Pub Date : 2024-12-13DOI: 10.3390/pathogens13121102
Mevlut Ulas, Seamus Hussey, Annemarie Broderick, Emer Fitzpatrick, Cara Dunne, Sarah Cooper, Anna Dominik, Billy Bourke
Metaproteomic analysis of microbiome post-translation modifications (PTMm) is challenging, and little is known about the effects of inflammation on the bacterial PTM landscape in IBD. Here, we adapted and optimised fluorescence in situ hybridisation-flow cytometry (FISH-FC) to study microbiome-wide tyrosine phosphorylation (p-Tyr) in children with and without inflammatory bowel disease (IBD). Microbial p-Tyr signal was significantly higher in children with IBD, compared to those without. Faecalibacterium prausnitzii, Bacteroidota, Gammaproteobacteria and Bifidobacteria tended to be more abundant in IBD than in non-IBD control children but there were only minor differences in p-Tyr among these bacterial communities in those with and without IBD. p-Tyr was significantly lower in non-IBD children older than 9 yrs compared with those less than 9 yrs, and the effect was seen in all four bacterial subgroups studied. The opposite trend was seen in patients with IBD. p-Tyr overall is higher in children with IBD but the effects of inflammation on p-Tyr vary according to the bacterial community. The overall microbiome p-Tyr signal changes with age in healthy children. FISH-FC can be used to study the microbiome-wide PTM landscape.
{"title":"FISH-Flow Cytometry Reveals Microbiome-Wide Changes in Post-Translational Modification and Altered Microbial Abundance Among Children with Inflammatory Bowel Disease.","authors":"Mevlut Ulas, Seamus Hussey, Annemarie Broderick, Emer Fitzpatrick, Cara Dunne, Sarah Cooper, Anna Dominik, Billy Bourke","doi":"10.3390/pathogens13121102","DOIUrl":"10.3390/pathogens13121102","url":null,"abstract":"<p><p>Metaproteomic analysis of microbiome post-translation modifications (PTMm) is challenging, and little is known about the effects of inflammation on the bacterial PTM landscape in IBD. Here, we adapted and optimised fluorescence in situ hybridisation-flow cytometry (FISH-FC) to study microbiome-wide tyrosine phosphorylation (p-Tyr) in children with and without inflammatory bowel disease (IBD). Microbial p-Tyr signal was significantly higher in children with IBD, compared to those without. <i>Faecalibacterium prausnitzii</i>, <i>Bacteroidota</i>, <i>Gammaproteobacteria</i> and <i>Bifidobacteria</i> tended to be more abundant in IBD than in non-IBD control children but there were only minor differences in p-Tyr among these bacterial communities in those with and without IBD. p-Tyr was significantly lower in non-IBD children older than 9 yrs compared with those less than 9 yrs, and the effect was seen in all four bacterial subgroups studied. The opposite trend was seen in patients with IBD. p-Tyr overall is higher in children with IBD but the effects of inflammation on p-Tyr vary according to the bacterial community. The overall microbiome p-Tyr signal changes with age in healthy children. FISH-FC can be used to study the microbiome-wide PTM landscape.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728554/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979495","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.3390/pathogens13121095
Sobur Ali, Marta Giovanetti, Catherine Johnston, Verónica Urdaneta-Páez, Taj Azarian, Eleonora Cella
The continual evolution of SARS-CoV-2 has significantly influenced the global response to the COVID-19 pandemic, with the emergence of highly transmissible and immune-evasive variants posing persistent challenges. The Omicron variant, first identified in November 2021, rapidly replaced the Delta variant, becoming the predominant strain worldwide. In Florida, Omicron was first detected in December 2021, leading to an unprecedented surge in cases that surpassed all prior waves, despite extensive vaccination efforts. This study investigates the molecular evolution and transmission dynamics of the Omicron lineages during Florida's Omicron waves, supported by a robust dataset of over 1000 sequenced genomes. Through phylogenetic and phylodynamic analyses, we capture the rapid diversification of the Omicron lineages, identifying significant importation events, predominantly from California, Texas, and New York, and exportation to North America, Europe, and South America. Variants such as BA.1, BA.2, BA.4, and BA.5 exhibited distinct transmission patterns, with BA.2 showing the ability to reinfect individuals previously infected with BA.1. Despite the high transmissibility and immune evasion of the Omicron sub-lineages, the plateauing of cases by late 2022 suggests increasing population immunity from prior infection and vaccination. Our findings underscore the importance of continuous genomic surveillance in identifying variant introductions, mapping transmission pathways, and guiding public health interventions to mitigate current and future pandemic risks.
{"title":"From Emergence to Evolution: Dynamics of the SARS-CoV-2 Omicron Variant in Florida.","authors":"Sobur Ali, Marta Giovanetti, Catherine Johnston, Verónica Urdaneta-Páez, Taj Azarian, Eleonora Cella","doi":"10.3390/pathogens13121095","DOIUrl":"https://doi.org/10.3390/pathogens13121095","url":null,"abstract":"<p><p>The continual evolution of SARS-CoV-2 has significantly influenced the global response to the COVID-19 pandemic, with the emergence of highly transmissible and immune-evasive variants posing persistent challenges. The Omicron variant, first identified in November 2021, rapidly replaced the Delta variant, becoming the predominant strain worldwide. In Florida, Omicron was first detected in December 2021, leading to an unprecedented surge in cases that surpassed all prior waves, despite extensive vaccination efforts. This study investigates the molecular evolution and transmission dynamics of the Omicron lineages during Florida's Omicron waves, supported by a robust dataset of over 1000 sequenced genomes. Through phylogenetic and phylodynamic analyses, we capture the rapid diversification of the Omicron lineages, identifying significant importation events, predominantly from California, Texas, and New York, and exportation to North America, Europe, and South America. Variants such as BA.1, BA.2, BA.4, and BA.5 exhibited distinct transmission patterns, with BA.2 showing the ability to reinfect individuals previously infected with BA.1. Despite the high transmissibility and immune evasion of the Omicron sub-lineages, the plateauing of cases by late 2022 suggests increasing population immunity from prior infection and vaccination. Our findings underscore the importance of continuous genomic surveillance in identifying variant introductions, mapping transmission pathways, and guiding public health interventions to mitigate current and future pandemic risks.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11679505/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142952677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.3390/pathogens13121096
Kyla Radke, Brandon Rivers, Mya Simpkins, Jacob Hardy, Jeffrey K Schachterle
Bacterial soft rot causes major crop losses annually and can be caused by several species from multiple genera. These bacteria have a broad host range and often infect produce through contact with soil. The main genera causing bacterial soft rot are Pectobacterium and Dickeya, both of which have widespread geographical distribution. Because of many recent renaming and reclassifications of bacteria causing soft rot, identification and characterization of the causative agents can be challenging. In this work, we surveyed commercially available produce exhibiting typical soft rot symptoms, isolating pectinolytic bacteria and characterizing them genetically and phenotypically. We found that in our sampling, many samples were from the genus Pectobacterium; however, other genera were also capable of eliciting symptoms in potatoes, including an isolate from the genus Chryseobacterium. Genomic analyses revealed that many of the Pectobacterium isolates collected share prophages not found in other soft rot species, suggesting a potential role for these prophages in the evolution or fitness of these isolates. Our Chryseobacterium isolate was most similar to C. scophthalmum, a fish pathogen, suggesting that this isolate may be a crossover pathogen.
{"title":"Characterization and Genomics of Pectinolytic Bacteria Isolated from Soft Rot Symptomatic Produce.","authors":"Kyla Radke, Brandon Rivers, Mya Simpkins, Jacob Hardy, Jeffrey K Schachterle","doi":"10.3390/pathogens13121096","DOIUrl":"10.3390/pathogens13121096","url":null,"abstract":"<p><p>Bacterial soft rot causes major crop losses annually and can be caused by several species from multiple genera. These bacteria have a broad host range and often infect produce through contact with soil. The main genera causing bacterial soft rot are <i>Pectobacterium</i> and <i>Dickeya</i>, both of which have widespread geographical distribution. Because of many recent renaming and reclassifications of bacteria causing soft rot, identification and characterization of the causative agents can be challenging. In this work, we surveyed commercially available produce exhibiting typical soft rot symptoms, isolating pectinolytic bacteria and characterizing them genetically and phenotypically. We found that in our sampling, many samples were from the genus <i>Pectobacterium</i>; however, other genera were also capable of eliciting symptoms in potatoes, including an isolate from the genus <i>Chryseobacterium</i>. Genomic analyses revealed that many of the <i>Pectobacterium</i> isolates collected share prophages not found in other soft rot species, suggesting a potential role for these prophages in the evolution or fitness of these isolates. Our <i>Chryseobacterium</i> isolate was most similar to <i>C. scophthalmum</i>, a fish pathogen, suggesting that this isolate may be a crossover pathogen.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728799/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.3390/pathogens13121098
Daniel H Fine
The purpose of this Editorial is to expose the gaps in the knowledge created by a decision by the World Workshop Consensus Conference (WWCC), held in 2017, which was focused on the re-classification of periodontal diseases [...].
{"title":"New Classification of Periodontal Diseases, the Obstacles Created and Opportunities for Growth.","authors":"Daniel H Fine","doi":"10.3390/pathogens13121098","DOIUrl":"10.3390/pathogens13121098","url":null,"abstract":"<p><p>The purpose of this Editorial is to expose the gaps in the knowledge created by a decision by the World Workshop Consensus Conference (WWCC), held in 2017, which was focused on the re-classification of periodontal diseases [...].</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728499/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142962364","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.3390/pathogens13121099
Piero Veronese, Simone Cella, Alessandra Giacometti, Irene Lapetina, Valentina Maffini, Marco Pappalardo, Monica Rubini, Maria Beatrice Ruozi, Icilio Dodi
In recent years, an increasing number of reports have described invasive infections caused by bacteria from Streptococcus anginosus group (SAGs). S. intermedius seems to be more related with pleuropulmonary infections and abscess of the brain and deep soft tissues, and it is more likely to cause suppurative and non-bacteremic infections compared to other members of the same genus. We present two clinical cases of invasive S. intermedius infections in pediatric patients: a liver abscess case and a pansinusitis case associated with bilateral otomastoiditis and parapharyngeal abscess complicated by acute mediastinitis, thrombophlebitis of the cavernous sinus, and thrombosis of the cranial tract of the ipsilateral jugular vein. In both cases, prompt broad-spectrum antibiotic therapy and operative drainage of the collections resulted in a good clinical response with full recovery.
{"title":"Invasive <i>Streptococcus intermedius</i> Infections in Children: Two Cases from a Pediatric Infectious Diseases Unit in Italy.","authors":"Piero Veronese, Simone Cella, Alessandra Giacometti, Irene Lapetina, Valentina Maffini, Marco Pappalardo, Monica Rubini, Maria Beatrice Ruozi, Icilio Dodi","doi":"10.3390/pathogens13121099","DOIUrl":"10.3390/pathogens13121099","url":null,"abstract":"<p><p>In recent years, an increasing number of reports have described invasive infections caused by bacteria from <i>Streptococcus anginosus group</i> (SAGs). <i>S. intermedius</i> seems to be more related with pleuropulmonary infections and abscess of the brain and deep soft tissues, and it is more likely to cause suppurative and non-bacteremic infections compared to other members of the same genus. We present two clinical cases of invasive <i>S. intermedius</i> infections in pediatric patients: a liver abscess case and a pansinusitis case associated with bilateral otomastoiditis and parapharyngeal abscess complicated by acute mediastinitis, thrombophlebitis of the cavernous sinus, and thrombosis of the cranial tract of the ipsilateral jugular vein. In both cases, prompt broad-spectrum antibiotic therapy and operative drainage of the collections resulted in a good clinical response with full recovery.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728730/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.3390/pathogens13121097
Grzegorz Tarasiuk, Marta D Remmenga, Kathleen C O'Hara, Marian K Talbert, Sarah Mielke, Marisa L Rotolo, Pam Zaabel, Danyang Zhang, Jeffrey J Zimmerman
Pen-based oral fluids are used extensively for surveillance and disease detection in swine, but there is sparse information on the sampling process itself. To address this shortcoming, we documented the pen-based oral fluid sampling process with the aim of optimizing the number of pigs in a pen that contributed to the sample. We quantified the effects of (1) previous experience with rope sampling (training), (2) the number of ropes suspended in the pen, and (3) sampling time on pig participation and pig-rope contact. A subset of pigs was clearly marked for individual identification and their interactions with ropes video recorded. Thereafter, pig-rope contacts were counted from the recordings, with "contact" defined as an individually identified pig clearly taking the rope into its mouth. Data were analyzed using appropriate models (R version 4.4.1 R core team 2024). Training, provision of additional ropes, and extended sampling time all increased pig participation across pen sizes. However, for routine oral fluid collection in the field, we recommend training pigs prior to hanging ropes for sample collection and increasing sampling time to maximize the pigs' contribution to the oral fluid sample. Importantly, these studies focused on pig behavior and not detection; thus, future studies should evaluate the impact of these same factors on the probability of detection.
{"title":"Optimizing Swine Oral Fluid Sampling Procedures for Growing Pigs in Commercial Settings.","authors":"Grzegorz Tarasiuk, Marta D Remmenga, Kathleen C O'Hara, Marian K Talbert, Sarah Mielke, Marisa L Rotolo, Pam Zaabel, Danyang Zhang, Jeffrey J Zimmerman","doi":"10.3390/pathogens13121097","DOIUrl":"10.3390/pathogens13121097","url":null,"abstract":"<p><p>Pen-based oral fluids are used extensively for surveillance and disease detection in swine, but there is sparse information on the sampling process itself. To address this shortcoming, we documented the pen-based oral fluid sampling process with the aim of optimizing the number of pigs in a pen that contributed to the sample. We quantified the effects of (1) previous experience with rope sampling (training), (2) the number of ropes suspended in the pen, and (3) sampling time on pig participation and pig-rope contact. A subset of pigs was clearly marked for individual identification and their interactions with ropes video recorded. Thereafter, pig-rope contacts were counted from the recordings, with \"contact\" defined as an individually identified pig clearly taking the rope into its mouth. Data were analyzed using appropriate models (R version 4.4.1 R core team 2024). Training, provision of additional ropes, and extended sampling time all increased pig participation across pen sizes. However, for routine oral fluid collection in the field, we recommend training pigs prior to hanging ropes for sample collection and increasing sampling time to maximize the pigs' contribution to the oral fluid sample. Importantly, these studies focused on pig behavior and not detection; thus, future studies should evaluate the impact of these same factors on the probability of detection.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11728740/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142979527","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-11DOI: 10.3390/pathogens13121094
Ana Cláudia Calchi, Charlotte O Moore, Lillianne Bartone, Emily Kingston, Marcos Rogério André, Edward B Breitschwerdt, Ricardo G Maggi
<p><p>More than one-hundred <i>Babesia</i> species that affect animals and humans have been described, eight of which have been associated with emerging and underdiagnosed zoonoses. Most diagnostic studies in humans have used serology or molecular assays based on the 18S rRNA gene. Because the 18S rRNA gene is highly conserved, obtaining an accurate diagnosis at the species level is difficult, particularly when the amplified DNA fragment is small. Also, due to its low copy number, sequencing of the product is often unsuccessful. In contrast, because the <i>Babesia</i> internal transcribed regions (ITS), between 18S rRNA and 5.8S rRNA, and between 5.8S rRNA and 28S rRNA, contain highly variable non-coding regions, the sequences in these regions provide a good option for developing molecular assays that facilitate differentiation at the species level. In this study, the complete ITS1 and ITS2 intergenic regions of different Piroplasmida species were sequenced to add to the existing GenBank database. Subsequently, ITS1 and ITS2 sequences were used to develop species-specific PCR assays and specific single-plex and multiplex conventional (c)PCR, quantitative real-time (q)PCR, and digital (d)PCR assays for four zoonotic <i>Babesia</i> species (<i>Babesia divergens</i>, <i>Babesia odocoilei</i>, <i>Babesia duncani</i>, and <i>Babesia microti</i>). The efficacy of the assay protocols was confirmed by testing DNA samples extracted from human blood or enrichment blood cultures. Primers were first designed based on the 18S rRNA-5.8S rRNA and 5.8S rRNA-28S rRNA regions to obtain the ITS1 and ITS2 sequences derived from different Piroplasmida species (<i>B. odocoilei</i>, <i>Babesia vulpes</i>, <i>Babesia canis</i>, <i>Babesia vogeli</i>, <i>Babesia gibsoni</i>, <i>Babesia lengau</i>, <i>Babesia divergens</i>-like, <i>B. duncani</i>, <i>B. microti</i>, <i>Babesia capreoli</i>, <i>Babesia negevi</i>, <i>Babesia conradae</i>, <i>Theileria bicornis</i>, and <i>Cytauxzoon felis</i>). Subsequently, using these sequences, single-plex or multiplex protocols were optimized targeting the ITS1 region of <i>B. divergens</i>, <i>B. microti</i>, and <i>B. odocoilei</i>. Each protocol proved to be sensitive and specific for the four targeted <i>Babesia</i> sp., detecting 10<sup>-2</sup> (for <i>B. microti</i> and <i>B. odocoilei</i>) and 10<sup>-1</sup> (for <i>B. divergens</i> and <i>B. duncani</i>) DNA copies per microliter. There was no cross-amplification among the <i>Babesia</i> species tested. Using 226 DNA extractions from blood or enrichment blood cultures obtained from 82 humans, <i>B. divergens</i> (seven individuals), <i>B. odocoilei</i> (seven individuals), and <i>B. microti</i> (two individuals) were detected and identified as a single infection, whereas co-infection with more than one <i>Babesia</i> sp. was documented by DNA sequencing in six (7.3%) additional individuals (representing a 26.8% overall prevalence). These newly developed protocols proved to be
{"title":"Development of Multiplex Assays for the Identification of Zoonotic <i>Babesia</i> Species.","authors":"Ana Cláudia Calchi, Charlotte O Moore, Lillianne Bartone, Emily Kingston, Marcos Rogério André, Edward B Breitschwerdt, Ricardo G Maggi","doi":"10.3390/pathogens13121094","DOIUrl":"https://doi.org/10.3390/pathogens13121094","url":null,"abstract":"<p><p>More than one-hundred <i>Babesia</i> species that affect animals and humans have been described, eight of which have been associated with emerging and underdiagnosed zoonoses. Most diagnostic studies in humans have used serology or molecular assays based on the 18S rRNA gene. Because the 18S rRNA gene is highly conserved, obtaining an accurate diagnosis at the species level is difficult, particularly when the amplified DNA fragment is small. Also, due to its low copy number, sequencing of the product is often unsuccessful. In contrast, because the <i>Babesia</i> internal transcribed regions (ITS), between 18S rRNA and 5.8S rRNA, and between 5.8S rRNA and 28S rRNA, contain highly variable non-coding regions, the sequences in these regions provide a good option for developing molecular assays that facilitate differentiation at the species level. In this study, the complete ITS1 and ITS2 intergenic regions of different Piroplasmida species were sequenced to add to the existing GenBank database. Subsequently, ITS1 and ITS2 sequences were used to develop species-specific PCR assays and specific single-plex and multiplex conventional (c)PCR, quantitative real-time (q)PCR, and digital (d)PCR assays for four zoonotic <i>Babesia</i> species (<i>Babesia divergens</i>, <i>Babesia odocoilei</i>, <i>Babesia duncani</i>, and <i>Babesia microti</i>). The efficacy of the assay protocols was confirmed by testing DNA samples extracted from human blood or enrichment blood cultures. Primers were first designed based on the 18S rRNA-5.8S rRNA and 5.8S rRNA-28S rRNA regions to obtain the ITS1 and ITS2 sequences derived from different Piroplasmida species (<i>B. odocoilei</i>, <i>Babesia vulpes</i>, <i>Babesia canis</i>, <i>Babesia vogeli</i>, <i>Babesia gibsoni</i>, <i>Babesia lengau</i>, <i>Babesia divergens</i>-like, <i>B. duncani</i>, <i>B. microti</i>, <i>Babesia capreoli</i>, <i>Babesia negevi</i>, <i>Babesia conradae</i>, <i>Theileria bicornis</i>, and <i>Cytauxzoon felis</i>). Subsequently, using these sequences, single-plex or multiplex protocols were optimized targeting the ITS1 region of <i>B. divergens</i>, <i>B. microti</i>, and <i>B. odocoilei</i>. Each protocol proved to be sensitive and specific for the four targeted <i>Babesia</i> sp., detecting 10<sup>-2</sup> (for <i>B. microti</i> and <i>B. odocoilei</i>) and 10<sup>-1</sup> (for <i>B. divergens</i> and <i>B. duncani</i>) DNA copies per microliter. There was no cross-amplification among the <i>Babesia</i> species tested. Using 226 DNA extractions from blood or enrichment blood cultures obtained from 82 humans, <i>B. divergens</i> (seven individuals), <i>B. odocoilei</i> (seven individuals), and <i>B. microti</i> (two individuals) were detected and identified as a single infection, whereas co-infection with more than one <i>Babesia</i> sp. was documented by DNA sequencing in six (7.3%) additional individuals (representing a 26.8% overall prevalence). These newly developed protocols proved to be","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11676916/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142952690","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-11DOI: 10.3390/pathogens13121093
Sabir Hussain, Abrar Hussain, Jeffery Ho, Jun Li, David George, Abdul Rehman, Jehan Zeb, Olivier Sparagano
There was an error in the original publication [...].
原文中有个错误[…]
{"title":"Correction: Hussain et al. An Epidemiological Survey Regarding Ticks and Tick-Borne Diseases among Livestock Owners in Punjab, Pakistan: A One Health Context. <i>Pathogens</i> 2021, <i>10</i>, 361.","authors":"Sabir Hussain, Abrar Hussain, Jeffery Ho, Jun Li, David George, Abdul Rehman, Jehan Zeb, Olivier Sparagano","doi":"10.3390/pathogens13121093","DOIUrl":"https://doi.org/10.3390/pathogens13121093","url":null,"abstract":"<p><p>There was an error in the original publication [...].</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11677401/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142952569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-10DOI: 10.3390/pathogens13121089
Maria Anele Romeo, Eliana Specchiarello, Cosmina Mija, Verdiana Zulian, Massimo Francalancia, Fabrizio Maggi, Anna Rosa Garbuglia, Daniele Lapa
Rift Valley Fever virus (RVFV) is a mosquito-borne virus with high pathogenic potential in ruminants and humans. Due to its high potential for spreading, it is considered a priority pathogen, and it is included in the Bluepoint list of the World Health Organization (WHO). Given the high pathogenic potential of the virus, it is crucial to develop a rapid heat-mediated inactivation protocol to create a safer working environment, particularly in medical facilities that lack a biosafety level 3 laboratory required for direct handling of RVFV. Our results reveal the broad tissue tropism of RVFV, showing the virus's capacity for replication in various cell lines. In terms of the thermal stability of RVFV, our findings showed that a 70 °C heat treatment did not fully inactivate the virus within 15 min. However, when exposed to 80 °C and 95 °C, the virus was completely inactivated after 15 min and 5 min, respectively. Additionally, our results indicated that heat-treatment only slightly decreased the integrity of the RVFV genome whether there is a high or low number of viral RNA copies. Overall, the study established a straightforward protocol for heat inactivation that may be beneficial in handling clinical and research samples of RVFV.
{"title":"Heat Treatment as a Safe-Handling Procedure for Rift Valley Fever Virus.","authors":"Maria Anele Romeo, Eliana Specchiarello, Cosmina Mija, Verdiana Zulian, Massimo Francalancia, Fabrizio Maggi, Anna Rosa Garbuglia, Daniele Lapa","doi":"10.3390/pathogens13121089","DOIUrl":"https://doi.org/10.3390/pathogens13121089","url":null,"abstract":"<p><p>Rift Valley Fever virus (RVFV) is a mosquito-borne virus with high pathogenic potential in ruminants and humans. Due to its high potential for spreading, it is considered a priority pathogen, and it is included in the Bluepoint list of the World Health Organization (WHO). Given the high pathogenic potential of the virus, it is crucial to develop a rapid heat-mediated inactivation protocol to create a safer working environment, particularly in medical facilities that lack a biosafety level 3 laboratory required for direct handling of RVFV. Our results reveal the broad tissue tropism of RVFV, showing the virus's capacity for replication in various cell lines. In terms of the thermal stability of RVFV, our findings showed that a 70 °C heat treatment did not fully inactivate the virus within 15 min. However, when exposed to 80 °C and 95 °C, the virus was completely inactivated after 15 min and 5 min, respectively. Additionally, our results indicated that heat-treatment only slightly decreased the integrity of the RVFV genome whether there is a high or low number of viral RNA copies. Overall, the study established a straightforward protocol for heat inactivation that may be beneficial in handling clinical and research samples of RVFV.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11676096/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142951879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-10DOI: 10.3390/pathogens13121092
Olga V Shevchenko, Alexander D Voropaev, Ivan V Bogdanov, Tatiana V Ovchinnikova, Ekaterina I Finkina
Today, Candida albicans is still the most common cause of both local and life-threatening systemic candidiasis. The spread of resistant fungal strains has resulted in an urgent need to search for new promising antimycotics. Here, we investigated the antifungal action of the tobacco defensin NaD1 against susceptible and resistant to azoles and echinocandins strains of C. albicans. We demonstrated that NaD1 was equally effective and fungicidal against all tested strains. The MIC and MFC values were 6.25 and 12.5 µM, respectively. We showed for the first time that NaD1 could act synergistically not only with caspofungin but also with human host defense antimicrobial peptides cathelicidin LL-37 and β-defensin-2 (HBD2) against susceptible and resistant fungal strains. Using flow cytometry, we demonstrated that NaD1 in combinations with LL-37 or HBD2 can reinforce each other by enhancing membrane disruption. Using the Caco-2 cell monolayer model, we demonstrated that NaD1 impaired the adhesion of C. albicans cells to the human epithelium. Moreover, NaD1 inhibited the formation of fungal biofilms in Sabouraud broth and less markedly in nutrient-rich RPMI-1640 medium, and enhanced the antibiofilm activity of caspofungin. Thus, we hypothesized that NaD1 might affect the development of candidiasis in vivo, including that caused by resistant fungal strains.
{"title":"Effects of the Tobacco Defensin NaD1 Against Susceptible and Resistant Strains of <i>Candida albicans</i>.","authors":"Olga V Shevchenko, Alexander D Voropaev, Ivan V Bogdanov, Tatiana V Ovchinnikova, Ekaterina I Finkina","doi":"10.3390/pathogens13121092","DOIUrl":"https://doi.org/10.3390/pathogens13121092","url":null,"abstract":"<p><p>Today, <i>Candida albicans</i> is still the most common cause of both local and life-threatening systemic candidiasis. The spread of resistant fungal strains has resulted in an urgent need to search for new promising antimycotics. Here, we investigated the antifungal action of the tobacco defensin NaD1 against susceptible and resistant to azoles and echinocandins strains of <i>C. albicans</i>. We demonstrated that NaD1 was equally effective and fungicidal against all tested strains. The MIC and MFC values were 6.25 and 12.5 µM, respectively. We showed for the first time that NaD1 could act synergistically not only with caspofungin but also with human host defense antimicrobial peptides cathelicidin LL-37 and β-defensin-2 (HBD2) against susceptible and resistant fungal strains. Using flow cytometry, we demonstrated that NaD1 in combinations with LL-37 or HBD2 can reinforce each other by enhancing membrane disruption. Using the Caco-2 cell monolayer model, we demonstrated that NaD1 impaired the adhesion of <i>C. albicans</i> cells to the human epithelium. Moreover, NaD1 inhibited the formation of fungal biofilms in Sabouraud broth and less markedly in nutrient-rich RPMI-1640 medium, and enhanced the antibiofilm activity of caspofungin. Thus, we hypothesized that NaD1 might affect the development of candidiasis in vivo, including that caused by resistant fungal strains.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"13 12","pages":""},"PeriodicalIF":3.3,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11678012/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142952696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}