AJTMH Tropical Medicine and Hygiene News
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 70(3), 2004, pp. 278-285
Copyright © 2004 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (8)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by MILLERON, R. S.
Right arrow Articles by LANZARO, G. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MILLERON, R. S.
Right arrow Articles by LANZARO, G. C.
Related Collections
Right arrow Vector Biology
Right arrow Leishmaniasis
Right arrow Sand Flies

NEGATIVE EFFECT OF ANTIBODIES AGAINST MAXADILAN ON THE FITNESS OF THE SAND FLY VECTOR OF AMERICAN VISCERAL LEISHMANIASIS

RANIA S. MILLERON, JOSE M. C. RIBEIRO, DIA ELNAIME, LYNN SOONG, AND GREGORY C. LANZARO
Department of Pathology and World Health Organization Collaborating Center for Tropical Diseases, University of Texas Medical Branch, Galveston, Texas; Medical Entomology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland

Lutzomyia longipalpis expresses a salivary protein called maxadilan (MAX) that functions to dilate vertebrate blood vessels and thereby to facilitate the sand fly’s acquisition of blood. We hypothesized that antibodies specific for one of many MAX variants would inhibit vasodilatory function of that variant. In vitro and in vivo experiments showed that antibodies against a specific MAX variant decreased vasodilatory function. More specifically, antibodies against MAX blocked vasodilation of a constricted rabbit aorta. Additionally, a strain of Lu. longipalpis, with a nearly uniform MAX genotype, obtained a larger blood meal from naive BALB/c mice compared with mice that were either immunized with a homologous MAX genotype or sensitized to bites of flies from the same strain. Those flies taking blood from mice sensitized by sand fly bites also laid significantly fewer eggs than when they took blood from naive mice. These results have potential epidemiologic importance in light of the potential use of MAX in a vaccine or as part of a diagnostic test because they imply that a uniform MAX genotype is selected against by the vertebrate host immune response and that antigenic diversity is selected for.


Received February 17, 2003. Accepted for publication September 3, 2003.

Acknowledgments: We thank Dr. Daniel Freeman (University of Texas Medical Branch) for discussing the statistical applications used in the manuscript.

Financial support: This work was funded by National Institutes of Health (grants T32 AI-075261 and AI-39540).

Authors’ addresses Rania S. Milleron, Center for Molecular and Cellular Toxicology, Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, 1 University Station, Austin, TX 78712-1074, Telephone: 512-471-3968, Fax: 512-471-5002, E-mail: rania{at}uts.cc.utexas.edu. Jose M. C. Ribeiro, Medical Entomology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 4 Center Drive, Bethesda, MD 20892-0425, Telephone: 301-496-3066, Fax: 301-402-4941, E-mail: jribeiro{at}nih.gov. Dia Elnaime, Department of Entomology, University of California, 1 Shields Avenue, Davis, CA, 95616-8579, Telephone: 530-752-55833, Fax: 530-752-1537, E-mail: daelnaiem{at}ucdavis.edu. Lynn Soong, Departments of Microbiology and Immunology, University of Texas Medical Branch at Galveston, 301 University Boulevard, MRB 3.142B, Galveston, TX 77555-1070, Telephone: 409-772-8149, Fax: 409-747-6869, E-mail: lysoong{at}utmb.edu. Gregory C. Lanzaro, Department of Entomology, University of California, 1 Shields Avenue, Davis, CA 95616-8579, Telephone: 530-752-5652, Fax: 530-752-1537, E-mail: gclanzaro{at}ucdavis.edu.




This article has been cited by other articles:


Home page
J. Immunol.Home page
W. H. Wheat, K. E. Pauken, R. V. Morris, and R. G. Titus
Lutzomyia longipalpis Salivary Peptide Maxadilan Alters Murine Dendritic Cell Expression of CD80/86, CCR7, and Cytokine Secretion and Reprograms Dendritic Cell-Mediated Cytokine Release from Cultures Containing Allogeneic T Cells
J. Immunol., June 15, 2008; 180(12): 8286 - 8298.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
T. M. Brodie, M. C. Smith, R. V. Morris, and R. G. Titus
Immunomodulatory Effects of the Lutzomyia longipalpis Salivary Gland Protein Maxadilan on Mouse Macrophages
Infect. Immun., May 1, 2007; 75(5): 2359 - 2365.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the American Society of Tropical Medicine and Hygiene.