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1.
Teneral Glossina morsitans centralis, G. m. morsitans and G. pallidipes were infected with three different clones of Trypanosoma brucei in blood containing D(+)-glucosamine, an inhibitor of tsetse midgut lectin. On average, 5 days of D(+)-glucosamine treatment tripled infection rates, without affecting the proportion of infections that matured. Total infection rates were equal in males and females, but twice as many infections matured in males. Counts of parasites in the guts and salivary glands of 277 flies revealed order of magnitude differences among flies, with females consistently having 2-3-times as many parasites as males. Parasite numbers varied in a sex-specific manner among tsetse-clone combinations, but these differences were not correlated with similar large differences in infection rates. D(+)-glucosamine treatment had no significant effect on parasite loads. 相似文献
2.
Identification and characterization of a novel PrfA-regulated gene in Listeria monocytogenes whose product, IrpA, is highly homologous to internalin proteins, which contain leucine-rich repeats.
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E Domann S Zechel A Lingnau T Hain A Darji T Nichterlein J Wehland T Chakraborty 《Infection and immunity》1997,65(1):101-109
3.
Screening for complement deficiency in bacterial meningitis 总被引:1,自引:0,他引:1
T Ernst PJ Späth C Aebi UB Schaad MG Bianchetti 《Acta paediatrica (Oslo, Norway : 1992)》1997,86(9):1009-1010
Seventy-seven children with bacterial meningitis were screened for complement deficiency. Both the classical and the alternate pathways were normal in 75 patients. Transiently reduced total haemolytic activity of the classical pathway was documented in a boy with meningococcal meningitis. Total haemolytic activity of both the classical and the alternate pathways were reduced in another patient with pneumococcal meningitis: individual complement components determination indicated predominant activation of the alternate pathway. 相似文献
4.
During studies to determine the main Trypanosoma brucei rhodesiense transmission sites in Lambwe Valley, Western Kenya, Glossina pallidipes were collected from two areas in the valley and examined for trypanosome infection. T. brucei isolated from infected flies were tested for their response to the lethal effects of human blood (Blood Incubation Infectivity Test, BIIT) and also characterized using isoenzyme electrophoresis. Six of the 26 T. brucei tested were BIIT positive, two of which had enzyme profiles identical to human isolates. The 26 isolates were grouped into 10 zymodemes. Two zymodemes were identical to T. b. rhodesiense isolated from sleeping sickness patients, one of which was identical to the predominant zymodemes among patients from Lambwe Valley area. The other zymodeme was identical to an isolate from a patient from the Busoga (Uganda) sleeping sickness epidemic focus. These two Zymodemes were BIIT positive. It is suggested that there has been an exchange of human infecting organisms between the Kenya and the Uganda foci. 相似文献
5.
The metabolism of inositol 1,4,5-trisphosphate and inositol 1,3,4,5-
tetrakisphosphate in homogenates and sub-fractions from normal rat liver
and premalignant liver nodules was investigated. The activities of
5-phosphatase, expressed as pmol converted substrate per minute and mg
protein, were equal when using the two substrates, and did not differ
between normal and nodular homogenates. Subcellular fractions were purified
by sequential steps of differential centrifugation and density gradient
fractionation procedures. The total phosphatase activity was found to be
distributed between cytosol (15%) and membraneous fractions (75%), with
most of the enzyme activity residing in the plasma membranes. A doubling of
phosphatase specific activity was seen in the nodular low density membrane
fraction, containing Golgi apparatus and endosomes, as compared with normal
liver. Inositol 1,4,5- trisphosphate 3-kinase activity was found to be
exclusively cytosolic. No difference in this enzyme was seen between the
two tissue types studied. Vasopressin (0.2 or 2 microM) had no effect
either on phosphatase or kinase activity. The compartmentalization of
inositol polyphosphate 5-phosphatase activity presents a possible
explanation of earlier findings that premalignant liver tissue was able to
respond with inositol 1,4,5-trisphosphate, but not inositol 1,3,4,5-
tetrakisphosphate formation after agonist stimulation.
相似文献
6.
Gotlib V Darji J Bloomfield K Chadburn A Patel A Braunschweig I 《Leukemia & lymphoma》2003,44(9):1609-1613
Eosinophilic variant of CML (eoCML) is a unique disease with a poor prognosis. Like the hypereosinophilic syndrome (HES), eoCML has no clinically identifiable reason for an increased eosinophil count in the peripheral blood. In contrast to HES, eoCML patients carry a distinct chromosomal abnormality. The bcr/abl fusion gene (Philadelphia chromosome) is the genetic basis of this clonal disease. Recently, eoCML has been separated from HES. Patients with eoCML frequently suffer organ damage including the heart and lungs. This damage is related to the release of eosinophilic granules in the blood, which results in fibrosis of the endothelial lining. We report a case of a peripheral vasculitis complicated by gangrene of the fingers in a patient with eoCML. Despite an almost complete response to CML treatment with Gleevac, combined with prednisone, aspirin and coumadin the patient sustained irreversible damage to the vascular lining of the distal arteries of the upper extremities. 相似文献
7.
M Sileghem A Darji L Remels R Hamers P De Baetselier 《European journal of immunology》1989,19(1):119-124
Lymph node cell populations derived from Trypanosoma brucei-infected mice failed to produce interleukin 2 (IL 2) in response to a potent mitogenic trigger and suppress the potential of normal lymph node cells to secrete IL 2 in co-culture assays. This suppression is promptly restored by the addition of indomethacin, which blocks prostaglandin synthesis, but is not markedly affected by the addition of catalase, which degrades H2O2. The suppression of the IL 2 receptor expression, on the other hand, is not restored by the addition of indomethacin, nor by the simultaneous supply of both indomethacin and catalase. This discrepancy is not caused by an extreme susceptibility of the receptor expression to low prostaglandin (PG) concentrations, but rather by the presence of suppressive cells that operate through a PG-independent mechanism. This suppressive mechanism accounts for the loss of the IL 2 receptors on both the Ly-2+ and the L3T4+ T cell compartment. The indomethacin-treated co-cultures, which manifest a normal IL 2 production but lack the IL 2 receptors, manifest an impaired DNA synthesis and contain a decreased number of T cell blasts. 相似文献
8.
lvaro Lpez-Valias Laura Baioni Lorena Crdoba Ayub Darji Chiara Chiapponi Joaquim Segals Llilianne Ganges Jos I. Núez 《Viruses》2022,14(9)
Swine influenza viruses (SIV) produce a highly contagious and worldwide distributed disease that can cause important economic losses to the pig industry. Currently, this virus is endemic in farms and, although used limitedly, trivalent vaccine application is the most extended strategy to control SIV. The presence of pre-existing immunity against SIV may modulate the evolutionary dynamic of this virus. To better understand these dynamics, the viral variants generated in vaccinated and nonvaccinated H3N2 challenged pigs after recovery from a natural A(H1N1) pdm09 infection were determined and analyzed. In total, seventeen whole SIV genomes were determined, 6 from vaccinated, and 10 from nonvaccinated animals and their inoculum, by NGS. Herein, 214 de novo substitutions were found along all SIV segments, 44 of them being nonsynonymous ones with an allele frequency greater than 5%. Nonsynonymous substitutions were not found in NP; meanwhile, many of these were allocated in PB2, PB1, and NS1 proteins. Regarding HA and NA proteins, higher nucleotide diversity, proportionally more nonsynonymous substitutions with an allele frequency greater than 5%, and different domain allocations of mutants, were observed in vaccinated animals, indicating different evolutionary dynamics. This study highlights the rapid adaptability of SIV in different environments. 相似文献
9.
Induced drug resistance inhibits selection of initiated cells and cancer development 总被引:1,自引:1,他引:0
Compounds exerting a mitoinhibitory effect on normal hepatocytes are potent
promoters in the resistant hepatocyte model of chemical carcinogenesis in
combination with stimulation of regenerative growth by partial hepatectomy
or treatment with carbon tetrachloride. 2- Acetylaminofluorene (2-AAF)
almost completely inhibits liver cell regeneration after partial
hepatectomy, allowing only resistant cells to participate in regenerative
growth. After initiation by diethylnitrosamine and promotion with 2-AAF and
partial hepatectomy (PH), focal growth of initiated cells generates liver
lesions which occupy 40% of the hepatic volume three weeks after PH. In
this work the mechanism for the anti promoting effects of phenobarbital and
3- methylcholantrene were investigated as well as their effects on the
development of malignant hepatocellular carcinoma in the resistant
hepatocyte model. Treatment with phenobarbital or, especially, 3-
methylcholanthrene rendered normal rat hepatocytes resistant to the
mitoinhibitory effect of 2-AAF. In combination with 2-AAF/PH, 3-
methylcholanthrene shortened the regenerative growth period to less than
one week. In the Solt-Farber protocol for experimental
hepatocarcinogenesis, treatment with phenobarbital or 3- methylcholanthrene
during promotion with 2-AAF/PH permitted hepatocytes surrounding the focal
lesions to respond with regenerative growth. The foci and surrounding liver
grew until the liver/body mass index reached the control value. With
phenobarbital treatment the total focal volume was 20% of the liver volume
three weeks after PH, whereas the corresponding value in the case of
3-methylcholanthrene was only 1%. Labelling index data supported the
conclusion that growth of the liver lesions in the resistant hepatocyte
model was dependent on differential inhibition of normal hepatocyte growth
by the promoter and that the size of the foci obtained was related to the
length of time after PH required to complete liver regeneration.
3-methylcholanthrene induced 2- AAF resistance prevented the development of
large persistent nodules and hepatocellular carcinoma while phenobarbital
delayed cancer development with several month. The data thus supports the
idea that the degree of clonal expansion during promotion determines the
size of the population at risk for malignant transformation, as well as the
final frequency of carcinomas.
相似文献
10.
Tsetse flies, Glossina morsitans morsitans, fed on rats infected with Trypanosoma brucei brucei showed wide fluctuations in total and differential haemocyte counts. Similar fluctuations occurred in controls fed on non-infected rats and also between the two groups without showing any difference which could be attributed to the infection. Trypanosome infection of the tsetse haemocoel occurred in 16.25% of the flies, starting from the second day after feeding on the infected rats, but salivary glands and proboscis became infected only after the eleventh day. About 2% of bloodstream forms of T. b. brucei injected into tsetse haemocoels completed their developmental cycle successfully. Injection of tsetse homogenates into teneral G. m. morsitans prior to exposure to trypanosome-infected feed increased T. b. brucei infections in the flies significantly. Injection of live Escherichia coli, Enterobacter cloacae and Acinetobacter calcoaceticus into tsetse induced a remarkable increase in two pre-existing haemolymph proteins with molecular weights of about 70 and 17 kilodaltons, while live Bacillus subtilis and Micrococcus luteus induced a very weak response or sometimes none at all. T. b. brucei also failed to induce any increase in these proteins. Inoculation of G. m. morsitans with live E. coli und T. b. brucei prior to feeding on trypanosome-infected rats had no effect on the salivary gland and proboscis infection rates by T. b. brucei. Injection of live T. b. brucei into the haemocoels of tsetse caused no change in total haemocyte counts, but the trypanosomes disappeared from the haemolymph so rapidly that by 48 h post-injection, only about 1% were left. 相似文献