Olga G Ovchinnikova, Bin Liu, Dan Guo, Nina A Kocharova, Magdalena Bialczak-Kokot, Alexander S Shashkov, Lu Feng, Antoni Rozalski, Lei Wang, Yuriy A Knirel
{"title":"Structural, serological, and genetic characterization of the O-antigen of Providencia alcalifaciens O40.","authors":"Olga G Ovchinnikova, Bin Liu, Dan Guo, Nina A Kocharova, Magdalena Bialczak-Kokot, Alexander S Shashkov, Lu Feng, Antoni Rozalski, Lei Wang, Yuriy A Knirel","doi":"10.1111/1574-695X.12002","DOIUrl":"https://doi.org/10.1111/1574-695X.12002","url":null,"abstract":"<p><p>The O-polysaccharide chain of the lipopolysaccharide (O-antigen) on the bacterial cell surface is one of the most structurally variable cell components and serves as a basis for serotyping of Gram-negative bacteria, including human opportunistic pathogens of the genus Providencia. In this work, the O-antigen of Providencia alcalifaciens O40 was obtained by mild acid degradation of the isolated lipopolysaccharide and studied by chemical methods and high-resolution NMR spectroscopy. The following structure of the O-polysaccharide was established: →4)-β-D-Quip3NFo-(1→3)-α-D-Galp-(1→3)-β-D-GlcpA-(1→3)-β-D-GalpNAc-(1→, where GlcA stands for glucuronic acid and Qui3NFo for 3,6-dideoxy-3-formamidoglucose. The O40-antigen was found to be structurally and serologically related to the O-antigens of P. alcalifaciens O5 and Providencia stuartii O18. The O40-antigen gene cluster between cpxA and yibK was sequenced, and the gene functions were predicted in silico. In agreement with the O-polysaccharide structure established, the genes for the synthesis of dTDP-D-Qui3NFo, UDP-D-Gal, UDP-D-GlcA, and UDP-D-GalNAc as well as those encoding three glycosyltransferases, flippase (Wzx), and O-antigen polymerase (Wzy) were recognized. In addition, homologues of wza, wzb, and wzc genes, which are required for the surface expression of capsular polysaccharides, were found within the gene cluster, suggesting that the O-polysaccharide studied is a part of the capsule-related form of the lipopolysaccharide called K(LPS).</p>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2012-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/1574-695X.12002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31058183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Molecular characteristics of community-acquired, methicillin-resistant Staphylococcus aureus isolated from Chinese children.","authors":"Wenjing Geng, Yonghong Yang, Dejing Wu, Guoying Huang, Chuanqing Wang, Li Deng, Yuejie Zheng, Zhou Fu, Changcong Li, Yunxiao Shang, Changan Zhao, Sangjie Yu, Xuzhuang Shen","doi":"10.1111/j.1574-695X.2010.00648.x","DOIUrl":"https://doi.org/10.1111/j.1574-695X.2010.00648.x","url":null,"abstract":"<p><p>The aim of this study was to investigate the molecular characteristics of community-acquired, methicillin-resistant Staphylococcus aureus (CA-MRSA) isolates from Chinese children. Ninety-nine isolates were collected from eight hospitals, and analyzed by multilocus sequence typing, staphylococcal chromosomal cassette mec (SCCmec) type, and spa typing. The Panton-Valentine leukocidin (PVL) gene was also detected. Overall, 14 sequence types (STs) were obtained, and ST59 (58.6%) was found to be the most prevalent, followed by ST1 (8%) and ST338 (8%). We also first registered the new ST1409. SCCmec type IV was the most predominant type at 67.7%, followed by SCCmec type V at 32.3%. SCCmec subtypes IVa, IVc, and IVg were found among the SCCmec type IV strains. Twenty-one spa types were also identified. Four new spa types were found by synchronization with the Ridom SpaServer and referring to the website (http://www.SeqNet.org). ST59-MRSA-IVa with t437 accounted for 40.4% of occurrences, making it the most prevalent clone. The prevalence of PVL genes was 58.6%, and multidrug resistance was observed in 95% of all isolates. This result indicates that CA-MRSA isolates in Chinese children are largely associated with the ST59-MRSA-IV clone, and that the predominant clones of CA-MRSA are spread all over the country.</p>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1574-695X.2010.00648.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28693933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nicholas Morin, Chelsea Tirling, Sabine M Ivison, Ajinder Pal Kaur, James P Nataro, Theodore S Steiner
{"title":"Autoactivation of the AggR regulator of enteroaggregative Escherichia coli in vitro and in vivo.","authors":"Nicholas Morin, Chelsea Tirling, Sabine M Ivison, Ajinder Pal Kaur, James P Nataro, Theodore S Steiner","doi":"10.1111/j.1574-695X.2010.00645.x","DOIUrl":"https://doi.org/10.1111/j.1574-695X.2010.00645.x","url":null,"abstract":"<p><p>Enteroaggregative Escherichia coli (EAEC) causes diarrhea in diverse populations worldwide. The AraC-like regulator AggR is a key virulence regulator in EAEC. AggR-regulated genes include those encoding the Aggregative Adherence Fimbria, the dispersin protein, and a type VI secretion system. This study characterizes the regulation of the aggR promoter (P(aggR)). Using primer extension analysis, the transcriptional start site of the aggR promoter was located 40 nucleotides upstream of the translational start. P(aggR) was found to be autoregulated and DNA footprinting revealed the presence of two AggR-binding sites: one upstream of the transcriptional start site and one downstream. Additionally, P(aggR) was found to be positively regulated by the DNA-binding protein FIS and negatively regulated by the global regulator H-NS. To further understand this complex regulation scheme, a bacterial luciferase reporter system was used with a mouse model of EAEC colonization. This allowed for the in vivo measurement of P(aggR), P(fis), and P(hns) activity. EAEC present in the mouse intestine possessed relatively high levels of P(fis) and P(aggR) activity and a low level of P(hns) when compared with in vitro experiments. The data provide significant insights into the regulation cascade leading to aggR expression in the mammalian intestine during EAEC infection.</p>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1574-695X.2010.00645.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28693935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jiufeng Sun, Xiqing Li, Hanxiang Zeng, Zhi Xie, Changming Lu, Liyan Xi, Gert S de Hoog
{"title":"Development and evaluation of loop-mediated isothermal amplification (LAMP) for the rapid diagnosis of Penicillium marneffei in archived tissue samples.","authors":"Jiufeng Sun, Xiqing Li, Hanxiang Zeng, Zhi Xie, Changming Lu, Liyan Xi, Gert S de Hoog","doi":"10.1111/j.1574-695X.2010.00647.x","DOIUrl":"https://doi.org/10.1111/j.1574-695X.2010.00647.x","url":null,"abstract":"<p><p>Penicillium marneffei is the etiologic agent of a severe systemic disease in immunocompromised hosts in Southeast Asia. In the present study, a novel method, known as loop-mediated isothermal amplification (LAMP), is described for the rapid and specific detection of the species, using a primer set derived from the internal transcribed spacer (ITS) region of the rRNA gene. Amplification products can be detected macroscopically by visual inspection in vials using SYBR Green I as well as by electrophoresis on agarose gel. The LAMP assay resulted in specific amplification of P. marneffei ITS using pure cultures after a 1-h reaction at 65 degrees C in a water bath; no cross-reactivity with other fungi including other biverticillate penicillia was observed. The detectable DNA limit was two copies. In addition, specific amplification was achieved using paraffin wax-embedded tissue samples from patients with penicilliosis marneffei and tissue samples from bamboo rats. The method provides a powerful tool for rapid diagnostics in the clinical lab, and has potential for use in ecological studies.</p>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1574-695X.2010.00647.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28678938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Toni Aebischer, André Fischer, Anna Walduck, Cord Schlötelburg, Mirko Lindig, Sören Schreiber, Thomas F Meyer, Stefan Bereswill, Ulf B Göbel
{"title":"Vaccination prevents Helicobacter pylori-induced alterations of the gastric flora in mice.","authors":"Toni Aebischer, André Fischer, Anna Walduck, Cord Schlötelburg, Mirko Lindig, Sören Schreiber, Thomas F Meyer, Stefan Bereswill, Ulf B Göbel","doi":"10.1111/j.1574-695X.2005.00024.x","DOIUrl":"https://doi.org/10.1111/j.1574-695X.2005.00024.x","url":null,"abstract":"<p><p>Molecular analysis of the gastric microflora in mice revealed that Helicobacter pylori infection causes an increase in microbial diversity. The stomachs of H. pylori-infected animals were colonized by bacteria which are naturally restricted to the lower intestinal tract. Clostridia, Bacteroides/Prevotella spp., Eubacterium spp., Ruminococcus spp., streptococci and Escherichia coli were detected exclusively in the stomachs of infected animals, whereas lactobacilli dominated the gastric flora in noninfected mice. The H. pylori-induced shifts in the gastric microbiota were independent from histological pathology and from changes in the gastric pH but were prevented by immunization of mice with live Salmonella expressing H. pylori urease. Immunized mice displayed reduced H. pylori levels in the gastric epithelium and developed a normal gastric microflora, indicating that vaccination may be protective against H. pylori-induced changes in the gastric flora.</p>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1574-695X.2005.00024.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25864037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"HIV Chemotherapy: A Critical Review","authors":"A. Belkum","doi":"10.1111/J.1574-695X.2005.00042.X","DOIUrl":"https://doi.org/10.1111/J.1574-695X.2005.00042.X","url":null,"abstract":"Edited by Salvatore T. Butera. Caister Academic Press, Norwich, UK. Printed by Cromwell Press. British Library Cataloguing-in-Publication Data. ISBN 0-9542464-9-7.\u0000\u0000HIV Chemotherapy: A Critical Review is a multi-authored book covering a variety of subjects that are essential for clinical management of HIV-positive patients. In such a book one would expect, in addition to an adequate historic review, a complete overview of the current treatment strategies with definitions of timely gold-standard chemotherapeutic regimens. The historic aspects are excellently covered by well-known authors: detailed descriptions of historic patient management protocols, assessment of the relevance of drug resistance, implementation of treatment in developing countries. In the remaining chapters, novel antiviral procedures and compounds and their implications for future treatment are, again, well explained. The only historic features that are not fully described are those concerning therapeutic trials in the various animal …","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81444351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ralf Bialek , Gloria M. González , Dominik Begerow , Ulrike E. Zelck
{"title":"Coccidioidomycosis and blastomycosis: Advances in molecular diagnosis","authors":"Ralf Bialek , Gloria M. González , Dominik Begerow , Ulrike E. Zelck","doi":"10.1016/j.femsim.2005.05.011","DOIUrl":"10.1016/j.femsim.2005.05.011","url":null,"abstract":"<div><p>Clinical isolates of <em>Coccidioides</em> spp. and <span><em>Blastomyces dermatitidis</em></span><span> can be identified by chemiluminescent DNA probes<span> and PCR assays targeting multicopy genes. In fixed tissue samples, cells of the two fungi are specified by in situ hybridization<span><span> and PCR assays targeting 18S rDNA but sequencing of the products is mandatory. </span>Nested PCR<span> assays targeting genes encoding species- or genus-specific proteins like proline rich antigen of </span></span></span></span><em>Coccidioides</em> spp. and <em>B. dermatitidis</em><span><span> adhesin facilitate amplification of specific DNA from fixed tissue samples. The value of </span>DNA amplification<span><span> from native specimens of suspected cases of coccidioidomycosis or </span>blastomycosis still needs to be determined.</span></span></p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2005-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.05.011","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25211920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
George S. Kobayashi (Guest editors), Maria Lucia Taylor, Eduardo Dei-Cas
{"title":"Editorial: Molecular genetic approaches to the study of human pathogenic fungi","authors":"George S. Kobayashi (Guest editors), Maria Lucia Taylor, Eduardo Dei-Cas","doi":"10.1016/j.femsim.2005.06.004","DOIUrl":"10.1016/j.femsim.2005.06.004","url":null,"abstract":"","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2005-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.06.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25222153","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cristina Elena Canteros , María Fernanda Zuiani , Viviana Ritacco , Diego E. Perrotta , María Rocío Reyes-Montes , Julio Granados , Gerardo Zúñiga , Maria Lucia Taylor , Graciela Davel
{"title":"Electrophoresis karyotype and chromosome-length polymorphism of Histoplasma capsulatum clinical isolates from Latin America","authors":"Cristina Elena Canteros , María Fernanda Zuiani , Viviana Ritacco , Diego E. Perrotta , María Rocío Reyes-Montes , Julio Granados , Gerardo Zúñiga , Maria Lucia Taylor , Graciela Davel","doi":"10.1016/j.femsim.2005.05.015","DOIUrl":"10.1016/j.femsim.2005.05.015","url":null,"abstract":"<div><p>Intact chromosomes of 19 clinical isolates of <span><em>Histoplasma capsulatum</em></span> recently obtained in Argentina, Mexico and Guatemala and the laboratory reference strain G186B from Panama were analyzed using pulsed-field gel electrophoresis. Chromosomal banding patterns of the human isolates revealed 5–7 bands, ranging from 1.3 to 10<!--> <!-->Mbp in size. Strain G186B showed five bands of approximately 1.1, 2.8, 3.3, 5.4 and 9.7<!--> <!-->Mbp. Thirteen different electrokaryotypes were identified, indicating that the genome of <em>H. capsulatum</em> varies widely in nature, as observed previously in laboratory strains. No definite association was found between electrokaryotype and geographical or clinical source.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2005-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.05.015","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25225741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Emilie Fréalle , Christophe Noël , Eric Viscogliosi , Daniel Camus , Eduardo Dei-Cas , Laurence Delhaes
{"title":"Manganese superoxide dismutase in pathogenic fungi: An issue with pathophysiological and phylogenetic involvements","authors":"Emilie Fréalle , Christophe Noël , Eric Viscogliosi , Daniel Camus , Eduardo Dei-Cas , Laurence Delhaes","doi":"10.1016/j.femsim.2005.06.003","DOIUrl":"10.1016/j.femsim.2005.06.003","url":null,"abstract":"<div><p><span>Manganese-containing superoxide dismutases (MnSODs) are ubiquitous metalloenzymes involved in cell defence against endogenous and exogenous reactive oxygen species. In fungi, using this essential enzyme for phylogenetic analysis of </span><span><em>Pneumocystis</em></span> and <span><em>Ganoderma</em></span><span> genera, and of species selected among Ascomycota<span>, Basidiomycota and Zygomycota, provided interesting results in taxonomy and evolution. The role of mitochondrial and cytosolic MnSODs was explored in some pathogenic Basidiomycota yeasts (</span></span><span><em>Cryptococcus neoformans</em></span> var. <em>grubii</em>, <em>Cryptococcus neoformans</em> var. <em>gattii</em>, <span><em>Malassezia sympodialis</em></span><span>), Ascomycota filamentous fungi (</span><span><em>Aspergillus fumigatus</em></span>), and Ascomycota yeasts (<span><em>Candida albicans</em></span>). MnSOD-based phylogenetic and pathogenic data are confronted in order to evaluate the roles of fungal MnSODs in pathophysiological mechanisms.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2005-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.06.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25220354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}