老年人单纯性尿路感染病原菌的分布及耐药性分析

目的 研究引起老年人单纯性尿路感染的病原菌的分布情况及其耐药性.方法 对新疆医科大学第一附属医院2009年至2012年期间患者尿培养分离出的1035株细菌进行鉴定,并采用K-B纸片扩散法进行耐药性分析.结果 致老年人单纯性尿路感染的病原菌以大肠埃希菌为主(54.0％),其次分别为粪肠球菌(15.1％)、肺炎克雷伯菌(8.7％)、金黄色葡萄球菌(7.2％);大肠埃希菌、肺炎克雷伯菌和变形杆菌除对亚胺培南保持100％敏感外,对其他抗生素的耐药率均呈上升的趋势;粪肠球菌、金黄色葡萄球菌和表皮葡萄球菌除同时对万古霉素保持100％敏感外,对其他抗生素的耐药率也较严重.结论 老年人单纯性尿路感染的病原菌耐药性严重,不能单凭经验选择抗生素,应该在细菌培养和药敏试验的指导下慎重选用敏感药物.     

457株尿路感染的病原菌及其耐药性研究

目的了解尿路感染的病原菌分布及耐药情况,为临床合理用药提供依据。方法用VITEK-AMS微生物自动分析仪鉴定菌种和药敏试验,同时对大肠埃希菌和肺炎克雷伯菌进行ESBLs检测,对肠球菌进行氨基糖苷类高水平耐药（HLAR）的筛选。结果尿路感染以大肠埃希菌检出率最高（50．5％）其余依次为肠球菌属（10．5％）,克雷伯菌属（8．6％）,真菌（7．9％）等,大肠埃希菌和肺炎克雷伯菌ESBLs检出率分别为24．2％和17．9％,HLAR肠球菌检出率为60．4％．尿路感染病原菌对喹诺酮类等常用药物的耐药性较高。结论明确尿路感染的病原菌及其耐药性对合理使用抗生素具有重要意义。     

老年脑梗死并发尿道感染患者病原菌分布及耐药性分析

目的:分析老年脑梗死并发尿道感染的病原菌分布及其耐药性。方法:选取2014年9月-2016年9月于我院治疗的240例老年脑梗死并发尿道感染患者为研究对象,收集患者中段尿标本进行细菌分离培养鉴定,分析病原菌分布情况并测定其耐药性。结果:共检出160株病原菌,其中革兰阴性菌108株,占67.50%,革兰阳性菌43株,占26.88%,真菌9株,占5.63%,前五位病原菌分别为大肠埃希菌、铜绿假单胞菌、肺炎克雷伯菌、溶血性葡萄球菌及粪肠球菌。在主要革兰阴性菌中,大肠埃希菌对头孢曲松耐药率最高(69.81%),对亚胺培南最敏感(3.77%);铜绿假单胞菌对环氧沙星耐药率最高(88.24%),对头孢曲松、头孢唑啉、头孢他啶、阿米卡星、哌拉西林、亚胺培南最敏感,耐药率均为0.00%;肺炎克雷伯菌对头孢唑林耐药率最高(75.00%),对呋喃妥因最敏感(6.25%)。在主要革兰阳性菌中,金黄色葡萄球菌对红霉素耐药率最高(85.71%);肠球菌属(粪肠球菌及屎肠球菌)对氨苄西林耐药率最高(70.00%);凝固酶阴性葡萄球菌(溶血性葡萄球菌及表皮葡萄球菌)对头孢曲松耐药率最高(93.75%);主要革兰阳性菌对万古霉素、利奈唑胺最敏感,耐药率均为0.00%。结论:老年脑梗死并发尿道感染病原菌种类多,应根据耐药性结果合理选用抗生素。     

医院血流感染病原菌分布及耐药性分析

目的了解医院血流感染病原菌的分布及其耐药性,为临床治疗提供参考。方法收集2013年1月至12月浙江中医药大学附属第一医院患者血培养标本,采用WHONET 5.6软件对所分离的病原菌及药敏结果进行统计分析。结果 2 017份血培养标本共检出病原菌370株,阳性率为18.34%,其中革兰阳性菌142株占38.38%,革兰阴性菌213株占57.57%,真菌15株,占4.05%。排名前5位病原菌依次是凝固酶阴性葡萄球菌、大肠埃希菌、肺炎克雷伯菌、肠球菌属和金黄色葡萄球菌,分别占19.73%、17.03%、13.51%、6.22%和4.59%。除哌拉西林/他唑巴坦对大肠埃希菌和铜绿假单胞菌仍保持较高的抗菌活性外,革兰阴性菌尤其是肺炎克雷伯菌对多种药物均产生了严重耐药性,其中产ESBLs大肠埃希菌和肺炎克雷伯菌分别占46.80%和20.00%。革兰阳性菌对利奈唑胺100%敏感,检出耐甲氧西林金黄色葡萄球菌(MRSA)4株,占25.00%,耐甲氧西林凝固酶阴性葡萄球菌(MRCNs)占92.00%,耐万古霉素的表皮葡萄球菌1株和耐万古霉素的粪肠球菌3株。结论血流感染病原菌分布复杂,以革兰阴性菌为主,耐药率高,且已出现耐万古霉素的表皮葡萄球菌和粪肠球菌,因此,进行早期监测和耐药性分析非常必要,对控制感染、指导合理使用抗菌药物,减缓耐药菌株的出现具有重要的临床意义。     

某三甲医院儿童和成年女性尿培养病原菌分布和耐药性分析

摘要 目的：了解尿路感染儿童和成年女性尿培养病原菌种类和耐药性的差异,为临床合理选用抗菌药物提供依据。方法：分别收集2018年1月~2019年12月期间在我院住院的尿路感染儿童的尿培养标本1618份和尿路感染成年女性的尿培养标本1044份,分析其病原菌的分布和耐药性。结果：1618份儿童尿培养标本中分离出267株病原菌,居首位的病原菌是屎肠球菌,占43.82%（117/267）;1044份成年女性尿培养标本中分离出139株病原菌,居首位的病原菌是粪肠球菌,占28.78%（40/139）。在两种人群尿培养病原菌中大肠埃希菌和肺炎克雷伯菌构成比均分别为第二位和第三位。儿童尿培养屎肠球菌对青霉素G、氨苄西林、环丙沙星等喹诺酮类药物的耐药率高于成年女性尿培养粪肠球菌,对克林霉素、奎奴普丁/达福普汀、四环素的耐药率低于成年女性尿培养粪肠球菌（P＜0.05）;未发现对高浓度庆大霉素、高浓度链霉素、利奈唑胺、万古霉素、替加环素耐药的肠球菌。儿童尿培养大肠埃希菌对氨苄西林/舒巴坦、头孢吡肟的耐药率均高于成年女性尿培养大肠埃希菌（P＜0.05）。儿童尿培养肺炎克雷伯菌对头孢哌酮/舒巴坦、氨苄西林/舒巴坦、哌拉西林/他唑巴坦、氨曲南、厄他培南、亚胺培南、美洛培南、呋喃妥因、头孢唑啉等头孢菌素类药物的耐药率高于成年女性尿培养肺炎克雷伯菌（P＜0.05）。结论：尿路感染儿童和成年女性尿培养病原菌均以肠球菌为主,大肠埃希菌和肺炎克雷伯菌构成比分别为第二位和第三位,两种人群尿培养主要病原菌耐药性均有不同程度的差异,临床医生应根据尿培养和药敏结果合理用药。     

2008年至2010年泌尿系统感染中病原菌的分布及耐药性分析

目的了解泌尿系统感染的病原菌分布及药物耐药性。方法采用法国生物梅里埃公司的VITEK60分析仪对2008年至2010年宁波市妇女儿童医院疑为泌尿系统感染患者的尿液标本进行细菌培养、菌株鉴定,纸片扩散确证试验检测ESBLs。结果 2008年至2010年尿标本中共分离出病原菌1 561株,以大肠埃希菌最多见,占27.2%,其次肺炎克雷伯菌、奇异变形菌、粪肠球菌(D群),各占6.34%、6.28%和6.21%,再次是表皮葡萄球、白色念珠菌和屎肠球菌(D群),各占4.48%、4.36%和3.91%。表皮葡萄球、粪肠球菌(D群)、屎肠球菌(D群)对万古霉素均敏感,对利奈唑烷仅1株粪肠球菌(D群)耐药。3年中,无1例大肠埃希菌对亚胺培南耐药,1株肺炎克雷伯菌和1株奇异变形菌对亚胺培南耐药,其他药物均有不同程度耐药。结论大肠埃希菌是导致泌尿系统感染最常见的致病菌,产ESBLs的菌株已达46.6%。治疗由产ESBLs细菌引起的尿路感染首选亚胺培南和哌拉西林/他唑巴坦;引起尿路感染的革兰阳性菌主要为肠球菌,青霉素可作为治疗粪肠球菌引起的尿路感染,但不适合治疗屎肠球菌引起的尿路感染,耐药率已达95%以上,呋喃妥因、利奈坐烷、万古霉素可作为首选。     

379株血培养病原菌的临床分布及耐药性分析

目的了解血培养病原菌种类、临床分布及耐药情况。方法对2008年6月至2009年6月的379株血培养病原菌及其药敏情况用WHONET5.4软件进行统计分析。结果 379株病原菌中,分离率从高到低依次是凝固酶阴性葡萄球菌(133/35.1%)、大肠埃希菌(44/11.6%)、肺炎克雷伯菌(32/8.4%)、鲍曼不动杆菌(30/7.9%)、铜绿假单胞菌(25/6.6%)、金黄色葡萄球菌(18/4.7%)、肠球菌(13/3.4%)和其他(75/22.2%)。这些菌株主要分布在ICU和普外科。药敏结果分析显示:革兰阳性球菌中,未发现利奈唑胺和万古霉素耐药株。金黄色葡萄球菌和凝固酶阴性葡萄球菌对苯唑西林的耐药率分别为61.1%和89.5%;屎肠球菌对多数抗生素耐药率超过80%,粪肠球菌对青霉素类抗生素敏感性较高。革兰阴性杆菌中,大肠埃希菌和肺炎克雷伯菌中产ESBLs菌株比例分别为36.4%和31.3%,且发现2株耐亚胺培南的肺炎克雷伯菌;鲍曼不动杆菌除对卡那霉素保持敏感外,对其他抗生素的耐药率为50%~100%;铜绿假单胞菌对头孢曲松的耐药率为100%,对其他β-内酰胺类抗生素、氨基糖苷类和喹诺酮类抗生素的耐药率相对较低。结论临床上应规范血培养标本留取方法以减少污染,加强细菌耐药监测、严格抗生素使用,以延缓细菌耐药情况的发生和发展。     

940株血培养分离菌的临床分布及抗菌药物敏感性分析

目的定期对医院血流感染分离菌的分布和抗菌药物敏感性进行分析,为菌血症的治疗提供可靠的药敏结果,提高治愈率。方法对大连市中心医院2010年1月至2013年12月8 277份血标本采用全自动血培养仪Bac T/Alert3D和Micro Scan Walk Away-40全自动细菌鉴定仪进行细菌培养、鉴定和抗生素敏感性试验。结果 8 277份血标本中检出病原菌940株,阳性率为11.4%。940株病原菌中革兰阳性菌441株,占46.9%;以金黄色葡萄球菌、凝固酶阴性葡萄球菌、屎肠球菌、粪肠球菌和肺炎链球菌为主;革兰阴性杆菌486株,占51.7%,以大肠埃希菌、肺炎克雷伯菌、阴沟肠杆菌、鲍曼不动杆菌和铜绿假单胞菌为主;真菌13株,占1.4%。大肠埃希菌、肺炎克雷伯菌对亚胺培南、美洛培南高度敏感;鲍曼不动杆菌对头孢哌酮/舒巴坦、米诺环素高度敏感;粪肠球菌、屎肠球菌、葡萄球菌对达托霉素、万古霉素、利奈唑胺、奎奴普丁/达福普汀高度敏感。结论血液培养意义重大,病原菌分布呈多样化趋势,且表现为多重耐药。     

孕产妇产后感染病原菌的构成及耐药性分析

目的了解孕产妇产后感染病原菌的分布及耐药现状,为临床抗感染治疗提供依据。方法采用法国生物梅里埃VITEK-2全自动细菌鉴定分析仪进行鉴定和药敏试验,采用WHONET5.6软件进行数据统计分析。结果 2012年1月至2015年12月我院产科病房孕产妇共60 229例,产后感染336例,感染主要部位为宫腔、切口、血液和尿液。主要病原菌依次为大肠埃希菌、粪肠球菌、B型链球菌和金黄色葡萄球菌。大肠埃希菌对头孢他啶、头孢吡肟、妥布霉素、阿米卡星、头孢替坦、哌拉西林/他唑巴坦、头孢哌酮/舒巴坦、亚胺培南耐药率均15.00%;粪肠球菌和无乳链球菌对氨苄西林、青霉素耐药率为0.00%,耐甲氧西林金黄色葡萄球菌(MRSA)耐药率高达19.05%。结论我院产科病房感染主要部位为宫腔(43.18%),减少剖宫产率可以降低产后感染发生率,感染的主要病原菌为大肠埃希菌和粪肠球菌(63.23%),在预防用药的选择上应选择对大肠埃希菌和粪肠球菌均有效的抗生素以减少产后感染的发生率,同时了解孕产妇产后感染病原菌的构成和耐药性,有助于临床更快速有效地治疗产后感染。     

尿路感染相关病原菌的分布及耐药性分析

目的调查尿路感染病原菌的分布和耐药特点,为临床的抗感染治疗提供依据。方法收集2013年至2015年荆州市中心医院门诊和住院患者中,尿路感染患者送检的尿培养和血培养标本中检出的病原菌,采用Vitek2 Compact全自动微生物检测仪进行细菌鉴定,采用纸片扩散法和仪器法分别对革兰阴性杆菌和革兰阳性球菌进行药敏试验,药敏结果的判断依照CLSI M100-S24标准。数据分析采用WHONET5.6和SPSS 19.0软件,统计分析采用x~2检验。结果从尿路感染患者送检的标本中共检出各类非重复病原菌2 306株,其中门诊患者中检出19种100株,住院患者检出56种2 206株。导致尿路感染最多的两种病原菌为大肠埃希菌和粪肠球菌,分别检出1 241株和232株。导致尿脓毒血症最多的两种病原菌为大肠埃希菌和肺炎克雷伯菌,分别检出36株和10株。大肠埃希菌产ESBL.s率达67.9%,其对多种抗菌药物的耐药性均高于60.0%。粪肠球菌对大多数抗菌药物的耐药性均高于50.0%,仅对呋喃妥因和高浓度链霉素的耐药性较低,分别为12.0%和38.7%;未检出对万古霉素、利奈唑胺和替加环素耐药的粪肠球菌。结论导致尿路感染的病原菌种类繁多,大肠埃希菌和粪肠球菌是主要病原菌,其耐药情况严重;为保证治疗的有效性,临床医生应注重相关病原学和药敏检查结果。     

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.     

Enterovirus 71 3C proteolytically processes the histone H3 N-terminal tail during infection

Highlights
1. The N-terminal tail of histone H3 is specifically cleaved during EV71 infection.
2. Viral protease 3C is identified as a protease responsible for proteolytically processing the N-terminal H3 tail.
3. Our finding reveals a new epigenetic regulatory mechanism for Enterovirus 71 in virus-host interactions.     

Detection of EBV and HHV6 in the Brain Tissue of Patients with Rasmussen’s Encephalitis

Rasmussen’s encephalitis (RE) is a rare pediatric neurological disorder, and the exact etiology is not clear. Viral infection may be involved in the pathogenesis of RE, but conflicting results have reported. In this study, we evaluated the expression of both Epstein-Barr virus (EBV) and human herpes virus (HHV) 6 antigens in brain sections from 30 patients with RE and 16 control individuals by immunohistochemistry. In the RE group, EBV and HHV6 antigens were detected in 56.7% (17/30) and 50% (15/30) of individuals, respectively. In contrast, no detectable EBV and HHV6 antigen expression was found in brain tissues of the control group. The co-expression of EBV and HHV6 was detected in 20.0% (6/30) of individuals. In particular, a 4-year-old boy had a typical clinical course, including a medical history of viral encephalitis, intractable epilepsy, and hemispheric atrophy. The co-expression of EBV and HHV6 was detected in neurons and astrocytes in the brain tissue, accompanied by a high frequency of CD8⁺ T cells. Our results suggest that EBV and HHV6 infection and the activation of CD8⁺ T cells are involved in the pathogenesis of RE.     

Perinatal Vertical Transmission of Chikungunya Virus in Ruili,a Town on the Border between China and Myanmar

正Dear Editor,Chikungunya virus (CHIKV), an arbovirus in the family of Togaviridae, genus Alphavirus, is transmitted by the A.aegyptii or A. albopictus mosquito, and causes disease in humans characterized by fever, rash, and arthralgia (Silva and Dermody 2017; Suhrbier 2019). It was first reported in 1953 in Tanzania, and caused only a few outbreaks and sporadic cases in Africa and Asia in last century. However, in the epidemic in 2004, CHIKV acquired mutations that conferred enhanced transmission by the A. albopictus mosquito(Schuffenecker et al. 2006). Since then, it has successively caused outbreaks in Africa, the Indian Ocean, South East Asia, the South America, and Europe (Zeller et al. 2016).     

Development of a Novel Reverse Transcription Loop-Mediated Isothermal Amplification Method for Rapid Detection of SARS-CoV-2

In conclusion, the novel visual RT-LAMP assay is a simple, rapid, and sensitive approach for detection of SARS-CoV-2, and it is ready for application in primary care and community hospitals or health care centers, and even patients' own houses in response to the current SARS-CoV-2 epidemic because the assay does not require sophisticated equipment and skilled personnel. Furthermore, it is also ready to be used in fields for screening samples from wild animals and environments to facilitate the identification of potential intermediate hosts that mediate the cross-species transmission of SARS-CoV-2 from bats to humans.