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1.
抗生素的不合理使用使得细菌耐药性快速产生及传播,细菌耐药性已然成为重大公共卫生问题。碳青霉烯类抗生素在临床治疗中表现良好,常作为治疗多重耐药菌感染的最后一道防线,碳青霉烯耐药菌的出现对公共卫生安全产生了极大的威胁。产碳青霉烯酶是碳青霉烯耐药菌耐药的主要机制,因此,对产碳青霉烯酶肠杆菌科细菌的检测至关重要。目前,对于碳青霉烯酶的检测手段以表型检测和分子生物学检测方法为主。表型检测一般易于操作,成本低廉,便于在临床进行,但在检测效率和检测用时方面差强人意。分子生物学及其他新型技术在保持高特异性和敏感性的基础上能做到快速、高通量检测,但试验检测的成本高,需专业设备和人员,部分技术在碳青霉烯酶检测领域仍有待开发。当前,多种碳青霉烯酶的检测方法可针对不同的需求和目的,并没有一项检测能满足所有情况。进行检测时,试验所需时间、操作难度、经济成本等都需列入考量,应根据实际情况选择合适的检测方法。笔者通过结合当前背景,归纳总结产碳青霉烯酶肠杆菌科细菌的检测方法,从试验特异性与敏感性、可操作性、检测时间、试验成本等方面分析比较各个方法特点,以期为之后新的检测方法的开发及现有方法的改良研究提供切入点,为临床监测与检测方案的制定和实行提供思路。  相似文献   
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Bacteria inhabiting the xylem of Norway spruce (Picea abies (L.) H. Karsten) were investigated. The trees had been wounded and artificially inoculated with fungi and bacteria obtained from wounds of naturally infected spruce. One and five growing seasons after inoculation the Gram‐negative bacterial population present in the stem of inoculated trees were analysed.

The Gram‐negative bacteria isolated from the trees were identified on the basis of morphological, biochemical and physiological tests and whole‐cell fatty acid composition. The predominant strains were Enterobacteriaceae fermenter strains (E. agglomerans or E. sakazakii), fluorescent and yellow pigmented Pseudomonas, Acinetobacter and Moraxella spp. All Gram‐positive bacteria were Bacillus species.

The Gram‐negative bacteria of Norway spruce differed from the Gram‐positive species in possessing stronger lipolytic activity and in their ability to utilize pine resins for growth. Gram‐positive bacteria were generally able to utilise cellulose and hemicellulose, whereas among the Gram‐negative bacteria only one xylanolytic (yellow Pseudomonas) strain was found.  相似文献   
3.
In recent years, the mobile metallo-β-lactamase (MBL) genes have been found to correspond to one of the most important resistance characters identified in Gram-negative bacteria, severely affecting clinical chemotherapy and threatening public health. The prevalence of mobile MBL genes and their flanking regions in Gram-negative bacteria from diseased pigs in China was investigated. A total of 334 lung samples from diseased pigs were screened for Gram-negative bacteria classified as non-susceptible to meropenem (MIC≥4 mg·L−1). Six isolates, including three Escherichia coli, two Acinetobacter baumanii and one A. calcoaeticus, exhibited MBL production and carried the blaNDM-1 gene. S1-PFGE and Southern blot analysis showed that the blaNDM-1 gene was located on the chromosome of one A. baumanii isolate and on plasmids of various sizes in the other five isolates. MIC testing using broth microdilution revealed that all blaNDM-1-carrying isolates and some of their transconjugants exhibited resistance to almost all β-lactams tested. Whole genome sequencing revealed that the flanking region of the blaNDM-1 gene from all porcine isolates had high levels of similarity with the corresponding regions in human isolates. One porcine E. coli isolate carrying blaNDM-1 was typed as ST48, a common sequence type in human E. coli isolates. These results suggest the possibility of human-to-food animal transfer of blaNDM-1-producing E. coli, highlighting the need for surveillance of carbapenemase producers among bacteria from food animals. In addition, the prudent use of antimicrobial agents to decrease the opportunities for co-selection of carbapenemase genes in food animals is also urgently needed.  相似文献   
4.
采用传统PCR法分析了不同季节城市污水处理厂进水、活性污泥和出水中耐四环素乳糖发酵型肠杆菌(TR-LFE)和乳糖发酵型肠杆菌(LFE)所含四环素耐药基因(tet-R基因)的多样性和数量。结果表明,在分离得到的528株TR-LFE和LFE中含有tet(A)、tet(B)、tet(C)、tet(D)、tet(E)、tet(M)、tet(G)和tet(X)等tet-R基因,检出比例为0~85.71%不等。  相似文献   
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Free-ranging browsing herbivores ingest a range of secondary plant compounds, such as tannins, with their natural diet. As many of these substances have been shown to have antibacterial properties, it could be speculated that a lack of such compounds in captive zoo diets could favour the growth of potentially pathogenic intestinal bacteria. The effect of a supplementation of a conventional diet (N, consisting mainly of grass hay and/or lucerne hay and pelleted compound feeds) fed to eight captive black rhinoceroses (Diceros bicornis) from three zoological institutions with either tannic acid (T), a source of hydrolysable tannins, or quebracho (Q), a source of condensed tannins, was investigated. The number of faecal colony forming units (CFU) of Enterobactericeae was determined by colony count of dilution series from fresh faeces applied to MacConkey agar plates. Tannins were added to the diets at approximately 5-15 g/kg dry matter, depending on the varying intake of roughage and compound feeds by the animals. There was no difference in the number of CFU between diets N (95.0 x 10(5) +/- 225.3 x 10(5)/g fresh faeces) and T (164.3 x 10(5) +/- 225.1 x 10(5)/g fresh faeces); in contrast, diet Q led to a significant reduction in CFU (4.3 x 10(5) +/- 6.5 x 10(5)/g fresh faeces) compared with the other diets. These findings suggest that condensed tannins could have the potential to reduce the number of potentially pathogenic intestinal bacteria, and that the deliberate inclusion of tannin sources in the diets of captive wild animals should be further investigated. The fact that tannic acid, shown to have antibacterial effects in various in vitro studies, did not have an effect in this study, emphasizes that the relevance of tannin supplementation for intestinal health must be verified in vivo.  相似文献   
7.
This report describes the first isolation of Moellerella wisconsensis from the lung of a goat in Italy and represents the fourth isolation of this rare enterobacterial species from non-human sources reported in the literature. In fact, since its first isolation, M. wisconsensis has only been described in a few other occasions and often in clinical samples associated with cases of human enteritis.  相似文献   
8.
Erwinia pyrifoliae, the causal pathogen of shoot blight in the Asian pear tree (Pyrus pyrifolia cv. Singo), is host-specific and endemic to Korea. To identify the genes associated with the hypersensitive response (HR) and pathogenicity, a genomic library of E. pyrifoliae WT3 was constructed, and the cosmid clone Escherichia coli (pCEP33) was selected. Sequence analysis of 19.7-kb pCEP33 determined disease-specific (dsp) region homolog and approximately 40% of the hrp genes, which included hrpW, hrpNEp, hrpV, hrpT, hrcC, hrpG, hrpF, and partial hrpE homologs, with respect to the cluster of Erwinia amylovora. Additionally, two open reading frames, ORFD and ORFE, were found downstream of the dspEF region. The results of the sequence analysis showed that the pCEP33 did not contain any hrp regulatory genes or most of the genes encoding components of the Hrp protein secretion system. The hrpNEp gene of E. pyrifoliae contained five intergenic nucleotide fragment insertions (INFIs) and produced the HR elicitor protein harpinEp, with a molecular mass of approximately 44kDa. The purified HrpNEp protein elicited faster and stronger HR when infiltrated into tobacco leaves than did HrpNEa from E. amylovora. To observe the role of the hrpL gene in the expression of HrpNEp, the pEL2 containing hrpL was used to transform E. coli (pCEP33). Expression of HrpNEp in E. coli (pCEP33 + pEPL2) was detected with an immunoblot using antiserum raised against HrpNEp, indicating a role of hrpL gene in enhancing the expression of HrpNEp.  相似文献   
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