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Volume 49(6); December 2011
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Research Support, Non-U.S. Gov'ts
Cupriavidus and Burkholderia Species Associated with Agricultural Plants that Grow in Alkaline Soils
Paulina Estrada-de los Santos , Nora Belinda Vacaseydel-Aceves , Lourdes Martínez-Aguilar , María Antonia Cruz-Hernández , Alberto Mendoza-Herrera , Jesús Caballero-Mellado
J. Microbiol. 2011;49(6):867-876.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1127-9
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AbstractAbstract PDF
The presence of Burkholderia, Cupriavidus, and Ralstonia species in northeastern Mexico was investigated. An analysis of the root surrounding soil from different agricultural plants led to the isolation of Burkholderia and Cupriavidus species but no Ralstonia strains. Most Cupriavidus species were unknown and grouped into two clusters according to ARDRA profiles. The 16S rRNA sequence analysis showed that the Cupriavidus isolates were highly related among them and with different Cupriavidus species with validated names. However, SDS-PAGE profiles were distinct among the different ARDRA profiles and to other Cupriavidus species examined, suggesting new species in the genus. This shows that Cupriavidus is more widely associated with plants than previously appreciated. The BCC isolate was 99% similar to B. cenocepacia by recA sequence analysis. Additionally, most Cupriavidus strains from the two largest groups grew on media containing up to 0.1 mg/ml of copper, 10.0 mg/ml arsenic and 1.0 mg/ml zinc. Burkholderia strains grew on media containing up to 10.0 mg/ml zinc, 5.0 mg/ml arsenic and 0.1 mg/ml copper.
Lactobacillus salivarius REN Counteracted Unfavorable 4-Nitroquinoline-1-Oxide-Induced Changes in Colonic Microflora of Rats
Ming Zhang , Xuewei Qiao , Liang Zhao , Lu Jiang , Fazheng Ren
J. Microbiol. 2011;49(6):877-883.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1137-7
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  • 11 Crossref
AbstractAbstract PDF
Probiotics and carcinogens both have a significant effect on the microfloral composition of the human intestine. The objective of this study was to investigate the impact of an important carcinogen, 4-Nitroquinoline-1- Oxide on colonic microflora and the efficacy of the probiotic Lactobacillus salivarius REN as an agent of counteracting these effects. Using denaturing gradient gel electrophoresis (DGGE) combined with redundancy analysis, we demonstrated that both 4-Nitroquinoline-1-Oxide and L. salivarius REN significantly altered the bacterial communities of rat colons. A total of 27 bacterial strains were identified as being affected by treatment with 4-Nitroquinoline-1-Oxide or L. salivarius REN using a t-value biplot combined with band sequencing. 4-Nitroquinoline-1-Oxide treatment increased the abundance of two potential pathogens (one Helicobacter strain and one Desulfovibrio strain), as well as reducing the abundance of two potentially beneficial strains (one Ruminococcaceae strain and one Rumen bacteria). The Helicobacter strain was initally detected in carcinogen-treated rat intestinal microflora, but L. salivarius REN treatment effectively suppressed the growth of the Helicobacter strain. These results suggested that L. salivarius REN may be a potential probiotic, efficiently acting against the initial infection with, and the growth of pathogenic bacteria.

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    Hao ZHANG, Jing SUN, Qing-yu WANG, Yu-tong HE, Hui-yong GU, Hui-yuan GUO, Qing-bo DING, Jun-si YANG, Fa-zheng REN
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    Mirko Rossi, Marja‐Liisa Hänninen
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The Use of Pseudomonas fluorescens P13 to Control Sclerotinia Stem Rot (Sclerotinia sclerotiorum) of Oilseed Rape
Hui Li , Huaibo Li , Yan Bai , Jing Wang , Ming Nie , Bo Li , Ming Xiao
J. Microbiol. 2011;49(6):884-889.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1261-4
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AbstractAbstract PDF
Sclerotinia stem rot (SSR) caused by the fungus Sclerotinia sclerotiorum has been an increasing threat to oilseed rape (Brassica napus L.) cultivation. Efficient and environment‐friendly treatments are much needed. Here we focus on microbial control. The Pseudomonas fluorescens P13 that was isolated from oilseed rape cultivation soil, proved to be a useful biocontrol strain for application. Morphology, physiological and biochemical tests and 16S rDNA analysis demonstrated that it was P. fluorescens P13 and that it had a broad antagonistic spectrum, significantly lessening the mycelial growth of S. sclerotiorum by 84.4% and suppressing sclerotial formation by 95‐100%. Scanning electron microscopy studies attested that P13 deformed S. sclerotiorum mycelia when they were cultured together. P13 did not produce chitinase but did produce hydrogen cyanide (HCN) which was likely one of the antagonistic mechanisms. The density of P13 remained at a high level (≥106 CFU/ml) during 5 weeks in the rhizosphere soil and roots. P13 reduced SSR severity at least by 59% in field studies and also promoted seedling growth (p<0.05) at the seedling stage. From these data, our work provided evidence that P13 could be a good alternative biological resource for biocontrol of S. sclerotiorum.
Complete Genome of Leptospirillum ferriphilum ML-04 Provides Insight into Its Physiology and Environmental Adaptation
Shuang Mi , Jian Song , Jianqun Lin , Yuanyuan Che , Huajun Zheng , Jianqiang Lin
J. Microbiol. 2011;49(6):890-901.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1099-9
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AbstractAbstract PDF
Leptospirillum ferriphilum has been identified as the dominant, moderately thermophilic, bioleaching microorganism in bioleaching processes. It is an acidic and chemolithoautrophic bacterium that gains electrons from ferrous iron oxidation for energy production and cell growth. Genetic information about this microorganism has been limited until now, which has hindered its further exploration. In this study, the complete genome of L. ferripilum ML-04 is sequenced and annotated. The bacterium has a single circular chromosome of 2,406,157 bp containing 2,471 coding sequences (CDS), 2 rRNA operons, 48 tRNA genes, a large number of mobile genetic elements and 2 genomic islands. In silico analysis shows L. ferriphilum ML-04 fixes carbon through a reductive citric acid (rTCA) cycle, and obtains nitrogen through ammonium assimilation. The genes related to “cell envelope biogenesis, outer membrane” (6.9%) and “DNA replication, recombination and repair” (5.6%) are abundant, and a large number of genes related to heavy metal detoxification, oxidative and acidic stress defense, and signal transduction pathways were detected. The genomic plasticity, plentiful cell envelope components, inorganic element metabolic abilities and stress response mechanisms found the base for this organism’s survival in the bioleaching niche.

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Characterization and Screening of Plant Probiotic Traits of Bacteria Isolated from Rice Seeds Cultivated in Argentina
Dante Ruiza , Betina Agaras , Patrice de Werrab , Luis G. Wall , Claudio Valverde
J. Microbiol. 2011;49(6):902-912.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1073-6
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AbstractAbstract PDF
Many seeds carry endophytes, which ensure good chances of seedling colonization. In this work, we have studied the seed-borne bacterial flora of rice varieties cultivated in the northeast of Argentina. Surface-sterilized husked seeds of the rice cultivars CT6919, El Paso 144, CAMBA, and IRGA 417 contained an average of 5×106 CFU/g of mesophilic and copiotrophic bacteria. Microbiological, physiological, and molecular characterization of a set of 39 fast-growing isolates from the CT6919 seeds revealed an important diversity of seed-borne mesophiles and potential plant probiotic activities, including diazotrophy and antagonism of fungal pathogens. In fact, the seed-borne bacterial flora protected the rice seedlings against Curvularia sp. infection. The root colonization pattern of 2 Pantoea isolates from the seeds was studied by fluorescence microscopy of the inoculated axenic rice seedlings. Both isolates strongly colonized the site of emergence of the lateral roots and lenticels, which may represent the entry sites for endophytic spreading. These findings suggest that rice plants allow grain colonization by bacterial species that may act as natural biofertilizers and bioprotectives early from seed germination.

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A Survey of the Geographic Distribution of Ophiocordyceps sinensis
Yi Li , Xiao-Liang Wang , Lei Jiao , Yi Jiang , Hui Li , Si-Ping Jiang , Ngarong Lhosumtseiring , Shen-Zhan Fu , Cai-Hong Dong , Yu Zhan , Yi-Jian Yao
J. Microbiol. 2011;49(6):913-919.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1193-z
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AbstractAbstract PDF
Ophiocordyceps sinensis is one of the best known fungi in Traditional Chinese Medicine. Many efforts have been devoted to locating the production areas of this species resulting in various reports; however, its geographic distribution remains incompletely understood. Distribution of O. sinensis at the county level is clarified in this work based on both a literature search and fieldwork. More than 3600 publications related to O. sinensis were investigated, including scientific papers, books, and online information. Herbarium specimens of O. sinensis and field collections made by this research group during the years 2000-2010 were examined to verify the distribution sites. A total of 203 localities for O. sinensis have been found, of which 106 are considered as confirmed distribution sites, 65 as possible distribution sites, 29 as excluded distribution sites and three as suspicious distribution sites. The results show that O. sinensis is confined to the Tibetan Plateau and its surrounding regions, including Tibet, Gansu, Qinghai, Sichuan, and Yunnan provinces in China and in certain areas of the southern flank of the Himalayas, in the countries of Bhutan, India and Nepal, with 3,000 m as the lowest altitude for the distribution. The fungus is distributed from the southernmost site in Yulong Naxi Autonomous County in northwestern Yunnan Province to the northernmost site in the Qilian Mountains in Qilian County, Qinghai Province, and from the east edge of the Tibetan Plateau in Wudu County, Gansu Province to the westernmost site in Uttarakhand, India. The clarification of the geographic distribution of O. sinensis will lay the foundation for conservation and sustainable use of the species.

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Journal Article
Assessment of Resistomycin, as an Anticancer Compound Isolated and Characterized from Streptomyces aurantiacus AAA5
Rajendran Vijayabharathi , Per Bruheim , Trygve Andreassen , Duraisamy Senthil Raja , Palanisamy Bruntha Devi , Sathyaseelan Sathyabama , Venkatesan Brindha Priyadarisini
J. Microbiol. 2011;49(6):920-926.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1260-5
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AbstractAbstract PDF
A new actinomycete strain, isolated from humus soils in the Western Ghats, was found to be an efficient pigment producer. The strain, designated AAA5, was identified as a putative Streptomyces aurantiacus strain based on cultural properties, morphology, carbon source utilization, and analysis of the 16S rRNA gene. The strain produced a reddish-brown pigmented compound during the secondary metabolites phase. A yellow compound was derived from the extracted pigment and was identified as the quinone-related antibiotic resistomycin based on ultraviolet–visible spectrophotometry, fourier transform infrared spectroscopy, liquid chromatography and mass spectroscopy, and nuclear magnetic resonance analyses. The AAA5 strain was found to produce large quantities of resistomycin (52.5 mg/L). It showed potent cytotoxic activity against cell lines viz. HepG2 (hepatic carcinoma) and HeLa (cervical carcinoma) in vitro, with growth inhibition (GI50) of 0.006 and 0.005 μg/ml, respectively. The strain also exhibited broad antimicrobial activities against both Gram-positive and Gram-negative bacteria. Therefore, AAA5 may have great potential as an industrial resistomycin-producing strain.

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Research Support, Non-U.S. Gov'ts
Comparative Genomic Analysis of Bacteriophage EP23 Infecting Shigella sonnei and Escherichia coli
Ho-Won Chang , Kyoung-Ho Kim
J. Microbiol. 2011;49(6):927-934.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1577-0
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AbstractAbstract PDF
Bacteriophage EP23 that infects Escherichia coli and Shigella sonnei was isolated and characterized. The bacteriophage morphology was similar to members of the family Siphoviridae. The 44,077 bp genome was fully sequenced using 454 pyrosequencing. Comparative genomic and phylogenetic analyses showed that EP23 was most closely related to phage SO-1, which infects Sodalis glossinidius and phage SSL-2009a, which infects engineered E. coli. Genomic comparison indicated that EP23 and SO-1 were very similar with each other in terms of gene order and amino acid similarity, even though their hosts were separated in the level of genus. EP23 and SSL-2009a displayed high amino acid similarity between their genes, but there was evidence of several recombination events in SSL-2009a. The results of the comparative genomic analyses further the understanding of the evolution and relationship between EP23 and its bacteriophage relatives.
Identification, Origin, and Evolution of Leaf Nodulating Symbionts of Sericanthe (Rubiaceae)
Benny Lemaire , Elmar Robbrecht , Braam van Wyk , Sandra Van Oevelen , Brecht Verstraete , Els Prinsen , Erik Smets , Steven Dessein
J. Microbiol. 2011;49(6):935-941.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1163-5
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AbstractAbstract PDF
Bacterial leaf symbiosis is an intimate association between bacteria and plants in which endosymbionts are housed within leaf nodules. This phenomenon has been reported in three genera of Rubiaceae (Pavetta, Psychotria, and Sericanthe), but the bacterial partner has only been identified in Psychotria and Pavetta. Here we report the identification of symbiotic bacteria in two leaf nodulating Sericanthe species. Using 16S rRNA data and common housekeeping genetic markers (recA and gyrB) we studied the phylogenetic relationships of bacterial endosymbionts in Rubiaceae. Endosymbionts of leaf nodulating Rubiaceae were found to be closely related and were placed as a monophyletic group within the genus Burkholderia (β-Proteobacteria). The phylogenetic analyses revealed a pattern of strict host specificity and placed the two investigated endosymbionts at two distinct positions in the topology of the tree, suggesting at least two different evolutionary origins. The degree of sequence divergence between the Sericanthe endosymbionts and their relatives was large enough to propose the Sericanthe endosymbionts as new species (‘Candidatus Burkholderia andongensis’ and ‘Candidatus Burkholderia petitii’). In a second part of this study, the pylogenetic relationships among nodulating and non-nodulating Sericanthe species were investigated using sequence data from six chloroplast regions (rps16, trnG, trnL-trnF, petD, petA-psbJ, and atpI-atpH). Overall, genetic variation among the plastid markers was insufficient to enable phylogenetic estimation. However, our results could not rule out the possibility that bacterial leaf symbiosis originated once in a common ancestor of the Sericanthe species.

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Isolation and Identification of Lipopeptide Antibiotics from Paenibacillus elgii B69 with Inhibitory Activity Against Methicillin-Resistant Staphylococcus aureus
Rui Ding , Xue-Chang Wu , Chao-Dong Qian , Yi Teng , Ou Li , Zha-Jun Zhan , Yu-Hua Zhao
J. Microbiol. 2011;49(6):942-949.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1153-7
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AbstractAbstract PDF
Two lipopeptide antibiotics, pelgipeptins C and D, were isolated from Paenibacillus elgii B69 strain. The molecular masses of the two compounds were both determined to be 1,086 Da. Mass-spectrometry, amino acid analysis and NMR spectroscopy indicated that pelgipeptin C was the same compound as BMY-28160, while pelgipeptin D was identified as a new antibiotic of the polypeptin family. These two peptides were active against all the tested microorganisms, including antibiotic-resistant pathogenic bacterial strains such as methicillin-resistant Staphylococcus aureus (MRSA). Time-kill assays demonstrated that pelgipeptin D exhibited rapid and effective bactericidal action against MRSA at 4×MIC. Based on acute toxicity test, the intraperitoneal LD50 value of pelgipeptin D was slightly higher than that of the structurally related antimicrobial agent polymyxin B. Pelgipeptins are highly potent antibacterial and antifungal agents, particularly against MRSA, and warrant further investigation as possible therapeutic agents for bacteria infections resistant to currently available antibiotics.

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Expression of the Lactobacillus plantarum malE Gene Is Regulated by CcpA and a MalR-Like Protein
Lidia Muscariello , Valeria Vastano , Rosa A. Siciliano , Margherita Sacco , Rosangela Marasco
J. Microbiol. 2011;49(6):950-955.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-0495-5
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AbstractAbstract PDF
Lactobacillus plantarum is commonly used in the food industry as a starter in various fermentations, especially in vegetable fermentations, in which starch is a common substrate. This polysaccharide, which is obtained from potatoes or corn and is hydrolysed mainly to maltose and glucose by acids or enzymes, is commercially used for the production of lactate by lactic acid fermentation. In this study, we describe the regulation of malE gene expression in L. plantarum. This gene, located in a 7-gene cluster, probably organized in an operon, encodes a putative maltose/maltodextrin-binding protein. We studied the expression of malE in L. plantarum LM3 (wild type) and in LM3-2 (ccpA1), which carries a null mutation in the ccpA gene, encoding the catabolite control protein A (CcpA). In the presence of glucose, expression of the MalE protein was higher in the mutant strain as compared to that in the wild-type strain. Transcription of the malE gene was induced by maltose and regulated by a CcpA-mediated carbon catabolite repression. Further, we isolated strains carrying mutations in 2 genes, lp_0172 and lp_0173, whose deduced amino acid sequences share significant identity with MalR, a regulator of the maltose operon in several gram-positive bacteria. A double mutant exhibited glucose-insensitive malE transcription, while absence of the functional Lp_0172 open reading frame had no effect on malE expression.
Responses in the Expression of Extracellular Proteins in Methicillin-Resistant Staphylococcus aureus Treated with Rhodomyrtone
Monton Visutthi , Potjanee Srimanote , Supayang Piyawan Voravuthikunchai
J. Microbiol. 2011;49(6):956-964.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1115-0
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AbstractAbstract PDF
Rhodomyrtone from a medicinal plant species, Rhodomyrtus tomentosa, is a challenged effective agent against Gram-positive bacteria, especially methicillin-resistant Staphylococcus aureus (MRSA). The present study was undertaken to provide insight into MRSA extracellular protein expression following rhodomyrtone treatment. Secreteomic approach was performed on a representative clinical MRSA isolate exposing to subinhibitory concentration rhodomyrtone (0.174 μg/ml). The identified extracellular proteins of a response of MRSA to rhodomyrtone treated condition were both suppressed and overexpressed. Staphylococcal antigenic proteins, immunodominant antigen A (IsaA) and staphylococcal secretory antigen (SsaA) involved in cell wall hydrolysis were downregulated after the treatment. The results suggested that rhodomyrtone may interfere with WalK/WalR (YycG/YycF) system. Other enzymes such as lipase precursor and another lipase, glycerophosphoryl diester phosphodiesterase, were absent. In contrast, cytoplasmic proteins such as SpoVG and glycerol phosphate lipoteichoic acid synthase, and ribosomal proteins were found in the treated sample. Appearance of several cytoplasmic proteins in the treated culture supernatant revealed that the bacterial cell wall biosynthesis was disturbed. This finding provides a proteomic mapping of extracellular proteins after rhodomytone treatment. Extensive investigation is required for this natural compound as it has a great potency as an alternative anti-MRSA drug.

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    International Journal of Molecular Sciences.2016; 17(5): 617.     CrossRef
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    S. Águila-Arcos, S. Ding, K. Aloria, J. M. Arizmendi, I. M. Fearnley, J. E. Walker, F. M. Goñi, I. Alkorta
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    Yeong-Hwan Han
    The Korean Journal of Microbiology.2015; 51(4): 444.     CrossRef
  • Rhodomyrtals A–D, four unusual phloroglucinol-sesquiterpene adducts from Rhodomyrtus psidioides
    Qingyao Shou, Joshua E. Smith, Htwe Mon, Zlatko Brkljača, Ana-Sunčana Smith, David M. Smith, Hans J. Griesser, Hans Wohlmuth
    RSC Adv..2014; 4(26): 13514.     CrossRef
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    Sukanlaya Leejae, Peter William Taylor, Supayang Piyawan Voravuthikunchai
    Journal of Medical Microbiology.2013; 62(1): 78.     CrossRef
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    Sukanlaya Leejae, Laila Hasap, Supayang Piyawan Voravuthikunchai
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Dynamical Analysis of Yeast Protein Interaction Network During the Sake Brewing Process
Mitra Mirzarezaee , Mehdi Sadeghi , Babak N. Araabi
J. Microbiol. 2011;49(6):965-973.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1194-y
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AbstractAbstract PDF
Proteins interact with each other for performing essential functions of an organism. They change partners to get involved in various processes at different times or locations. Studying variations of protein interactions within a specific process would help better understand the dynamic features of the protein interactions and their functions. We studied the protein interaction network of Saccharomyces cerevisiae (yeast) during the brewing of Japanese sake. In this process, yeast cells are exposed to several stresses. Analysis of protein interaction networks of yeast during this process helps to understand how protein interactions of yeast change during the sake brewing process. We used gene expression profiles of yeast cells for this purpose. Results of our experiments revealed some characteristics and behaviors of yeast hubs and non-hubs and their dynamical changes during the brewing process. We found that just a small portion of the proteins (12.8 to 21.6%) is responsible for the functional changes of the proteins in the sake brewing process. The changes in the number of edges and hubs of the yeast protein interaction networks increase in the first stages of the process and it then decreases at the final stages.

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  • Synergistic regulation mechanism of iperoxo and LY2119620 for muscarinic acetylcholine M2 receptor
    Quan Li, Hai-Feng Chen
    RSC Advances.2018; 8(24): 13067.     CrossRef
Molecular Characterization of Chloranilic Acid Degradation in Pseudomonas putida TQ07
Luis G. Treviño-Quintanilla , Julio A. Freyre-González , Rosa A. Guillén-Garcés , Clarita Olvera
J. Microbiol. 2011;49(6):974-980.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1507-1
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AbstractAbstract PDF
Pentachlorophenol is the most toxic and recalcitrant chlorophenol because both aspects are directly proportional to the halogenation degree. Biological and abiotic pentachlorophenol degradation generates p-chloranil, which in neutral to lightly alkaline environmental conditions is hydrolyzed to chloranilic acid that present a violet-reddish coloration in aqueous solution. Several genes of the degradation pathway, cadR-cadCDX, as well as other uncharacterized genes (ORF5 and 6), were isolated from a chloranilic acid degrading bacterium, Pseudomonas putida strain TQ07. The disruption by random mutagenesis of the cadR and cadC genes in TQ07 resulted in a growth deficiency in the presence of chloranilic acid, indicating that these genes are essential for TQ07 growth with chloranilic acid as the sole carbon source. Complementation assays demonstrated that a transposon insertion in mutant CAD82 (cadC) had a polar effect on other genes contained in cosmid pLG3562. These results suggest that at least one of these genes, cadD and cadX, also takes part in chloranilic acid degradation. Based on molecular modeling and function prediction, we strongly suggest that CadC is a pyrone dicarboxylic acid hydrolase and CadD is an aldolase enzyme like dihydrodipicolinate synthase. The results of this study allowed us to propose a novel pathway that offers hypotheses on chloranilic acid degradation (an abiotic by-product of pentachlorophenol) by means of a very clear phenotype that is narrowly related to the capability of Pseudomonas putida strain TQ07 to degrade this benzoquinone.

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  • Insights into the generation of hydroxyl radicals from H2O2 decomposition by the combination of Fe2+ and chloranilic acid
    M. I. Ahmad, N. Bensalah
    International Journal of Environmental Science and Technology.2022; 19(10): 10119.     CrossRef
  • Effective synthesis of sulfate metabolites of chlorinated phenols
    Hans-Joachim Lehmler, Xianran He, Xueshu Li, Michael W. Duffel, Sean Parkin
    Chemosphere.2013; 93(9): 1965.     CrossRef
Shift of Phylogenic Position in Megalocytiviruses Based on Three Different Genes
Se Ryun Kwon , Toyohiko Nishizawa , Jong-Won Park , Myung-Joo Oh
J. Microbiol. 2011;49(6):981-986.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1500-8
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AbstractAbstract PDF
Major capsid protein (MCP), the adenosine triphosphatase (ATPase), and the PstI fragment genes from five Japanese and three Korean megalocytivirus isolates were sequenced and phylogenetically analyzed with known megalocytiviruses. Phylogenetic trees formed three major clusters (M1, M2, and M3 or P1, P2, and P3), and genogroup I was divided into two minor clusters (M1a/M1b and P1a/P1b) using three target genes. Sequence identity was >97% within each cluster, except cluster II of the PstI fragment (>94% of sequence identity). Interestingly, different genotyping patterns were observed for the same isolates depending on the gene analyzed. The JPN-YelTail and JPN-BfTuna isolates located in the minor M1a cluster, based on MCP and ATPase nucleotide sequences, appeared in the minor P1b cluster based on the PstI fragment, suggesting a shift of phylogenic position in megalocytiviruses. Further study will be conducted to compare the viral antigenicity and pathogenicity between the two isolates showing the shift of phylogenic position and the other isolates clustered within genogroup I.

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  • Analysis of the transcriptomic profiles of Mandarin fish (Siniperca chuatsi) infected with red sea bream iridovirus (RSIV)
    Yanbing Zhang, Chunjie Zhang, Zheling Zhang, Wei Sun, Xiaojun Zhang, Xiaodan Liu
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    AA Fonseca, M Laguardia-Nascimento, AP Scotá Ferreira, CA Pinto, TR Pereira Freitas, AV Rivetti Júnior, VS Ferreira Homem, MF Camargos
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    So-Young Oh, Toyohiko Nishizawa
    Journal of Virological Methods.2016; 238: 1.     CrossRef
  • Potential for a live red seabream iridovirus (RSIV) vaccine in rock bream Oplegnathus fasciatus at a low rearing temperature
    So-Young Oh, Myung-Joo Oh, Toyohiko Nishizawa
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    Fan Shuang, Yongwen Luo, Xiao-peng Xiong, Shaoping Weng, Yiming Li, Jianguo He, Chuanfu Dong
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Frequency of Antibiotic Resistance in Helicobacter pylori Strains Isolated from the Northern Population of Iran
Amin Talebi Bezmin Abadi , Tarang Taghvaei , Ashraf Mohabbati Mobarez , Beth M. Carpenter , D. Scott Merrell
J. Microbiol. 2011;49(6):987-993.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1170-6
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AbstractAbstract PDF
The purpose of this study was to evaluate the primary resistance rates of recent clinical Helicobacter pylori isolates to the most commonly used antibiotics in Iran. Two hundreds and ten patients presenting with gastric maladies between January and July of 2009 were enrolled in this study. Endoscopy was performed, and biopsy specimens were collected from each patient for subsequent bacterial culture of H. pylori. Single colony isolates from each patient were then used for antimicrobial susceptibility testing. The disk diffusion method was used to determine susceptibility patterns. One hundred and ninety-seven of the patients were H. pylori positive (93.8%). The rates of resistance to tetracycline, amoxicillin, ciprofloxacin, metronidazole, clarithromycin, and furizoladone were 37.1%, 23.9%, 34.5%, 65.5%, 45.2%, and 61.4%, respectively. A significant association between amoxicillin resistance and disease state (P<0.05) was identified. Furthermore, some double, triple, quadruple, and quintuple combinations of antibiotic resistance were found to be associated with disease state. This study evaluated the prevalence of H. pylori resistance to the most commonly prescribed antibiotics used in Iran and showed that resistance rates were generally higher than previously reported. This data adds to the growing body of evidence that suggests there is increasing antibiotic resistance among H. pylori isolates, which likely is responsible for the decreasing efficacy of anti-H. pylori therapy at the local and global level. Hence, there is a need for continued monitoring of resistance patterns, especially at the local level, and for incorporation of that information into treatment regimens for H. pylori infections.

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Antibacterial Efficacy of Lytic Pseudomonas Bacteriophage in Normal and Neutropenic Mice Models
Birendra R. Tiwari , Shukho Kim , Marzia Rahman , Jungmin Kim
J. Microbiol. 2011;49(6):994-999.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1512-4
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AbstractAbstract PDF
Recently, lytic bacteriophages (phages) have been focused on treating bacterial infectious diseases. We investigated the protective efficacy of a novel Pseudomonas aeruginosa phage, PA1Ø, in normal and neutropenic mice. A lethal dose of P. aeruginosa PAO1 was administered via the intraperitoneal route and a single dose of PA1Ø with different multiplicities of infection (MOI) was treated into infected mice. Immunocompetent mice infected with P. aeruginosa PAO1 were successfully protected by PA1Ø of 1 MOI, 10 MOI or 100 MOI with 80% to 100% survival rate. No viable bacteria were found in organ samples after 48 h of the phage treatment. Phage clearing patterns were different in the presence or absence of host bacteria but PA1Ø disappeared from all organs after 72 h except spleen in the presence of host bacteria. On the contrary, PA1Ø treatment could not protect neutropenic mice infected with P. aeruginosa PAO1 even though could extend their lives for a short time. In in vitro phage-neutrophil bactericidal test, a stronger bactericidal effect was observed in phage-neutrophil co-treatment than in phage single treatment without neutrophils, suggesting phage-neutrophil co-work is essential for the efficient killing of bacteria in the mouse model. In conclusion, PA1Ø can be possibly utilized in future phage therapy endeavors since it exhibited strong protective effects against virulent P. aeruginosa infection.

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Functional Definition of LuxS, an Autoinducer-2 (AI-2) Synthase and Its Role in Full Virulence of Streptococcus suis Serotype 2
Min Cao , Youjun Feng , Changjun Wang , Feng Zheng , Ming Li , Hui Liao , Yinghua Mao , Xiuzhen Pan , Jing Wang , Dan Hu , Fuquan Hu , Jiaqi Tang
J. Microbiol. 2011;49(6):1000-1011.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1523-1
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AbstractAbstract PDF
Quorum sensing is a widespread chemical communication in response to fluctuation of bacterial population density, and has been implicated into bacterial biofilm formation and regulation of expression of virulence factors. The luxS gene product, S-ribosylhomocysteinase, catalizes the last committed step in biosynthetic pathway of autoinducer 2 (AI-2), a signaling molecule for inter-species quorum sensing. We found a luxS homologue in 05ZYH33, an epidemic strain of Streptococcus suis serotype 2 (SS2) in China. A luxS null mutant (ΔluxS) of 05ZYH33 strain was obtained using an approach of homologous recombination. LuxS was determined to be required for AI-2 production in 05ZYH33 strain of S. suis 2. Inactivation of luxS gene led to a wide range of phenotypic changes including thinner capsular walls, increased tolerance to H2O2, reduced adherence capacity to epithelial cells, etc. In particular, loss of LuxS impaired dramatically its full virulence of SS2 in experimental model of piglets, and functional complementation restored it nearly to the level of parent strain. Genome-wide transcriptome analyses suggested that some known virulence factors such as CPS are down-regulated in the ΔluxS mutant, which might in part explain virulence attenuation by luxS deletion. Similarly, 29 of 71 genes with different expression level were proposed to be targets candidate regulated by LuxS/AI-2-dependent quorum sensing.

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NOTE] Functional Analysis of a Hansenula polymorpha MNN2-2 Homologue Encoding a Putative UDP-N-acetylglucosamine Transporter Localized in the Endoplasmic Reticulum
Jeong-Nam Park , Jinho Choo , Hyun Ah Kang
J. Microbiol. 2011;49(6):1012-1017.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1520-4
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AbstractAbstract PDF
The Kluyveromyces lactis UDP-GlcNAc transporter (KlMnn2-2p) is responsible for the biosynthesis of N-glycans containing N-acetylglucosamine. A putative gene of Hansenula polymorpha encoding a KlMnn2-2p homologue, HpMNN2-2, was identified and investigated for its function. The deletion mutant strain of HpMNN2-2 (Hpmnn2-2Δ) showed increased sensitivity to geneticin, hygromycin B, and tunicamycin. However, the Hpmnn2-2Δ strain exhibited increased resistance to Calcofluor white, an inhibitor of chitin biosynthesis, along with a reduced chitin content. The localization of HpMnn2-2p at the endoplasmic reticulum-enriched membrane, different from the Golgi localization of a K. lactis homologue, further supports the involvement of HpMnn2-2p in cell wall chitin biosynthesis.

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    Yizhou Gao, Xiaohui Xiong, Hui Wang, Jiajing Wang, Yan Bi, Yuqing Yan, Zhongye Cao, Dayong Li, Fengming Song
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    João Heitor Colombelli Manfrão-Netto, Enzo Bento Queiroz, Kelly Assis Rodrigues, Cintia M. Coelho, Hugo Costa Paes, Elibio Leopoldo Rech, Nádia Skorupa Parachin
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    Seon Ah Cheon, Hyunah Kim, Doo-Byoung Oh, Ohsuk Kwon, Hyun Ah Kang
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NOTE] Detection of a Unique Fibrinolytic Enzyme in Aeromonas sp. JH1
Han-Young Cho , Min Jeong Seo , Jeong Uck Park , Byoung Won Kang , Gi-Young Kim , Woo Hong Joo , Young-Choon Lee , Yong Kee Jeong
J. Microbiol. 2011;49(6):1018-1021.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1376-7
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AbstractAbstract PDF
A fibrinolytic enzyme was found in a Gram-negative bacterium, Aeromonas sp. JH1. SDS-PAGE and fibrinzymography showed that it was a 36 kDa, monomeric protein. Of note, the enzyme was highly specific for fibrinogen molecules and the hydrolysis rate of fibrinogen subunits was highest for α, β, and γ chains in that order. The first 15 amino acids of N-terminal sequence were X-D-A-T-G-P-G-G-N-V-X-T-G-K-Y, which was distinguishable from other fibrinolytic enzymes. The optimum pH and temperature of the enzyme were approximately 8.0 and 40°C, respectively. Therefore, these results provide a fibrinolytic enzyme with potent thrombolytic activity from the Aeromonas genus.

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  • Purification and Characterization of a Fibrinolytic Enzyme from Marine Bacillus velezensis Z01 and Assessment of Its Therapeutic Efficacy In Vivo
    Yuting Zhou, Huizhen Chen, Bo Yu, Guiguang Chen, Zhiqun Liang
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    Shihai Huang, Shihan Pan, Guiguang Chen, Shan Huang, Zhaofeng Zhang, Yan Li, Zhiqun Liang
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NOTE] Gramella jeungdoensis sp. nov., Isolated from a Solar Saltern in Korea
Yochan Joung , Haneul Kim , Taeyong Jang , Tae-Seok Ahn , Kiseong Joh
J. Microbiol. 2011;49(6):1022-1026.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1192-0
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AbstractAbstract PDF
A non-motile, Gram- stain-negative, yellow pigmented, rod-shaped bacterium, strain HMD3159T, was isolated from a solar saltern in Korea. The major fatty acids were iso-C15:0 (26.3%), iso-C17:0 3OH (12.1%), iso-C16:0 (12.0%), summed feature 3 (comprising C16:1 ω7c and/or C16:1 ω6c; 11.0%) and summed feature 9 (iso-C17:1 ω9c and/or 10-methyl C16:0; 10.0%). The major respiratory quinone was MK-6. The DNA G+C content was 40.9 mol%. The phylogenetic tree based on 16S rRNA gene sequences showed that strain HMD3159T formed a lineage within the genus Gramella and closely related to Gramella gaetbulicola (95.5% sequence similarity), Gramella portivictoriae (94.9%), Gramella echinicola (94.6%), and Gramella marina (93.6%). On the basis of the evidence presented in this study, strain HMD3159T represents a novel species of the genus Gramella, for which the name Gramella jeungdoensis sp. nov., is proposed. The type strain is HMD3159T (=KCTC 32123T =CECT 7683T).

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    Lin Yang, Haolei Shi, Qian Li, Minggang Zheng, Qiliang Lai, Li Zheng
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    Hui-Jing Niu, Kai-Shi Dong, Li Guan, Li-Ping Sun, Qin Wang, Yan-Jiao Zhang, Yi Li, Cheng-Qiang Xia, Cai-Xia Pei
    International Journal of Systematic and Evolutionary Microbiology.2022;[Epub]     CrossRef
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    Kristin M Rath, Noah Fierer, Daniel V Murphy, Johannes Rousk
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    Sae Hyun Hwang, Woon Mo Hwang, Keunsoo Kang, Tae-Young Ahn
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    An-zhang Li, Xi-bin Han, Long-zhen Lin, Ming-xia Zhang, Hong-hui Zhu
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    Jaewoo Yoon, Yujin Jo, Geum Jin Kim, Hyukjae Choi
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    Mariyam Shahina, Asif Hameed, Shih-Yao Lin, Ren-Jye Lee, Maw-Rong Lee, Chiu-Chung Young
    Antonie van Leeuwenhoek.2014; 105(4): 771.     CrossRef
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    Asif Hameed, Mariyam Shahina, Shih-Yao Lin, You-Cheng Liu, Wei-An Lai, Chiu-Chung Young
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NOTE] Bacillus manliponensis sp. nov., a New Member of the Bacillus cereus Group Isolated from Foreshore Tidal Flat Sediment
Min Young Jung , Joong-Su Kim , Woon Kee Paek , Jeongheui Lim , Hansoo Lee , Pyoung Il Kim , Jin Yeul Ma , Wonyong Kim , Young-Hyo Chang
J. Microbiol. 2011;49(6):1027-1032.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1049-6
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AbstractAbstract PDF
A Gram-positive, endospore-forming, new Bacillus species, strain BL4-6T, was isolated from tidal flat sediment of the Yellow Sea. Strain BL4-6T is a straight rod, with motility by peritrichate flagella. The cell wall contains meso-diaminopimelic acid, and the major respiratory quinone is menaquinone-7. The major fatty acids are iso-C15:0 and summed feature 3 (containing C16:1 ω7c/ iso-C15:0 2OH, and/or iso-C15:0 2OH/C16:1 ω7c). Cells are catalase-positive and oxidase-negative. The G+C content of the genomic DNA is 38.0 mol%. Based on a comparative 16S rRNA gene sequence analysis, the isolate belongs to the genus Bacillus, forms a clade with the Bacillus cereus group, and is closely related to Bacillus mycoides (98.5%), Bacillus cereus (98.5%), Bacillus anthracis (98.4%), Bacillus thuringiensis (98.4%), Bacillus weihenstephanensis (98.1%), and Bacillus pseudomycoides (97.5%). The isolate showed less than 85% similarity of the gyrA gene sequence and below 95% similarity of the rpoB gene sequence to the members of this group. DNA-DNA relatedness between strain BL4-6T and B. cereus group was found to be in a range of 22.8-42.3%, and thus BL4-6T represents a unique species. On the basis of these studies, strain BL4-6T (=KCTC 13319T =JCM 15802T) is proposed to represent the type strain of a novel species, Bacillus manliponensis sp. nov.

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NOTE] Cohnella soli sp. nov. and Cohnella suwonensis sp. nov. Isolated from Soil Samples in Korea
Soo-Jin Kim , Hang-Yeon Weon , Yi-Seul Kim , Soon-Wo Kwon
J. Microbiol. 2011;49(6):1033-1038.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1071-8
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AbstractAbstract PDF
Two bacterial isolates from soil samples taken in Korea, strains YM2-7T and WD2-19T, were characterized using a polyphasic approach. The cells were strictly aerobic, Gram-positive, motile with peritrichous flagella, and rod-shaped. Both strains formed ellipsoidal bulging positioned subterminal spores. Phylogenetic analysis of their 16S rRNA gene sequences revealed a clear affiliation with the Firmicutes. The 16S rRNA gene sequence similarity between YM2-7T and WD2-19T was 96.5%. Strains YM2-7T and WD2-19T showed 16S rRNA gene sequence similarities of 93.0-96.5% to type strains of recognized Cohnella species. The G+C contents of the DNA of strains YM2-7T and WD2-19T were 52.2 and 55.6 mol%, respectively. The major fatty acids of strains YM2-7T and WD2-19T were anteiso-C15:0 (44.4%), C16:0 (19.2%), and iso-C16:0 (16.8%) and anteiso-C15:0 (46.5%), iso-C16:0 (21.8%), and C16:0 (11.2%), respectively. Both strains contained menaquinone with seven isoprene units (MK-7) as the predominant quinone. Both strains had diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine and lysophosphatidylglycerol as the major polar lipids. Comparative analysis of phenotypic and phylogenetic traits indicated that strains YM2-7T and WD2-19T represented two novel species of the genus Cohnella. The names Cohnella soli sp. nov. (type strain YM2-7T =KACC 13346T =NBRC 106486T), and Cohnella suwonensis sp. nov. (type strain WD2-19T =KACC 13347T =NBRC 106485T) are proposed for these organisms.

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    Antonie van Leeuwenhoek.2019; 112(7): 1029.     CrossRef
  • Cohnella faecalis sp. nov., isolated from animal faeces in a karst cave
    Hai-Zhen Zhu, Xiao-Dong Liu, Cheng-Ying Jiang, Shuang-Jiang Liu
    International Journal of Systematic and Evolutionary Microbiology.2019; 69(2): 572.     CrossRef
  • Cohnella lubricantis sp. nov., isolated from a coolant lubricant solution
    Peter Kämpfer, Stefanie P. Glaeser, Hans-Jürgen Busse
    International Journal of Systematic and Evolutionary Microbiology .2017; 67(2): 466.     CrossRef
  • Airborne bacteria associated with corrosion of mild steel 1010 and aluminum alloy 1100
    Aruliah Rajasekar, Wang Xiao, Manivannan Sethuraman, Punniyakotti Parthipan, Punniyakotti Elumalai
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  • Cohnella capsici sp. nov., a novel nitrogen-fixing species isolated from Capsicum annuum rhizosphere soil, and emended description of Cohnella plantaginis
    Li-Ying Wang, Tian-Shu Wang, San-Feng Chen
    Antonie van Leeuwenhoek.2015; 107(1): 133.     CrossRef
  • Cohnella collisoli sp. nov., isolated from lava forest soil
    Keun Chul Lee, Kwang Kyu Kim, Jong-Shik Kim, Dae-Shin Kim, Suk-Hyung Ko, Seung-Hoon Yang, Jung-Sook Lee
    International Journal of Systematic and Evolutionary Microbiology .2015; 65(Pt_9): 3125.     CrossRef
  • Cohnella nanjingensis sp. nov., an extracellular polysaccharide-producing bacterium isolated from soil
    Zhi Huang, Ya-jun Yu, Yuan-yuan Bao, Li Xia, Xia-fang Sheng, Lin-yan He
    International Journal of Systematic and Evolutionary Microbiology .2014; 64(Pt_9): 3320.     CrossRef
  • Cohnella lupini sp. nov., an endophytic bacterium isolated from root nodules of Lupinus albus
    José David Flores-Félix, Lorena Carro, Martha-Helena Ramírez-Bahena, Carmen Tejedor, José M. Igual, Alvaro Peix, Encarna Velázquez
    International Journal of Systematic and Evolutionary Microbiology .2014; 64(Pt_1): 83.     CrossRef
  • Cohnella formosensis sp. nov., a xylanolytic bacterium isolated from the rhizosphere of Medicago sativa L
    Asif Hameed, Mei-Hua Hung, Shih-Yao Lin, Yi-Han Hsu, You-Cheng Liu, Mariyam Shahina, Wei-An Lai, Hsin-Chieh Huang, Li-Sen Young, Chiu-Chung Young
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  • List of new names and new combinations previously effectively, but not validly, published

    International Journal of Systematic and Evolutionary Microbiology .2012; 62(Pt_3): 473.     CrossRef
  • Cohnella plantaginis sp. nov., a novel nitrogen-fixing species isolated from plantain rhizosphere soil
    Li-Ying Wang, San-Feng Chen, Lei Wang, Yu-Guang Zhou, Hong-Can Liu
    Antonie van Leeuwenhoek.2012; 102(1): 83.     CrossRef
NOTE] Mitochondrial Phylogeny Reveals Intraspecific Variation in Peronospora effusa, the Spinach Downy Mildew Pathogen
Young-Joon Choi , Marco Thines , Jae-Gu Han , Hyeon-Dong Shin
J. Microbiol. 2011;49(6):1039-1043.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1069-2
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AbstractAbstract PDF
Since about two hundred years, downy mildew caused by Peronospora effusa is probably the most economically important disease of spinach (Spinacia oleracea). However, there is no information on the global phylogeographic structure of the pathogen and thus it is unclear whether a single genotype occurs worldwide
or whether some local genetic variation exists. To investigate the genetic variability of this pathogen, a sequence analysis of two partial mitochondrial DNA genes, cox2 and nad1, was carried out. Thirty-three specimens of Peronospora effusa from four continents were analyzed, including samples from Australia, China, Japan, Korea, Mexico, Russia, Sweden, and the USA. Despite the potential anthropogenic admixture of genotypes, a phylogeographic pattern was observed, which corresponds to two major groups, an Asian/Oceanian clade and another group, which includes American/European specimens. Notably, two of six Japanese specimens investigated did not belong to the Asian/Oceanian clade, but were identical to three of the specimens from the USA, suggestive of a recent introduction from the USA to Japan. As similar introduction events may be occurring as a result of the globalised trade with plant and seed material, a better knowledge of the phylogeographic distribution of pathogens is highly warranted for food security purposes.

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    Young‐Joon Choi, Gordon Beakes, Sally Glockling, Julia Kruse, Bora Nam, Lisa Nigrelli, Sebastian Ploch, Hyeon‐Dong Shin, Roger G. Shivas, Sabine Telle, Hermann Voglmayr, Marco Thines
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  • Coupling Spore Traps and Quantitative PCR Assays for Detection of the Downy Mildew Pathogens of Spinach (Peronospora effusa) and Beet (P. schachtii)
    Steven J. Klosterman, Amy Anchieta, Neil McRoberts, Steven T. Koike, Krishna V. Subbarao, Hermann Voglmayr, Young-Joon Choi, Marco Thines, Frank N. Martin
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NOTE] Leucobacter kyeonggiensis sp. nov., a New Species Isolated from Dye Waste Water
Hyun-jung Kim , Sang-Seob Lee
J. Microbiol. 2011;49(6):1044-1049.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1548-5
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AbstractAbstract PDF
A Gram-positive, aerobic, non-motile bacterium designated F3-P9T, was isolated from dye waste water in Korea and was characterized using a polyphasic taxonomic approach. Comparative 16S rRNA gene sequence analysis showed that strain F3-P9T belongs to genus Leucobacter. The 16S rRNA gene sequence similarities
among strain F3-P9T and validated representatives of the genus Leucobacter ranged from 95.9-97.4%. Strain F3-P9T exhibited DNA-DNA relatedness values below 48% with respect to Leucobacter species. The G+C content of the genomic DNA was 67.5 mol%. F3-P9T contained MK-11 as the major respiratory quinone. The major fatty acids were anteiso-C15:0 (48.5%), anteiso-C17:0 (22.7%), and iso-C16:0 (14.5%). The peptidoglycan was composed of L-2,4-diaminbutyric acid, alanine, glycine, and glutamic acid. The polar lipid profile showed a major amount of diphosphatidylglycerol (DPG), a moderate amount of phosphatidylglycerol (PG), and two unknown glycolipids. On the basis of its phenotypic and genotypic properties and its phylogenetic distinctiveness, strain F3-P9T (KEMC 211-128T =KACC 16572T =JCM 17539T) should be classified in the genus Leucobacter as the type strain of a novel species, for which the name Leucobacter kyeonggiensis sp. nov. is proposed.
NOTE] IL-10 Suppresses Bactericidal Response of Macrophages against Salmonella Typhimurium
Kyoung-Sun Lee , Eui-Suk Jeong , Seung-Ho Heo , Jin-Hee Seo , Dong-Gu Jeong , Yang-Kyu Choi
J. Microbiol. 2011;49(6):1050-1053.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1043-z
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AbstractAbstract PDF
We report, herein, an attempt to determine whether an IL-10-induced immunological state affects the response of macrophages against Salmonella Typhimurium (ST). Pretreatment with mrIL-10 induced the intracellular invasion of ST into macrophages in a dose-dependent manner. It also activated AKT phosphorylation, cyclin D1, Bcl-XL, and COX-2 upon ST infection, which may correlate with Salmonella’s survival within the macrophages. However, I-κB phosphorylation was shown to be inhibited, along with the expression of TNF-α and MIP-2α mRNA. Therefore, IL-10 not only suppresses the bactericidal response of macrophages against ST, but also ultimately causes infected macrophages to function as hosts for ST replication.

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    Geraldyne A. Salazar, Hernán F. Peñaloza, Catalina Pardo-Roa, Bárbara M. Schultz, Natalia Muñoz-Durango, Roberto S. Gómez, Francisco J. Salazar, Daniela P. Pizarro, Claudia A. Riedel, Pablo A. González, Manuel Alvarez-Lobos, Alexis M. Kalergis, Susan M. B
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    Elisa Deriu, Gayle M. Boxx, Xuesong He, Calvin Pan, Sammy David Benavidez, Lujia Cen, Nora Rozengurt, Wenyuan Shi, Genhong Cheng, Renée M. Tsolis
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    Soumi De Montijo-Prieto, Encarnación Moreno, Triana Bergillos-Meca, Agustín Lasserrot, María-Dolores Ruiz-López, Alfonso Ruiz-Bravo, María Jiménez-Valera
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NOTE] Isolation and Characterization of Self-Fertile Suppressors from the Sterile nsdD Deletion Mutant of Aspergillus nidulans
Dong-Beom Lee , Lee Han Kim , Jin-Pyo Kim , Kap-Hoon Han , Dong-Min Han
J. Microbiol. 2011;49(6):1054-1057.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1111-4
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AbstractAbstract PDF
To identify downstream and/or interactive factors of the nsdD gene, which encodes a positive regulator of sexual development of Aspergillus nidulans, suppressor mutants displaying a self-fertile phenotype were isolated from a sterile nsdD deletion mutant. At least five different loci (sndA-E) were identified and genetically analyzed. In the nsdD+ background, most of the suppressors showed a marked increment of sexual development, even under the stress conditions that normally inhibited sexual development. The common phenotype of the suppressor mutants suggested the involvement of the snd genes in the negative regulation of sexual development in response to the environmental factors.

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  • Inactivation of the global regulator LaeA in Monascus ruber results in a species-dependent response in sporulation and secondary metabolism
    Qingpei Liu, Li Cai, Yanchun Shao, Youxiang Zhou, Mu Li, Xiaohong Wang, Fusheng Chen
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  • A putative APSES transcription factor is necessary for normal growth and development of Aspergillus nidulans
    Ji-Yeon Lee, Lee-Han Kim, Ha-Eun Kim, Jae-Sin Park, Kap-Hoon Han, Dong-Min Han
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NOTE] Molecular Characterization of Two Strains of Porcine Group C Rotavirus
Sung-Geun Lee , Soo-Hyun Youn , Mi-Hwa Oh , Ok-Jae Rhee , Sangsuk Oh , Soon-Young Paik
J. Microbiol. 2011;49(6):1058-1062.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1088-z
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AbstractAbstract PDF
Group C rotaviruses are an important cause of acute gastroenteritis in humans and animals. Fecal samples were collected from a porcine herd in July, 2009. Group C rotavirus RNA was detected using RT-PCR for the VP6 gene. The identified strain was further characterized by sequencing and phylogenetic analysis of the partial VP4, and complete VP6 and VP7 gene sequences. The partial VP4 and complete VP6 gene sequences of the CUK-5 strain were most closely related to those of the CUK-6 strain of group C rotaviruses. Phylogenetic analysis of the VP7 gene of the 2 strains (CUK-5 and CUK-6) and reference strains of group G rotavirus by the neighbor-joining method also confirmed that CUK-5 and CUK-6 belonged to type G5 and G1 strains, respectively. This study provides useful data for the prediction of newly appearing variants of porcine group C rotaviruses in neighboring countries through comparisons with GCRVs and fundamental research for vaccine development.

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