Infection of newborn piglets with Bordetella pertussis:: a new model for pertussis

被引:50
作者
Elahi, S
Brownlie, R
Korzeniowski, J
Buchanan, R
O'Connor, B
Peppler, MS
Halperin, SA
Lee, SF
Babiuk, LA
Gerdts, V
机构
[1] Univ Saskatchewan, VIDO, Saskatoon, SK S7N 5E3, Canada
[2] Univ Saskatchewan, Prairie Diagnost Serv, Saskatoon, SK, Canada
[3] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB, Canada
[4] Dalhousie Univ, Dept Pediat, Fac Med, Halifax, NS, Canada
[5] Dalhousie Univ, Fac Dent, Dept Appl Oral Sci, Halifax, NS B3H 3J5, Canada
关键词
D O I
10.1128/IAI.73.6.3636-3645.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bordetella pertussis is the causative agent of pertussis or whooping cough. This bacterium is a human pathogen that under experimental conditions also infects selected rodents and primates. Here, we show for the first time that newborn piglets can be infected with B. pertussis when it is delivered intrapulmonarily. Infected piglets displayed fever and respiratory symptoms, such as nasal discharge, nonparoxysmal coughing, and breathing difficulties. Eventually, all infected animals developed severe bronchopneumonia, which in some cases was combined with a fibrinous pleuritits. Immunohistochemical staining revealed the presence of large numbers of B. pertussis cells within airways, adhering to the epithelial lining or phagocytosed by macrophages and neutrophils. Viable bacteria were reisolated from bronchoalveolar lavages and lung lesions for more than 10 days postinfection. The systemic presence of pertussis toxin was shown by hypoglycemia, lymphocytosis, and induction of a clustered pattern of CHO cells by serum and bronchoalveolar lavage samples. Thus, a large-animal model for pertussis was developed, which should complement existing rodent models for identifying the immune responses relevant to the design of new vaccines. In particular, this model should help researchers analyze the roles of both maternal and mucosal immunity in disease protection against pertussis and should ultimately assist in the design of new vaccines for early life protection.
引用
收藏
页码:3636 / 3645
页数:10
相关论文
共 51 条
[1]   Innate immunity in the lung: how epithelial cells fight against respiratory pathogens [J].
Bals, R ;
Hiemstra, PS .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (02) :327-333
[2]  
BARAFF LJ, 1984, PEDIATRICS, V73, P37
[3]   Immunogenicity of a three-component acellular pertussis vaccine administered at birth [J].
Belloni, C ;
De Silvestri, A ;
Tinelli, C ;
Avanzini, MA ;
Marconi, M ;
Strano, F ;
Rondini, G ;
Chirico, G .
PEDIATRICS, 2003, 111 (05) :1042-1045
[4]  
*CDCP, 1995, MMWR-MORBID MORTAL W, V44, P525
[5]   Bordetella species are distinguished by patterns of substantial gene loss and host adaptation [J].
Cummings, CA ;
Brinig, MM ;
Lepp, PW ;
van de Pas, S ;
Relman, DA .
JOURNAL OF BACTERIOLOGY, 2004, 186 (05) :1484-1492
[6]   Pertussis: an important target for maternal immunization [J].
Edwards, KM .
VACCINE, 2003, 21 (24) :3483-3486
[7]   Are pertussis fatalities in infants on the rise? What can be done to prevent them? [J].
Edwards, KM .
JOURNAL OF PEDIATRICS, 2003, 143 (05) :552-553
[8]  
EDWARDS KM, 1999, VACCINES, P293
[9]  
ENGLUND JA, 1995, PEDIATRICS, V96, P580
[10]   Autotoxicity of nitric oxide in airway disease [J].
Flak, TA ;
Goldman, WE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (04) :S202-S206