CHANGES IN THE ULTRASTRUCTURE OF CHLAMYDIA-PSITTACI PRODUCED BY TREATMENT OF THE HOST-CELL WITH DEAE-DEXTRAN AND CYCLOHEXIMIDE

被引:13
作者
SPEARS, P
STORZ, J
机构
[1] Department of Microbiology, Colorado State University, Fort Collins
来源
JOURNAL OF ULTRASTRUCTURE RESEARCH | 1979年 / 67卷 / 02期
关键词
D O I
10.1016/S0022-5320(79)80004-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ultrastructure of two Chlamydia psittaci serotypes was investigated in infected L-cell monolayers fixed and embedded in situ. This preparation preserved the relationship of the parasite to the internal structure of the host cells. Chlamydial inclusions in cells treated with diethylaminoethyl-dextran (DEAE-D) and cycloheximide were compared to inclusions in untreated cells. C. psittaci serotype 1 had the same or larger yields of infectious progeny per infected cell in treated cells as in untreated cells. This serotype developed normal inclusions following both treatments. C. psittaci serotype 2 had decreased infectivity yields per infected cell and developed aberrant chlamydial forms in treated cell monolayers. Serotype 2 inclusions contained pycnotic chlamydial forms and numerous miniature reticulate bodies in cycloheximide-treated cells. In DEAE-Dtreated cells, some serotype 2 reticulate bodies were abnormally pleomorphic and contained amorphous material of intermediate electron density. Other reticulate bodies had lost electron density, degenerated, and contained only fragments of the reticulum. Maturation of reticulate bodies into infectious elementary bodies was greatly decreased in serotype 2 inclusions that contained aberrant forms. © 1979 Academic Press, Inc.
引用
收藏
页码:152 / 160
页数:9
相关论文
共 14 条
[1]   PROCEDURE FOR EMBEDDING IN SITU SELECTED CELLS CULTURED IN VITRO [J].
BRINKLEY, BR ;
MURPHY, P ;
RICHARDSON, LC .
JOURNAL OF CELL BIOLOGY, 1967, 35 (01) :279-+
[2]  
CUTLIP R C, 1970, Infection and Immunity, V1, P499
[3]   ENHANCING EFFECT OF DEAE-DEXTRAN ON INCLUSION COUNTS OF AN OVINE CHLAMYDIA (BEDSONIA) IN CELL CULTURE [J].
HARRISON, MJ .
AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1970, 48 :207-&
[4]   COMPETITION BETWEEN CHLAMYDIA-PSITTACI AND L-CELLS FOR HOST ISOLEUCINE POOLS - LIMITING FACTOR IN CHLAMYDIAL MULTIPLICATION [J].
HATCH, TP .
INFECTION AND IMMUNITY, 1975, 12 (01) :211-220
[5]   GROWTH OF EWE ABORTION CHLAMYDIAL AGENT IN MCCOY CELL-CULTURES [J].
HOBSON, D ;
JOHNSON, FWA ;
BYNG, RE .
JOURNAL OF COMPARATIVE PATHOLOGY, 1977, 87 (01) :155-159
[6]   INTERACTION OF CHLAMYDIA-TRACHOMATIS ORGANISMS AND HELA 229 CELLS [J].
KUO, CC ;
GRAYSTON, JT .
INFECTION AND IMMUNITY, 1976, 13 (04) :1103-1109
[7]   INTRACELLULAR PARASITISM - LIFE IN AN EXTREME ENVIRONMENT [J].
MOULDER, JW .
JOURNAL OF INFECTIOUS DISEASES, 1974, 130 (03) :300-306
[8]   USE OF LEAD CITRATE AT HIGH PH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY [J].
REYNOLDS, ES .
JOURNAL OF CELL BIOLOGY, 1963, 17 (01) :208-&
[9]   SEROTYPING OF CHLAMYDIA - ISOLATES OF BOVINE ORIGIN [J].
SCHACHTER, J ;
BANKS, J ;
SUGG, N ;
SUNG, M ;
STORZ, J ;
MEYER, KF .
INFECTION AND IMMUNITY, 1975, 11 (05) :904-907
[10]   SEROTYPING OF CHLAMYDIA .1. ISOLATES OF OVINE ORIGIN [J].
SCHACHTER, J ;
BANKS, J ;
SUGG, N ;
SUNG, M ;
STORZ, J ;
MEYER, KF .
INFECTION AND IMMUNITY, 1974, 9 (01) :92-94