女性泌尿生殖道支原体感染患者药敏状况

目的探讨女性泌尿生殖道感染患者中支原体的感染状况及其对不同药物的敏感性,为临床合理用药提供参考。方法对516例女性泌尿生殖道拭子进行支原体培养,并对阳性菌株进行10种常用抗生素药敏试验。结果 516例患者中,支原体培养阳性263例,检出率为50.97%,其中解脲支原体(Ureaplasma urealyticum,UU)为237例(45.93%),人型支原体(Mycoplasma hominis,MH)仅9例(1.74%),UU+MH 17例(6.46%);三种类型感染均对交沙霉素、强力霉素、美满霉素比较敏感。结论 UU为沈阳医学院附属第二医院泌尿生殖道支原体感染的主要病原体,交沙霉素、强力霉素及美满霉素可作为治疗的经验用药,其中交沙霉素为首选抗生素。     

乌鲁木齐女性泌尿生殖道支原体感染状况及其 耐药性探讨

目的探讨新疆乌鲁木齐市女性泌尿生殖道感染支原体的状况及其耐药情况。方法采用支原体分离培养药敏试剂盒检测2013年7月至2017年8月间7 899例在本院首次就诊的女性患者的泌尿生殖道分泌物样本,分析支原体培养及药敏结果。结果 7 899例女性泌尿生殖道样本中,支原体阳性1 913例,总阳性率为24.22%,其中单纯解脲脲原体(MH-UU+)1 772例,占支原体感染阳性构成比92.63%。民族中,汉族、维吾尔族、回族、哈萨克族、蒙古族中支原体感染率分别为24.18%、22.85%、24.34%、27.94%、24.21%,差异无统计学意义(P0.05)。单纯人型支原体(MH+UU-)感染对左氧氟沙星、氧氟沙星的耐药率均高于MH-UU+与解脲脲原体和人型支原体混合感染(MH+UU+)(P0.05)。MH+UU+感染对司巴沙星的耐药率高于MH-UU+和MH+UU-感染(P0.05)。结论本地区女性泌尿生殖道支原体以MH-UU+感染为主,首选抗生素为交沙霉素,目前在这5个民族感染的支原体体外抗生素耐药性差异不明显。     

长沙地区1409例泌尿生殖道支原体感染者的感染状况及药敏分析

目的了解长沙地区普通人群泌尿生殖道支原体感染的现状及药敏情况,为临床合理用药提供依据。方法收集并回顾性分析湖南省人民医院1 409例门诊泌尿生殖道感染者的支原体培养鉴定结果及其药物敏感试验结果。结果 1 409例门诊样本中,支原体总阳性率为15.3%(215/1409);其中,解脲脲原体(Uu)和人型支原体(Mh)阳性率为11.5%和6.2%,单独感染Uu、单独感染Mh和混合感染Uu+Mh阳性率分别为9.1%、3.8%和2.4%;女性支原体阳性率为22.3%,明显高于男性的3.3%(χ~2=92.378,P0.01);药物敏感性较高的为强力霉素、美满霉素和交沙霉素,耐药性较高的有喹诺酮类和罗红霉素;女性感染者对交沙霉素和壮观霉素的敏感性高于男性,对其他药物的敏感性则明显低于男性。单独Uu感染者对各抗菌药物(环丙沙星和壮观霉素除外)的敏感性均高于单独Mh感染者,而混合Uu+Mh感染者则为药物敏感性最低的一组(对大部分药物的敏感性低于40%)。结论长沙地区普通人群泌尿生殖道支原体感染的阳性率总体较低,但耐药问题依然突出,临床用药时可把四环素类药物和交沙霉素纳入首选,同时依据感染者的性别、感染类型等选择适宜药物进行治疗。     

韶关地区NGU支原体感染情况及药敏结果分析

目的：了解近年来韶关地区非淋菌性尿道(宫颈)炎(NGU)患者支原体感染情况及药敏情况，为临床提供治疗支原体感染和抗生素选抒提供参考依据。方法：对300例NGU患者进行支原体培养．并对阳性标本做10种抗生素药敏试验。采用支原体培养、鉴定、药敏一体化试剂盒进行检测。结果：300例支原体中阳性107例，感染率为35．7％。解脲支原体(UU)、人型支原体(MH)及UU MH混合感染阳性率分别为27．3％(82例)、1．7％(5例)、6．7％(20例)。UU对10种抗生素药敏敏感性最高是交沙霉素(96．3％)，其次是克拉霉素(92．7％)；耐药性最高是甲枫霉素(37．8%)和可乐必妥(37．8％)。结论：性病门诊支原体感染率高达35．7％，主要以UU为主(占76．6％82／107)：交沙霉素是治疗尿道(宫颈)炎UU感染的首选药物。     

泌尿生殖道支原体感染检测及药敏试验

目的了解本地区泌尿生殖道解脲脲原体（Uu）和人型支原体（Mh）感染状况及药物敏感性,指导临床医生合理应用抗生素。方法应用法国生物梅里埃公司提供的IST试剂盒进行支原体鉴定及9种药物敏感检测,并对结果进行统计分析。结果1210例门诊患者检出支原体阳性683例,总感染率为56.4%,其中Uu单独感染占628例（占51.9%）,Mh单独感染14例（占1.2%）,Uu和Mh混合感染41例（占3.4%）。交沙霉素和原始霉素敏感率最高,对Uu分别为98.5%和97.0%,对Uu和Mh混合感染率都为100%;氧氟沙星敏感率最低,分别为1.5%和0.0%。结论泌尿生殖道系统感染主要由解脲支原体引起,交沙霉素和原始霉素敏感率最高,氧氟沙星敏感率最低。临床应选用培养敏感的抗菌药物,提高治疗效果。     

绍兴地区男女泌尿生殖道支原体感染特点及药敏差异分析

目的 了解绍兴地区男女泌尿生殖道支原体属感染的特点,比较男女两性对几种抗菌药物的耐药情况的差异.方法 应用法国生物梅里埃公司MycoplasmaISI试剂盒对2010年1月至201 1年10月男女两性泌尿生殖道标本进行支原体培养及药敏试验,统计解脲脲支原体和人支原体的检出率及耐药情况.结果 共1722例泌尿生殖道感染病例中,支原体属阳性869例,总阳性率50.46％,其中单纯解脲脲原体(Uu)感染702例,单纯人型支原体(Mh)感染29例,Uu及Mh混合感染138例;714例男性中支原体阳性190例,阳性率26.61％,1008例女性中支原体阳性679例,阳性率67.36％;男性单纯Uu感染耐药率较高的主要是:环丙沙星(80.50％)、氧氟沙星(63.60％),女性单纯Uu感染耐药率较高的主要是:环丙沙星(91.97％)、氧氟沙星(73.72％)、红霉素(47.81％).男女两性单纯Uu感染对红霉素、阿奇霉素、克拉霉素和交沙霉素的敏感性差异有统计学意义(P＜0.05).结论 男女两性泌尿生殖道支原体感染以Uu为主,且两者对多种抗菌药物的敏感性具有显著性差异,临床应根据药敏结果合理选取使用抗菌药物.     

2006～2010年泌尿生殖道炎症患者支原体感染率检测与耐药性分析

目的 了解杭州市萧山区2006～ 2010年泌尿生殖道炎症患者支原体感染及耐药情况.方法 对4 023例泌尿生殖道炎症患者用支原体鉴定及药敏试剂盒进行支原体培养及药敏试验.结果 支原体总检出率为48.1％,女性检出率51.2％明显高于男性41.8％ (P ＜0.05).支原体培养阳性患者中Uu单独感染1701例(88.0％),Mh单独感染57例(2.9％),Uu+ Mh混合感染176例(9.1％),Uu单独感染明显高于Mh单独感染和Uu+ Mh混合感染(P＜0.05).5年间支原体阳性检出率从2006年的39.4％到2010年的58.1％逐年增高,感染模式观察期内无明显变化.支原体对交沙霉素、原始霉素和强力霉素均敏感(敏感率≥91.4％),对四环素、红霉素、氧氟沙星和环丙沙星的耐药率高,均大于50％.比较2006年至2010年各种支原体对9种药物的耐药率,除四环素外耐药率呈不同程度上升,四环素耐药率2007年和2008年较高,后逐年下降,2010年为53.5％.混合感染总体耐药率比Uu或Mh单独感染耐药率高.结论 泌尿生殖道炎症患者支原体感染Uu比较常见,且女性检出率显著高于男性.临床分离支原体大多具有多重耐药性,临床治疗需根据药敏结果加以选择.     

女性泌尿生殖道支原体感染及耐药性观察

目的了解女性泌尿生殖道感染患者解脲支原体(Uu)和人支原体(Mh)感染及耐药情况,指导临床合理应用抗菌药物。方法采用法国梅里埃公司生产的IST2支原体培养及药敏试剂盒,对932例女性泌尿生殖道感染患者进行培养及药敏试验。结果 932例患者中支原体阳性426例,总检出率45.7%,其中Uu阳性354例(37.9%),Mh阳性14例(1.5%),Uu+Mh阳性58例(6.2%);药敏结果表明,Uu与Mh对多西环素、交沙霉素、四环素较为敏感,Uu对环丙沙星、氧氟沙星耐药率较高,而Mh对克拉霉素、红霉素、阿奇霉素耐药率较高。结论女性泌尿生殖道支原体检出率较高,主要以Uu为主,Uu和Mh对多种抗菌药物耐药,应引起临床重视。     

2011—2015年不同年龄段男女患者泌尿生殖道支原体感染状况及耐药性调查

摘要：目的 了解本地区男女患者泌尿生殖道支原体感染状况及耐药特征,为临床诊疗及合理用药提供依据。方法 选取2011年1月—2015年12月门诊及住院患者,采集泌尿生殖道标本做支原体培养,并对阳性标本进行药敏试验,对阳性标本及其药敏结果进行分析。结果 2011年—2015年男女患者的感染率和总感染率呈逐年递增趋势（P＜0.01）,女性感染者高于男性,男女患者均以Uu单纯感染为主,不同年度均以21岁～30岁年龄段患者为主,占合计中51.0%,药敏试验表明Uu+Mh混合感染的耐药率明显高于Uu、Mh单纯感染,Uu+Mh混合感染对克拉霉素、阿奇霉素、罗红霉素、环丙沙星的耐药率均＞90.0%,Uu、Mh和Uu+Mh对美满霉素、强力霉素、交沙霉素的耐药率较低,均＜10.0%。结论 本地区支原体感染呈逐年上升趋势,女性感染率高于男性,年龄21～30岁患者居多,并以Uu单纯感染为主,治疗支原体感染首选美满霉素、强力霉素、交沙霉素。     

887例宫颈分泌物支原体培养及耐药性分析

目的 了解女性泌尿生殖道感染患者支原体感染及耐药情况.方法 采用生物梅里埃IST2试剂盒,对887例宫颈分泌物进行培养及药敏试验.结果 887例标本中检出Uu阳性401例(45.2％),Mh阳性4例(0.5％),Uu+Mh阳性137例(15.4％),共检出542例(61.1％).药敏结果表明,Uu与Mh对原始霉素、交沙霉素、强力霉素、四环素较为敏感,对环丙沙星耐药率最高.结论 女性泌尿生殖道Uu和Mh感染率很高,主要以Uu为主,Uu和Mh对多种抗菌药物耐药,其中以环丙沙星为最高,单纯Uu、Mh和Uu+ Mh的耐药率存在一定差异,治疗支原体感染首选交沙霉素、四环素.     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

A Unique Protease Cleavage Site Predicted in the Spike Protein of the Novel Pneumonia Coronavirus (2019-nCoV) Potentially Related to Viral Transmissibility

正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

Synthesis and antimicrobial studies of hydrazone derivatives of 4-[3-(2,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid and 4-[3-(3,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid

Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.

     

Novel compounds with potent CDK9 inhibitory activity for the treatment of myeloma

Cyclin-dependent kinases (CDKs) and Polo-like kinases (PLKs) play key role in the regulation of the cell cycle. The aim of our study was originally the further development of our recently discovered polo-like kinase 1 (PLK1) inhibitors. A series of new 2,4-disubstituted pyrimidine derivatives were synthesized around the original hit, but their PLK1 inhibitory activity was very poor. However the novel compounds showed nanomolar CDK9 inhibitory activity and very good antiproliferative effect on multiple myeloma cell lines (RPMI-8226).