Background: Multidrug-resistant Klebsiella pneumoniae (MDR-KP) leads global health concerns as an infectious agent due to many virulence factors, including biofilm formation. The growing urgency for alternative treatment strategies beyond antibiotics has renewed interest in bacteriophages. Pathogen evolution is dynamic and can lead to phage resistance.
Methods: Bacteriophages were isolated from environmental sources and screened against a panel of 280 MDR- K. pneumoniae clinical isolates (74 from 2018 to 2020 and 167 from 2022-23 and 39 environmental KP isolates). Phages were grouped by host range and DNA fingerprinting. Five candidate phages with unique and broad host coverage were selected for further characterization and genome sequencing.
Results: Five candidate phages exhibited diverse host range patterns, strong bacteriolytic activity and significant antibiofilm activity even at low multiplicity of infection. Whole genome sequencing analysis revealed phage KPØ6 to be a novel Taipevirus species with low intergenomic similarity to known phages, and it showed the broadest host range on isolates from the 2018-2020 panel. A significant rise in phage resistance among MDR-KP isolate panels of 2018-2020 and 2022-2023 was observed.
Conclusion: Lytic bacteriophages offer a promising alternative for tackling MDR-KP infections, especially within healthcare environments. The phages characterized in this study demonstrate strong potential for both biocontrol and therapeutic use against MDR-KP, including infections involving biofilms. However, the dynamic nature of bacterial evolution over five years reiterates the need to update phage banks.
{"title":"Updated phage banks essential to cope with pathogen evolution: Lessons from Klebsiella pneumoniae and their phages.","authors":"Pallavi Bhat Ajakkala, Apoorva R Kenjar, Sujana Prabell, Sushma Bhandarkar, Shreya Bhat, Akhila Dharnappa Sannejal, Anusha Karunasagar, Ashwini Chauhan, Indrani Karunasagar, Juliet Roshini Mohan Raj","doi":"10.1016/j.jmii.2025.08.022","DOIUrl":"https://doi.org/10.1016/j.jmii.2025.08.022","url":null,"abstract":"<p><strong>Background: </strong>Multidrug-resistant Klebsiella pneumoniae (MDR-KP) leads global health concerns as an infectious agent due to many virulence factors, including biofilm formation. The growing urgency for alternative treatment strategies beyond antibiotics has renewed interest in bacteriophages. Pathogen evolution is dynamic and can lead to phage resistance.</p><p><strong>Methods: </strong>Bacteriophages were isolated from environmental sources and screened against a panel of 280 MDR- K. pneumoniae clinical isolates (74 from 2018 to 2020 and 167 from 2022-23 and 39 environmental KP isolates). Phages were grouped by host range and DNA fingerprinting. Five candidate phages with unique and broad host coverage were selected for further characterization and genome sequencing.</p><p><strong>Results: </strong>Five candidate phages exhibited diverse host range patterns, strong bacteriolytic activity and significant antibiofilm activity even at low multiplicity of infection. Whole genome sequencing analysis revealed phage KPØ6 to be a novel Taipevirus species with low intergenomic similarity to known phages, and it showed the broadest host range on isolates from the 2018-2020 panel. A significant rise in phage resistance among MDR-KP isolate panels of 2018-2020 and 2022-2023 was observed.</p><p><strong>Conclusion: </strong>Lytic bacteriophages offer a promising alternative for tackling MDR-KP infections, especially within healthcare environments. The phages characterized in this study demonstrate strong potential for both biocontrol and therapeutic use against MDR-KP, including infections involving biofilms. However, the dynamic nature of bacterial evolution over five years reiterates the need to update phage banks.</p>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144994726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-29DOI: 10.1016/j.jmii.2025.08.019
Anastasios Smyrnaios, Sidsel Krokstad, Turid Follestad, Andreas Christensen, Kari Risnes, Svein Arne Nordbø, Henrik Døllner
Objectives: Diagnosing paediatric Community-Acquired Pneumonia (CAP) is challenging due to the difficulty in obtaining lung specimens. Studies suggest that the upper-airway density of Streptococcus pneumoniae is related to the risk and severity of CAP. We studied the association between S. pneumoniae and its density in the upper airways with CAP and its severity. Additionally, we examined the relationship between respiratory viral load and severe CAP.
Methods: Seven hundred fifteen children with radiologically confirmed CAP and 673 controls were enrolled over 11 years. Nasopharyngeal aspirates (NPA) were tested for 20 viruses and bacteria using semi-quantitative polymerase chain reaction (PCR). NPAs positive for S. pneumoniae were further analysed by quantitative PCR. Adjusted odds ratios (aORs) and 95 % confidence intervals (CIs) were calculated to assess the association between S. pneumoniae density and CAP and CAP severity.
Results: Fewer cases than controls were colonised with S. pneumoniae (culture: 37.6 % vs 51.9 %, p < .001; PCR: 55.3 % vs 69.1 %, p < .001), and the median density was lower (6.20 log10 copies/mL vs 6.62 log10 copies/mL, p < .001). No association was found between S. pneumoniae density and CAP severity. CAP severity was significantly associated with high Respiratory Syncytial Virus (RSV) load (aOR 2.26, 95 % CI 1.43-3.57, p < .001) or high Human Metapneumovirus (HMPV) load (aOR 4.32, 95 % CI 2.19-8.48, p < .001), adjusted by pneumococcal density, other pathogens, age, sex, comorbidities, prior antibiotics and season.
Conclusions: Detection and density of S. pneumoniae in the upper airways do not correlate with CAP presence or severity. High RSV and HMPV loads were linked to severe CAP.
目的:诊断儿童社区获得性肺炎(CAP)是具有挑战性的,因为难以获得肺标本。研究表明,肺炎链球菌的上气道密度与CAP的风险和严重程度有关。我们研究了肺炎链球菌及其上气道密度与CAP及其严重程度的关系。此外,我们研究了呼吸道病毒载量与严重CAP之间的关系。方法:在11年的时间里,715名经放射学证实患有CAP的儿童和673名对照组被纳入研究。采用半定量聚合酶链反应(PCR)对鼻咽吸出液(NPA)进行20种病毒和细菌检测。肺炎链球菌NPAs阳性进一步采用定量PCR分析。计算校正优势比(aORs)和95%置信区间(CIs)来评估肺炎链球菌密度与CAP和CAP严重程度之间的关系。结果:与对照组相比,感染肺炎链球菌的病例较少(培养:37.6% vs 51.9%, p10拷贝/mL vs 6.62 log10拷贝/mL)。结论:上呼吸道肺炎链球菌的检测和密度与CAP的存在或严重程度无关。高RSV和HMPV载量与严重的CAP有关。
{"title":"The significance of upper airway density of Streptococcus pneumoniae and respiratory viruses in the aetiology and severity of paediatric community-acquired pneumonia in Norway: An observational study.","authors":"Anastasios Smyrnaios, Sidsel Krokstad, Turid Follestad, Andreas Christensen, Kari Risnes, Svein Arne Nordbø, Henrik Døllner","doi":"10.1016/j.jmii.2025.08.019","DOIUrl":"10.1016/j.jmii.2025.08.019","url":null,"abstract":"<p><strong>Objectives: </strong>Diagnosing paediatric Community-Acquired Pneumonia (CAP) is challenging due to the difficulty in obtaining lung specimens. Studies suggest that the upper-airway density of Streptococcus pneumoniae is related to the risk and severity of CAP. We studied the association between S. pneumoniae and its density in the upper airways with CAP and its severity. Additionally, we examined the relationship between respiratory viral load and severe CAP.</p><p><strong>Methods: </strong>Seven hundred fifteen children with radiologically confirmed CAP and 673 controls were enrolled over 11 years. Nasopharyngeal aspirates (NPA) were tested for 20 viruses and bacteria using semi-quantitative polymerase chain reaction (PCR). NPAs positive for S. pneumoniae were further analysed by quantitative PCR. Adjusted odds ratios (aORs) and 95 % confidence intervals (CIs) were calculated to assess the association between S. pneumoniae density and CAP and CAP severity.</p><p><strong>Results: </strong>Fewer cases than controls were colonised with S. pneumoniae (culture: 37.6 % vs 51.9 %, p < .001; PCR: 55.3 % vs 69.1 %, p < .001), and the median density was lower (6.20 log<sup>10</sup> copies/mL vs 6.62 log<sup>10</sup> copies/mL, p < .001). No association was found between S. pneumoniae density and CAP severity. CAP severity was significantly associated with high Respiratory Syncytial Virus (RSV) load (aOR 2.26, 95 % CI 1.43-3.57, p < .001) or high Human Metapneumovirus (HMPV) load (aOR 4.32, 95 % CI 2.19-8.48, p < .001), adjusted by pneumococcal density, other pathogens, age, sex, comorbidities, prior antibiotics and season.</p><p><strong>Conclusions: </strong>Detection and density of S. pneumoniae in the upper airways do not correlate with CAP presence or severity. High RSV and HMPV loads were linked to severe CAP.</p>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Acinetobacter seifertii, a recently identified member of the Acinetobacter calcoaceticus-Acinetobacter baumannii (Acb) complex, has emerged as a cause of severe human infections. It is closely related to Acinetobacter nosocomialis, a major pathogen of the Acb complex. Here, we aimed to explore the clinical and molecular differences between these two species.
Methods: This retrospective study enrolled 83 adults with A. seifertii bacteremia and 402 adults with A. nosocomialis bacteremia from four medical centers over a 9-year period. Species identification was confirmed using matrix-assisted laser desorption ionization-time of flight mass spectrometry and rpoB sequencing. Clinical information, antimicrobial susceptibility, and carbapenem resistance determinants were analyzed.
Results: There were no significant differences in the underlying diseases or mortality between patients with A. seifertii and A. nosocomialis bacteremia. However, A. seifertii bacteremia was more frequently associated with intensive care unit (ICU) admission, recent ICU stay, central venous catheter use, ventilator use at bacteremia onset, and pneumonia as the primary infection source than A. nosocomialis bacteremia. A. seifertii exhibited significantly lower susceptibility to colistin, amikacin, gentamicin, ceftazidime, and cefepime than A. nosocomialis. Carbapenem resistance was primarily mediated by ISAba1-blaOXA-51-like in A. seifertii and IS1006-ΔISAba3-blaOXA-58-like in A. nosocomialis.
Conclusion: A. seifertii and A. nosocomialis exhibit distinct antimicrobial susceptibility profiles and carbapenem resistance mechanisms but share similar mortality rates. The ability of both species to act as reservoirs of carbapenem resistance highlights the importance of accurate identification, antimicrobial stewardship, and infection control strategies to mitigate the spread of resistant strains.
{"title":"Comparison of clinical manifestations, antimicrobial susceptibility patterns, and carbapenem resistance determinants between Acinetobacter seifertii and Acinetobacter nosocomialis isolated in Taiwan.","authors":"Yi-Tzu Lee, Jun-Ren Sun, Li-Hua Li, Ya-Sung Yang, Hao-Ming Chang, Pei-Yin Lin, Po-Hsiang Liao, Fang-Yu Kang, Te-Li Chen, Yung-Chih Wang","doi":"10.1016/j.jmii.2025.08.025","DOIUrl":"https://doi.org/10.1016/j.jmii.2025.08.025","url":null,"abstract":"<p><strong>Background: </strong>Acinetobacter seifertii, a recently identified member of the Acinetobacter calcoaceticus-Acinetobacter baumannii (Acb) complex, has emerged as a cause of severe human infections. It is closely related to Acinetobacter nosocomialis, a major pathogen of the Acb complex. Here, we aimed to explore the clinical and molecular differences between these two species.</p><p><strong>Methods: </strong>This retrospective study enrolled 83 adults with A. seifertii bacteremia and 402 adults with A. nosocomialis bacteremia from four medical centers over a 9-year period. Species identification was confirmed using matrix-assisted laser desorption ionization-time of flight mass spectrometry and rpoB sequencing. Clinical information, antimicrobial susceptibility, and carbapenem resistance determinants were analyzed.</p><p><strong>Results: </strong>There were no significant differences in the underlying diseases or mortality between patients with A. seifertii and A. nosocomialis bacteremia. However, A. seifertii bacteremia was more frequently associated with intensive care unit (ICU) admission, recent ICU stay, central venous catheter use, ventilator use at bacteremia onset, and pneumonia as the primary infection source than A. nosocomialis bacteremia. A. seifertii exhibited significantly lower susceptibility to colistin, amikacin, gentamicin, ceftazidime, and cefepime than A. nosocomialis. Carbapenem resistance was primarily mediated by ISAba1-bla<sub>OXA-51</sub>-like in A. seifertii and IS1006-ΔISAba3-bla<sub>OXA-58</sub>-like in A. nosocomialis.</p><p><strong>Conclusion: </strong>A. seifertii and A. nosocomialis exhibit distinct antimicrobial susceptibility profiles and carbapenem resistance mechanisms but share similar mortality rates. The ability of both species to act as reservoirs of carbapenem resistance highlights the importance of accurate identification, antimicrobial stewardship, and infection control strategies to mitigate the spread of resistant strains.</p>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145014431","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-27DOI: 10.1016/j.jmii.2025.08.018
Po-Kai Chen, Po-Liang Lu, Etsuro Ito, Tsung-Ying Yang
Sexually transmitted infections (STIs) continue to pose major public health challenges globally, with millions of new cases reported annually. The asymptomatic characteristic of many STIs makes accurate and cost-effective diagnostic methods essential for screening and diagnosis. This paper evaluates the utility of enzyme-linked immunosorbent assays (ELISAs) in diagnoses of HIV, HPV, HSV, HBV, HCV, Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis and Treponema pallidum. Compared to nucleic acid amplification tests (NAATs), ELISAs have advantages that include minimal training requirements, lower costs, and suitability for community screening programs. Despite their practical advantages, conventional ELISAs face key performance limitations, cross-reactivity, lower sensitivity, and delayed detection, that have restricted their broader adoption, reducing the potential for ELISAs to become a standard STI detection method. Currently, advancements in ultrasensitive and digital ELISA technologies have greatly improved their accuracy and may improve the dilemma. This review describes current ELISA methodologies, efficacies, and limitations as observed in and reported for clinical applications and offers a comprehensive perspective on essential STI diagnostic improvements, motivated by the belief that ELISA techniques can significantly contribute to the early detection, treatment, and containment of STIs.
{"title":"Enzyme-linked immunosorbent STI assays: development, current status and future perspective.","authors":"Po-Kai Chen, Po-Liang Lu, Etsuro Ito, Tsung-Ying Yang","doi":"10.1016/j.jmii.2025.08.018","DOIUrl":"https://doi.org/10.1016/j.jmii.2025.08.018","url":null,"abstract":"<p><p>Sexually transmitted infections (STIs) continue to pose major public health challenges globally, with millions of new cases reported annually. The asymptomatic characteristic of many STIs makes accurate and cost-effective diagnostic methods essential for screening and diagnosis. This paper evaluates the utility of enzyme-linked immunosorbent assays (ELISAs) in diagnoses of HIV, HPV, HSV, HBV, HCV, Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis and Treponema pallidum. Compared to nucleic acid amplification tests (NAATs), ELISAs have advantages that include minimal training requirements, lower costs, and suitability for community screening programs. Despite their practical advantages, conventional ELISAs face key performance limitations, cross-reactivity, lower sensitivity, and delayed detection, that have restricted their broader adoption, reducing the potential for ELISAs to become a standard STI detection method. Currently, advancements in ultrasensitive and digital ELISA technologies have greatly improved their accuracy and may improve the dilemma. This review describes current ELISA methodologies, efficacies, and limitations as observed in and reported for clinical applications and offers a comprehensive perspective on essential STI diagnostic improvements, motivated by the belief that ELISA techniques can significantly contribute to the early detection, treatment, and containment of STIs.</p>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980094","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-27DOI: 10.1016/j.jmii.2025.08.024
Tien-Heng Ku, Yi-Pei Lin, Chia-Yu Tsai, Po-Liang Lu, Shin-Huei Kuo, Shih-Hao Lo, Chun-Yuan Lee
Background: Adherence to antiretroviral therapy (ART) is critical for successful viral suppression in people living with HIV (PLHIV). The comparative effectiveness of two-drug regimens (2DRs) versus three-drug regimens (3DRs)-particularly in Asian populations-is an underexplored topic.
Methods: This retrospective cross-sectional study was conducted at two hospitals in Taiwan between November 2023 and January 2025. Adherence was measured in terms of the proportion of days covered (PDC) over 365 days. Logistic regression analyses were used to evaluate the effectiveness of viral suppression and factors associated with regimen selection.
Results: Of the 628 PLHIV included, most were men, aged between 30 and 50 years, identified as lesbian, gay, bisexual, or transgender, and had received their diagnosis of HIV >5 years prior to this study. Among the participants receiving 3DRs (81.37 %), 3.72 % had viral loads exceeding 200 copies/mL. Regarding those receiving 2DRs (18.63 %), 2.56 % exhibited similar viral loads (p = 0.781). Multivariable analysis indicated that PDC ≥75 % was strongly associated with viral suppression (adjusted odds ratio [aOR] = 45.80, p < 0.0001), with no significant difference in viral suppression rates between regimens. The participants receiving 3DRs were less likely to have >75 % adherence (aOR = 0.18, p = 0.018) and to have a long HIV history (>5 years; aOR = 0.22, p = 0.041).
Conclusion: Adherence, not regimen type, is the key factor affecting viral suppression. Nevertheless, the findings should be cautiously interpreted because of potential bias and small subgroup sizes. Further prospective studies should evaluate the comparative efficacy of these regimens.
背景:坚持抗逆转录病毒治疗(ART)对于HIV感染者(PLHIV)成功抑制病毒至关重要。双药方案(2DRs)与三药方案(3DRs)的比较有效性——特别是在亚洲人群中——是一个未被充分探讨的话题。方法:本研究于2023年11月至2025年1月在台湾两家医院进行回顾性横断面研究。依从性是根据365天内覆盖天数(PDC)的比例来衡量的。采用Logistic回归分析来评估病毒抑制的有效性和与方案选择相关的因素。结果:在纳入的628例HIV感染者中,大多数是男性,年龄在30至50岁之间,被确定为女同性恋、男同性恋、双性恋或变性人,并且在本研究之前5年接受了HIV诊断。在接受3dr的参与者中(81.37%),3.72%的病毒载量超过200拷贝/mL。在接受2dr治疗的患者(18.63%)中,2.56%表现出相似的病毒载量(p = 0.781)。多变量分析表明,PDC≥75%与病毒抑制(校正优势比[aOR] = 45.80, p = 75%)、依从性(aOR = 0.18, p = 0.018)和HIV病史长(bbb50年;aOR = 0.22, p = 0.041)密切相关。结论:影响病毒抑制的关键因素是依从性,而非方案类型。然而,由于潜在的偏倚和较小的亚组规模,研究结果应谨慎解释。进一步的前瞻性研究应评估这些方案的相对疗效。
{"title":"Real-world viral effectiveness of two-drug versus three-drug regimens for HIV in Taiwan: Impact of adherence and treatment selection.","authors":"Tien-Heng Ku, Yi-Pei Lin, Chia-Yu Tsai, Po-Liang Lu, Shin-Huei Kuo, Shih-Hao Lo, Chun-Yuan Lee","doi":"10.1016/j.jmii.2025.08.024","DOIUrl":"https://doi.org/10.1016/j.jmii.2025.08.024","url":null,"abstract":"<p><strong>Background: </strong>Adherence to antiretroviral therapy (ART) is critical for successful viral suppression in people living with HIV (PLHIV). The comparative effectiveness of two-drug regimens (2DRs) versus three-drug regimens (3DRs)-particularly in Asian populations-is an underexplored topic.</p><p><strong>Methods: </strong>This retrospective cross-sectional study was conducted at two hospitals in Taiwan between November 2023 and January 2025. Adherence was measured in terms of the proportion of days covered (PDC) over 365 days. Logistic regression analyses were used to evaluate the effectiveness of viral suppression and factors associated with regimen selection.</p><p><strong>Results: </strong>Of the 628 PLHIV included, most were men, aged between 30 and 50 years, identified as lesbian, gay, bisexual, or transgender, and had received their diagnosis of HIV >5 years prior to this study. Among the participants receiving 3DRs (81.37 %), 3.72 % had viral loads exceeding 200 copies/mL. Regarding those receiving 2DRs (18.63 %), 2.56 % exhibited similar viral loads (p = 0.781). Multivariable analysis indicated that PDC ≥75 % was strongly associated with viral suppression (adjusted odds ratio [aOR] = 45.80, p < 0.0001), with no significant difference in viral suppression rates between regimens. The participants receiving 3DRs were less likely to have >75 % adherence (aOR = 0.18, p = 0.018) and to have a long HIV history (>5 years; aOR = 0.22, p = 0.041).</p><p><strong>Conclusion: </strong>Adherence, not regimen type, is the key factor affecting viral suppression. Nevertheless, the findings should be cautiously interpreted because of potential bias and small subgroup sizes. Further prospective studies should evaluate the comparative efficacy of these regimens.</p>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-02-28DOI: 10.1016/j.jmii.2025.02.010
Cong Zhou , Wencai Ke , Hui Zhang , Maosuo Xu , Baoyu Yuan , Yong Lin , Fang Shen
Background
KL1, KL2 CR-hvKP and KL64, KL47 hv-CRKP all exhibit overlapping multidrug resistance and hypervirulence phenotypes, but the differences in epidemiological, phenotypic and genotypic characteristics between them remains unclear.
Methods
In this study, we collected non-repeated hv-CRKP/CR-hvKP isolates in a tertiary hospital in Shanghai, China from January 2019 to December 2022. Furthermore, we selected four typical hypervirulent and carbapenem-resistant Klebsiella pneumoniae, including ST23-KL1/ST86-KL2 CR-hvKP (WYKP3 and WYKP194) and ST11-KL64/ST11-KL47 hv-CRKP (WYKP589 and WYKP188), and tried to clarify and compare their differences in virulence and drug resistance characteristics and plasmid distribution.
Results
Our study found that ST23-KL1 and ST86-KL2 CR-hvKP exhibited less plasmid diversity than that of ST11-KL64 and ST11-KL47 hv-CRKP. Compared with ST11-KL64 and ST11-KL47 hv-CRKP, ST23-KL1/ST86-KL2 CR-hvKP harbored significantly fewer antimicrobial resistance genes but more virulence genes, which contributed to the higher virulence of these strains and exhibited resistance to fewer antibiotics. ST11-KL64 hv-CRKP has emerged as the most prevalent hypervirulent and carbapenem-resistant Klebsiella pneumoniae probably due to its clonal transmission within hospitals as well as the transmission of virulence plasmids with the help of conjugative resistance plasmids.
Conclusions
Due to the different evolutionary mechanisms of hypervirulent and carbapenem-resistant Klebsiella pneumoniae with different capsular serotypes, the epidemiological, phenotypic and genotypic characteristics of KL1, KL2 CR-hvKP and KL64, KL47 hv-CRKP are different.
{"title":"Epidemiological, phenotypic and genotypic characteristics difference of hypervirulent and carbapenem-resistant Klebsiella pneumoniae with different capsular serotypes","authors":"Cong Zhou , Wencai Ke , Hui Zhang , Maosuo Xu , Baoyu Yuan , Yong Lin , Fang Shen","doi":"10.1016/j.jmii.2025.02.010","DOIUrl":"10.1016/j.jmii.2025.02.010","url":null,"abstract":"<div><h3>Background</h3><div>KL1, KL2 CR-hvKP and KL64, KL47 hv-CRKP all exhibit overlapping multidrug resistance and hypervirulence phenotypes, but the differences in epidemiological, phenotypic and genotypic characteristics between them remains unclear.</div></div><div><h3>Methods</h3><div>In this study, we collected non-repeated hv-CRKP/CR-hvKP isolates in a tertiary hospital in Shanghai, China from January 2019 to December 2022. Furthermore, we selected four typical hypervirulent and carbapenem-resistant <em>Klebsiella pneumoniae</em>, including ST23-KL1/ST86-KL2 CR-hvKP (WYKP3 and WYKP194) and ST11-KL64/ST11-KL47 hv-CRKP (WYKP589 and WYKP188), and tried to clarify and compare their differences in virulence and drug resistance characteristics and plasmid distribution.</div></div><div><h3>Results</h3><div>Our study found that ST23-KL1 and ST86-KL2 CR-hvKP exhibited less plasmid diversity than that of ST11-KL64 and ST11-KL47 hv-CRKP. Compared with ST11-KL64 and ST11-KL47 hv-CRKP, ST23-KL1/ST86-KL2 CR-hvKP harbored significantly fewer antimicrobial resistance genes but more virulence genes, which contributed to the higher virulence of these strains and exhibited resistance to fewer antibiotics. ST11-KL64 hv-CRKP has emerged as the most prevalent hypervirulent and carbapenem-resistant <em>Klebsiella pneumoniae</em> probably due to its clonal transmission within hospitals as well as the transmission of virulence plasmids with the help of conjugative resistance plasmids.</div></div><div><h3>Conclusions</h3><div>Due to the different evolutionary mechanisms of hypervirulent and carbapenem-resistant <em>Klebsiella pneumoniae</em> with different capsular serotypes, the epidemiological, phenotypic and genotypic characteristics of KL1, KL2 CR-hvKP and KL64, KL47 hv-CRKP are different.</div></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"58 4","pages":"Pages 444-454"},"PeriodicalIF":4.5,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143586835","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-03-17DOI: 10.1016/j.jmii.2025.03.001
Carmen Hidalgo-Tenorio , Svetlana Sadyrbaeva-Dolgova , Eduardo Aparicio-Minguijón , Arístides Alarcón , Antonio Plata , Francisco Javier Martínez Marcos , Beatriz Álvarez-Álvarez , Belén Loeches , Benedetta Varisco , Agustín Estévez , Carmen Herrero , Francesc Escrihuela-Vidal , Lucia Boix-Palop , Yvon Ruch , Florent Valour , Nahéma Issa , Pauline Thill , Sophie Nguyen , Samantha Poloni , Romain Millot , David Luque-Paz
Enterococcal endocarditis (EIE) affects elderly patients, with high rates of complications and mortality, and dalbavancin (DBV) exhibits significant antimicrobial activity against most enterococci. However, data are lacking on the use of DBV in EIE. The main objective was to evaluate the outcomes of treatment with DBV in the consolidation therapy of IE by Enterococcus spp.
Methods
Spanish-French retrospective observational study of patients with EIE enrolled between November 2016 and June 30, 2022 receiving DBV in consolidation phase and followed for ≥12 months.
Results
Ninety-eight patients were enrolled, 69.4 % male, with mean age of 71.2 (±12.51) years and median Charlson index of 5 (IQR 3–7). Criteria for definite IE were met by 84.7%; 60.2 % had IE on native valve, 26.5 % late prosthetic IE, 8.2 % early prosthetic IE, 2 % cardiovascular implantable electronic-IE (CIE-IE), and 3.1 % CIE-IE and valve. Aortic valve involvement was observed in 66.3 %. E. faecalis was isolated in 86.7 %, E. faecium in 11.2 %; 32.6 % underwent surgery, and these had a higher cure rate (100 % vs 75.8 %; p = 0.005) and lower mortality (0 vs 13.6 %; p = 0.029). DBV was administered to facilitate discharge in 88.8 %. Total dose was 2500 mg (1500–3000) over 3.5 weeks (2–4). Loss to follow-up was 0 %, relapse rate 8.2 %, 1-year IE-related mortality 3.1 %, and clinical cure rate 81.2 %. Severe adverse events affected 1 % (acute tubular necrosis). Hospital stay was reduced by 21 days (14–28).
Conclusions
DBV appears to be highly effective, safe, and cost-effective as consolidation therapy in patients with IE caused by Enterococcus spp., with minimal adverse events.
肠球菌性心内膜炎(EIE)影响老年患者,并发症和死亡率高,dalbavancin (DBV)对大多数肠球菌具有显著的抗菌活性。然而,关于DBV在EIE中的使用的数据缺乏。方法:西班牙-法国回顾性观察研究,纳入2016年11月至2022年6月30日在巩固期接受DBV治疗的EIE患者,随访≥12个月。结果:98例患者入组,男性69.4%,平均年龄71.2(±12.51)岁,中位Charlson指数5 (IQR 3-7)。84.7%的人符合明确的IE标准;60.2%的患者有先天性IE, 26.5%的患者有晚期假体IE, 8.2%的患者有早期假体IE, 2%的患者有心血管植入式电子IE (IE-IE), 3.1%的患者有IE-IE和瓣膜。66.3%的患者受累于主动脉瓣。分离出粪肠杆菌86.7%,分离出粪肠杆菌11.2%;32.6%的患者接受了手术治疗,治愈率更高(100% vs 75.8%;P = 0.005)和较低的死亡率(0 vs 13.6%;p = 0.029)。88.8%的患者使用DBV方便出院。总剂量为2500毫克(1500-3000),持续3.5周(2-4周)。随访损失为0%,复发率为8.2%,1年ie相关死亡率为3.1%,临床治愈率为81.2%。严重不良事件占1%(急性肾小管坏死)。住院时间缩短21天(14 ~ 28天)。结论:作为肠球菌引起的IE患者的巩固治疗,DBV似乎是非常有效、安全且具有成本效益的,并且不良事件最少。
{"title":"Real-world evidence of dalbavancin effectiveness as consolidation therapy in infective endocarditis due to Enterococcus spp.","authors":"Carmen Hidalgo-Tenorio , Svetlana Sadyrbaeva-Dolgova , Eduardo Aparicio-Minguijón , Arístides Alarcón , Antonio Plata , Francisco Javier Martínez Marcos , Beatriz Álvarez-Álvarez , Belén Loeches , Benedetta Varisco , Agustín Estévez , Carmen Herrero , Francesc Escrihuela-Vidal , Lucia Boix-Palop , Yvon Ruch , Florent Valour , Nahéma Issa , Pauline Thill , Sophie Nguyen , Samantha Poloni , Romain Millot , David Luque-Paz","doi":"10.1016/j.jmii.2025.03.001","DOIUrl":"10.1016/j.jmii.2025.03.001","url":null,"abstract":"<div><div>Enterococcal endocarditis (EIE) affects elderly patients, with high rates of complications and mortality, and dalbavancin (DBV) exhibits significant antimicrobial activity against most enterococci. However, data are lacking on the use of DBV in EIE. The main objective was to evaluate the outcomes of treatment with DBV in the consolidation therapy of IE by <em>Enterococcus</em> spp.</div></div><div><h3>Methods</h3><div>Spanish-French retrospective observational study of patients with EIE enrolled between November 2016 and June 30, 2022 receiving DBV in consolidation phase and followed for ≥12 months.</div></div><div><h3>Results</h3><div>Ninety-eight patients were enrolled, 69.4 % male, with mean age of 71.2 (±12.51) years and median Charlson index of 5 (IQR 3–7). Criteria for definite IE were met by 84.7%; 60.2 % had IE on native valve, 26.5 % late prosthetic IE, 8.2 % early prosthetic IE, 2 % cardiovascular implantable electronic-IE (CIE-IE), and 3.1 % CIE-IE and valve. Aortic valve involvement was observed in 66.3 %. <em>E. faecalis</em> was isolated in 86.7 %, <em>E. faecium</em> in 11.2 %; 32.6 % underwent surgery, and these had a higher cure rate (100 % vs 75.8 %; p = 0.005) and lower mortality (0 vs 13.6 %; p = 0.029). DBV was administered to facilitate discharge in 88.8 %. Total dose was 2500 mg (1500–3000) over 3.5 weeks (2–4). Loss to follow-up was 0 %, relapse rate 8.2 %, 1-year IE-related mortality 3.1 %, and clinical cure rate 81.2 %. Severe adverse events affected 1 % (acute tubular necrosis). Hospital stay was reduced by 21 days (14–28).</div></div><div><h3>Conclusions</h3><div>DBV appears to be highly effective, safe, and cost-effective as consolidation therapy in patients with IE caused by <em>Enterococcus</em> spp., with minimal adverse events.</div></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"58 4","pages":"Pages 429-436"},"PeriodicalIF":4.5,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143744515","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-02-10DOI: 10.1016/j.jmii.2025.02.003
Shuangyan Li , Mingming Pan , Hui Zhao , Yanming Li
Respiratory virus infection is an important cause of both community acquired pneumonia and hospital-acquired pneumonia. Various respiratory viruses, including influenza virus, avian influenza virus, respiratory syncytial virus (RSV), SARS-CoV, MERS-CoV, and SARS-CoV-2, result in severe fibrosis sequelae after the acute phase. Since the COVID-19 pandemic, respiratory virus infection, as an important cause of pulmonary fibrosis, has attracted increasing attention around the world. Respiratory virus infection usually triggers robust inflammation responses, leading to large amounts of proinflammatory mediator production, such as chemokine (C-C motif) ligand 2 (CCL2), a critical chemokine involved in the recruitment of various inflammatory cells. Moreover, CCL2 plays a pivotal role in the pathogenesis of fibrosis progression, through regulating recruitment of bone marrow-derived monocytes and increasing the expression of extracellular matrix proteins. This review provided a concise overview of the common fibrosis sequelae after virus infection. Then we discussed the elevated levels of CCL2 in various respiratory virus infection, underscoring its potent profibrotic role. Targeting the CCL2/CCR2 axis holds promise for alleviating fibrosis sequelae post-acute virus infection and warrants further investigation.
{"title":"Role of CCL2/CCR2 axis in pulmonary fibrosis induced by respiratory viruses","authors":"Shuangyan Li , Mingming Pan , Hui Zhao , Yanming Li","doi":"10.1016/j.jmii.2025.02.003","DOIUrl":"10.1016/j.jmii.2025.02.003","url":null,"abstract":"<div><div>Respiratory virus infection is an important cause of both community acquired pneumonia and hospital-acquired pneumonia. Various respiratory viruses, including influenza virus, avian influenza virus, respiratory syncytial virus (RSV), SARS-CoV, MERS-CoV, and SARS-CoV-2, result in severe fibrosis sequelae after the acute phase. Since the COVID-19 pandemic, respiratory virus infection, as an important cause of pulmonary fibrosis, has attracted increasing attention around the world. Respiratory virus infection usually triggers robust inflammation responses, leading to large amounts of proinflammatory mediator production, such as chemokine (C-C motif) ligand 2 (CCL2), a critical chemokine involved in the recruitment of various inflammatory cells. Moreover, CCL2 plays a pivotal role in the pathogenesis of fibrosis progression, through regulating recruitment of bone marrow-derived monocytes and increasing the expression of extracellular matrix proteins. This review provided a concise overview of the common fibrosis sequelae after virus infection. Then we discussed the elevated levels of CCL2 in various respiratory virus infection, underscoring its potent profibrotic role. Targeting the CCL2/CCR2 axis holds promise for alleviating fibrosis sequelae post-acute virus infection and warrants further investigation.</div></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"58 4","pages":"Pages 397-405"},"PeriodicalIF":4.5,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143425779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-03-27DOI: 10.1016/j.jmii.2025.03.012
Thi Nhu Le Tran , Ngoc-Niem Bui , Vu Trung Nguyen , Ngoc Anh Tran
Background
The escalating antibiotic resistance in Helicobacter pylori (H. pylori) has become a significant concern in the management of infections. This study aimed to investigate the mutations associated with levofloxacin resistance in H. pylori isolated from southern Vietnam.
Methods
Levofloxacin-resistant H. pylori strains were isolated from peptic ulcer patients and DNA sequencing of DNA gyrase (gyrA and gyrB) genes was performed.
Results
We found that 97 % of resistant isolates bearing at least one mutation in GyrA and 32.3 % had a simultaneous mutation in GyrB. Additionally, we identified three previously known mutations, G85C (1.5 %), N87 (34.3 %), and D91 (14.9 %), within the quinolone-resistance-determining region (QRDR) region of GyrA, which confer resistance through natural transformation and were the most prevalent in our study. Notably, we demonstrated a mutation (A88V MIC 4 μg/mL) in GyrA and four novel mutations (E422R MIC 16 μg/mL, A426G MIC 32 μg/mL, S429E MIC 4 μg/mL, and P443A MIC 4 μg/mL) in GyrB, belonging to the QRDR. Additionally, several mutations outside the QRDR were observed, including R190K (16.4 %), P219A/G (13.4 %), L45F (9 %), P220E (6 %), Y28I (4.5 %), A27L (3 %) in GyrA, and S457A (7.5 %), A382F (5.9 %), L389F (4.5 %), D412R (1.5 %), L460P (1.5 %), I482V (1.5 %), and L518E (1.5 %) that have not been documented in any previous studies and were not functionally validated.
Conclusion
These results highlight the high genetic diversity and prevalence of levofloxacin-resistant H. pylori strains in southern Vietnam and provide valuable insights into levofloxacin resistance mechanisms for future diagnostic and treatment advancements.
背景:幽门螺杆菌(Helicobacter pylori, H. pylori)的抗生素耐药性不断上升,已成为感染管理中的一个重要问题。本研究旨在调查越南南部分离的幽门螺杆菌中与左氧氟沙星耐药性相关的突变。方法:从消化性溃疡患者中分离出左氧氟沙星耐药幽门螺杆菌,对其DNA旋切酶(gyrA和gyrB)基因进行测序。结果:我们发现97%的耐药菌株至少携带一种GyrA突变,32.3%的耐药菌株同时携带GyrB突变。此外,我们在GyrA的喹诺酮类耐药决定区(QRDR)区域内发现了三个已知的突变,G85C (1.5%), N87(34.3%)和D91(14.9%),它们通过自然转化赋予耐药性,在我们的研究中最为普遍。值得注意的是,我们在GyrA中发现了一个突变(A88V MIC 4 μg/mL),在GyrB中发现了四个新的突变(E422R MIC 16 μg/mL, A426G MIC 32 μg/mL, S429E MIC 4 μg/mL和P443A MIC 4 μg/mL),属于QRDR。此外,还观察到QRDR外的一些突变,包括GyrA中的R190K(16.4%)、P219A/G(13.4%)、L45F(9%)、P220E(6%)、Y28I(4.5%)、A27L(3%),以及S457A(7.5%)、A382F(5.9%)、L389F(4.5%)、D412R(1.5%)、L460P(1.5%)、I482V(1.5%)和L518E(1.5%),这些突变在以往的研究中没有记录,也没有功能验证。结论:这些结果突出了越南南部左氧氟沙星耐药幽门螺杆菌菌株的高遗传多样性和患病率,并为进一步研究左氧氟沙星耐药机制提供了有价值的见解。
{"title":"Novel DNA gyrase mutations in levofloxacin-resistant Helicobacter pylori isolates from southern Vietnam","authors":"Thi Nhu Le Tran , Ngoc-Niem Bui , Vu Trung Nguyen , Ngoc Anh Tran","doi":"10.1016/j.jmii.2025.03.012","DOIUrl":"10.1016/j.jmii.2025.03.012","url":null,"abstract":"<div><h3>Background</h3><div>The escalating antibiotic resistance in <em>Helicobacter pylori</em> (<em>H. pylori</em>) has become a significant concern in the management of infections. This study aimed to investigate the mutations associated with levofloxacin resistance in <em>H. pylori</em> isolated from southern Vietnam.</div></div><div><h3>Methods</h3><div>Levofloxacin-resistant <em>H. pylori</em> strains were isolated from peptic ulcer patients and DNA sequencing of DNA gyrase (<em>gyrA</em> and <em>gyrB</em>) genes was performed.</div></div><div><h3>Results</h3><div>We found that 97 % of resistant isolates bearing at least one mutation in GyrA and 32.3 % had a simultaneous mutation in GyrB. Additionally, we identified three previously known mutations, G85C (1.5 %), N87 (34.3 %), and D91 (14.9 %), within the quinolone-resistance-determining region (QRDR) region of GyrA, which confer resistance through natural transformation and were the most prevalent in our study. Notably, we demonstrated a mutation (A88V MIC 4 μg/mL) in GyrA and four novel mutations (E422R MIC 16 μg/mL, A426G MIC 32 μg/mL, S429E MIC 4 μg/mL, and P443A MIC 4 μg/mL) in GyrB, belonging to the QRDR. Additionally, several mutations outside the QRDR were observed, including R190K (16.4 %), P219A/G (13.4 %), L45F (9 %), P220E (6 %), Y28I (4.5 %), A27L (3 %) in GyrA, and S457A (7.5 %), A382F (5.9 %), L389F (4.5 %), D412R (1.5 %), L460P (1.5 %), I482V (1.5 %), and L518E (1.5 %) that have not been documented in any previous studies and were not functionally validated.</div></div><div><h3>Conclusion</h3><div>These results highlight the high genetic diversity and prevalence of levofloxacin-resistant <em>H. pylori</em> strains in southern Vietnam and provide valuable insights into levofloxacin resistance mechanisms for future diagnostic and treatment advancements.</div></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"58 4","pages":"Pages 455-462"},"PeriodicalIF":4.5,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143756177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-03-17DOI: 10.1016/j.jmii.2025.03.007
Tian-Yu You , Nan-Yao Lee , Tai-Hua Yang , Po-Lin Chen , Ming-Chi Li , Shu-Li Su , Yu-Wei Hsu , Wen-Chien Ko
{"title":"Culture-negative orthopedic implant-associated infection due to Mycoplasma hominis: A case report","authors":"Tian-Yu You , Nan-Yao Lee , Tai-Hua Yang , Po-Lin Chen , Ming-Chi Li , Shu-Li Su , Yu-Wei Hsu , Wen-Chien Ko","doi":"10.1016/j.jmii.2025.03.007","DOIUrl":"10.1016/j.jmii.2025.03.007","url":null,"abstract":"","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"58 4","pages":"Pages 493-495"},"PeriodicalIF":4.5,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143694636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}