Background and
Research Interests
Dr. Jenifer Turco received her M.S. in Biology and her Ph.D. in Medical Microbiology from West Virginia University. She then did postdoctoral research at the University of South Alabama. Dr. Turco’s professional interests include microbiology, immunology, and infectious diseases. Her research focuses on Rickettsia prowazekii, an obligate intracellular bacterium that causes epidemic typhus in humans.
R. prowazekii is transmitted by human body lice; thus, outbreaks of disease due to this organism have been associated with poor hygiene, overcrowding, and other living conditions that promote body louse infestation. At present, louse-borne typhus is most likely an underreported disease. However, it has been documented in parts of Africa, Asia, and Latin America during the past two decades. In the United States, flying squirrels may harbor R. prowazekii bacteria, and there have been sporadic cases of flying squirrel-associated typhus in humans.
Within the human body, R. prowazekii grows mainly inside the endothelial cells that line the small blood vessels, although the organism can also grow within macrophages. R. prowazekii bacteria may persist in individuals who recover from typhus and later cause an illness known as Brill-Zinsser disease (recrudescent typhus).
Dr. Turco is studying how cytokines such as interferons and tumor necrosis factor alpha limit the intracellular growth of rickettsiae and thus contribute to defending the host against the rickettsiae. Questions being addressed include:
(1) What are the cellular signaling pathways through which these cytokines induce their antirickettsial effects?
(2) Is rickettsial growth inhibited in cytokine-treated host cells because the rickettsiae cannot obtain required nutrients such as nucleotides and iron?
(3) How do cytokine-resistant R. prowazekii isolates avoid the antirickettsial effects of cytokines?
Selected Publications
Turco,
J.,
and H. H. Winkler. 1991.
Comparison of properties of virulent, avirulent, and
interferon-resistant Rickettsia
prowazekii strains. Infect. Immun. 59:1647-1655.
Gao, Q., J. Turco, and H. H. Winkler. 1993.
Synthesis of DNA, rRNA, and protein by Rickettsia
prowazekii growing in untreated or gamma interferon-treated
mouse L929 cells. Infect. Immun. 61:2383-2389.
Winkler, H. H., L. C. Day, R. M.
Daugherty, and J. Turco. 1993.
Effect of gamma interferon on phospholipid hydrolysis and fatty
acid
incorporation in L929 cells infected with Rickettsia
prowazekii. Infect. Immun. 61:3412-3415.
Turco, J.,
and H. H. Winkler. 1993.
Role of the nitric oxide synthase pathway in the inhibition of
growth of
interferon-sensitive and interferon-resistant Rickettsia
prowazekii strains in L929 cells treated with tumor necrosis
factor alpha and gamma interferon.
Infect. Immun. 61: 4317-4325.
Turco, J.,
and H. H. Winkler. 1994.
Relationship of tumor necrosis factor alpha, the nitric oxide
synthase
pathway, and lipopolysaccharide to the killing of gamma
interferon-treated
macrophagelike RAW264.7 cells by Rickettsia
prowazekii. Infect. Immun. 62:
2568-2574.
Turco, J.,
and H. H. Winkler. 1994.
Cytokine sensitivity and methylation of lysine in Rickettsia
prowazekii EVir and interferon-resistant Rickettsia
prowazekii strains. Infect. Immun. 62:
3172-3177.
Turco, J.,
and H. H. Winkler. 1997.
Cytokines influencing infections by Rickettsia
species, p. 29-52. In B.
Anderson, H. Friedman, and M. Bendinelli (ed.), Rickettsial
Infection and Immunity. Plenum
Publishing Corp.,
Turco, J.,
H. Liu, S. F. Gottlieb, and H. H.
Winkler. 1998. Nitric
oxide-mediated inhibition of the
ability of Rickettsia prowazekii to
infect mouse fibroblasts and mouse macrophagelike cells.
Infect. Immun. 66: 558-566.
Turco, J., and M. Byrd. 2001.
An interdisciplinary perspective: infectious diseases and
history. American Biology Teacher 63:
325-335.
Turco, J.
2005. Rickettsia
prowazekii-infected, cultured human fibroblasts.
Microbe Library (American Society for Microbiology)
[Online]. Available: http://www.microbelibrary.org.
The
image is a light micrograph of R. prowazekii-infected,
cultured human fibroblasts that
were stained by the Giménez method.