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microtis/inflammation
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Multiple granulomas in three squirrel monkeys (Saimiri sciureus) caused by Mycobacterium microti.
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Mycobacterium microti, a member of the Mycobacterium tuberculosis complex, causes tuberculosis in small rodents and occasionally in other mammals including man. Three adult male squirrel monkeys, two with a history of lethargy, weakness and stridor and one with paralysis of the hind legs, were
Pathomorphologic findings in short-tailed voles (Microtus agrestis) experimentally-infected with Frenkelia microti.
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Following oral infection of Microtus agrestis with sporocysts of Frenkelia microti, transient focal necrosis and cellular infiltrations in the liver, hyperplasia of lymphoid organs, and inflammatory infiltrations in the heart, pulmonary veins, skeletal muscles and brain occurred during the first
Regulation of macrophage accessory cell activity by mycobacteria. II. In vitro inhibition of Ia expression by Mycobacterium microti.
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In our preceding study, we showed that infection of mice with Mycobacterium microti leads to a dramatic increase in Ia expression on local inflammatory macrophage populations. However, the majority of these cells did not contain intracellular organisms. To evaluate the effect of parasitism of
Helper T cell and antibody responses to infection of CBA mice with Babesia microti.
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Helper T cell cytokine and antibody responses were investigated in mice after infection with Babesia microti (King strain). Infection of CBA mice with 106 parasitized erythrocytes resulted in the development of a transitory high parasitaemia which peaked 14 days post infection (DPI), and was
Hepatic tissue changes in rats due to chronic invasion of Babesia microti.
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The etiological agents of babesiosis are intraerythrocytic parasites of the genus Babesia, which are transmitted by ticks. The course of disease is characterized by variable severity. The risk of a complicated course of babesiosis occurs in premature infants, the elderly, splenectomized patients and
Effects of Trypanosoma brucei and Babesia microti infections on the primary granulomatous reaction to Schistosoma eggs in mice.
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Mouse infection with the blood protozoa Trypanosoma brucei suppressed significantly the frequency and intensity of the primary granulomatous inflammatory response to eggs of the blood flukes Schistosoma mansoni and S. bovis injected into the pulmonary microvasculature. In addition, the dynamics of
Histopathologic responses of the jird, Meriones unguiculatus, to the bile duct and pancreatic trematode, Brachylaime microti.
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Biliary tract histopathologic responses of the Mongolian jird, Meriones unguiculatus, were monitored during infection with Brachylaime microti. At 15 days postinoculation (PI), an inflammatory cell (polymorphonuclear and band neutrophil) response occurred in periductal tissue of the common bile duct
Toll-Like Receptors 2 and 4 Cooperate in the Control of the Emerging Pathogen Brucella microti.
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Toll-like receptors (TLRs) recognize pathogen-derived molecules and play a critical role during the host innate and adaptive immune response. Brucella spp. are intracellular gram-negative bacteria including several virulent species, which cause a chronic zoonotic infection in a wide range of
Protozoan Parasite Babesia microti Subverts Adaptive Immunity and Enhances Lyme Disease Severity.
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Lyme disease is the most prominent tick-borne disease in the United States. Co-infections with the tick-transmitted pathogens Babesia microti and Borrelia burgdorferi sensu stricto are becoming a serious health problem. B. burgdorferi is an extracellular spirochete that causes
Age-Related Differential Stimulation of Immune Response by Babesia microti and Borrelia burgdorferi During Acute Phase of Infection Affects Disease Severity.
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Lyme disease is the most prominent tick-borne disease with 300,000 cases estimated by CDC every year while ~2,000 cases of babesiosis occur per year in the United States. Simultaneous infection with Babesia microti and Borrelia burgdorferi are now the most common tick-transmitted
Induction of IL-10-producing CD1dhighCD5+ regulatory B cells following Babesia microti-infection.
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BACKGROUND
Understanding the induction of immune regulatory cells upon helminth infection is important for understanding the control of autoimmunity and allergic inflammation in helminth infection. Babesia microti, an intraerythrocytic protozoan of the genus Babesia, is a major cause of the emerging
Comparative pathogenesis of human WA1 and Babesia microti isolates in a Syrian hamster model.
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The pathogenesis of a newly recognized, molecularly and antigenically distinct human babesial isolate (WA1) and Babesia microti, the common cause of human babesiosis in the United States, were compared in a Syrian hamster model. A group of 33 adult female hamsters were inoculated intraperitoneally
Suppression of Plasmodium cynomolgi in rhesus macaques by coinfection with Babesia microti.
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Both Plasmodium and Babesia species are intraerythrocytic protozoans that infect a wide range of hosts, including humans, and they elicit similar inflammatory responses and clinical manifestations that differ markedly in severity. We recently reported that a rhesus macaque that was chronically
Babesia microti Confers Macrophage-Based Cross-Protective Immunity Against Murine Malaria.
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Malaria and babesiosis, the two primary intraerythrocytic protozoan diseases of humans, have been reported in multiple cases of co-infection in endemic regions. As the geographic range and incidence of arthropod-borne infectious diseases is being affected by climate change, co-infection cases with
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