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The Risk Factors Associated with the Incidence of Genital Warts in Iran 与伊朗生殖器疣发病率相关的危险因素
Pub Date : 2023-08-02 DOI: 10.33696/genetics.2.013
Sara Talebipour Nikoo, A. Lotfi
Objective: Prevention of sexually transmitted diseases is an essential factor in managing diseases in the human population and increasing individuals’ and society’s health levels. Thus to increase our insufficient knowledge about proper prevention methods, we performed this study to assess the risk factors of the incidence of genital warts (GW).Methods: In this case-control study, we enrolled 120 women and divided them into two groups. Sixty women with GW were set in the case group, and 60 healthy women were set in the control group. Afterwards, a questionnaire consisting of 13 questions regarding their life habituates was filled. The answers were analyzed using T-tests and chi-square test. Findings: There was a statistically significant correlation between the incidence of GW and age (P-value ≤ 0.001*), the years passed from first intercourse (P-value =0.02*), and the history of venereal diseases (P-value =0.03*). However, the correlation between this disease and smoking, use of contraceptive medications, use of barrier and gravidity methods, marriage, education, the job of the individual and her partner, and the type of intercourse was not statistically significant.Conclusion: It is interesting that although some factors may increase the risk of GW, some factors that one might reason should affect the prevalence of GW such as the use of barriers, marriage, and socioeconomics of the individuals had no significant effect on the prevalence of GW in this study.
目的:预防性传播疾病是控制人口疾病和提高个人和社会健康水平的一个重要因素。因此,为了增加我们对正确预防方法的不足认识,我们进行了这项研究来评估生殖器疣(GW)发生的危险因素。方法:在本病例对照研究中,我们招募了120名妇女,并将其分为两组。60名GW妇女被设为病例组,60名健康妇女被设为对照组。之后,他们填写了一份由13个问题组成的问卷,内容涉及他们的生活习惯。采用t检验和卡方检验对答案进行分析。结果:GW发病率与年龄(p值≤0.001*)、首次性行为年龄(p值=0.02*)、性病史(p值=0.03*)有统计学意义相关。然而,这种疾病与吸烟、使用避孕药物、使用屏障和妊娠方法、婚姻、教育、个人及其伴侣的工作以及性交类型之间的相关性在统计上没有显著意义。结论:有趣的是,尽管一些因素可能会增加GW的风险,但一些可能会影响GW患病率的因素,如使用屏障、婚姻和个体的社会经济因素,在本研究中对GW患病率没有显著影响。
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引用次数: 0
Allelic Variants on SLC6A3 Neurotransmitter Gene and Their Relationship with Personality Traits Scales in Egyptian Athletes 埃及运动员SLC6A3神经递质基因等位变异及其与人格特质量表的关系
Pub Date : 2023-05-22 DOI: 10.33696/genetics.2.012
A. EL-Seedy, Mariam H. Botros, Guylène Page, V. Ladevèze
Human dopamine transporter gene (SLC6A3) is one of the neurotransmission genes that plays an important role in controlling the behavior and psychological reactions toward various physical activities. The aim of the present study is to evaluate the associations between SLC6A3 3’-UTR VNTR (3’VNTR) genotypes and eight personality traits in Egyptian athletes. One hundred athletes (50 males and 50 females) and one hundred non-athletes participated in this investigation either in individual or team games. The Freiburg Personality inventory-Revised questionnaire was applied to athletes to evaluate personality traits according to the scale, at a scheduled time, using descriptive analysis. Genotyping for SLC6A3 3’-UTR VNTR polymorphism in athletes was realized to detect the different genotypes by PCR amplifications using desired primers. Three different genotypes of the 3’VNTR polymorphism; namely (9/9), (9/10), (10/10) were identified. The 9/10 and 10/10 genotypes of SLC6A3 gene were significantly higher in players than those in the control group. There were no statistically significant differences in personality traits values among males and females. The Cronbach’s alpha stability coefficient for four items is higher than 0.7 suggesting that these items (Neuroticism, Aggressiveness, Depression and Excitability) have a good reliability and support the used personality dimensions for this investigation. Our findings revealed a significant association between the genotypes of 3’VNTR and the personality traits in Egyptian athletes. These data shed light on the role of SLC6A3 gene in athletes’ behavioral performance and could serve as the basis for further characterization in the large number of Egyptian athletes.
人多巴胺转运蛋白基因(SLC6A3)是一种神经传递基因,在控制人对各种体育活动的行为和心理反应中起重要作用。本研究的目的是评估SLC6A3 3 ' -UTR VNTR (3 ' VNTR)基因型与埃及运动员八种人格特征之间的关系。100名运动员(男女各50名)和100名非运动员参加了个人或团体比赛。采用弗莱堡人格量表-修正问卷对运动员进行人格特征评估,在规定的时间,采用描述性分析。对运动员SLC6A3 3′-UTR VNTR多态性进行基因分型,利用所需引物进行PCR扩增,检测不同基因型。3'VNTR多态性的三种不同基因型即(9/9)、(9/10)、(10/10)。运动员SLC6A3基因的9/10和10/10基因型明显高于对照组。男性和女性在人格特质价值上没有统计学上的差异。四个项目的Cronbach’s alpha稳定系数大于0.7,表明神经质、攻击性、抑郁和兴奋性具有较好的信度,支持本调查所使用的人格维度。我们的研究结果揭示了3'VNTR基因型与埃及运动员人格特征之间的显著关联。这些数据揭示了SLC6A3基因在运动员行为表现中的作用,可以作为进一步表征大量埃及运动员的基础。
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引用次数: 0
Comparison of Horizontal blaCTX-M Gene Transfer via Conjugation among Extended Spectrum β-Lactamases Producing Escherichia coli Isolates from Patients with Urinary Tract Infection, Their Animals, and Environment. 尿路感染患者、其动物和环境中产生β-内酰胺酶的大肠杆菌分离株的偶联水平blaCTX-M基因转移的比较。
Pub Date : 2023-01-01 DOI: 10.33696/genetics.2.011
Adam A Mwakyoma, Benson R Kidenya, Caroline A Minja, Martha F Mushi, Alison Sandeman, Wilber Sabiti, Mathew T G Holden, Stephen E Mshana

Background: The dissemination of the extended spectrum β-lactamases (ESBL) producing E. coli poses a significant public health problem. Understanding the efficiency and frequency of horizontal gene transfer via conjugation of ESBL producing E. coli is imperative towards devising prevention and control measures. This study compared the frequencies and efficiencies of horizontal blaCTX-M gene transfer via conjugation among Escherichia coli isolates from urine and gastrointestinal tract (GIT) of patients with urinary tract infection (UTI), their animals and environment.

Methods: Horizontal blaCTX-M gene transfer via conjugation by a broth mating experiment was performed using 50 confirmed ESBL producing E. coli isolates as donors and Escherichia coli J53 (F-, met, pro, Azr), as the recipient. The transconjugants were detected and their frequencies and efficiencies of conjugation were measured and compared between ESBL producing E. coli isolates multi-sourced from urine, GIT, animals and environment. Antimicrobial susceptibility testing of all resulting transconjugants was performed. DNA was extracted from all transconjugants to confirm the presence and the acquisition of blaCTX-M gene.

Results: Out of 50 ESBL producing E. coli isolates harboring blaCTX-M gene, 37 (74.0%) successfully exercised horizontal gene transfer through conjugation. All transconjugants were confirmed phenotypically and genotypically by PCR. Of note, all of the isolates from environment 100.0% (7/7) performed conjugation, exhibiting the highest transfer efficiency, followed by isolates from urine and animals, with the conjugation transfer efficiency of 77.8% (14/18) and 76.1% (10/13), respectively. The isolates from the environment conjugated with a significant more efficiency than those from the GIT [Two-sample test of proportions; p-value = 0.0119]. The overall conjugation transfer frequencies ranged from 0.4 × 10-14 - 5.5 × 10-11 per donor cells with the highest median conjugation transfer frequency observed among isolates from animal (3.23 × 10-12 [IQR: 0.70 × 10-12 - 7.22 × 10-12]) followed by that of isolates from the environment (1.60 × 10-12 [IQR: 0.30 × 10-12 - 5.0 × 10-12]).

Conclusion: ESBL producing E. coli from human, animals and environment exercises horizontal blaCTX-M gene transfer efficiently with the highest occurrence among isolates from the environment and animals. The antimicrobial resistance control and prevention strategies should be widened up to explore strategies to prevent horizontal AMR gene transfer.

背景:产超广谱β-内酰胺酶大肠杆菌的传播是一个严重的公共卫生问题。了解通过结合产生ESBL的大肠杆菌进行水平基因转移的效率和频率对于制定预防和控制措施至关重要。本研究比较了尿路感染(UTI)患者、其动物和环境中来自尿液和胃肠道(GIT)的大肠杆菌分离株之间通过偶联进行水平blaCTX-M基因转移的频率和效率。方法:以50株产ESBL的大肠杆菌为供体,大肠杆菌J53(F-、met、pro、Azr)为受体,通过肉汤交配实验进行水平结合blaCTX-M基因转移。检测了来自尿液、GIT、动物和环境的多来源产ESBL大肠杆菌分离株之间的跨偶联剂,并测量和比较了它们的偶联频率和偶联效率。对所有产生的跨偶联物进行了抗菌药物敏感性测试。从所有转导偶联物中提取DNA以确认blaCTX-M基因的存在和获得。结果:在50株携带blaCTX-M基因的产ESBL大肠杆菌中,有37株(74.0%)通过偶联成功地进行了水平基因转移。所有的转导偶联物均通过PCR进行表型和基因型确认。值得注意的是,所有来自环境的分离株100.0%(7/7)都进行了接合,表现出最高的转移效率,其次是来自尿液和动物的分离株,接合转移效率分别为77.8%(14/18)和76.1%(10/13)。来自环境的分离物结合的效率明显高于来自GIT的分离物[比例的双样本检验;p值=0.019]。每个供体细胞的总结合转移频率在0.4×10-14-5.5×10-11之间,在动物分离物中观察到的中位结合转移频率最高(3.23×10-12[IQR:0.70×10-12-7.22×10-12])其次是环境分离株(1.60×10-12[IQR:30×10-12-5.0×10-12])。应拓宽耐药性控制和预防策略,探索防止AMR基因水平转移的策略。
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引用次数: 0
Commentary on “Type II Toxin-antitoxin Systems Have a Peculiar Localization in Escherichia Coli Cells II型毒素-抗毒素系统在大肠杆菌细胞中具有特殊的定位
Pub Date : 2022-11-07 DOI: 10.33696/genetics.1.009
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引用次数: 0
Impact of Sleep on Autophagy and Neurodegenerative Disease: Sleeping Your Mind Clear 睡眠对自噬和神经退行性疾病的影响:睡眠使头脑清醒
Pub Date : 2022-11-07 DOI: 10.33696/genetics.1.007
{"title":"Impact of Sleep on Autophagy and Neurodegenerative Disease: Sleeping Your Mind Clear","authors":"","doi":"10.33696/genetics.1.007","DOIUrl":"https://doi.org/10.33696/genetics.1.007","url":null,"abstract":"","PeriodicalId":72286,"journal":{"name":"Archives of molecular biology and genetics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75225500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Actors of ROS Homeostasis in Stigmatic Cells Essential for Plant Reproduction 植物生殖所必需的柱头细胞中活性氧稳态的参与者
Pub Date : 2022-11-07 DOI: 10.33696/genetics.1.006
{"title":"Actors of ROS Homeostasis in Stigmatic Cells Essential for Plant Reproduction","authors":"","doi":"10.33696/genetics.1.006","DOIUrl":"https://doi.org/10.33696/genetics.1.006","url":null,"abstract":"","PeriodicalId":72286,"journal":{"name":"Archives of molecular biology and genetics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90279306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SARS-CoV-2 Mutations, Diagnosis and Their Concern SARS-CoV-2突变、诊断及其关注
Pub Date : 2022-11-07 DOI: 10.33696/genetics.1.008
{"title":"SARS-CoV-2 Mutations, Diagnosis and Their Concern","authors":"","doi":"10.33696/genetics.1.008","DOIUrl":"https://doi.org/10.33696/genetics.1.008","url":null,"abstract":"","PeriodicalId":72286,"journal":{"name":"Archives of molecular biology and genetics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80004244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Risk Management Implemented by Turkey during the COVID-19 Pandemic Disaster 土耳其在COVID-19大流行灾难期间实施的风险管理
Pub Date : 2022-11-07 DOI: 10.33696/genetics.1.010
{"title":"Risk Management Implemented by Turkey during the COVID-19 Pandemic Disaster","authors":"","doi":"10.33696/genetics.1.010","DOIUrl":"https://doi.org/10.33696/genetics.1.010","url":null,"abstract":"","PeriodicalId":72286,"journal":{"name":"Archives of molecular biology and genetics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80172628","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The Nature of Radiation-induced Inherited Recessive Gene Mutations in Drosophila Melanogaster 辐射诱导黑腹果蝇遗传隐性基因突变的性质
Pub Date : 2022-03-16 DOI: 10.33696/genetics.1.003
I. Alexandrov, M. Alexandrova, K. Afanasyeva
Analysis of early [1] and current [2] data on epidemiology and genetics of inherited developmental anomalies and other disorders allows us to note an interesting and important fact that among the various detected genetic changes, point mutations underlie almost one-half of the recessive Mendelian diseases [1] circulating in modern human populations. At the same time, the results of molecular analysis showed that the DNA changes underlying these mutations are represented mainly by base substitutions, indels, extended deletions or insertions and duplications [3-5]. Taking into account the well-known and important fact that the most dangerous mutagen for human is ionizing radiation with which humans are increasingly exposed on Earth (nuclear power station, radiotherapy, neutron research, nuclear disaster etc.) and in outer space. Therefore, it is important to know: (i) does ionizing radiation induces point mutations in germ cells in general, (ii) if so, what is the efficiency of sparsely and densely ionizing radiation in induction of such mutations, and (iii) what DNA changes underlie these mutations.
对早期[1]和当前[2]关于遗传性发育异常和其他疾病的流行病学和遗传学数据的分析使我们注意到一个有趣而重要的事实,即在各种检测到的遗传变化中,点突变是现代人群中传播的近一半隐性孟德尔病[1]的基础。同时,分子分析结果表明,这些突变背后的DNA变化主要表现为碱基替换、索引、延伸缺失或插入和重复[3-5]。考虑到众所周知的重要事实,即对人类最危险的诱变剂是电离辐射,人类在地球上(核电站、放射治疗、中子研究、核灾难等)和外层空间日益受到电离辐射的影响。因此,重要的是要知道:(i)电离辐射是否在一般情况下诱导生殖细胞的点突变,(ii)如果是这样,稀疏和密集的电离辐射在诱导这种突变中的效率是多少,以及(iii)哪些DNA变化是这些突变的基础。
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引用次数: 0
Constitutively Active Death Receptor Induces Apoptosis in Mammalian Cells 组成型活性死亡受体诱导哺乳动物细胞凋亡
Pub Date : 2022-03-16 DOI: 10.33696/genetics.1.004
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引用次数: 0
期刊
Archives of molecular biology and genetics
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