Pathogens and disease最新文献

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Being the Alice of academia: lessons from the Red Queen hypothesis. 成为学术界的爱丽丝:来自红皇后假说的教训。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-11-02 DOI: 10.1093/femspd/ftac034
S G Negatu, M C Arreguin, K A Jurado, C Vazquez
{"title":"Being the Alice of academia: lessons from the Red Queen hypothesis.","authors":"S G Negatu,&nbsp;M C Arreguin,&nbsp;K A Jurado,&nbsp;C Vazquez","doi":"10.1093/femspd/ftac034","DOIUrl":"https://doi.org/10.1093/femspd/ftac034","url":null,"abstract":"<p><p>Viruses and hosts must navigate environments in which each tries to outcompete the other for survival or to coexist within the same spaces. In Lewis Carrol's Through the Looking Glass, the Red Queen tells Alice, \"Now, here, you see, it takes all the running you can do, to keep in the same place. If you want to get somewhere else, you must run at least twice as fast as that!\" Borrowing from this idea, the Red Queen hypothesis asserts that organisms, such as viruses, must continuously adapt to environmental pressures to survive. In this commentary, we draw parallels between the Red Queen hypothesis and the experiences scientists of color navigate to thrive in academic spaces. In both phenomena, adapting to environmental pressures is necessary for survival. We identify the various pressures and bottlenecks faced by historically underrepresented groups in academia, as well as the adaptation strategies they must implement to persist in academia.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629500/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40357568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Phages, anti-CRISPR proteins, and drug-resistant bacteria: what do we know about this triad? 噬菌体、抗crispr蛋白和耐药细菌:我们对这三位一体了解多少?
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-29 DOI: 10.1093/femspd/ftac039
Andres Ceballos-Garzon, Angela B Muñoz, Juan D Plata, Zilpa A Sanchez-Quitian, Jose Ramos-Vivas
{"title":"Phages, anti-CRISPR proteins, and drug-resistant bacteria: what do we know about this triad?","authors":"Andres Ceballos-Garzon,&nbsp;Angela B Muñoz,&nbsp;Juan D Plata,&nbsp;Zilpa A Sanchez-Quitian,&nbsp;Jose Ramos-Vivas","doi":"10.1093/femspd/ftac039","DOIUrl":"https://doi.org/10.1093/femspd/ftac039","url":null,"abstract":"<p><p>Phages are viruses that infect bacteria, relying on their genetic machinery to replicate. To survive the constant attack of phages, bacteria have developed diverse defense strategies to act against them. Nevertheless, phages rapidly co-evolve to overcome these barriers, resulting in a constant, and often surprising, molecular arms race. Thus, some phages have evolved protein inhibitors known as anti-CRISPRs (∼50-150 amino acids), which antagonize the bacterial CRISPR-Cas immune response. To date, around 45 anti-CRISPRs proteins with different mechanisms and structures have been discovered against the CRISPR-Cas type I and type II present in important animal and human pathogens such as Escherichia, Morganella, Klebsiella, Enterococcus, Pseudomonas, Staphylococcus, and Salmonella. Considering the alarming growth of antibiotic resistance, phage therapy, either alone or in combination with antibiotics, appears to be a promising alternative for the treatment of many bacterial infections. In this review, we illustrated the biological and clinical aspects of using phage therapy; furthermore, the CRISPR-Cas mechanism, and the interesting activity of anti-CRISPR proteins as a possible weapon to combat bacteria.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40338420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adjuvants to increase immunogenicity of SARS-CoV-2 RBD and support maternal-fetal transference of antibodies in mice. 佐剂增加SARS-CoV-2 RBD的免疫原性并支持小鼠抗体的母胎转移
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-19 DOI: 10.1093/femspd/ftac038
Gabrielle Gimenes Lima, Amanda Izeli Portilho, Elizabeth De Gaspari
{"title":"Adjuvants to increase immunogenicity of SARS-CoV-2 RBD and support maternal-fetal transference of antibodies in mice.","authors":"Gabrielle Gimenes Lima,&nbsp;Amanda Izeli Portilho,&nbsp;Elizabeth De Gaspari","doi":"10.1093/femspd/ftac038","DOIUrl":"https://doi.org/10.1093/femspd/ftac038","url":null,"abstract":"<p><p>Adjuvants are important components of vaccines, increasing immunogenicity and modulating the immune response. SARS-CoV-2 vaccines are still being developed in order to improve worldwide access to immunization. Specific populations should be addressed in these investigations, such as pregnant women-to protect both mothers and neonates. In this study, female adult mice were immunized with Receptor-binding domain (RBD) from SARS-CoV-2 adjuvanted by a mixture of DDA and Saponin and put to mating to verify the maternal transference of IgG. For comparison, other group received RBD adjuvanted by OMVs from Neisseria meningitidis and Alum. The adjuvants enhanced IgG production and neutralization. DDA/Sap contributed to increase IgG1, IgG2a, IgG2b, and IgG3 isotypes. Total IgG avidity was considered high, as well as IgG1, IgG2a, and IgG2b avidity. IgG antibodies were effectively transferred to the offspring, predominantly IgG2a, IgG2b, and IgG3. The passive transferred immunoglobulin maintained the neutralizing ability, although it lost avidity. ELISA data was confirmed in Dot-ELISA and immunoblotting assays. DDA and Saponin seem a promising adjuvant mixture to enhance the humoral response of SARS-CoV-2 antigens. Further studies considering the effects of maternal immunization in the protection of offspring are needed, regardless the platform used in COVID-19 vaccines.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620730/pdf/ftac038.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9254779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Construction and characterization of the full-length cDNA of an infectious clone of emerging porcine teschovirus-2. 新发猪teschovirus-2传染性克隆cDNA的构建与鉴定。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-12 DOI: 10.1093/femspd/ftac033
Yuying Li, Shengnan Chen, Yaokai Shi, Haixin Huang, Wei Wang, Min Zheng, Chenchen Zhao, Xinyu Zhang, Xiaoxiao Lei, Wenchao Sun, Hao Liu, Tian Lan
{"title":"Construction and characterization of the full-length cDNA of an infectious clone of emerging porcine teschovirus-2.","authors":"Yuying Li,&nbsp;Shengnan Chen,&nbsp;Yaokai Shi,&nbsp;Haixin Huang,&nbsp;Wei Wang,&nbsp;Min Zheng,&nbsp;Chenchen Zhao,&nbsp;Xinyu Zhang,&nbsp;Xiaoxiao Lei,&nbsp;Wenchao Sun,&nbsp;Hao Liu,&nbsp;Tian Lan","doi":"10.1093/femspd/ftac033","DOIUrl":"https://doi.org/10.1093/femspd/ftac033","url":null,"abstract":"<p><p>Porcine teschovirus (PTV) is a causative agent of polioencephalomyelitis, encephalomyelitis, reproductive disorders and gastrointestinal and respiratory diseases in swine. In the present study, the PTV2 GX/2020 strain was isolated from pig intestinal tissue through the use of ST cells. Phylogenetic analysis of VP1 nucleotide sequences indicated that the GX/2020 isolate is closely related to PTV2. Furthermore, the full-length cDNA of an infectious GX/2020 clone was constructed using seamless ligation technology. The genome sequence of the rescued virus is largely consistent with the sequence of the parental virus, and it exhibits viral growth properties. The PTV2 virus was successfully isolated in the present study, and the reverse-genetic platform provides a foundation for studies of the pathogenic mechanisms of porcine teschovirus.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40334836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study on antibacterial effect of halicin (SU3327) against Enterococcus faecalis and Enterococcus faecium. 盐酸素(SU3327)对粪肠球菌和粪肠球菌的抑菌作用研究。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-06 DOI: 10.1093/femspd/ftac037
Zubair Hussain, She Pengfei, Li Yimin, Liu Shasha, Li Zehao, Yang Yifan, Li Linhui, Zhou Linying, Wu Yong
{"title":"Study on antibacterial effect of halicin (SU3327) against Enterococcus faecalis and Enterococcus faecium.","authors":"Zubair Hussain,&nbsp;She Pengfei,&nbsp;Li Yimin,&nbsp;Liu Shasha,&nbsp;Li Zehao,&nbsp;Yang Yifan,&nbsp;Li Linhui,&nbsp;Zhou Linying,&nbsp;Wu Yong","doi":"10.1093/femspd/ftac037","DOIUrl":"https://doi.org/10.1093/femspd/ftac037","url":null,"abstract":"<p><p>Enterococci are important pathogens of nosocomial infections and are increasingly difficult to treat due to their intrinsic and acquired resistance to a range of antibiotics. Therefore, there is an urgent need to develop novel antibacterial agents, while drug repurposing is a promising approach to address this issue. Our study aimed to determine the antimicrobial efficacy of halicin against enterococci and found that the minimum inhibitory concentrations (MIC) of halicin against different strains of Enterococcus faecalis and Enterococcus faecium ranged from 4 to 8 μg/ml. In addition, the synergistic antibacterial effect between halicin and doxycycline (DOX) against Enterococcus was observed through the checkerboard method, and it was observed that halicin and DOX could significantly synergistically inhibit biofilm formation and eradicate preformed biofilms at sub-MICs. Moreover, the electron microscope results revealed that halicin could also disrupt the bacterial cell membrane at high concentrations. Furthermore, it is also confirmed that the combination of halicin and DOX has no significant cytotoxic effect on erythrocytes and other human-derived cells. In addition, the mouse subcutaneous model and H&E staining showed that the combination of halicin and DOX could effectively reduce the bacterial load and inflammatory infiltration without obvious side effects. In nutshell, these results demonstrate the potential of halicin in combination with DOX as a novel therapy against infections by Enterococcus.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33492560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Involvement of the Noncanonical Polyadenylation Polymerase Cid14 in Fungal Azole Resistance in the Pathogen Cryptococcus neoformans. 非典型聚腺苷酸聚合酶Cid14在新型隐球菌真菌抗唑中的作用。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-06 DOI: 10.1093/femspd/ftac036
Chenxi Li, Sihui Zhen, Xiaoyu Ma, Lan Ma, Zhen Wang, Ping Zhang, Xudong Zhu
{"title":"Involvement of the Noncanonical Polyadenylation Polymerase Cid14 in Fungal Azole Resistance in the Pathogen Cryptococcus neoformans.","authors":"Chenxi Li,&nbsp;Sihui Zhen,&nbsp;Xiaoyu Ma,&nbsp;Lan Ma,&nbsp;Zhen Wang,&nbsp;Ping Zhang,&nbsp;Xudong Zhu","doi":"10.1093/femspd/ftac036","DOIUrl":"https://doi.org/10.1093/femspd/ftac036","url":null,"abstract":"<p><p>The yeast noncanonical polyadenylation polymerase Cid14 was originally identified from fission yeast and plays a critical role in the TRAMP complex. This protein is a cytoplasmic cofactor and regulator of RNA-degrading exosomes. Cid14 is highly conserved from yeast to animals and has been demonstrated to play key roles in the regulation of RNA surveillance, nutrition metabolism, and growth in model organisms, but not yet in Cryptococcus neoformans (C. neoformans). Here, we report the identification of a gene encoding an equivalent Cid14 protein, named CID14, in the fungal pathogen C. neoformans. To obtain insights into the function of Cid14, we created a mutant strain, cid14Δ, with the CRISPR-Cas9 editing tool. Disruption of CID14 impaired cell membrane stability. Further investigations revealed the defects of the cid14Δ mutant in resistance to low carbohydrate levels. Meanwhile, significantly, the ability to grow under flucytosine stress was decreased in the cid14Δ mutant. More importantly, our results showed that the cid14Δ mutant does not affect yeast virulence but exhibits multidrug resistance to azole. Our work is the first to suggest that Cid14 plays critical roles in azole resistance by affecting Afr1, which is chiefly responsible for azole excretion in the ABC (ATP-binding cassette) transporter.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40374799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Differential vaccine-induced kinetics of humoral and cellular immune responses in SARS-CoV-2 naive and convalescent health care workers. 差异疫苗诱导的SARS-CoV-2初诊和恢复期医护人员体液和细胞免疫反应动力学
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-03 DOI: 10.1093/femspd/ftac035
Wouter Smit, Steven Thijsen, Robert van der Kieft, Sophie van Tol, Johan Reimerink, Chantal Reusken, Lidewij Rümke, Ailko Bossink, Gijs Limonard, Michiel Heron
{"title":"Differential vaccine-induced kinetics of humoral and cellular immune responses in SARS-CoV-2 naive and convalescent health care workers.","authors":"Wouter Smit,&nbsp;Steven Thijsen,&nbsp;Robert van der Kieft,&nbsp;Sophie van Tol,&nbsp;Johan Reimerink,&nbsp;Chantal Reusken,&nbsp;Lidewij Rümke,&nbsp;Ailko Bossink,&nbsp;Gijs Limonard,&nbsp;Michiel Heron","doi":"10.1093/femspd/ftac035","DOIUrl":"https://doi.org/10.1093/femspd/ftac035","url":null,"abstract":"<p><p>Effective vaccination is a key element in the exit strategy from the current severe acute respiratory syndrome-CoV coronavirus-2 (SARS-CoV-2) pandemic, and may also offer protection against severe disease from future variants of concern. Here, we prospectively monitored T-cell responses over time, using ELISpot interferon-γ (INF-y) release assays, and B-cell responses, using serological tests, after vaccination and booster with BioNTech/Pfizer mRNA (Pfizer) and Janssen vector (Janssen/Johnson & Johnson) vaccines in hospital health care workers. Vaccine recipients were divided into seropositive and seronegative individuals at baseline, in order to determine the effect of natural immunity on vaccine-induced immune kinetics. We found that convalescent individuals mounted higher spike-specific INF-y-secreting T-cell responses and B-cell-mediated IgG responses, after receiving the Janssen vaccine or the first dose of the Pfizer vaccine. IgG levels corresponded to the virus neutralization capacity as measured by VNT assay. At 8 months postvaccination, spike-specific cellular immunity waned to low levels in individuals with or without prior natural immunity, whereas waning of humoral immunity occurred predominantly in naive individuals. The booster shot effectively reinduced both cellular and humoral immune responses. To conclude, our data supports the implemented single-dose mRNA booster strategy employed in the Netherlands. Furthermore, the level of pre-existing natural immunity may be factored into determining the optimal time window between future booster vaccines.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494413/pdf/ftac035.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33458897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Mycobacterial response to an acidic environment: protective mechanisms. 分枝杆菌对酸性环境的反应:保护机制。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-10-03 DOI: 10.1093/femspd/ftac032
Rupal Rai, Vinayak Singh, Bijina J Mathew, Anirudh K Singh, Shivendra K Chaurasiya
{"title":"Mycobacterial response to an acidic environment: protective mechanisms.","authors":"Rupal Rai,&nbsp;Vinayak Singh,&nbsp;Bijina J Mathew,&nbsp;Anirudh K Singh,&nbsp;Shivendra K Chaurasiya","doi":"10.1093/femspd/ftac032","DOIUrl":"https://doi.org/10.1093/femspd/ftac032","url":null,"abstract":"<p><p>Given the emergence and spread of multidrug-resistant and extensively drug-resistant strains of Mycobacterium tuberculosis (Mtb), the world faces the urgency of finding new drugs to combat tuberculosis. Understanding the biochemical/physiological processes enabling Mtb to survive the stressful environment within macrophages and acquire tolerance, resistance and persistence against the stresses are the key to developing new approaches to tackle this health problem. As Mtb gains entry into the respiratory tract and is engulfed by macrophages, lowering pH acts as a primary defence of phagosomes within macrophages and also in the centres of caseating granulomas. It becomes essential for the pathogen to maintain pH homeostasis for survival in these conditions. Acid resistance mechanisms are well known and extensively studied in other bacteria such as Escherichia coli, Lactobacillus spp., Brucella spp., Helicobacter pylori and Listeria monocytogenes. However, in the case of Mtb, acid tolerance and resistance mechanisms still need to be explored in detail. This review aims to describe the current understanding of underlying mechanisms involved in countering low pH faced by Mtb as the acid resistance/tolerance mechanisms contribute to the pathogenesis of the disease.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40711092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Treponema pallidum outer membrane proteins: current status and prospects. 梅毒螺旋体外膜蛋白:现状与展望。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-09-27 DOI: 10.1093/femspd/ftac023
Jinlin Chen, Jielite Huang, Zhuoran Liu, Yafeng Xie
{"title":"Treponema pallidum outer membrane proteins: current status and prospects.","authors":"Jinlin Chen,&nbsp;Jielite Huang,&nbsp;Zhuoran Liu,&nbsp;Yafeng Xie","doi":"10.1093/femspd/ftac023","DOIUrl":"https://doi.org/10.1093/femspd/ftac023","url":null,"abstract":"<p><p>The outer membrane proteins (OMPs) of Treponema pallidum subsp. pallidum (T. pallidum), the etiological agent of the sexually transmitted disease syphilis, have long been a hot research topic. Despite many hurdles to studying the pathogen, especially the inability to manipulate T. pallidum in vitro genetically, considerable progress has been made in elucidating the structure, pathogenesis and functions of T. pallidum OMPs. In this review, we integrate this information to garner fresh insights into the role of OMPs in the diagnosis, pathogenicity and vaccine development of T. pallidum. Collectively, the essential scientific discussions herein should provide a framework for understanding the current status and prospects of T. pallidum OMPs.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40639895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Burden of bacterial bloodstream infections and recent advances for diagnosis. 细菌性血流感染的负担及诊断的最新进展。
IF 3.3 4区 医学
Pathogens and disease Pub Date : 2022-09-27 DOI: 10.1093/femspd/ftac027
Susana P Costa, Carla M Carvalho
{"title":"Burden of bacterial bloodstream infections and recent advances for diagnosis.","authors":"Susana P Costa,&nbsp;Carla M Carvalho","doi":"10.1093/femspd/ftac027","DOIUrl":"https://doi.org/10.1093/femspd/ftac027","url":null,"abstract":"<p><p>Bloodstream infections (BSIs) and subsequent organ dysfunction (sepsis and septic shock) are conditions that rank among the top reasons for human mortality and have a great impact on healthcare systems. Their treatment mainly relies on the administration of broad-spectrum antimicrobials since the standard blood culture-based diagnostic methods remain time-consuming for the pathogen's identification. Consequently, the routine use of these antibiotics may lead to downstream antimicrobial resistance and failure in treatment outcomes. Recently, significant advances have been made in improving several methodologies for the identification of pathogens directly in whole blood especially regarding specificity and time to detection. Nevertheless, for the widespread implementation of these novel methods in healthcare facilities, further improvements are still needed concerning the sensitivity and cost-effectiveness to allow a faster and more appropriate antimicrobial therapy. This review is focused on the problem of BSIs and sepsis addressing several aspects like their origin, challenges, and causative agents. Also, it highlights current and emerging diagnostics technologies, discussing their strengths and weaknesses.</p>","PeriodicalId":19795,"journal":{"name":"Pathogens and disease","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40573204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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