Samuel J. Black

Professor of Veterinary and Animal Sciences, University of Massachusetts

Email: sblack@bio.umass.edu
S. Black Veterinary & Animal Sciences Web Site

Ph.D.: University of Edinburgh, Scotland
Postdoctoral Training: Cologne University, Germany; Stanford University; International Laboratory for Research in Animal Diseases, Kenya

Molecular Basis of Innate Immunity Against Parasitic Protozoa

We are studying host control of African trypanosomes, tsetse fly-transmitted flagellate protozoa that live and replicate in the fluid compartment of host blood. The organisms cause fatal disease in people and domestic animals. Human trypanosomiasis is restricted to a few regions of Africa but likened to a sleeping dragon that can awake and spread like wildfire. Cattle trypanosomiasis is endemic in and excludes cattle from about 10 million square kilometers of Africa lying between 15° North and 20° South and comprising much of the humid and semi-humid zones. This region is haven to Cape buffalo which are resistant to trypanosomiasis.

Our investigations show that control of trypanosome infection in Cape buffalo correlates with broad-acting anti-trypanosome serum activity involving oxygen radicals generated during catabolism of purines by serum xanthine oxidase. Two features of the buffalo response are noteworthy. First, the presence of a high concentration of serum xanthine oxidase ensures the extracellular capability of producing significant quantities of reactive oxygen radicals. Secondly, an infection-associated decline in blood catalase activity occurs co-incident with clearance of the first parasitemic wave and augments the efficacy of the oxidative response by limiting the rate of catabolism of hydrogen peroxide which is the trypanocidal radical.

We want to characterize features of xanthine oxidase that affect its presence and concentration in serum, the sources and regulation of purine substrates in serum, and how infection causes the decline in serum and erythrocyte-associated catalase. These questions are of fundamental interest because whilst oxygen radicals can slay dragons they can also turn on their maker.

Representative publications:

Black, S.J. , Lunn, DP., Hwang, M., Yin, C., Lenz, SD., Belknap, JK. 2006. Leukocyte emigration in the early stages of laminitis. Veterinary Immunology and Immunopathology. 109: 161-166.

Black, S.J., Seed, J.R. 2005. African Trypanosomiasis, In: Topley and Wilson 's Microbiology and Microbial Infections 10 th Edition, Ed, Frank Fox, Edward Arnold Ltd., Hodder Arnold Publishers ISBN 0 340 88568 8

Kitani H., Black S.J., Nakamura Y., Naessens J., Murphy N.B., Yokomizo Y., Gibson J., and F. Iraqi. (2002) Recombinant tumor necrosis factor alpha does not inhibit the growth of African trypanosomes in axenic cultures. Infect. Immun. 70:2210-4.

Wang, J., A.Van Praagh, E. Hamilton, Q. Wang, B. Zou, M. Muranjan, N.B. Murphy, S.J. Black. 2002, Serum xanthine oxidase: Origin, regulation and
contribution to control of trypanosome parasitemia. Antioxidants and Redox Signaling. 4:161-178.

Hatada, S., Seed, J.R., Barker, C., Hadjuk, S.L., Black, S.J. and Maeda, M. 2002. No trypanosoma lytic activity in sera of mice producing human
haptoglobin-related protein. Molecular and Biochemical parasitology, 119: 291-294.

Sathiyaseelan, T., Naiman, B., Welte, S., MacHugh, N., Black, S.J. and Baldwin, C.L. 2002. Immunological characterization of a gamma delta T cell
stimulatory ligand on autologous monocytes. Immunology, 105:181-189.

Rogers, A.N., Welte, S., Black, S.J. and Baldwin, C.L. 2002. Genetic identification of homologues of CD72 and CD166/ALCAM, ligands for SRCR
family accessory molecules of CD5 and CD6. Veterinary Immunology and Immunopathology, 85:233-239.

Kitani, H., Black, S.J., Nakamura, Y., Naessens, J., Iraqi, F., Gibson, J., Murphy, N. and Yokomizo, Y. 2002. Recombinant tumor necrosis factor alpha
does not inhibit the growth of African trypanosomes in axenic cultures.Infection and Immunity, 70:2210-2214.

Baldwin, C.L., Black S.J. 2002. Immunology, In. Microbial Life. Eds.J.J. Jerry, J.T. Staley, S. Lory. Chapter 27, p 639-676. Sinauer Associates.

Black, S.J., N. Murphy, D. Nolan, 2001 Control of trypanosome parasitemia in Cape buffalo. Int. J. Parasitol. 31:562-565.

Black, S.J., N. B. Murphy, D. Nolan. 2001. Towards a trypanosomiasis vaccine. In: The African Trypanosomes, S,J. Black, J.R. Seed Eds. Pp.
159-174. Kluwer Academic Publishers.

Wu, H., Smyth, J., Luzzi, V., Fukami, K., Takenawa, T., Black, S.J., Allbriton, N.L. and Fissore, R.A. 2001. Sperm factor induces
intracellular free calcium oscillations by stimulating the phosphoinositide pathway. Biology of Reproduction. 64:1338-1349.

Wang, Q., E. Hamilton and S. J. Black (2000). "Purine requirements for the expression of Cape buffalo serum trypanocidal activity." Comp Biochem Physiol C Toxicol Pharmacol 125(1): 25-32.

Black, S. J., Q. Wang, T. Makadzange, Y. L. Li, A. Van Praagh, M. Loomis and J. R. Seed (1999). "Anti-Trypanosoma brucei activity of nonprimate zoo sera." J Parasitol 85(1): 48-53.

Seed, J. R. and S. J. Black (1999). "A revised arithmetic model of long slender to short stumpy transformation in the African trypanosomes." J Parasitol 85(5): 850-4.

Wang, Q., N. Murphy and S. J. Black (1999). "Infection-associated decline of cape buffalo blood catalase augments serum trypanocidal activity." Infect Immun 67(6): 2797-803.

Black, S.J., Wang, Q., Makadzange, T., Li, Y-L., Van Praagh, A., Loomis, M. and Seed, J.R. (1998) Anti-Trypanosoma brucei activity of non-primate zoo sera. J. Parasitol., in press.

Muranjan, M., Wang, Q., Li, Y-l., Hamilton, E., Otieno-Omondi, F.P., Wang, J., Van Praagh, A., Grootenhuis, J.G. and Black, S.J. (1997) The trypanocidal Cape buffalo serum protein is xanthine oxidase. Infect. Immun. 65, 3806-3814.

Reduth, D., Grootenhuis, J.G., Olubayo, R.O., Maranjan, M., Otieno-Omondi, F.P., Morgan, G.A., Brun, R., Williams, D.J.L. and Black, S.J. (1994) African buffalo serum contains novel trypanocidal protein. J. Eukaryotic Microbiol. 41, 95-103.