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Adel Almogren
Abstract: Host defense against Mycobacterium tuberculosis (MTB) is essentially a cell mediated immune response. The aim of this study is to assess immune abnormalities in the peripheral blood lymphocyte subsets in patients with pulmonary tuberculosis. Flowcytometry data for peripheral blood lymphocyte subsets in ten patients (mean age of 27 ± 6 years) with pulmonary tuberculosis were compared with similar data from 25 normal healthy individuals (mean age 24 ± 6 years) retrospectively in Immunology Unit at King Khalid University Hospital, Riyadh. The absolute numbers (523.7 ± 360.9 vs 177.1 ± 133.7, p = 0.0000) and % (28 ± 12.8% vs 9.9 ± 5.6%, p = 0.0000) of the natural killer cells and B lymphocytes (426.8 ± 452.1 vs 205.7 ± 69 p = 0.0000 and 18.2 ± 8.1% vs 11 ± 2.5%, p = 0.0000, respectively) were significantly higher in patients with PTB than the normal healthy individuals. A marked reduction in the absolute numbers (542.9 ± 350.3 vs 775.7 ± 225.4, p = 0.0250) and the percentage (30.8 ± 10.7% vs 44.01 ± 5.4%, p = 0.0000) of CD4 + cells in patients with pulmonary tuberculosis was also noted. Elevated natural killer and B cells with CD4 + lymphopenia in pulmonary tuberculosis prompt further investigations to gain a better understanding of host defense against M. tuberculosis.[...] Read More.
Keywords: Mycobacterium tuberculosis, natural killer cells, lymphocyte subsets, pulmonary tuberculosis.
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文章
Yang Lin,*, Baohua Wang*, Yijun Liu, Zhigang Yu, Manhua Cui and Haichun Ma
Abstract: The nucleocapsid (N) protein of SARS coronavirus (SARS-CoV) is a major structural component of virions, which appears to be a multifunctional protein involved in viral RNA replication and translation. However, how N protein interacts with host protein remains largely elusive. To identify cellular proteins that interact with the N protein and to elucidate the possible involvement of N protein in SARS-Cov replication and translation, a human lung cDNA library was screened using a yeast two-hybrid system assay. In this study, we have identified Macrophage migration inhibitory factor protein (MIF) as a novel interaction partner of N protein by yeast two-hybrid system. The direct interaction and co-localization of N protein with MIF were confirmed by immunoprecipitation and confocal microscopy analysis, respectively. The mapping studies localized the critical N sequences for this interaction to amino acid 140-210 including SR motif by yeast two -hybrid system. To the best of our knowledge, this is the first report that SARS-N protein interacts with the MIF within host cells, which enhance our understanding of the molecular mechanisms of SARS replication.[...] Read More.
Keywords: Severe acute respiratory syndrome (SARS) coronavirus, nucleocapsid protein, Macro|phage migration inhibitory factor protein, yeast two-hybrid.
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Ana Marta de los Ángeles Lobo-Sánchez, Patricia Lozano-Zaraín, Ygnacio Martínez-Laguna, Zita Gutiérrez-Cázarez, Antonio Rivera-Tapia, Carmen Torres and Rosa del Carmen Rocha-Gracia,*
Abstract: We investigated the prevalence of methicillin-resistant staphylococci (MRS) and evaluated the antimicrobial resistance patterns of 284 Staphylococcus strains isolated from two hospitals, as well as from community and the environment in Puebla City, Mexico. Isolates were identified by Gram-stain and biochemical reactions and antimicrobial susceptibility testing was performed by Kirby-Bauer and in some cases by determination of minimal inhibitory concentrations of antimicrobial agents. Result showed that from 284 strains studied, 32% (90 strains) were multidrug-resistant, of which 82% (74 strains) were methicillin-resistant. From 154 Staphylococcus aureus isolates tested, 41 strains showed methicillin-resistance (27%) and 84 of 130 coagulase-negative staphylococci showed methicillin-resistance (65%). The mecA gene was detected in 38 of 43 oxacillin-resistant staphylococci tested (14/14 S. aureus and 24/29 coagulase negative staphylococci). Nevertheless, this gene was also identified in 14 S. aureus that exhibited oxacillin and cefoxitin susceptibility. The percentages of resistance detected among S. aureus and coagulase negative staphylococcal isolates were: penicillin (79 and 67%, respectively), oxacillin (27 and 65%), erythromycin (18 and 36%), tetracycline (6 and 24%), gentamicin (71 and 45%), and trimethoprim sulfamethoxazole (19 and 37%). The b-lactamase production was positive in more than 80% of isolates. These results show the presence of multiresistant strains in these three sources, which supports the control measures taken by health authorities with respect to avoiding the misuse and abuse of antibiotics.[...] Read More.
Keywords: Staphylococcus, methicillin resistance Staphylococcus aureus (MRSA), methicillin resistance coagulase-negative staphylococci (MRCoNS), emerging infections.
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文章
Shiping He*, Ya-Wen Chang and Ya-Ling Lin
Abstract: To determine the relations between Haemophilus influenzae (Hi) genotypes (antibiotic resistance and active IgA1 protease) and infectious diseases, strains from infected blood, pus, sputum, bronchial washing and thorax patient samples with invasive diseases were cloned, and assayed for IgA1 protease activity and the enzymic subtype, as well as antibiotic resistance. Clinic samples of patients aged 1 to over 71 with invasive diseases of pneumonia, sinusitis, bacteremia, bronchitis, chronic obstructive of pulmonary diseases (COPD), conjunctivitis or otitis media were analyzed. Results showed that all Hi isolates contained IgA gene, but only 80% contained active IgA1 protease. Majority of Hi isolates (84%) are non-typable Haemophilus influenzae (NTHi), suggesting that NTHi had become major population in causing invasive diseases. Protease assays showed that 76% NTHi and 85% Haemophilus influenzae (THi) contained active IgA1 protease. Pulse-field agarose gel electrophoresis (PFGE) analysis showed that none of the Hi isolates had identical genome. Phenotypic comparison of bacterial strains showed a weak relation between active IgA1 protease and antibiotic resistance. Deoxyribonucleic acid (DNA) sequencing showed that mutations in silent IgA gene are common in Hi isolates. In conclusion, the antibiotic resistance and active IgA1 protease are two essential but independent phenotypes for NTHi infection and colonization.[...] Read More.
Keywords: Haemophilus influenzae (Hi), IgA1 protease, invasive diseases, non-typable Haemophilus influenzae (NTHi), typable Haemophilus influenzae (THi).
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文章
Vladimir S. Kurcubic*, Nenad S. Milic, Radojica D. Djokovic and Zoran Z. Ilic
Abstract: This study is aimed at evaluating the immunogenicity of two inactivated (mono- and polyvalent) vaccines containing bovine virus diarrhea virus (BVDV) reference and field strains. Three experimental groups were formed: 10 calves vaccinated twice (days 1 and 28) subcutaneously (s/c) with 2 ml of inactivated polyvalent vaccine per animal (Group 1); 10 calves vaccinated twice (days 1 and 28) subcutaneously (s/c) with 2 ml of inactivated monovalent vaccine per animal (Group 2) and 9 unvaccinated calves (Control, Group C). Blood sera were obtained from immunized animals (standard procedure: on days 0, 14, 28, 42 and 56 post-immunization). Geometric mean titer (GMT) values for BVDV neutralizing antibodies were substantially higher in blood sera of calves receiving the inactivated monovalent vaccine. The immune response developed more rapidly in calves immunized with the monovalent vaccine.[...] Read More.
Keywords: Bovine virus diarrhea virus, immunogenic properties, inactivated vaccines.
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Full Length Research Paper
Abstract: A newly isolated Aspergillus awamori MTCC 9997 strain from spoiled cooked rice was cultured under solid state using cassava peel powder to produce α-amylase. The effect of extraction medium, solid to solvent ratio, extraction time, temperature and physical state on α-amylase recovery was examined. Among various organic, inorganic solvents and buffer solutions tested, maximum extraction of α-amylase was achieved when phosphate buffer of pH 7.0 was added. A solid to solvent ratio (cassava peel : phosphate buffer) of 1:10 (w/v) resulted in maximum yield of α-amylase. The optimum extraction time was 30 min. At 30°C, α-amylase recovery was found to be the maximum. An appreciable amount of α-amylase was recovered under agitated conditions of the fermented biomass at 150 rpm compared with the quantum recovered under stationary conditions.[...] Read More.
Keywords: α-Amylase, Aspergillus awamori, solid-state fermentation, extraction.
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Mojdeh Hakemi Vala, Jinous Asgarpanah*, Mohammad Hossein Hedayati, Jeilan Shirali and Fatemeh Bagheri Bejestani
Abstract: Traditional medicine has a key role in health care worldwide. Obtaining scientific information about the efficacy and safety of the plants is one of the researcher's goals. In this research, the flowering aerial parts of Eremurus persicus were collected from Golpayegan (Isfahan, Iran) in May 2010. The extract was tested for its antibacterial activity against 4 Gram- positive bacteria strains (Staphylococcus aureus, Staphylococcus epidermidis and Bacillus cereus, Streptococcus pyogenes) and 5 Gram-negative bacterial strains (Escherichia coli, Salmonella typhi, Shigella dysantriae, Klebsiella pneumoniae, Pseudomonas aeruginosa). Its cytotoxic activity was also investigated using MTT assay. Here we reported the antibacterial activity of E. persicus against S. aureus (MIC = 125 mg/ml), B. cereus (MIC = 15.62 mg/ml), E. coli (MIC = 125 mg/ml), S. typhi (MIC = 31.25 mg/ml), S. dysantriae (MIC = 0.48 mg/ml) for the first time. Furthermore the cytotoxic potentials of E. persicus on two cell lines, HeLa and Caco-2, were studied.[...] Read More.
Keywords: Eremurus persicus, antibacterial activity, cytotoxic activity.
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文章
Full Length Research Paper
Abstract: Buruli ulcer (BU) is caused by a mycobacterium called Mycobacterium ulcerans . The events of BU are the skin lesions. The lack of early diagnosis and treatment cause severe disability. Today the emergence to BU in Africa and particularly in Côte d’Ivoire needs faster diagnosis to control and to prevent the infection by M. ulcerans. The surveillance of BU is difficult, because the transmission of M. ulcerans occurs in rural regions where the transport of fresh collected sample is long, and the detection with culture technique needs several months. This study has allowed the application of polymerase chain reaction (PCR) technique in real time with two targets for molecular diagnosis of BU in Côte d©Ivoire. 63 samples (clinical, environmental, local strains and reference strains) were analyzed in real-time PCR by comparing the target of the Insertion Sequence (IS) 2404 and the sequence Ketoreductase-B (KR-B), located respectively on the chromosome and on the virulence plasmid. 49 samples (76%) were positive in real-time for both targets. The sensitivity of the PCR shows a detection limit of 0.25 genome copy for both targets. The capacity, speed and sensitivity of real-time PCR assays improve the diagnosis and contribute to strengthening the eradication of BU in Côte d’Ivoire.[...] Read More.
Keywords: Buruli ulcer, Mycobacterium ulcerans, real-time, insertion sequence, ketoreductase, Côte d’Ivoire.
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文章
Amina Hssaine, Jawhar Gharbi, Rafik Harrath, Rajae Harrak, Abderrahman Chait, Mahjoub Aouni and Jamal Hafid*
Abstract: Enteroviruses are among the most common viruses infecting the human intestine; they are very widespread in nature and resistant to external agents. They are eliminated in the faeces and contaminate water and food. These viruses cause various clinical syndromes and constitute a big public health problem. The aim of our study was to search for enteroviruses in the water samples. For this, a total of 225 L of tap water coming from the national network office for drinking water (ONEP) and 18 samples of waste water originating from Marrakech city were studied. These samples were concentrated, treated with polyethylene glycol 6000 and then analyzed by RT-PCR. Only two samples were found to be positive for enteroviruses by RT- PCR among the 18 waste water samples analyzed, which gave a rate of 11.11%. On the other hand, no positive samples were found in the tap water. This study made it possible on the one hand to apply for the first time RT-PCR for the detection of enteroviruses in water samples originating from Marrakech city, and on the other hand to show that tap water of this city does not present any risk of contamination by this type of germ.[...] Read More.
Keywords: Drinking water, waste water, enterovirus, RT-PCR, Marrakech.
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文章
Pan-Chen Liu, Ching-Fu Cheng, Chen-Hsuan Chang, Shiun-Long Lin, Way-Shyan Wang*, Shao-Wen Hung, Ming-Hui Chen, Cheng-Chung Lin, Ching-Yu Tu, and Yu-Hsing Lin
Abstract: In Taiwan, a fish conservation farm had about 6,250 Taiwan paradise fishes, Macropodus opercularis (L.), which were separately cultivated in an outdoor tank containing 3,250 fishes, and an indoor tank containing the rest. The water supplying both tanks was the same running water source from the adjacent hills. Following a change in the fish feed (the commercial aquaculture feed became eel’s feed) to all fishes in May 2010, rotten body surfaces were only found in diseased and dead fishes in the outdoor tank. Interestingly, no sick fishes were found in the indoor tank. The clinical findings of the diseased fishes were bleeding at basal fins, peripheral site of genital pore, and bilateral surface of the abdomen. Additionally, we discovered whitish-mucus gills, edema of the intestines, and multi-focal white tubercles in infected fishes during gross examination. The results of the histopathology study showed that there were numerous multi-focal granulomas in the spleen, posterior kidney, and liver. Furthermore, Photobacterium damselae subsp. piscicida was isolated from lesions of the ailing fishes. We conducted an experimental animal virulence test, and our data revealed that P. damselae subsp. piscicida was a highly virulent pathogen. Fortunately, P. damselae subsp. piscicida appeared to be susceptible to most commonly used antimicrobial agents, according to the results of the antibiotic sensitivity study. We recommended a treatment with oxolinic acid (20 mg/kg/day) in the feed for 7 days for all Taiwan paradise fishes. The fishes’ condition significantly improved and the disease appeared to be controlled.[...] Read More.
Keywords: Conservation, photobacteriosis, Taiwan paradise fish, virulence.
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