The infectivity of sarcoid clinical material and its bacterial content inoculated in CBA mice.
نویسندگان
چکیده
BACKGROUND Sarcoidosis is a multisystemic disorder that is currently viewed as the consequence of chronic immunological response associating genetic susceptibility and specific environmental or transmissible agents. Relevant evidence, although conflicting, justifies a concern about the involvement of specific pathogens to disease causation. In this study we assessed the infectivity of sarcoid clinical material, and of the pathogens found in it, to normal CBA mice used as a model of an immuno-competent host. MATERIALS AND METHODS One hundred and eleven mice were inoculated into their footpads with fresh, filtered, and autoclaved, sputum and bronchoalveolar lavage homogenates, collected from patients with sarcoidosis, and with the mycobacterial and propionibacterial pathogens isolated from this material. RESULTS The total number of positive reactors of the animals that received raw clinical material and the pathogens it contained was statistically significant compared to those of the control groups. However, the number of affected mice per group was in most cases less than 50% and inflammation was almost always mild and local. CONCLUSION Based on the evidence provided by inoculation of normal CBA mice, some of the material under study, although of mild potency, can be infectious to an immuno-competent host.
منابع مشابه
تأثیر محلولهای نگهدارندهی مختلف در فرایند انجماد بر عفونتزایی لیشمانیاماژور در مدل موشی
Background and Aim: Leishmanization (LZ) is an effective tool to prevent cutaneous leishmaniasis. Standardization of Leishmania is the main drawback of LZ. The aim of this study was to assess the effect of various preservatives on the infectivity of Leishmania.Methods: L.major harvested at different stages of growth logarithmic, early and late stationary phases were frozen using various pr...
متن کاملDiverse pathogenicity of equine herpesvirus 1 (EHV-1) isolates in CBA mouse model.
The pathogenicity of equine herpesvirus 1 (EHV-1) isolates of Japan were evaluated by using the CBA mouse model. CBA mice were inoculated with eight Japanese EHV-1 strains (89c1, 90c16, 90c18, 97c11, 98c12, 00c19, 01c1 and HH-1) and one British strain (Ab4p). 89c1 caused slight body weight loss and nervous signs in mice at 8 days post infection (dpi). Severe weight loss and nervous signs were o...
متن کاملResistance to erythroleukemia in immunodeficient xid- CBA/N mice with susceptibility after immune stimulation.
CBA/N (xid-) mice failed to develop erythroleukemia when inoculated with an NB-tropic, anemia-causing Friend virus stock (FVA), while Fv-2ss mouse strains succumbed rapidly to the characteristic Friend disease, even after a virus dose 30-fold lower than that given to CBA/N mice. Immunization with bacterial antigens or with spleen cell allografts prior to FVA inoculation rendered CBA/N mice high...
متن کاملاثر سویههای بومی ازتوباکتر کروکوکوم بر رشد، جذب نیتروژن و فسفر گیاه گندم در شرایط گلخانهای
Azotobacter chroococcum can improve mineral nutrition of plants through N2 fixation and plant growth promoting capabilities. Fourteen strains of A. chroococcum were isolated from rhizosphere of wheat plants grown in different field conditions around Tabriz, northwest of Iran. In a pot culture experiment with sterile soil, wheat plants (Triticum aestivum cv. Falat) were inoculated with 14 bacter...
متن کاملThe effect of ZnO nanoparticles on bacterial load of experimental infectious wounds contaminated with Staphylococcus aureus in mice
Objective (s): Bacterial infection is an important cause of delayed wound healing. Staphylococcus aureus (S. aureus) is the main agent causing these infections. Zinc Oxide (ZnO) nanoparticles have antibacterial activity and also accelerate the wound healing process. The aim of the present study is to evaluate the effect of ZnO nanoparticles on bacterial load reduction of the wound infection. M...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- In vivo
دوره 20 6B شماره
صفحات -
تاریخ انتشار 2006