Infection of murine precision cut lung slices (PCLS) with respiratory syncytial virus (RSV) and chlamydophila pneumoniae using the Krumdieck technique

被引:28
作者
Ebsen, M
Mogilevski, G
Anhenn, O
Maiworm, V
Theegarten, D
Schwarze, J
Morgenroth, K
机构
[1] Ruhr Univ Bochum, Dept Pathol, D-44801 Bochum, Germany
[2] Ruhr Univ Bochum, St Josef Hosp, Dept Pediat, D-4630 Bochum, Germany
关键词
Krumdieck technique; RSV; chlamydophila pneumoniae; in vitro technique; transmission electron microscopy;
D O I
10.1078/0344-0338-00331
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The Krumdieck technique allows the investigation of the so-called precision cut lung slices (PCLS) with a special microtome. It is thus possible to evaluate morphologic changes over a longer period of time using only a small group of animals. Chlamydophila pneumoniae (Cp) and respiratory syncytial virus (RSV) proved to be important causes of pneumonia, rhinitis and exacerbations of asthma bronchiale, as well as of lower respiratory tract infections in young children. PCLS should be tested for their suitability as an in vitro model for these infections. The PCLS were infected with Cp and RSV over different periods of time. Investigations were carried out by light and transmission electron microscopy (TEM). Furthermore, immunofluorescence (IF) studies with antibodies against bacterial or viral proteins and cell-specific markers were done using confocal laser scanning microscopy (CLSM). Non-infected and infected PCLS showed a well-preserved morphology up to 72 hours. After short infection intervals, typical inclusions of Cp or RSV were detected in vacuoles of different cell types. Infection and cell types could be verified using IF. Cytopathic effects were not prominent. Ciliary beat was detectable up to 96 hours after infection. This in vitro technique offers the possibility of studying mechanisms and effects of bacterial and viral infections on viable tissue complexes.
引用
收藏
页码:747 / 753
页数:7
相关论文
共 27 条
[1]  
BACHI T, 1973, J VIROL, V12, P1173
[2]  
BAURIEDEL G, 1998, DEUT MED WOCHENSCHR, V123, P375
[3]   Airway epithelial cell-induced activation of monocytes and eosinophils in respiratory syncytial viral infection [J].
Becker, S ;
Soukup, JM .
IMMUNOBIOLOGY, 1999, 201 (01) :88-106
[4]   Drug-metabolizing activity of human and rat liver, lung, kidney and intestine slices [J].
De Kanter, R ;
De Jager, MH ;
Draaisma, AL ;
Jurva, JU ;
Olinga, P ;
Meijer, DKF ;
Groothuis, GMM .
XENOBIOTICA, 2002, 32 (05) :349-362
[5]   Rabbit model for Chlamydia pneumoniae infection [J].
Fong, IW ;
Chiu, B ;
Viira, E ;
Fong, MW ;
Jang, D ;
Mahony, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) :48-52
[6]   CYTOPLASMIC INCLUSIONS OF RESPIRATORY SYNCYTIAL VIRUS-INFECTED CELLS - FORMATION OF INCLUSION-BODIES IN TRANSFECTED CELLS THAT COEXPRESS THE NUCLEOPROTEIN, THE PHOSPHOPROTEIN, AND THE 22K PROTEIN [J].
GARCIA, J ;
GARCIABARRENO, B ;
VIVO, A ;
MELERO, JA .
VIROLOGY, 1993, 195 (01) :243-247
[7]   Medical progress - Respiratory syncytial virus and parainfluenza virus. [J].
Hall, CB .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (25) :1917-1928
[8]   LONG-TERM PROSPECTIVE-STUDY IN CHILDREN AFTER RESPIRATORY SYNCYTIAL VIRUS-INFECTION [J].
HALL, CB ;
HALL, WJ ;
GALA, CL ;
MAGILL, FB ;
LEDDY, JP .
JOURNAL OF PEDIATRICS, 1984, 105 (03) :358-364
[9]   Characterization of airway and vascular responses in murine lungs [J].
Held, HD ;
Martin, C ;
Uhlig, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 126 (05) :1191-1199
[10]   STRUCTURE OF RESPIRATORY SYNCYTIAL VIRUS [J].
JONCAS, J ;
BERTHIAUME, L ;
PAVILANIS, V .
VIROLOGY, 1969, 38 (03) :493-+