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PMID: 3919118 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Phagocytosis and killing of Brucella by human polymorphonuclear leukocytes.

The Journal of infectious diseases ·Vol. 151 ·No. 4 ·1985-04-00 ·Pages 682-90

Young EJ, Borchert M, Kretzer FL, Musher DM

Abstract

Although cellular immunity involving activated macrophages is important in resistance to Brucella, serum factors and polymorphonuclear leukocytes (PMNLs) play some role in the initial response to infection. The interaction between human PMNLs and virulent and attenuated strains of Brucella abortus and Brucella melitensis was studied by in vitro techniques. Virulent and attenuated strains of both species were rapidly phagocytosed after opsonization with normal human serum (NHS); nonopsonized bacteria were not phagocytosed. In contrast, NHS devoid of detectable antibodies was bactericidal for strains of B. abortus but not of B. melitensis. In addition, intracellular killing of ingested bacteria was shown for virulent B. abortus but not for B. melitensis. Ultrastructural studies revealed morphological alterations in about one-half of phagocytosed B. abortus and B. melitensis after incubation for 10 min; thereafter, nearly 100% of B. abortus showed some degree of degeneration, whereas B. melitensis remained intact during 120 min of observation.

MeSH Terms
Adult Brucella/immunology,pathogenicity,ultrastructure Brucella abortus/immunology,pathogenicity,ultrastructure Cytoplasm/ultrastructure Humans In Vitro Techniques Kinetics Microscopy, Electron Neutrophils/immunology,ultrastructure Opsonin Proteins Phagocytosis Vacuoles/ultrastructure Virulence
Chemicals
Opsonin Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Young E J
Borchert M
Kretzer F L
Musher D M
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
0022-1899
Published
1985-04-00
Pages
682-90
Language
English
Region
United States
NLM ID
0413675
Subset
IM
Grants
NEI NIH HHS · EY-02607 · United States
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