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Advances and perspectives for animal models of chikungunya virus infection 基孔肯雅病毒感染动物模型的研究进展与展望
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.09.008
Meng Zou, Zhihui Zheng, Wei Wang, Hongqi Liu
With the global warming, the expansion of transportation networks, a tremendous increase in international travel and exchange, and the ongoing evolution of viruses, chikungunya virus (CHIKV) has spread beyond its African origins and achieved global distribution, posing a significant threat to public health worldwide. Under such circumstances, animal models serve as indispensable tools for elucidating CHIKV pathogenesis and developing antiviral strategies. The currently established animal models of CHIKV infection can recapitulate various aspects of the clinical disease at different levels of complexity. However, each model possesses distinct advantages and limitations, rendering them suitable for rather specific research applications. Furthermore, the clinical realities of CHIKV infection in patients with comorbidities or coinfections with other viruses, coupled with emerging initiatives to reduce animal model reliance, present substantial challenges for the future development and application of these models. This review summarizes the natural history and susceptible host of CHIKV, recent advances in understanding the pathogenesis and animal model development, and prospects for animal models of CHIKV infection. The aim is to provide a reference for the selection, utilization, and development of appropriate animal models for CHIKV research.
随着全球变暖、交通网络的扩大、国际旅行和交流的大量增加以及病毒的不断演变,基孔肯雅病毒(CHIKV)已超越其非洲起源传播并实现全球分布,对全世界的公共卫生构成重大威胁。在这种情况下,动物模型是阐明CHIKV发病机制和制定抗病毒策略不可或缺的工具。目前建立的CHIKV感染动物模型可以在不同复杂程度上概括该临床疾病的各个方面。然而,每种模型都有其独特的优点和局限性,使得它们适合于相当特定的研究应用。此外,伴有合并症或与其他病毒共感染的患者感染CHIKV的临床现实,加上减少对动物模型依赖的新举措,为这些模型的未来开发和应用提出了重大挑战。本文综述了CHIKV的自然历史、易感宿主、发病机制和动物模型的研究进展,并展望了CHIKV感染动物模型的发展前景。旨在为选择、利用和开发适宜的CHIKV动物模型提供参考。
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引用次数: 0
Harnessing a high-quality Salmonella genome catalog to combat antimicrobial resistance and inform outbreak responses 利用高质量沙门氏菌基因组目录来对抗抗菌素耐药性并为疫情应对提供信息
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.09.009
Beiwen Zheng , Yi Liu , Yonghong Xiao
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引用次数: 0
Sustained circulation of Aedes albopictus-derived novel almendraviruses in the urban parks 城市公园中白纹伊蚊衍生的新型阿尔门德拉病毒持续传播
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.10.003
Xi Zhang , Chengyu Liu , Yang Han , Junying She , Wanqi Wu , Lili Wang , Jingdong Song , George F. Gao , Ziqian Xu , Hao Liang , Jun Liu
The Rhabdoviridae family comprises a diverse range of negative-sense single-stranded ribonucleic acid (RNA) viruses, including significant human and mammalian viruses transmitted by various arthropod species. Herein, using Aedes albopictus (Ae. albopictus) samples collected in two urban parks during 2023 and 2024, through metagenomics sequencing, 16 sequences were identified as putative novel viruses, showing closest homology to insect-specific viruses, mycoviruses, or plant-associated viruses. Notably, two novel viruses, Aedes albopictus almendravirus GCCDC15 (Aealb-AlmV GCCDC15) and Aedes albopictus almendravirus GCCDC16 (Aealb-AlmV GCCDC16) were identified and successfully isolated. Both of these viruses belong to the genus Almendravirus within the Rhabdoviridae family. Phylogenetic analysis revealed that Aealb-AlmV GCCDC15 and GCCDC16 are distantly related to Coot Bay virus (the United States of America, 2013) and Menghai rhabdovirus (Yunnan Province, China, 2017). The genetic distances between these two viruses and their most similar viruses are marked by 59.85 % and 87.20 % of amino acid identity in the L protein, respectively, supporting their classification as two new species in the Rhabdoviridae family. Cytopathic effects and rod-like virions were observed in mosquito cells (C6/36) after inoculating with supernatants from the Ae. albopictus samples. To investigate the natural distribution and persistence of the novel almendraviruses, we conducted a specific reverse transcription-polymerase chain reaction (RT-PCR) screening of Ae. albopictus mosquitoes collected from two urban parks across different time points. The assays confirmed the presence of both Aealb-AlmV GCCDC15 and GCCDC16 in mosquito populations. Critically, these viruses were detected repeatedly over successive sampling periods and in mosquitoes from geographically distinct sites within the urban environment. In summary, our study delineates the virome characteristics of Aedes mosquitoes in the urban ecosystem and successfully isolated two novel rhabdoviruses. The recurrent detection provides clear evidence for the sustained circulation of Ae. albopictus-derived almendraviruses in urban parks, highlighting their ongoing transmission and establishment in these habitats.
横纹肌病毒科包括多种负义单链核糖核酸(RNA)病毒,包括由各种节肢动物物种传播的重要的人类和哺乳动物病毒。本文采用白纹伊蚊(伊蚊;2023年和2024年在两个城市公园采集白纹伊蚊样本,通过元基因组测序,鉴定出16个序列为假定的新型病毒,与昆虫特异性病毒、分枝病毒或植物相关病毒具有最密切的同源性。值得注意的是,鉴定并成功分离到了白纹伊蚊阿尔门德拉病毒GCCDC15 (aalb - almv GCCDC15)和白纹伊蚊阿尔门德拉病毒GCCDC16 (aalb - almv GCCDC16)两种新型病毒。这两种病毒都属于弹状病毒科的阿尔门德拉病毒属。系统发育分析显示,aalb - almv GCCDC15和GCCDC16与库特湾病毒(美国,2013)和勐海横纹病病毒(中国,云南省,2017)有远亲关系。这两种病毒与它们最相似的病毒在L蛋白上的遗传距离分别为59.85%和87.20%,支持它们作为Rhabdoviridae科两个新种的分类。用伊蚊上清液接种蚊子细胞(C6/36)后,观察到细胞病变效应和杆状病毒粒子。排样品。为了研究新型阿尔门德拉病毒的自然分布和持久性,我们对伊蚊进行了特异性的逆转录聚合酶链反应(RT-PCR)筛选。在不同时间点从两个城市公园采集白纹伊蚊。检测结果证实,蚊子种群中存在aalb - almv GCCDC15和GCCDC16。关键的是,这些病毒是在连续的采样期间和在城市环境中地理位置不同的蚊子中反复检测到的。总之,我们的研究描绘了城市生态系统中伊蚊的病毒学特征,并成功分离出两种新的横纹病病毒。反复检测为伊蚊的持续传播提供了明确的证据。在城市公园中发现白纹伊蚊衍生的阿尔门德拉病毒,突出了它们在这些栖息地中的持续传播和建立。
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引用次数: 0
An explainable artificial intelligence framework reveals mutations associated with drug resistance in Mycobacterium tuberculosis 一个可解释的人工智能框架揭示了与结核分枝杆菌耐药性相关的突变
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.11.001
Hui Cen , Peng Zhang , Yunchao Ling , Guoping Zhao , Guoqing Zhang
Understanding the mechanisms of drug resistance in Mycobacterium tuberculosis (MTB) is essential for the rapid detection of resistance and for guiding effective treatment, ultimately contributing to reducing the global burden of tuberculosis (TB). Under anti-TB drugs pressure, MTB continues to accumulate resistance loci. The current repertoire of known resistance-associated mutations requires further refinement, necessitating efficient methods for the timely identification of potential resistance sites. Here, we introduce xAI-MTBDR, an explainable artificial intelligence framework designed to identify potential resistance-associated mutations and predict drug resistance in MTB. It outperforms state-of-the-art methods in predicting drug resistance for all first-line drugs, and scoring each mutation’s contribution to resistance. By leveraging public whole-genome sequencing data from nearly 40,000 MTB isolates, the framework identified 788 candidate resistance-related mutations and revealed 27 potential resistance markers, several of which are positioned closer to their respective drugs in protein structures than known resistance mutations, suggesting a potentially more direct role in mediating resistance. Furthermore, these scores enabled the framework to efficiently subgroup isolates with different resistance mechanisms and reflect varying levels of resistance. The framework serves as a valuable tool for accurate detection of drug-resistant MTB and offers new insights into its underlying mechanisms.
了解结核分枝杆菌(MTB)的耐药机制对于快速发现耐药性和指导有效治疗至关重要,最终有助于减轻结核病的全球负担。在抗结核药物的压力下,结核分枝杆菌继续积累耐药位点。目前已知的耐药相关突变需要进一步完善,需要有效的方法来及时识别潜在的耐药位点。在这里,我们介绍了xai -MTB - dr,这是一个可解释的人工智能框架,旨在识别潜在的耐药性相关突变并预测MTB的耐药性。它在预测所有一线药物的耐药性方面优于最先进的方法,并对每个突变对耐药性的贡献进行评分。通过利用来自近4万株MTB分离株的公开全基因组测序数据,该框架确定了788个候选耐药相关突变,并揭示了27个潜在的耐药标记,其中一些在蛋白质结构上比已知的耐药突变更接近各自的药物,这表明它们在介导耐药中可能更直接地起作用。此外,这些分数使该框架能够有效地对具有不同抗性机制的分离株进行亚组,并反映不同的抗性水平。该框架是准确检测耐药MTB的宝贵工具,并为其潜在机制提供了新的见解。
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引用次数: 0
Attribution of super-spreaders to the COVID-19 outbreak 超级传播者与COVID-19疫情的关系
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.09.010
Rui Wang, Jianping Huang, Xinbo Lian, Yingjie Zhao, Shujuan Hu, Beidou Zhang
The explosive growth during the early stages and the sustained transmission in the later phases of the coronavirus disease 2019 (COVID-19) pandemic may be closely linked to superspreading events (SSEs), yet in-depth research into their specific mechanisms and quantitative effects remains limited. This study, based on data from 4,519 COVID-19 cases across eight regions in China, reconstructed transmission chains and quantified key parameters such as the basic reproduction number (R0) and dispersion parameter (k), revealing a high degree of heterogeneity in COVID-19 transmission. The results showed that the majority of COVID-19 cases were mild, with female cases in some regions being significantly older than males. Epidemic curves were highly similar in geographically proximal areas, with the longest transmission chain reaching nine generations. The transmission parameters revealed a serial interval of 1.27–4.71 days, R0 ranging from 0.87 to 2.65, and k values between 0.50–2.04, demonstrating that super-spreaders serve as critical drivers of epidemic spread. We found that 1.35 % of cases identified as super-spreaders directly responsible for 40.09 % of secondary cases. Occupationally, students and catering staff were identified as high-risk groups for super-spreading. Geographically, household or community transmission served as the main driver of SSEs in six regions, while school-based transmission dominated in one region. These findings provide crucial scientific evidence for advancing our understanding of COVID-19 transmission dynamics and informing precision prevention strategies.
2019冠状病毒病(COVID-19)大流行早期的爆发式增长和后期的持续传播可能与超级传播事件密切相关,但对其具体机制和定量效应的深入研究仍然有限。本研究基于中国8个地区4519例新冠肺炎病例数据,重构传播链,量化基本复制数(R0)、扩散参数(k)等关键参数,发现新冠肺炎传播具有高度异质性。结果显示,新冠肺炎病例以轻症为主,部分地区女性发病年龄明显大于男性。地理上邻近地区的流行曲线高度相似,最长的传播链可达9代。传播参数序列间隔为1.27 ~ 4.71 d, R0值为0.87 ~ 2.65,k值为0.50 ~ 2.04,表明超级传播者是疫情传播的关键驱动因素。我们发现1.35%的病例被确定为超级传播者,直接导致了40.09%的继发性病例。职业上,学生和餐饮人员被确定为超级传播的高危人群。从地理上看,6个地区的家庭或社区传播是ssi的主要驱动因素,而一个地区的学校传播占主导地位。这些发现为增进我们对COVID-19传播动态的理解和为精确预防战略提供了重要的科学证据。
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引用次数: 0
Chikungunya virus: Current situation and future challenges 基孔肯雅病毒:现状和未来挑战
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.10.001
Teng Zhao , Teng Chen , Jie Zhang , Chunxiao Li , Chengfeng Qin
Chikungunya virus (CHIKV), a mosquito-borne alphavirus first identified in Tanzania in 1952, has expanded to more than 100 countries posing increasing global health risks. The 2025 epidemic in Réunion Island and local transmission in Foshan City, Guangdong Province, China, illustrated the growing risk of global dissemination. For primary vectors Aedes aegypti and Aedes albopictus, their behavioral traits (such as daytime biting, skip oviposition, and multiple-host feeding) substantially increased transmission potential and complicate control. Two vaccines, IXCHIQ® (live-attenuated) and VIMKUNYATM (virus-like particle), have been licensed in Europe and the United States, and multiple candidates including inactivated, subunit, viral-vectored, and messenger ribonucleic acid (mRNA) vaccines are under development. This review summarized current knowledge on CHIKV virology, epidemiology, evolution, vaccines, and vector control, to provide insights for effective management of this re-emerging arboviral threat.
基孔肯雅病毒(CHIKV)是1952年首次在坦桑尼亚发现的一种蚊媒甲病毒,现已扩展到100多个国家,构成越来越大的全球卫生风险。2025年在雷姆联岛的疫情和中国广东省佛山市的本地传播表明,全球传播的风险日益增加。对于主要媒介埃及伊蚊和白纹伊蚊,它们的行为特征(如白天叮咬、跳过产卵和多宿主取食)大大增加了传播可能性,并使控制复杂化。两种疫苗IXCHIQ®(减毒活疫苗)和VIMKUNYATM(病毒样颗粒疫苗)已在欧洲和美国获得许可,多种候选疫苗,包括灭活疫苗、亚基疫苗、病毒载体疫苗和信使核糖核酸(mRNA)疫苗正在开发中。本综述总结了目前关于CHIKV病毒学、流行病学、进化、疫苗和媒介控制的知识,为有效管理这一再次出现的虫媒病毒威胁提供见解。
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引用次数: 0
TempSnap-Trace: A temporal snapshot-based framework for haplotype network tracing TempSnap-Trace:用于单倍型网络跟踪的基于临时快照的框架
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.11.003
Jiajun Liu , Decheng Li , Yixue Li , Tao Huang
To address the challenge of tracking large-scale viral evolutionary history, this study introduces TempSnap-Trace, a novel computational framework designed for this purpose. The methodology processes genomic data to generate variant-featured haplotype strings. Subsequently, the minimum-cost arborescence network (McAN) algorithm is employed to infer phylogenetic relationships, from which weighted temporal snapshot networks are constructed. Core evolutionary nodes are then identified using community detection approach. This method integrates mutation sites, network topology, and directional information to reconstruct backbone evolutionary pathways based on inter-community similarity over time. Compared to community detection methods based on unweighted graphs, this approach increased modularity by 17.4 % and reduced code length by 30.1 %. This approach was validated on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) data, where it successfully identified the French B.1 lineage as a key transmission hub and accurately traced the backbone evolutionary paths of major variants, including Beta (B.1.351) and Zeta (P.2). Its utility was further demonstrated by delineating the evolutionary trajectory of the Mpox IIb B.1 variant. Furthermore, through extensive parallelization and algorithmic optimizations, the framework exhibits exceptional computational efficiency and scalability: in benchmark tests against the viral genome evolutionary analysis system (VENAS) workflow, our end-to-end pipeline demonstrated a 27-fold speedup (55.1 s vs. 1,492.6 s) and successfully processed a massive dataset in 23.6 h that caused VENAS to fail due to memory limitations. These findings validate the utility of TempSnap-Trace for large-scale viral surveillance, highlighting its distinct advantages in cross-border transmission warning and variant origin tracing. The code of TempSnap-Trace is available at https://github.com/Jiajun0413/TempSnap-Trace.
为了解决追踪大规模病毒进化史的挑战,本研究引入了TempSnap-Trace,这是一种为此目的设计的新型计算框架。该方法处理基因组数据以生成具有变异特征的单倍型字符串。然后,利用最小代价树形网络(McAN)算法推断系统发育关系,并以此为基础构建加权时间快照网络。然后使用社区检测方法确定核心进化节点。该方法结合突变位点、网络拓扑和方向信息,基于群落间相似性重构主干进化路径。与基于未加权图的社区检测方法相比,该方法的模块化程度提高了17.4%,代码长度减少了30.1%。这种方法在严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)数据上得到了验证,成功地确定了法国B.1谱系是一个关键的传播枢纽,并准确地追踪了主要变异的主干进化路径,包括Beta (B.1.351)和Zeta (P.2)。通过描述Mpox IIb B.1变异的进化轨迹,进一步证明了其实用性。此外,通过广泛的并行化和算法优化,该框架显示出卓越的计算效率和可扩展性:在针对病毒基因组进化分析系统(VENAS)工作流的基准测试中,我们的端到端管道显示出27倍的加速(55.1秒对1492.6秒),并在23.6小时内成功处理了大量数据集,导致VENAS因内存限制而失败。这些发现验证了TempSnap-Trace在大规模病毒监测中的实用性,突出了其在跨境传播预警和变异起源追踪方面的独特优势。TempSnap-Trace的代码可从https://github.com/Jiajun0413/TempSnap-Trace获取。
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引用次数: 0
Clinical characteristics of SARS-CoV-2 infection in patients with chronic hepatitis B during interferon antiviral therapy 慢性乙型肝炎患者干扰素抗病毒治疗期间SARS-CoV-2感染的临床特征
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-01 DOI: 10.1016/j.bsheal.2025.10.002
Shiyu Wang , Ziyu Zhang , Xinxin Li , Wen Deng , Yaqin Zhang , Weihua Cao , Xin Wei , Zixuan Gao , Linmei Yao , Shuojie Wang , Yao Xie , Minghui Li
To investigate the clinical characteristics of coronavirus disease 2019 (COVID-19) infection in patients with chronic hepatitis B (CHB) during interferon antiviral therapy and to explore the correlation between interferon use and COVID-19 infection and clinical indicators in these patients. A retrospective study was conducted on 477 Patient with CHB who visited the Second Hepatology Department of Ditan Hospital from December 2022 to February 2023. Patients were divided into an interferon group and a nucleoside analogue group based on whether they received interferon treatment. COVID-19 infection and fever duration were the primary indicators, while blood routine and liver function were the secondary indicators. Differences in COVID-19 infection rate, fever duration, and related laboratory tests between the two groups were compared. There were 184 patients in the interferon group and 293 patients in the nucleoside analogue group. The COVID-19 infection rate was 73.91 % (136/184) in the interferon group and 92.15 % (270/293) in the nucleoside analogue group, with a statistically significant difference (χ2 = 29.67, P < 0.001). After COVID-19 infection, the fever duration was shorter in the interferon group than in the nucleoside analogue group, with a statistically significant difference (χ2 = 130.15, P < 0.001). Logistic regression analysis showed that interferon use was an independent influencing factor for COVID-19 (odds ratio = 0.25, 95 % confidence interval: 0.14–0.43, P < 0.001). Compared with the nucleoside analogue group, the levels of white blood cells, neutrophils, lymphocytes, platelets, and aminotransferases were significantly different in the interferon group (P < 0.05). There were no differences between the two groups in creatinine and cardiac enzymes (P > 0.05). Interferon therapy can reduce the COVID-19 infection rate in patient with CHB and shorten the fever duration to a certain extent.
探讨干扰素抗病毒治疗期间慢性乙型肝炎(CHB)患者冠状病毒病2019 (COVID-19)感染的临床特点,探讨干扰素使用与慢性乙型肝炎(CHB)患者COVID-19感染及临床指标的相关性。对2022年12月至2023年2月在地坛医院第二肝病科就诊的477例慢性乙型肝炎患者进行回顾性研究。根据是否接受干扰素治疗,将患者分为干扰素组和核苷类似物组。新冠肺炎感染和发热时间为主要指标,血常规和肝功能为次要指标。比较两组患者COVID-19感染率、发热持续时间及相关实验室检查的差异。干扰素组184例,核苷类似物组293例。干扰素组和核苷类似物组的COVID-19感染率分别为73.91%(136/184)和92.15%(270/293),差异有统计学意义(χ2 = 29.67, P < 0.001)。新冠病毒感染后,干扰素组发热持续时间短于核苷类似物组,差异有统计学意义(χ2 = 130.15, P < 0.001)。Logistic回归分析显示,干扰素使用是COVID-19的独立影响因素(优势比= 0.25,95%可信区间:0.14-0.43,P < 0.001)。干扰素组白细胞、中性粒细胞、淋巴细胞、血小板、转氨酶水平与核苷类似物组比较差异均有统计学意义(P < 0.05)。两组患者肌酐、心肌酶比较差异无统计学意义(P > 0.05)。干扰素治疗可降低慢性乙型肝炎患者的COVID-19感染率,并在一定程度上缩短发热时间。
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引用次数: 0
Application progress and biosafety challenges of gene editing and synthetic biotechnology in diagnosis, treatment and prevention of infectious diseases 基因编辑和合成生物技术在传染病诊断、治疗和预防中的应用进展及生物安全挑战
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-10-01 DOI: 10.1016/j.bsheal.2025.09.002
Zixuan Gao , Yuanjiao Gao , Shuojie Wang , Xinxin Li , Weihua Cao , Wen Deng , Linmei Yao , Xin Wei , Ziyu Zhang , Shiyu Wang , Yaqin Zhang , Minghui Li , Yao Xie
Global infectious disease prevention faces escalating challenges due to the continual emergence of novel pathogens and rapid viral mutations. Synthetic biology has revolutionized this field by enabling precise diagnostics, innovative vaccine platforms, and targeted therapeutics, yet it simultaneously raises concerns regarding dual-use potential, biosafety, and ethical governance. This systematic review (2015–2025, PubMed, Web of Science, Scopus) focuses on CRISPR-based diagnostics, synthetic vaccines, and engineered probiotics. CRISPR/Cas systems such as DETECTR (Cas12a) and SHERLOCK (Cas13a) demonstrate high sensitivity and rapid pathogen detection (e.g., SARS-CoV-2, Ebola), but their misuse could enhance pathogen virulence or enable bioweapon development. mRNA and viral vector vaccines offer flexible and rapid responses to emerging infections but encounter limitations in molecular stability, delivery system toxicity, and ecological safety. Engineered probiotics, designed as “living therapeutics,” can detect pathogens and modulate immune responses, yet pose potential risks of horizontal gene transfer and host-specific variability. Overall, while synthetic biology provides transformative tools for infectious disease control, it necessitates robust global regulatory frameworks, standardized biosafety practices, and ethical oversight to ensure responsible and sustainable application.
由于新型病原体的不断出现和病毒的快速突变,全球传染病预防面临着不断升级的挑战。合成生物学通过实现精确诊断、创新疫苗平台和靶向治疗,彻底改变了这一领域,但同时也引起了对双重用途潜力、生物安全和伦理治理的关注。本系统综述(2015-2025,PubMed, Web of Science, Scopus)重点关注基于crispr的诊断、合成疫苗和工程益生菌。DETECTR (Cas12a)和SHERLOCK (Cas13a)等CRISPR/Cas系统显示出高灵敏度和快速病原体检测(例如SARS-CoV-2、埃博拉病毒),但它们的滥用可能会增强病原体的毒力或促进生物武器的开发。mRNA和病毒载体疫苗对新出现的感染提供灵活和快速的反应,但在分子稳定性、递送系统毒性和生态安全性方面存在局限性。工程益生菌被设计为“活疗法”,可以检测病原体并调节免疫反应,但存在水平基因转移和宿主特异性变异的潜在风险。总体而言,虽然合成生物学为传染病控制提供了变革性工具,但它需要强有力的全球监管框架、标准化的生物安全做法和道德监督,以确保负责任和可持续的应用。
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引用次数: 0
Evaluating viral inactivation in the liquid waste stream from a viral total nucleic acid extraction kit for safe disposal 评估病毒总核酸提取试剂盒的废液流中病毒灭活的安全性
IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-10-01 DOI: 10.1016/j.bsheal.2025.09.001
Charles Gan , Melissa Pitton , Lea Caduff , Timothy R. Julian
Safe laboratory processing requires mitigating risks from the release of pathogens into the environment through generated waste streams. This study evaluated the inactivation kinetics of bacteriophage MS2 as a surrogate for infectious viruses in liquid waste produced from total nucleic acid extractions of wastewater. The goal was to determine a waste handling protocol that ensures sufficient viral infectivity loss (i.e., inactivation) for safe disposal. Liquid waste was generated using a viral total nucleic acid extraction kit (Wizard® Enviro Total Nucleic Acid Kit, Promega, The United States of America) containing guanidinium chloride, isopropanol, ethanol, and other residual reagents. MS2 phage was artificially added into liquid waste, and inactivation was monitored over 24 h using double agar layer plaque assays. A one-phase exponential decay model was applied to estimate the time required for safe disposal, showing MS2 inactivation followed an exponential decay pattern, achieving a predicted 6-log10 reduction at an average of 2.41 h (145 min), with a 95 % confidence interval of 1.34 h (80 min) to 4.05 h (243 min). However, only the 24-hour holding time was observed to significantly exceed the 6-log10 reduction threshold, supporting its recommendation as a conservative and practical holding time after which the waste can be safely disposed of as chemical solvent waste without additional decontamination measures such as autoclaving, as viral infectivity is reduced by at least 6-log10.
安全的实验室处理需要减轻通过产生的废物流将病原体释放到环境中的风险。本研究评估了噬菌体MS2在废水总核酸提取液中作为感染性病毒替代品的失活动力学。目的是确定一种废物处理方案,以确保足够的病毒传染性损失(即灭活),以便安全处置。使用含有氯化胍、异丙醇、乙醇和其他残留试剂的病毒总核酸提取试剂盒(Wizard®Enviro total nucleic acid kit, Promega, United States of America)产生废液。将MS2噬菌体人工添加到废液中,用双琼脂层菌斑法监测24 h的失活情况。采用一相指数衰减模型来估计安全处理所需的时间,结果显示MS2失活遵循指数衰减模式,平均2.41 h (145 min)预测减少6-log10, 95%置信区间为1.34 h (80 min)至4.05 h (243 min)。然而,只有24小时的保温时间被观察到显著超过6-log10的还原阈值,支持其作为保守和实用的保温时间的建议,之后的废物可以作为化学溶剂废物安全处理,而不需要额外的去污染措施,如高压灭菌,因为病毒传染性至少降低了6-log10。
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Biosafety and Health
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