,2 Robert W. Walters,3,4 Joseph Zabner,3 and John A. Chiorini1,*

Gene Therapy and Therapeutics Branch, National Institute of Dental and Craniofacial Research,1 and Hematology Branch, National Heart, Lung, and Blood Institute,2 National Institutes of Health, Bethesda, Maryland, and Departments of Internal Medicine3 and Physiology and Biophysics,4 University of Iowa College of Medicine, Iowa City, Iowa

Received 31 January 2001/Accepted 3 May 2001

Adeno-associated virus serotype 4 (AAV4) and AAV5 have different tropisms compared to AAV2 and to each other. We recently reported that alpha 2-3 sialic acid is required for AAV5 binding and transduction. In this study, we characterized AAV4 binding and transduction and found it also binds sialic acid, but the specificity is significantly different from AAV5. AAV4 can hemagglutinate red blood cells from several species, whereas AAV5 hemagglutinates only rhesus monkey red blood cells. Treatment of red blood cells with trypsin inhibited hemagglutination for both AAV4 and AAV5, suggesting that the agglutinin is a protein. Treatment of Cos and red blood cells with neuraminidases also indicated that AAV4 bound alpha 2-3 sialic acid. However, resialylation experiments with neuraminidase-treated red blood cells demonstrated that AAV4 binding required alpha 2-3 O-linked sialic acid, whereas AAV5 required N-linked sialic acid. Similarly, resialylation of sialic acid-deficient CHO cells supported this same conclusion. The difference in linkage specificity for AAV4 and AAV5 was confirmed by binding and transduction experiments with cells incubated with either N-linked or O-linked inhibitors of glycosylation. Furthermore, AAV4 transduction was only blocked with soluble alpha 2-3 sialic acid, whereas AAV5 could be blocked with either alpha 2-3 or alpha 2-6 sialic acid. These results suggest that AAV4 and AAV5 require different sialic acid-containing glycoproteins for binding and transduction of target cells and they further explain the different tropism of AAV4 and AAV5.

* Corresponding author. Mailing address: NIH 10/IN113, 10 Center Dr., MSC 1190, Bethesda, MD 20902-1190. Phone: (301) 496-4279. Fax: (301) 402-1228. E-mail: Jchiorini{at}dir.nidcr.nih.gov.

Journal of Virology, August 2001, p. 6884-6893, Vol. 75, No. 15
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.15.6884-6893.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.


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