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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of medicinal chemistry 26 (1983), S. 1300-1307 
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] CD1d-restricted T cells are implicated as key players in host defense against various microbial infections. However, the mechanisms involved and the role they play, if any, at the mucosal surfaces where pathogenic infections are initiated is unknown. In a murine pneumonia model established by ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS immunology and medical microbiology 22 (1998), S. 0 
    ISSN: 1574-695X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: In both batch and continuous culture, Peptostreptococcus anaerobius was able to grow in vaginal defined medium with Prevotella bivia, but not in pure culture. Growth of P. anaerobius was increased by 238% (P〈0.001) in peptone-supplemented vaginal defined medium conditioned by prior growth of P. bivia. Analysis of P. bivia culture supernatants showed a net accumulation of amino acids and subsequent growth of P. anaerobius in the conditioned supernatants resulted generally in amino acid utilization. Supplementation of peptone-supplemented vaginal defined medium with amino acids in concentrations similar to those available after prior growth with P. bivia were growth-stimulatory (246%, P=0.006) for P. anaerobius. Increased availability of amino acids by P. bivia is proposed as a mechanism to support the observed in vitro commensal symbiosis between P. bivia and P. anaerobius.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 30 (1985), S. 40S 
    ISSN: 1573-2568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Animal model systems have been used extensively to study both experimental and naturally occurring ulcerative colitis syndromes. Interestingly, despite a variety of different animal species and a broad range of inducing agents, the response of the large intestine has been somewhat predictable. Although there is suggestive evidence for transmissible agents in several of these animal model systems, documentation of a bacterial or viral etiology has remained elusive. Perhaps the best evidence to suggest that bacteria play a role in the development of naturally occurring ulcerative colitis resides in the studies utilizing the rabbitdinitrochlorobenzine model and the carrageenininduced ulcerative colitis model in the guinea pig, The evidence for microbial involvement in these model systems includes the use of single bacterial species in the carrageenin model to produce an ulcerative colitis like disease and the use of antimicrobial agents to alter the experimental model system in the guinea pig and hamster with proliferative ileitis and evidence of transmissibility. Recent reports of transmissible agents for both ulcerative colitis and Crohn's disease in studies utilizing immunologically deficient mice also suggest that the search for the “agent” and mechanism should continue in model systems. The many differences between animal model systems and the human disease cannot be ignored. These differences make establishing what appears to be a complicated etiology even more difficult. Despite the difference in anatomy, physiology, and nutritional factors between animal model systems and the human disease process, the fact remains that one or more of these model systems may reflect the same mechanism or etiologic agent which occurs in the human disease. It is important that future studies include animal model systems, regardless of whether or not they absolutely reflect all of the requirements of the naturally occurring disease.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-7411
    Keywords: abscess ; host response ; intraabdominal ; B.fragilis ; microbiological synergy ; capsular polysaccharide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Obligate anaerobes are known to play a significant role in the development of intraabdominal abscesses. Much of our knowledge about these organisms is based on observations made using an animal model developed by this laboratory in 1974 [1,2]. The basic model system employs Wistar rats surgically implanted with an inoculum of intestinal contents from other rats. The inoculum is prepared in a manner which simulates the microbiologic parameters of the human colon. This is accomplished by placing rats on a diet of lean ground beef for two weeks and then harvesting, homogenizing and freezing aliquots of prepared intestinal contents for subsequent use. Following implantation of the intestinal contents, animals develop a characteristic bi-phasic infection. The first phase of the disease is peritonitis associated with positive blood and peritoneal cultures, death of approximately 50% of implanted animals, free flowing peritoneal exudates and an increase in peripheral white blood cell counts. Animals that survive the initial stage of disease appear to recover within five days of surgery. However, all surviving recipients of the intestinal content inoculum develop intraabdominal abscesses. This second phase of the disease is more chronic and is characterized by the presence of abscesses, adhesions and negative blood cultures. Abscesses contain a polymicrobic flora consisting of both obligate anaerobes and facultative species. The clinical end points for evaluation in this model are mortality and abscess formation, while microbiologic end points include blood, peritoneal and abscess cultures. The two phases of this disease are associated with distinctly different bacterial populations. During the early, acute peritonitis stage, Escherichia coli and other Gram negative organisms are numerically dominant and are responsible for the early mortality. The second more chronic stage of the disease, abscess formation, requires the presence of obligate anaerobes, such as Bacteroides fragilis. It has also been shown that abscess development in this model is associated with either a synergistic combination of obligate anaerobes and facultative species [3], or can be experimentally reproduced with the capsular polysaccharide of B.fragilis [4]. The unique properties of the capsular polysaccharide of B.fragilis and it’s role in both the induction and prevention of abscesses has been well documented in the literature [5–15]. It is the second phase of this experimental disease process that will be discussed in this chapter.
    Type of Medium: Electronic Resource
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