Oxidant generation by single infected monocytes after short-term fluorescence labeling of a protozoan parasite

Haeok K. Chang, Colin Thalhofer, Breck A. Duerkop, Joanna S. Mehling, Shilpi Verma, Kenneth J. Gollob, Roque Almeida, Mary E. Wilson

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Leishmania spp. are intracellular protozoa residing in mononuclear phagocytes. Leishmania organisms are susceptible to microbicidal responses generated in response to phagocytosis. Assuming that both phagocyte and parasite populations are heterogeneous, it is advantageous to examine the response of individual cells phagocytosing living parasites. Because Leishmania spp. lose virulence during the raising of transfectants, we developed a method to label live Leishmania chagasi short-term with fluorescent dyes. Up to six parasite divisions were detected by flow cytometry after labeling with carboxyfluorescein diacetate succinimidyl ester (CFSE), dioctadecyl-tetramethylindo carbocyanine perchlorate, or chloromethyl tetramethylrhodamine. Labeled parasites entered mononuclear phagocytes as determined by confocal and time-lapse microscopy. Dihydroethidium (DHE) was used to detect macrophage-derived oxidants generated during phagocytosis. Presumably Leishmania organisms are opsonized with host serum/tissue components such as complement prior to phagocytosis. Therefore, we investigated the effects of opsonization and found that this increased the efficiency of CFSE-labeled parasite entry into monocytes (84.6% ± 8.8% versus 20.2% ± 3.8% monocytes infected; P < 0.001). Opsonization also increased the percentage of phagocytes undergoing a respiratory burst (66.0% ± 6.3% versus 41.0% ± 8.3% of monocytes containing CFSE-labeled parasites; P < 0.001) and the magnitude of oxidant generation by each infected monocyte. Inhibitor data indicated that DHE was oxidized by products of the NADPH oxidase. These data suggest that opsonized serum components such as complement lead to more efficient entry of Leishmania into their target cells but at the same time activate the phagocyte oxidase to generate microbicidal products in infected cells. The parasite must balance these positive and negative survival effects in order to initiate a viable infection.

Original languageEnglish (US)
Pages (from-to)1017-1024
Number of pages8
JournalInfection and Immunity
Volume75
Issue number2
DOIs
StatePublished - Feb 2007

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Oxidants
Monocytes
Parasites
Leishmania
Fluorescence
Phagocytes
Phagocytosis
Carbocyanines
Leishmania infantum
Cytophagocytosis
Respiratory Burst
NADPH Oxidase
Serum
Fluorescent Dyes
Virulence
Microscopy
Flow Cytometry
Oxidoreductases
Macrophages
Infection

ASJC Scopus subject areas

  • Immunology

Cite this

Chang, H. K., Thalhofer, C., Duerkop, B. A., Mehling, J. S., Verma, S., Gollob, K. J., ... Wilson, M. E. (2007). Oxidant generation by single infected monocytes after short-term fluorescence labeling of a protozoan parasite. Infection and Immunity, 75(2), 1017-1024. https://doi.org/10.1128/IAI.00914-06

Oxidant generation by single infected monocytes after short-term fluorescence labeling of a protozoan parasite. / Chang, Haeok K.; Thalhofer, Colin; Duerkop, Breck A.; Mehling, Joanna S.; Verma, Shilpi; Gollob, Kenneth J.; Almeida, Roque; Wilson, Mary E.

In: Infection and Immunity, Vol. 75, No. 2, 02.2007, p. 1017-1024.

Research output: Contribution to journalArticle

Chang, HK, Thalhofer, C, Duerkop, BA, Mehling, JS, Verma, S, Gollob, KJ, Almeida, R & Wilson, ME 2007, 'Oxidant generation by single infected monocytes after short-term fluorescence labeling of a protozoan parasite', Infection and Immunity, vol. 75, no. 2, pp. 1017-1024. https://doi.org/10.1128/IAI.00914-06
Chang, Haeok K. ; Thalhofer, Colin ; Duerkop, Breck A. ; Mehling, Joanna S. ; Verma, Shilpi ; Gollob, Kenneth J. ; Almeida, Roque ; Wilson, Mary E. / Oxidant generation by single infected monocytes after short-term fluorescence labeling of a protozoan parasite. In: Infection and Immunity. 2007 ; Vol. 75, No. 2. pp. 1017-1024.
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