Establishment of lethal inhalational infection with Francisella tularensis (tularaemia) in the common marmoset (Callithrix jacchus)

被引:34
作者
Nelson, Michelle [1 ]
Lever, Mark S. [1 ]
Savage, Victoria L. [1 ]
Salguero, Francisco Javier [2 ]
Pearce, Peter C. [1 ]
Stevens, Daniel J. [1 ]
Simpson, Andrew J. H. [1 ]
机构
[1] Dstl, Salisbury, Wilts, England
[2] Vet Labs Agcy, Surrey, England
关键词
Francisella tularensis; inhalation; marmoset; tularaemia; AIRBORNE TULAREMIA; BODY-TEMPERATURE; MACACA-MULATTA; PATHOGENESIS; MONKEYS; AEROSOL; MICE; DIAGNOSIS; EXPOSURE; DISEASE;
D O I
10.1111/j.1365-2613.2008.00631.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Susceptibility and lethality studies of inhalational tularaemia were undertaken using the common marmoset (Callithrix jacchus) to determine its suitability as a nonhuman primate model, Pairs of marmosets were exposed to varying challenge doses of Francisella tularensis by the airborne route and monitored for up to 14 days post- challenge (p.c.). Lethal infection was achieved following a retained dose of less than 10 bacterial colony-forming units (CFU). However, precise LD50 determination was not possible. The model was characterized using a target challenge dose of approximately 100 CFU. Increased core body temperature was the first indicator of disease, at approximately 2.5 days p.c. Overt clinical signs were first observed 12-18 h after the temperature increase. Significantly decreased activity was observed after approximately 3 days. All animals succumbed to infection between 4.5 and 7 days p.c. At postmortem examination, gross pathology was evident in the liver, spleen and lungs of all animals and high bacterial numbers were detected in all the organs assessed. Bacteraemia was demonstrated in all animals postmortem. Histopathological observations included severe suppurative bronchopneumonia, severe multifocal pyogranulomatous hepatitis, splenitis and lymphadenitis. Tularaemia disease progression in the common marmoset therefore appears to be consistent with the disease seen in humans and other animal models. The common marmoset may therefore be considered a suitable model for further studies of inhalational tularaemia.
引用
收藏
页码:109 / 118
页数:10
相关论文
共 31 条
[1]  
AVERY FW, 1967, AM REV RESPIR DIS, V95, P584
[2]  
BASKERVILLE A, 1978, BRIT J EXP PATHOL, V59, P615
[3]  
*CDC, 2008, CDC EM PREP RESP WEB
[4]   Tularemia in BALB/c and C57BL/6 mice vaccinated with Francisella tularensis LVS and challenged intradermally, or by aerosol with virulent isolates of the pathogen:: protection varies depending on pathogen virulence, route of exposure, and host genetic background [J].
Chen, WX ;
Shen, H ;
Webb, A ;
KuoLee, R ;
Conlan, JW .
VACCINE, 2003, 21 (25-26) :3690-3700
[5]   Expression of cyclooxygenase-2 in swine naturally infected with Actinobacillus pleuropneumoniae [J].
Cho, WS ;
Chae, C .
VETERINARY PATHOLOGY, 2003, 40 (01) :25-31
[6]   Experimental tularemia in mice challenged by aerosol or intradermally with virulent strains of Francisella tularensis:: bacteriologic and histopathologic studies [J].
Conlan, JW ;
Chen, WX ;
Shen, H ;
Webb, A ;
KuoLee, R .
MICROBIAL PATHOGENESIS, 2003, 34 (05) :239-248
[7]   EXPERIMENTAL TULAREMIA IN MACACA-MULATTA - RELATIONSHIP OF AEROSOL PARTICLE SIZE TO INFECTIVITY OF AIRBORNE PASTEURELLA-TULARENSIS [J].
DAY, WC ;
BERENDT, RF .
INFECTION AND IMMUNITY, 1972, 5 (01) :77-+
[8]   Tularemia as a biological weapon - Medical and public health management [J].
Dennis, DT ;
Inglesby, TV ;
Henderson, DA ;
Bartlett, JG ;
Ascher, MS ;
Eitzen, E ;
Fine, AD ;
Friedlander, AM ;
Hauer, J ;
Layton, M ;
Lillibridge, SR ;
McDade, JE ;
Osterholm, MT ;
O'Toole, T ;
Parker, G ;
Perl, TM ;
Russell, PK ;
Tonat, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (21) :2763-2773
[9]  
DIXON WJ, 1993, DRUG INF J, V27, P741
[10]   A MOBILE FORM OF HENDERSON APPARATUS [J].
DRUETT, HA .
JOURNAL OF HYGIENE-CAMBRIDGE, 1969, 67 (03) :437-+