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Tick-, flea- and mite-borne pathogens and associated diseases of public health importance in Bangladesh: a review
Pub Date : 2024-12-01 DOI: 10.1016/j.imj.2024.100146
Marina E. Eremeeva, Shobhan Das

Background

This scoping review provides a baseline summary of the current records of the ticks, fleas, and mites of public health importance that are present in Bangladesh. It summarizes their geographic distributions and reports the levels of their infestation of livestock, pets, wildlife, and humans, and the clinical and epidemiological studies pertinent to these vectors and their pathogens.

Methods

Sixty-one articles were identified in a literature search, including 43 published since 2011.

Results

Twelve articles contained reliable information on ticks and their associated hosts. However, information on fleas and mites in Bangladesh is very limited. Seventeen species of ixodid ticks that commonly parasitize peridomestic animals and can bite humans are described: Rhipicephalus microplus, R. appendiculatus, R. sanguineus, Haemaphysalis bispinosa, Hyalomma anatolicum, and Amblyomma testudinarium. Thirty-eight veterinary articles describe livestock pathogens, including Babesia, Anaplasma, and Theileria, and the diseases they cause. Few of those studies used modern molecular techniques to identify these pathogens. Eleven articles reported human diseases or surveillance studies, 10 from the last 10 years. Two country-wide serosurveys of 1,209 and 720 patients, using Enzyme Linked Immunosorbent Assay (ELISA) and Indirect Immunofluorescence Assay (IFA), respectively, reported human exposure to Orientia tsutsugamushi (8.8%–23.7%), typhus and spotted-fever group rickettsiae (19.7%–66.6%), and Coxiella burnetii (3%). The seropositivity rates varied regionally. PCR-based studies confirmed that febrile patients in Bangladesh may be infected with O. tsutsugamushi, Rickettsia typhi, Rickettsia felis, or Bartonella elizabethae. Only limited molecular research has been done with dogs and cats. These studies have reported PCR-confirmed canine infections with Babesia gibsoni (30%), Anaplasma bovis (58%), or Rickettsia monacenis (14%, n=50), and feline infections with Rickettsia felis (21%, n=100). Similarly, fleas from cats tested positive for Rickettsia felis (20.6%).

Conclusions

These findings indicate that diseases borne by non-mosquito vectors in Bangladesh urgently require more attention from public health, medical, and veterinary specialists to establish their true occurrence.
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引用次数: 0
Molecular epidemiology of Burkholderia pseudomallei in Hainan Province of China based on O-antigen
Pub Date : 2024-12-01 DOI: 10.1016/j.imj.2024.100150
Jinzhu Huang , Shiwei Wang , Xiaoxue Lu , Liangpeng Suo , Minyang Wang , Juanjuan Yue , Rong Lin , Xuhu Mao , Qian Li , Jingmin Yan

Background

Burkholderia pseudomallei is a gram-negative bacterium widely found in Southeast Asia and northern Australia. This bacterium, which lacks an available vaccine, is the causative agent of melioidosis and has properties that potentially enable its exploitation as a bioweapon.

Methods

Polymerase chain reaction assays targeting each of the lipopolysaccharide (LPS) genetic types were used to investigate genotype frequencies in B. pseudomallei populations. Silver staining, gas chromatography-mass spectrometry (GC-MS), and immunofluorescence were used to characterize LPS.

Results

In our study, a total of 169 clinical B. pseudomallei isolates were collected from Hainan Province, China between 2004 and 2016. The results showed that LPS genotype A was the predominant type, comprising 91.1% of the samples, compared with only 8.9% of LPS genotype B. The majority of patients were male and were diagnosed with sepsis or pneumonia. Silver staining and GC-MS demonstrated that LPS genotypes A and B exhibited distinct phenotypes and molecular structures. Immunofluorescence tests showed there was no cross-reaction between LPS genotypes A and B.

Conclusions

This is the first report on the molecular epidemiology of B. pseudomallei based on O-antigen in China. Tracking the regional distribution of different LPS genotypes offers significant insights relevant to the development and administration of LPS-based vaccines.
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引用次数: 0
Leveraging computer-aided design and artificial intelligence to develop a next-generation multi-epitope tuberculosis vaccine candidate
Pub Date : 2024-12-01 DOI: 10.1016/j.imj.2024.100148
Li Zhuang , Awais Ali , Ling Yang , Zhaoyang Ye , Linsheng Li , Ruizi Ni , Yajing An , Syed Luqman Ali , Wenping Gong

Background

Tuberculosis (TB) remains a global public health challenge. The existing Bacillus Calmette–Guérin vaccine has limited efficacy in preventing adult pulmonary TB, necessitating the development of new vaccines with improved protective effects.

Methods

Computer-aided design and artificial intelligence technologies, combined with bioinformatics and immunoinformatics approaches, were used to design a multi-epitope vaccine (MEV) against TB. Comprehensive bioinformatics analyses were conducted to evaluate the physicochemical properties, spatial structure, immunogenicity, molecular dynamics (MD), and immunological characteristics of the MEV.

Results

We constructed a MEV, designated ZL12138L, containing 13 helper T lymphocyte epitopes, 12 cytotoxic T lymphocyte epitopes, 8 B-cell epitopes, as well as Toll-like receptor (TLR) agonists and helper peptides. Bioinformatics analyses revealed that ZL12138L should exhibit excellent immunogenicity and antigenicity, with no toxicity or allergenicity, and had potential to induce robust immune responses and high solubility, the immunogenicity score was 4.14449, the antigenicity score was 0.8843, and the immunological score was 0.470. Moreover, ZL12138L showed high population coverage for human leukocyte antigen class I and II alleles, reaching 92.41% and 90.17%, respectively, globally. Molecular docking analysis indicated favorable binding affinity of ZL12138L with TLR-2 and TLR-4, with binding energies of −1173.4 and −1360.5 kcal/mol, respectively. Normal mode analysis and MD simulations indicated the stability and dynamic properties of the vaccine construct. Immune simulation predictions suggested that ZL12138L could effectively activate innate and adaptive immune cells, inducing high levels of Type 1 T helper cell cytokines.

Conclusions

This study provides compelling evidence for ZL12138L as a promising TB vaccine candidate. Future research will focus on experimental validation and further optimization of the vaccine design.
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引用次数: 0
The critical role of health policy and management in epidemic control: COVID-19 and beyond 卫生政策和管理在流行病控制中的关键作用:COVID-19 及其后
Pub Date : 2024-11-09 DOI: 10.1016/j.imj.2024.100151
Zeyu Zhang , You Wu
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引用次数: 0
Vagal nerve stimulation for the management of long COVID symptoms 迷走神经刺激疗法用于治疗长期 COVID 症状
Pub Date : 2024-11-08 DOI: 10.1016/j.imj.2024.100149
Malik W.Z. Khan , Muhammad Ahmad , Salma Qudrat , Fatma Afridi , Najia Ali Khan , Zain Afridi , Fahad , Touba Azeem , Jibran Ikram
This review investigates the therapeutic potential of vagal nerve stimulation (VNS) in managing long COVID, a condition marked by persistent symptoms following acute SARS-CoV-2 infection. Long COVID manifests as ongoing fatigue, cognitive impairment, and autonomic dysfunction, hypothesized to arise from sustained inflammatory and neurological dysregulation. The vagus nerve, central to modulating systemic inflammation and autonomic homeostasis, represents a promising therapeutic target for symptom alleviation through VNS. A comprehensive literature search was conducted across PubMed, Scopus, and Web of Science to identify studies evaluating VNS in the context of long COVID. Preliminary evidence from small-scale pilot studies suggests VNS may attenuate systemic inflammation through activation of the cholinergic anti-inflammatory pathway (CAP), thus restoring autonomic balance and ameliorating symptoms such as fatigue, cognitive dysfunction, and anxiety. In targeting the inflammatory cascade that underlies both acute COVID-19 pathophysiology and its prolonged sequelae, VNS holds potential as an innovative intervention for persistent post-viral symptoms. While these initial findings indicate promise, current data remain limited in scope and robustness, underscoring the need for larger, controlled trials to validate the efficacy and mechanisms of VNS in long COVID management. Establishing a clearer understanding of VNS's impact on inflammation and autonomic regulation in this context is crucial to inform clinical guidelines and therapeutic strategies for long COVID, potentially offering a targeted approach for mitigating this disabling condition.
长期COVID是一种急性SARS-CoV-2感染后出现的持续症状,本综述探讨了迷走神经刺激(VNS)在治疗长期COVID方面的潜力。长期COVID表现为持续的疲劳、认知障碍和自主神经功能障碍,据推测是由持续的炎症和神经失调引起的。迷走神经是调节全身炎症和自律神经平衡的中枢神经,是通过 VNS 缓解症状的治疗靶点。我们在 PubMed、Scopus 和 Web of Science 上进行了全面的文献检索,以确定在长 COVID 的背景下对 VNS 进行评估的研究。小规模试点研究的初步证据表明,VNS 可通过激活胆碱能抗炎通路 (CAP) 减轻全身炎症反应,从而恢复自律神经平衡并改善疲劳、认知功能障碍和焦虑等症状。VNS 针对的炎症级联既是 COVID-19 急性病理生理学的基础,也是其长期后遗症的基础,因此有可能成为治疗病毒后持续症状的创新干预措施。虽然这些初步研究结果表明了前景,但目前的数据在范围和稳健性方面仍然有限,这突出表明需要进行更大规模的对照试验,以验证 VNS 在长期 COVID 治疗中的疗效和机制。在这种情况下,更清楚地了解 VNS 对炎症和自律神经调节的影响至关重要,这将为长程 COVID 的临床指南和治疗策略提供依据,并有可能为缓解这种致残性疾病提供有针对性的方法。
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引用次数: 0
Nipah virus resurgence: a call for preparedness across states 尼帕病毒卷土重来:呼吁各州做好准备
Pub Date : 2024-10-22 DOI: 10.1016/j.imj.2024.100145
Manya Soni , Vijay Kumar , Mahendra Pratap Singh , Muhammed Shabil , Sanjit Sah
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引用次数: 0
Vascular fibrosis and extracellular matrix remodelling in post-COVID 19 conditions 后 COVID 19 条件下的血管纤维化和细胞外基质重塑
Pub Date : 2024-10-19 DOI: 10.1016/j.imj.2024.100147
Anna Kamdar , Robert Sykes , Cameron R. Thomson , Kenneth Mangion , Daniel Ang , Michelle AW Lee , Tom Van Agtmael , Colin Berry
Causal associations between viral infections and acute myocardial injury are not fully understood, with mechanisms potentially involving direct cardiovascular involvement or systemic inflammation. This review explores plausible mechanisms of vascular fibrosis in patients with post-COVID-19 syndrome, focusing on extracellular matrix remodelling. Despite global attention, significant mechanistic or translational breakthroughs in the management of post-viral syndromes remain limited. No effective pharmacological or non-pharmacological interventions are currently available for patients experiencing persistent symptoms following COVID-19 infection. The substantial expansion of scientific knowledge resulting from collaborative efforts by medical experts, scientists, and government organisations in undertaking COVID-19 research could inform treatment strategies for other post-viral syndromes and respiratory illnesses. There is a critical need for clinical trials to evaluate potential therapeutic candidates, providing evidence to guide treatment decisions for post-COVID-19 syndromes.
病毒感染与急性心肌损伤之间的因果关系尚未完全明了,其机制可能涉及直接心血管参与或全身炎症。本综述探讨了 COVID-19 后综合征患者血管纤维化的合理机制,重点关注细胞外基质重塑。尽管全球都在关注病毒后综合征的治疗,但在机制或转化方面取得的重大突破仍然有限。对于感染 COVID-19 后出现持续症状的患者,目前尚无有效的药物或非药物干预措施。医学专家、科学家和政府组织在开展 COVID-19 研究的过程中通力合作,极大地丰富了科学知识,可为其他病毒后综合征和呼吸道疾病的治疗策略提供参考。目前亟需开展临床试验来评估潜在的候选疗法,为 COVID-19 后综合征的治疗决策提供指导证据。
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引用次数: 0
Protection conferred by booster vaccine doses in hospitalized patients with COVID-19 during the SARS-CoV-2 Omicron BA.2 and BA.5 epidemics from 2022 to 2023 in Greece 2022 至 2023 年 SARS-CoV-2 Omicron BA.2 和 BA.5 在希腊流行期间,COVID-19 强化疫苗剂量对住院患者的保护作用
Pub Date : 2024-10-18 DOI: 10.1016/j.imj.2024.100144
Helena C. Maltezou , Maria N. Gamaletsou , Maria Chini , Vasileios Petrakis , Vasiliki Rapti , Theodoros V. Giannouchos , Eleni Karantoni , Konstantinos Kounouklas , Panagiota Stamou , Αmalia Karapanou , Dimitrios Basoulis , Andrianna-Chrysovalanto Verykokkou , Kyriakos Souliotis , Periklis Panagopoulos , Dimitrios Hatzigeorgiou , Garyfalia Poulakou , Konstantinos N. Syrigos , Nikolaos V. Sipsas

Background

To estimate the protection that coronavirus disease 2019 (COVID-19) vaccine doses conferred to hospitalized patients with COVID-19 against adverse outcomes and longer length of stay during the Omicron BA.2 and BA.5 subvariant epidemics in Greece.

Methods

The study was conducted from November 2022 to May 2023. Multivariable logistic and negative binomial regression models were applied to estimate the association between any adverse outcomes and length of stay with the number of COVID-19 vaccine doses.

Results

We studied 962 patients (median age: 78 years; mean length of stay: 9.2 days), of whom 847 (88.0%) had ≥ 1 comorbidity. Of these, 39 (4.0%) were admitted to the intensive care unit, 44 (4.6%) received invasive mechanical ventilation, and 110 (11.4%) died in hospital. There were 184 (19.1%) unvaccinated patients, 125 (13.0%) with one or two vaccine doses, and 653 (67.9%) with ≥ 3 doses. In multivariable analyses, patients with ≥ 3 doses had lower odds of experiencing any adverse outcomes (adjusted odds ratio: 0.57; 95% confidence interval [CI]: 0.37–0.86) compared with unvaccinated patients. On average, patients with one or two doses and those with ≥ 3 had decreased length of hospital stay (−1.5 days [95% CIs: −2.6 to −0.4] and −2.8 days [95% CIs: −4.1 to −1.4], respectively] compared with unvaccinated patients. Other characteristics consistently associated with adverse outcomes and longer length of stay included older age, having three or more comorbidities compared with none, and being admitted to the hospital two or more weeks post-diagnosis.

Conclusions

A history of ≥ 3 vaccine doses conferred significant protection against any adverse outcome and longer length of stay in hospitalized patients with COVID-19.
背景为了估计在希腊Omicron BA.2和BA.5亚变种流行期间,冠状病毒病2019(COVID-19)疫苗剂量对COVID-19住院患者的保护作用,以避免不良后果和更长的住院时间。结果我们研究了 962 名患者(中位年龄:78 岁;平均住院时间:9.2 天),其中 847 人(88.0%)合并症≥ 1 种。其中 39 人(4.0%)住进了重症监护室,44 人(4.6%)接受了有创机械通气,110 人(11.4%)在住院期间死亡。184名(19.1%)患者未接种疫苗,125名(13.0%)患者接种了1或2剂疫苗,653名(67.9%)患者接种了≥3剂疫苗。在多变量分析中,与未接种疫苗的患者相比,接种疫苗剂量≥3 剂的患者出现任何不良后果的几率较低(调整后的几率比:0.57;95% 置信区间 [CI]:0.37-0.86)。平均而言,与未接种疫苗的患者相比,接种一到两次疫苗和接种≥3次疫苗的患者住院时间缩短(分别为-1.5天[95% CIs:-2.6至-0.4]和-2.8天[95% CIs:-4.1至-1.4])。与不良结局和住院时间延长相关的其他特征还包括年龄较大、有三种或三种以上并发症而非无并发症、确诊后住院两周或两周以上。
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引用次数: 0
Diagnostic and prognostic value of disulfidptosis-related genes in sepsis 败血症中与二硫化硫相关基因的诊断和预后价值
Pub Date : 2024-10-17 DOI: 10.1016/j.imj.2024.100143
Wenlu Zou, Lintao Sai, Wen Sai, Li Song, Gang Wang

Background

Sepsis is a disease associated with high morbidity and mortality rates, especially among the elderly and patients in intensive care units. Disulfidptosis, a newly identified form of cell death triggered by disulfide stress, is emerging as a significant factor in disease progression. This study aimed to explore the diagnostic and prognostic value of disulfidptosis-related genes in sepsis.

Methods

We obtained two datasets from the Gene Expression Omnibus (GEO) database to conduct our analysis. Functional enrichment analysis was performed to identify relevant biological pathways. A protein-protein interaction network was constructed to identify hub genes critical to sepsis. Additionally, we analyzed the immune infiltration status in sepsis patients. The diagnostic value of these hub genes for sepsis was evaluated using nomograms, receiver operating characteristic (ROC) curves, and calibration curves in both training and validation datasets. Finally, a miRNA-immune-related hub genes (miRNA-IHGs) regulatory network was developed to elucidate the synergistic interactions between miRNAs and their target genes.

Results

A total of 3,469 differentially expressed genes (DEGs) were identified, of which seven were related to disulfidptosis (DR-DEGs). Functional enrichment analysis showed that DR-DEGs were significantly enriched in pathways related to actin dynamics. Five hub genes (MYH10, ACTN4, MYH9, FLNA, and IQGAP1) were identified as central to these processes. The analysis of immune infiltration revealed significantly lower levels of 11 immune cell types, while macrophages and regulatory T cells were significantly elevated in sepsis patients. The area under the ROC curves (AUCs) of the IHGs risk prediction model were 0.917 and 0.894 for the training and validation sets, respectively. A miRNA-IHGs regulatory network, comprising 17 nodes and 27 edges, was constructed, with MYH9 being the most frequently regulated by miRNAs.

Conclusion

The pathophysiological process of sepsis appears to involve disulfidptosis, highlighting it as a potential new therapeutic targets for sepsis management.
背景败血症是一种发病率和死亡率都很高的疾病,尤其是在老年人和重症监护病房的病人中。二硫化物中毒是一种新发现的由二硫化物应激引发的细胞死亡形式,正在成为疾病进展的一个重要因素。本研究旨在探讨脓毒症中与二硫化物中毒相关基因的诊断和预后价值。我们进行了功能富集分析,以确定相关的生物学通路。我们构建了一个蛋白质-蛋白质相互作用网络,以确定对败血症至关重要的枢纽基因。此外,我们还分析了败血症患者的免疫浸润状态。在训练数据集和验证数据集中,我们使用提名图、接收者操作特征曲线(ROC)和校准曲线评估了这些枢纽基因对败血症的诊断价值。最后,研究人员建立了一个 miRNA-免疫相关枢纽基因(miRNA-IHGs)调控网络,以阐明 miRNA 与其靶基因之间的协同作用。功能富集分析表明,DR-DEGs 在肌动蛋白动力学相关通路中显著富集。五个中心基因(MYH10、ACTN4、MYH9、FLNA 和 IQGAP1)被确定为这些过程的中心基因。对免疫浸润的分析表明,脓毒症患者体内 11 种免疫细胞类型的水平明显降低,而巨噬细胞和调节性 T 细胞则明显升高。IHGs风险预测模型的训练集和验证集的ROC曲线下面积(AUC)分别为0.917和0.894。结论脓毒症的病理生理过程似乎涉及二硫化血症,这突出表明二硫化血症是脓毒症治疗的潜在新靶点。
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引用次数: 0
Multiple-site decontamination in critically ill patients requires careful implementation 重症患者的多部位净化需要谨慎实施
Pub Date : 2024-10-16 DOI: 10.1016/j.imj.2024.100142
Yuetian Yu , Bin Lin , Lihui Wang , Chunhui Xu , Cheng Zhu , Yuan Gao
The EPIC III study showed that 52% of patients admitted to the intensive care unit (ICU) have infectious diseases and that the incidence of ICU-acquired infections is increasing, leading to longer ICU stays and higher mortality rates. Multiple-site decontamination, a type of selective decontamination program, has been associated with a reduction in the incidence of ICU-acquired infection and decreased mortality rates in some critically ill patients. However, the standardized implementation and actual effectiveness of multiple-site decontamination require further investigation.
EPIC III 研究表明,重症监护室(ICU)收治的病人中有 52% 患有感染性疾病,重症监护室获得性感染的发病率正在上升,导致重症监护室住院时间延长和死亡率升高。多部位净化是一种选择性净化计划,与降低重症监护室获得性感染的发病率和降低一些重症患者的死亡率有关。然而,多部位净化的标准化实施和实际效果还需要进一步研究。
{"title":"Multiple-site decontamination in critically ill patients requires careful implementation","authors":"Yuetian Yu ,&nbsp;Bin Lin ,&nbsp;Lihui Wang ,&nbsp;Chunhui Xu ,&nbsp;Cheng Zhu ,&nbsp;Yuan Gao","doi":"10.1016/j.imj.2024.100142","DOIUrl":"10.1016/j.imj.2024.100142","url":null,"abstract":"<div><div>The EPIC III study showed that 52% of patients admitted to the intensive care unit (ICU) have infectious diseases and that the incidence of ICU-acquired infections is increasing, leading to longer ICU stays and higher mortality rates. Multiple-site decontamination, a type of selective decontamination program, has been associated with a reduction in the incidence of ICU-acquired infection and decreased mortality rates in some critically ill patients. However, the standardized implementation and actual effectiveness of multiple-site decontamination require further investigation.</div></div>","PeriodicalId":100667,"journal":{"name":"Infectious Medicine","volume":"3 4","pages":"Article 100142"},"PeriodicalIF":0.0,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142578458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Infectious Medicine
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