Journal Article
- Vaccine Development for Severe Fever with Thrombocytopenia Syndrome Virus in Dogs
-
Seok-Chan Park, Da-Eun Jeong, Sun-Woo Han, Joon-Seok Chae, Joo-Yong Lee, Hyun-Sook Kim, Bumseok Kim, Jun-Gu Kang
-
J. Microbiol. 2024;62(4):327-335. Published online April 18, 2024
-
DOI: https://doi.org/10.1007/s12275-024-00119-y
-
-
59
View
-
0
Download
-
1
Web of Science
-
Abstract
-
Severe fever with thrombocytopenia syndrome (SFTS) is a life-threatening viral zoonosis. The causative agent of this disease is the Dabie bandavirus, which is usually known as the SFTS virus (SFTSV). Although the role of vertebrates in SFTSV transmission to humans remains uncertain, some reports have suggested that dogs could potentially transmit SFTSV to humans. Consequently, preventive measures against SFTSV in dogs are urgently needed. In the present study, dogs were immunized three times at two-week intervals with formaldehyde-inactivated SFTSV with two types of adjuvants. SFTSV (KCD46) was injected into all dogs two weeks after the final immunization. Control dogs showed viremia from 2 to 4 days post infection (dpi), and displayed white pulp atrophy in the spleen, along with a high level of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling assay (TUNEL) positive area. However, the inactivated SFTSV vaccine groups exhibited rare pathological changes and significantly reduced TUNEL positive areas in the spleen. Furthermore, SFTSV viral loads were not detected at any of the tested dpi. Our results indicate that both adjuvants can be safely used in combination with an inactivated SFTSV formulation to induce strong neutralizing antibodies. Inactivated SFTSV vaccines effectively prevent pathogenicity and viremia in dogs infected with SFTSV. In conclusion, our study highlighted the potential of inactivated SFTSV vaccination for SFTSV control in dogs.
Review
- Searching for a Reliable Viral Indicator of Faecal Pollution in Aquatic Environments
-
Felana Harilanto Andrianjakarivony , Yvan Bettarel , Christelle Desnues
-
J. Microbiol. 2023;61(6):589-602. Published online June 1, 2023
-
DOI: https://doi.org/10.1007/s12275-023-00052-6
-
-
54
View
-
0
Download
-
2
Web of Science
-
1
Crossref
-
Abstract
-
The disposal of sewage in significant quantities poses a health hazard to aquatic ecosystems. These effluents can contain
a wide range of pathogens, making faecal contamination a leading source of waterborne diseases around the world. Yet
monitoring bacteria or viruses in aquatic environments is time consuming and expensive. The standard indicators of faecal
pollution all have limitations, including difficulty in determining the source due to lack of host specificity, poor connection
with the presence of non-bacterial pathogens, or low environmental persistence. Innovative monitoring techniques are sorely
needed to provide more accurate and targeted solutions. Viruses are a promising alternative to faecal indicator bacteria for
monitoring, as they are more persistent in ambient water, more abundant in faeces, and are extremely host-specific. Given
the range of viruses found in diverse contexts, it is not easy to find one “ideal” viral indicator of faecal pollution; however,
several are of interest. In parallel, the ongoing development of molecular techniques coupled with metagenomics and bioinformatics
should enable improved ways to detect faecal contamination using viruses. This review examines the evolution
of faecal contamination monitoring with the following aims (i) to identify the characteristics of the main viral indicators of
faecal contamination, including human enteric viruses, bacteriophages, CRESS and plant viruses, (ii) to assess how these
have been used to monitor water pollution in recent years, (iii) to evaluate the reliability of recent detection methods of such
viruses, and (iv) to tentatively determine which viruses may be most effective as markers of faecal pollution.
-
Citations
Citations to this article as recorded by

- Review of carbon dot–hydrogel composite material as a future water-environmental regulator
Minghao Jiang, Yong Wang, Jichuan Li, Xing Gao
International Journal of Biological Macromolecules.2024; 269: 131850. CrossRef
Journal Articles
- The velvet repressed vidA gene plays a key role in governing development in Aspergillus nidulans
-
Min-Ju Kim , Won-Hee Jung , Ye-Eun Son , Jae-Hyuk Yu , Mi-Kyung Lee , Hee-Soo Park
-
J. Microbiol. 2019;57(10):893-899. Published online August 28, 2019
-
DOI: https://doi.org/10.1007/s12275-019-9214-4
-
-
46
View
-
0
Download
-
14
Web of Science
-
12
Crossref
-
Abstract
-
Fungal development is regulated by a variety of transcription
factors in Aspergillus nidulans. Previous studies demonstrated
that the NF-κB type velvet transcription factors regulate certain
target genes that govern fungal differentiation and cellular
metabolism. In this study, we characterize one of the
VosA/VelB-inhibited developmental genes called vidA, which
is predicted to encode a 581-amino acid protein with a C2H2
zinc finger domain at the C-terminus. Levels of vidA mRNA
are high during the early and middle phases of asexual development
and decrease during the late phase of asexual development
and asexual spore (conidium) formation. Deletion
of either vosA or velB results in increased vidA mRNA accumulation
in conidia, suggesting that vidA transcript accumulation
in conidia is repressed by VosA and VelB. Phenotypic
analysis demonstrated that deletion of vidA causes decreased
colony growth, reduced production of asexual spores,
and abnormal formation of sexual fruiting bodies. In addition,
the vidA deletion mutant conidia contain more trehalose
and β-glucan than wild type. Overall, these results suggest
that VidA is a putative transcription factor that plays a
key role in governing proper fungal growth, asexual and sexual
development, and conidia formation in A. nidulans.
-
Citations
Citations to this article as recorded by

- Regulators of the Asexual Life Cycle of Aspergillus nidulans
Ye-Eun Son, Jae-Hyuk Yu, Hee-Soo Park
Cells.2023; 12(11): 1544. CrossRef - The Forkhead Gene fkhB is Necessary for Proper Development in Aspergillus nidulans
Seo-Yeong Jang, Ye-Eun Son, Dong-Soon Oh, Kap-Hoon Han, Jae-Hyuk Yu, Hee-Soo Park
Journal of Microbiology and Biotechnology.2023; 33(11): 1420. CrossRef - The function of a conidia specific transcription factor CsgA in Aspergillus nidulans
He-Jin Cho, Hee-Soo Park
Scientific Reports.2022;[Epub] CrossRef - The Putative C2H2 Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
Xiaoyu Li, Yanxia Zhao, Heungyun Moon, Jieyin Lim, Hee-Soo Park, Zhiqiang Liu, Jae-Hyuk Yu
Cells.2022; 11(24): 3998. CrossRef - The Role of Chromatin and Transcriptional Control in the Formation of Sexual Fruiting Bodies in Fungi
Minou Nowrousian
Microbiology and Molecular Biology Reviews.2022;[Epub] CrossRef - Functions of PUF Family RNA-Binding Proteins in Aspergillus nidulans
Sung-Hun Son, Seo-Yeong Jang, Hee-Soo Park
Journal of Microbiology and Biotechnology.2021; 31(5): 676. CrossRef - The putative sensor histidine kinase VadJ coordinates development and sterigmatocystin production in Aspergillus nidulans
Yanxia Zhao, Mi-Kyung Lee, Jieyin Lim, Heungyun Moon, Hee-Soo Park, Weifa Zheng, Jae-Hyuk Yu
Journal of Microbiology.2021; 59(8): 746. CrossRef - Unveiling the Functions of the VosA-VelB Target GenevidDinAspergillus nidulans
Ye-Eun Son, Hee-Soo Park
Mycobiology.2021; 49(3): 258. CrossRef - Velvet activated McrA plays a key role in cellular and metabolic development in Aspergillus nidulans
Mi-Kyung Lee, Ye-Eun Son, Hee-Soo Park, Ahmad Alshannaq, Kap-Hoon Han, Jae-Hyuk Yu
Scientific Reports.2020;[Epub] CrossRef - The role of the VosA-repressed dnjA gene in development and metabolism in Aspergillus species
Ye-Eun Son, He-Jin Cho, Wanping Chen, Sung-Hun Son, Mi-Kyung Lee, Jae-Hyuk Yu, Hee-Soo Park
Current Genetics.2020; 66(3): 621. CrossRef - Homeobox proteins are essential for fungal differentiation and secondary metabolism in Aspergillus nidulans
Sung-Hun Son, Ye-Eun Son, He-Jin Cho, Wanping Chen, Mi-Kyung Lee, Lee-Han Kim, Dong-Min Han, Hee-Soo Park
Scientific Reports.2020;[Epub] CrossRef - The brlA Gene Deletion Reveals That Patulin Biosynthesis Is Not Related to Conidiation in Penicillium expansum
Chrystian Zetina-Serrano, Ophélie Rocher, Claire Naylies, Yannick Lippi, Isabelle P. Oswald, Sophie Lorber, Olivier Puel
International Journal of Molecular Sciences.2020; 21(18): 6660. CrossRef
- Expression of sexual genes in Aspergillus fumigatus homogeneous culture produced by vegetative mass mating
-
Joo-Yeon Lim , Hee-Moon Park
-
J. Microbiol. 2019;57(8):688-693. Published online May 11, 2019
-
DOI: https://doi.org/10.1007/s12275-019-9094-7
-
-
51
View
-
0
Download
-
3
Web of Science
-
3
Crossref
-
Abstract
-
There are presently no studies on the genes for sexual development
of Aspergillus fumigatus in situ using mating culture,
primarily because of challenging experimental conditions
that require a significantly long period of induction and produce
developmentally heterogenous culture, harboring very
few sexual organs. In order to overcome these challenges, we
developed an efficient and convenient procedure called ‘vegetative
mass mating (VeM)’ for study at a molecular level.
The VeM method enabled production of a developmentally
homogenous A. fumigatus culture, harboring many sexual
organs in a plate within a short period of two weeks. Feasibility
of the use of VeM for functional study of genes during
A. fumigatus sexual development was evaluated by analyzing
the transcription pattern of genes involved in pheromone signal
transduction and regulation of sexual development. Here,
we present for the first time, an in situ expression pattern of
sexual genes during the mating process, induced by the VeM
method
, which will enable and promote the sexual development
study of A. fumigatus at the molecular level.
-
Citations
Citations to this article as recorded by

- The Gβ-like Protein AfCpcB Affects Sexual Development, Response to Oxidative Stress and Phagocytosis by Alveolar Macrophages in Aspergillus fumigatus
Joo-Yeon Lim, Yeon-Ju Kim, Hee-Moon Park
Journal of Fungi.2022; 8(1): 56. CrossRef - The LAMMER Kinase, LkhA, Affects Aspergillus fumigatus Pathogenicity by Modulating Reproduction and Biosynthesis of Cell Wall PAMPs
Joo-Yeon Lim, Yeon Ju Kim, Seul Ah Woo, Jae Wan Jeong, Yu-Ri Lee, Cheol-Hee Kim, Hee-Moon Park
Frontiers in Cellular and Infection Microbiology.2021;[Epub] CrossRef - Global Sexual Fertility in the Opportunistic Pathogen Aspergillus fumigatus and Identification of New Supermater Strains
Sameira S. Swilaiman, Céline M. O’Gorman, Wenyue Du, Janyce A. Sugui, Joanne Del Buono, Matthias Brock, Kyung J. Kwon-Chung, George Szakacs, Paul S. Dyer
Journal of Fungi.2020; 6(4): 258. CrossRef
- Cecal microbiome divergence of broiler chickens by sex and body weight
-
Kyu-Chan Lee , Dong Yong Kil , Woo Jun Sul
-
J. Microbiol. 2017;55(12):939-945. Published online December 7, 2017
-
DOI: https://doi.org/10.1007/s12275-017-7202-0
-
-
47
View
-
0
Download
-
71
Crossref
-
Abstract
-
The divergence of gut bacterial community on broiler chickens
has been reported as potentially possible keys to enhancing
nutrient absorption, immune systems, and increasing
poultry health and performance. Thus, we compared cecal
bacterial communities and functional predictions by sex and
body weight regarding the association between cecal microbiota
and chicken growth performance. In this study, a total
of 12 male and 12 female 1-day-old broiler chickens were
raised for 35 days in 2 separate cages. Chickens were divided
into 3 subgroups depending on body weight (low, medium,
and high) by each sex. We compared chicken cecal microbiota
compositions and its predictive functions by sex and body
weight difference. We found that bacterial 16S rRNA genes
were classified as 3 major phyla (Bacteroidetes, Firmicutes,
and Proteobacteria), accounting for > 98% of the total bacterial
community. The profiling of different bacterial taxa and
predictive metagenome functions derived from 16S rRNA
genes were performed over chicken sex and bodyweight. Male
chickens were related to the enrichment of Bacteroides while
female chickens were to the enrichment of Clostridium and
Shigella. Male chickens with high body weight were associated
with the enrichment of Faecalibacterium and Shuttleworthia.
Carbohydrate and lipid metabolisms were suggested as candidate
functions for weight gain in the males. This suggests
that the variation of cecal bacterial communities and their
functions by sex and body weight may be associated with the
differences in the growth potentials of broiler chickens.
-
Citations
Citations to this article as recorded by

- Dietary ethylenediamine dihydroiodide mitigated Escherichia coli O78-induced immune and intestinal damage of ducks via suppression of NF-κB signal
Yanru Liang, Yaqi Chang, Yueqin Xie, Qinteng Hou, Hua Zhao, Guangmang Liu, Xiaoling Chen, Gang Tian, Jingyi Cai, Gang Jia
Poultry Science.2024; 103(5): 103610. CrossRef - The effect of sex and dietary crude protein level on nutrient transporter gene expression and cecal microbiota populations in broiler chickens
Ashley D. England, Sara de las Heras-Saldana, Kosar Gharib-Naseri, Sarbast K. Kheravii, Shu-Biao Wu
Poultry Science.2024; 103(2): 103268. CrossRef - Morphological features of the feral pigeon’s (Columba livia f. urbana) digestive system
I. O. Кolomak
Journal for Veterinary Medicine, Biotechnology and Biosafety.2024; 10(1): 7. CrossRef - Microbial community profiling in intestinal tract of indigenous chickens from different villages
Mokoma Eunice Mootane, Thendo Mafuna, Tondani Madeleine Ramantswana, Dikeledi Petunia Malatji
Scientific Reports.2024;[Epub] CrossRef - The Effect of including a Mixed-Enzyme Product in Broiler Diets on Performance, Metabolizable Energy, Phosphorus and Calcium Retention
Harriet Walker, Suvi Vartiainen, Juha Apajalahti, Jules Taylor-Pickard, Ivana Nikodinoska, Colm A. Moran
Animals.2024; 14(2): 328. CrossRef - Integrating microbial 16S rRNA sequencing and non-targeted metabolomics to reveal sexual dimorphism of the chicken cecal microbiome and serum metabolome
Yongxian Yang, Fuping Zhang, Xuan Yu, Liqi Wang, Zhong Wang
Frontiers in Microbiology.2024;[Epub] CrossRef - Dynamic effects of black soldier fly larvae meal on the cecal bacterial microbiota and prevalence of selected antimicrobial resistant determinants in broiler chickens
Calvin Ho-Fung Lau, Sabrina Capitani, Yuan-Ching Tien, Lou Ann Verellen, Munene Kithama, Hellen Kang, Elijah G. Kiarie, Edward Topp, Moussa S. Diarra, Michael Fruci
Animal Microbiome.2024;[Epub] CrossRef - Assessing the impact of hatching system and body weight on the growth performance, caecal short-chain fatty acids, and microbiota composition and functionality in broilers
Muhammad Zeeshan Akram, Ester Arévalo Sureda, Luke Comer, Matthias Corion, Nadia Everaert
Animal Microbiome.2024;[Epub] CrossRef - Are there consistent effects of gut microbiota composition on performance, productivity and condition in poultry?
Kateřina Marková, Jakub Kreisinger, Michal Vinkler
Poultry Science.2024; 103(6): 103752. CrossRef - Sex‐specific genetic parameter estimates of body weight in Mazandaran indigenous chickens
Mohammad Esmaeili, Mohsen Gholizadeh, Hasan Hafezian, Ayoub Farhadi
Journal of Animal Breeding and Genetics.2024; 141(4): 465. CrossRef - A catalog of microbial genes and metagenome-assembled genomes from the quail gut microbiome
Xinwei Xiong, Yousheng Rao, Jinge Ma, Zhangfeng Wang, Qin He, Jishang Gong, Wentao Sheng, Jiguo Xu, Xuenong Zhu, Yuwen Tan, Yanbei Yang
Poultry Science.2023; 102(10): 102931. CrossRef - Plant essential oils improve growth performance by increasing antioxidative capacity, enhancing intestinal barrier function, and modulating gut microbiota in Muscovy ducks
Chaoyue Ge, Xinyu Luo, Lianchi Wu, Yujie Lv, Zhaoying Hu, Dongyou Yu, Bing Liu
Poultry Science.2023; 102(8): 102813. CrossRef - The Development of Gut Microbiota and Its Changes Following C. jejuni Infection in Broilers
Walid Ghazi Al Hakeem, Keila Y. Acevedo Villanueva, Ramesh K. Selvaraj
Vaccines.2023; 11(3): 595. CrossRef - Growing Patterns of the Branca Chicken Breed—Concentrate vs. Maize-Based Diet
Laura Soares, Fernando Mata, Joaquim L. Cerqueira, José Araújo
Agriculture.2023; 13(12): 2282. CrossRef - Regulation of poultry lipid metabolism by dietary fibre: a review
Hua Zhou, Lei Yang, Tiande Zou, Qiufen Li, Mingren Qu, Jingming You, Guanhong Li
World's Poultry Science Journal.2023; 79(3): 485. CrossRef - Effect of water supplementation of Magic oil at different growing periods on growth performance, carcass traits, blood biochemistry, and ileal histomorphology of broiler chickens
Elsayed O.S. Hussein, Gamaleldin M. Suliman, Abdullah N. Al-Owaimer, Hani H. Al-Baadani, Maged A. Al-Garadi, Hani A. Ba-Awadh, Mohammed M. Qaid, Ayman A. Swelum
Poultry Science.2023; 102(8): 102775. CrossRef - Versatile, vigilance, and gut microbiome support the priority of high-ranking hens
Zhijiang Xie, Limin Xing, Mengqiao Zhao, Lei Zhao, Jinling Liu, Yushan Li, Jiankang Gan, Siyu Chen, Hua Li
Frontiers in Veterinary Science.2023;[Epub] CrossRef - Anaerobutyricum and Subdoligranulum Are Differentially Enriched in Broilers with Disparate Weight Gains
Jing Liu, Kelsy Robinson, Wentao Lyu, Qing Yang, Jing Wang, Karen D. Christensen, Guolong Zhang
Animals.2023; 13(11): 1834. CrossRef - Inonotus obliquus polysaccharide are linear molecules that alter the abundance and composition of intestinal microbiota in Sprague Dawley rats
Songqing Liu, Wenjing Zhou, Xin Deng, Wei Jiang, Yanping Wang, Jiasui Zhan, Binhong Hu
Frontiers in Nutrition.2023;[Epub] CrossRef - Host genotype affects endotoxin release in excreta of broilers at slaughter age
F. Marcato, J. M. J. Rebel, S. K. Kar, I. M. Wouters, D. Schokker, A. Bossers, F. Harders, J. W. van Riel, M. Wolthuis-Fillerup, I. C. de Jong
Frontiers in Genetics.2023;[Epub] CrossRef - Phenotype Alterations in the Cecal Ecosystem Involved in the Asymptomatic Intestinal Persistence of Paratyphoid Salmonella in Chickens
Michael H. Kogut, Mariano Enrique Fernandez Miyakawa
Animals.2023; 13(18): 2824. CrossRef - Long-Term Dietary Fish Meal Substitution with the Black Soldier Fly Larval Meal Modifies the Caecal Microbiota and Microbial Pathway in Laying Hens
Junliang Zhao, Takuma Ban, Hironori Miyawaki, Hirofumi Hirayasu, Akihisa Izumo, Shun-ichiro Iwase, Koji Kasai, Kiyonori Kawasaki
Animals.2023; 13(16): 2629. CrossRef - Sex-based responses of heat stress and subsequent recovery on the growth performance, metabolic changes, and redox status of broilers at market age
Ding Jinxue, Sun Shiang, Song Kai, Xiong Yongjie, He Shaojun
International Journal of Biometeorology.2023; 67(10): 1669. CrossRef - Dietary fiber modulates abdominal fat deposition associated with cecal microbiota and metabolites in yellow chickens
Xiaoyan Cui, Zhongyong Gou, Zongyong Jiang, Long Li, Xiajing Lin, Qiuli Fan, Yibing Wang, Shouqun Jiang
Poultry Science.2022; 101(4): 101721. CrossRef - Microbiota and Transcriptomic Effects of an Essential Oil Blend and Its Delivery Route Compared to an Antibiotic Growth Promoter in Broiler Chickens
Samson Oladokun, K. Fraser Clark, Deborah I. Adewole
Microorganisms.2022; 10(5): 861. CrossRef - Effect of stocking density on performance, meat quality and cecal bacterial communities of yellow feather broilers
Laidi Wang, Lingling Kong, Xiaodan Hu, Hao Bai, Zhixiu Wang, Yong Jiang, Yulin Bi, Guobin Chang, Guohong Chen
Animal Biotechnology.2022; 33(6): 1322. CrossRef - Potential Probiotics Role in Excluding Antibiotic Resistance
Irfan Ahmed, Zhengtian Li, Sharoon Shahzad, Saima Naveed, Ahmad Kamran Khan, Ayesha Ahmed, Zahid Kamran, Muhammad Yousaf, Shakeel Ahmad, Gulnaz Afzal, Hafiz Ishfaq Ahmad, Nasim Ahmad Yasin, Junjing Jia, Mubashir Hussain, Shahzad Munir, Ali Akbar
Journal of Food Quality.2022; 2022: 1. CrossRef - Delayed access to feed early post-hatch affects the development and maturation of gastrointestinal tract microbiota in broiler chickens
Monika Proszkowiec-Weglarz, Katarzyna B. Miska, Laura E. Ellestad, Lori L. Schreier, Stanislaw Kahl, Nadia Darwish, Philip Campos, Jonathan Shao
BMC Microbiology.2022;[Epub] CrossRef - Effect of Two Soybean Varieties Treated with Different Heat Intensities on Ileal and Caecal Microbiota in Broiler Chickens
Florian Hemetsberger, Benjamin Zwirzitz, Nadia Yacoubi, Wolfgang Kneifel, Karl Schedle, Konrad J. Domig
Animals.2022; 12(9): 1109. CrossRef - Comparison of organic acids supplementation on the growth performance, intestinal characteristics and morphology, and cecal microflora in broilers fed corn-soybean meal diet
Hao Yang Sun, Hong Bin Zhou, Yang Liu, Yue Wang, Cheng Zhao, Liang Mei Xu
Animal Bioscience.2022; 35(11): 1689. CrossRef - Centennial Review: Factors affecting the chicken gastrointestinal microbial composition and their association with gut health and productive performance
Yugal Raj Bindari, Priscilla F. Gerber
Poultry Science.2022; 101(1): 101612. CrossRef - A carvacrol-based product reduces Campylobacter jejuni load and alters microbiota composition in the caeca of chickens
Marion Allaoua, Elsa Bonnafé, Pierre Etienne, Virginie Noirot, Jean-François Gabarrou, Adrien Castinel, Géraldine Pascal, Vincent Darbot, Michel Treilhou, Sylvie Combes
Journal of Applied Microbiology.2022; 132(6): 4501. CrossRef - The replacement of bacitracin methylene disalicylate with Bacillus subtilis PB6 in the diet of male Cherry Valley Ducks reduces the feed conversion ratio by improving intestinal health and modulating gut microbiota
Qianqian Zhang, Jian Li, Guixiang Wang, Lizhi Wang, Zhiming Zhang, Zhengfeng Fang, Yan Lin, Shengyu Xu, Bin Feng, Yong Zhuo, Lun Hua, Xuemei Jiang, Xilun Zhao, De Wu, Lianqiang Che
Poultry Science.2022; 101(11): 102155. CrossRef - Novel strategies to improve chicken performance and welfare by unveiling host-microbiota interactions through hologenomics
Núria Tous, Sofia Marcos, Farshad Goodarzi Boroojeni, Ana Pérez de Rozas, Jürgen Zentek, Andone Estonba, Dorthe Sandvang, M. Thomas P. Gilbert, Enric Esteve-Garcia, Robert Finn, Antton Alberdi, Joan Tarradas
Frontiers in Physiology.2022;[Epub] CrossRef - Role of Physiology, Immunity, Microbiota, and Infectious Diseases in the Gut Health of Poultry
Samiru S. Wickramasuriya, Inkyung Park, Kyungwoo Lee, Youngsub Lee, Woo H. Kim, Hyoyoun Nam, Hyun S. Lillehoj
Vaccines.2022; 10(2): 172. CrossRef - The avian gut microbiota: Diversity, influencing factors, and future directions
Fengfei Sun, Junfeng Chen, Kai Liu, Meizhen Tang, Yuewei Yang
Frontiers in Microbiology.2022;[Epub] CrossRef - A Probabilistic Structural Equation Model to Evaluate Links between Gut Microbiota and Body Weights of Chicken Fed or Not Fed Insect Larvae
Johann Detilleux, Nassim Moula, Edwin Dawans, Bernard Taminiau, Georges Daube, Pascal Leroy
Biology.2022; 11(3): 357. CrossRef - Feed Safety and the Development of Poultry Intestinal Microbiota
Dragana Stanley, Yadav Sharma Bajagai
Animals.2022; 12(20): 2890. CrossRef - Factors Affecting Breast Myopathies in Broiler Chickens and Quality of Defective Meat: A Meta-Analysis
Francesco Bordignon, Gerolamo Xiccato, Marija Boskovic Cabrol, Marco Birolo, Angela Trocino
Frontiers in Physiology.2022;[Epub] CrossRef - Effects of therapeutic levels of dietary antibiotics on the cecal microbiome composition of broiler chickens
Seyed Hossien Kairmi, Khaled Taha-Abdelaziz, Alexander Yitbarek, Mehdi Sargolzaei, Heidi Spahany, Jake Astill, Bahram Shojadoost, Mohammadali Alizadeh, Raveendra R. Kulkarni, John Parkinson, Shayan Sharif
Poultry Science.2022; 101(6): 101864. CrossRef - Taxonomic and predicted functional signatures reveal linkages between the rumen microbiota and feed efficiency in dairy cattle raised in tropical areas
Priscila Fregulia, Mariana Magalhães Campos, Roberto Júnio Pedroso Dias, Junhong Liu, Wei Guo, Luiz Gustavo Ribeiro Pereira, Marco Antônio Machado, Daniele Ribeiro de Lima Reis Faza, Le Luo Guan, Phil C. Garnsworthy, André Luis Alves Neves
Frontiers in Microbiology.2022;[Epub] CrossRef - Effect of Salmonella Typhimurium Colonization on Microbiota Maturation and Blood Leukocyte Populations in Broiler Chickens
Kelsy Robinson, Anna L. F. V. Assumpcao, Komala Arsi, Gisela F. Erf, Annie Donoghue, Palmy R. R. Jesudhasan
Animals.2022; 12(20): 2867. CrossRef - Caecal microbial communities, functional diversity, and metabolic pathways in Ross 308 broiler chickens fed with diets containing different levels of Marama (Tylosema esculentum) bean meal
Peter Kotsoana Montso, Caven Mguvane Mnisi, Ayansina Segun Ayangbenro
Frontiers in Microbiology.2022;[Epub] CrossRef - Microbiota populations and short-chain fatty acids production in cecum of immunosuppressed broilers consuming diets containing γ-irradiated Astragalus polysaccharides
Y.S. Liu, S. Li, X.F. Wang, T. Xing, J.L. Li, X.D. Zhu, L. Zhang, F. Gao
Poultry Science.2021; 100(1): 273. CrossRef - Effects of Clostridium butyricum, Sodium Butyrate, and Butyric Acid Glycerides on the Reproductive Performance, Egg Quality, Intestinal Health, and Offspring Performance of Yellow-Feathered Breeder Hens
Yibing Wang, Yang Wang, Xiajing Lin, Zhongyong Gou, Qiuli Fan, Shouqun Jiang
Frontiers in Microbiology.2021;[Epub] CrossRef - The link between broiler flock heterogeneity and cecal microbiome composition
Randi Lundberg, Christian Scharch, Dorthe Sandvang
Animal Microbiome.2021;[Epub] CrossRef - Changes in the ceca microbiota of broilers vaccinated for coccidiosis or supplemented with salinomycin
C. Orso, T.B. Stefanello, C.H. Franceschi, M.B. Mann, A.P.M. Varela, I.M.S. Castro, J. Frazzon, A.P.G. Frazzon, I. Andretta, A.M.L. Ribeiro
Poultry Science.2021; 100(4): 100969. CrossRef - Highly Fermentable Fiber Alters Fecal Microbiota and Mitigates Swine Dysentery Induced by Brachyspira hyodysenteriae
Emma T. Helm, Nicholas K. Gabler, Eric. R. Burrough
Animals.2021; 11(2): 396. CrossRef - Sex differences in growth performance are related to cecal microbiota in chicken
Lei Cui, Xiaolong Zhang, Ranran Cheng, Abdur Rahman Ansari, Abdelmotaleb A. Elokil, Yafang Hu, Yan Chen, Abdallah A. Nafady, Huazhen Liu
Microbial Pathogenesis.2021; 150: 104710. CrossRef - Metagenomic Analysis Identifies Sex-Related Cecal Microbial Gene Functions and Bacterial Taxa in the Quail
Jing-E Ma, Xin-Wei Xiong, Ji-Guo Xu, Ji-Shang Gong, Jin Li, Qiao Xu, Yuan-Fei Li, Yang-Bei Yang, Min Zhou, Xue-Nong Zhu, Yu-Wen Tan, Wen-Tao Sheng, Zhang-Feng Wang, Xu-Tang Tu, Cheng-Yao Zeng, Xi-Quan Zhang, You-Sheng Rao
Frontiers in Veterinary Science.2021;[Epub] CrossRef - The digestive and reproductive tract microbiotas and their association with body weight in laying hens
Yuan Su, Yile Ge, Zhongxian Xu, Dejing Zhang, Diyan Li
Poultry Science.2021; 100(11): 101422. CrossRef - Factors Influencing the Succession of the Fecal Microbiome in Broilers
Dirkjan Schokker, Britt de Klerk, Randy Borg, Alex Bossers, Johanna M.J. Rebel
Livestock Science.2021; 247: 104486. CrossRef - Effects of Xylanase in Corn- or Wheat-Based Diets on Cecal Microbiota of Broilers
Jian Wang, Heng Cao, Chengling Bao, Yajing Liu, Bing Dong, Chunlin Wang, Zhenda Shang, Yunhe Cao, Suozhu Liu
Frontiers in Microbiology.2021;[Epub] CrossRef - Effects of rearing system (floor vs. cage) and sex on performance, meat quality and enteric microorganism of yellow feather broilers
Lai-di WANG, Yang ZHANG, Ling-ling KONG, Zhi-xiu WANG, Hao BAI, Yong JIANG, Yu-lin BI, Guo-bin CHANG, Guo-hong CHEN
Journal of Integrative Agriculture.2021; 20(7): 1907. CrossRef - A reasonable correlation between cloacal and cecal microbiomes in broiler chickens
Nadia A. Andreani, Caroline J. Donaldson, Matthew Goddard
Poultry Science.2020; 99(11): 6062. CrossRef - Green Tea and Pomegranate Extract Administered During Critical Moments of the Production Cycle Improves Blood Antiradical Activity and Alters Cecal Microbial Ecology of Broiler Chickens
Vera Perricone, Marcello Comi, Carlotta Giromini, Raffaella Rebucci, Alessandro Agazzi, Giovanni Savoini, Valentino Bontempo
Animals.2020; 10(5): 785. CrossRef - Respiratory and Gut Microbiota in Commercial Turkey Flocks with Disparate Weight Gain Trajectories Display Differential Compositional Dynamics
Kara J. M. Taylor, John M. Ngunjiri, Michael C. Abundo, Hyesun Jang, Mohamed Elaish, Amir Ghorbani, Mahesh KC, Bonnie P. Weber, Timothy J. Johnson, Chang-Won Lee, Edward G. Dudley
Applied and Environmental Microbiology.2020;[Epub] CrossRef - Metagenomic analysis reveals linkages between cecal microbiota and feed efficiency in Xiayan chickens
Wenya Du, Jixian Deng, Zhuliang Yang, Linghu Zeng, Xiurong Yang
Poultry Science.2020; 99(12): 7066. CrossRef - Effects of Rearing Conditions and Sex on Cecal Microbiota in Ducks
Chunhong Zhu, Wenjuan Xu, Zhiyun Tao, Weitao Song, Hongxiang Liu, Shuangjie Zhang, Huifang Li
Frontiers in Microbiology.2020;[Epub] CrossRef - Effects of Eimeria maxima and Clostridium perfringens infections on cecal microbial composition and the possible correlation with body weight gain in broiler chickens
Mingmin Lu, Robert W. Li, Hongyan Zhao, Xianghe Yan, Hyun S. Lillehoj, Zhifeng Sun, SungTak Oh, Yueying Wang, Charles Li
Research in Veterinary Science.2020; 132: 142. CrossRef - Family matters: skin microbiome reflects the social group and spatial proximity in wild zebra finches
Kathrin Engel, Helga Pankoke, Sebastian Jünemann, Hanja B. Brandl, Jan Sauer, Simon C. Griffith, Jörn Kalinowski, Barbara A. Caspers
BMC Ecology.2020;[Epub] CrossRef - Dissection of the cecal microbial community in chickens after Eimeria tenella infection
Hong-Liang Chen, Xin-Yu Zhao, Guang-Xun Zhao, Hai-Bin Huang, Hao-Rui Li, Chun-Wei Shi, Wen-Tao Yang, Yan-Long Jiang, Jian-Zhong Wang, Li-Ping Ye, Quan Zhao, Chun-Feng Wang, Gui-Lian Yang
Parasites & Vectors.2020;[Epub] CrossRef - Dietary supplementation with fermented defatted “alperujo” induces modifications of the intestinal mucosa and cecal microbiota of broiler chickens
Agustín Rebollada-Merino, María Ugarte-Ruiz, Marta Hernández, Pedro Miguela-Villoldo, David Abad, Pedro Cuesta-Álvaro, David Rodríguez-Lázaro, Lucía de Juan, Lucas Domínguez, Antonio Rodríguez-Bertos
Poultry Science.2020; 99(11): 5308. CrossRef - Changes in the gut microbiota mediate the differential regulatory effects of two glucose oxidases produced by Aspergillus niger and Penicillium amagasakiense on the meat quality and growth performance of broilers
Shengru Wu, Xiaodong Chen, Taohuan Li, Hao Ren, Lixin Zheng, Xiaojun Yang
Journal of Animal Science and Biotechnology.2020;[Epub] CrossRef - Sanguinarine modulate gut microbiome and intestinal morphology to enhance growth performance in broilers
Zhu-Ying Liu, Xiao-Long Wang, Shu-Qi Ou, De-Xing Hou, Jian-Hua He, Michael H. Kogut
PLOS ONE.2020; 15(6): e0234920. CrossRef - Characterization of heat stress affecting the growth performance, blood biochemical profile, and redox status in male and female broilers at market age
Shaojun He, Qirun Yin, Yongjie Xiong, Jing Li, Deyi Liu
Tropical Animal Health and Production.2020; 52(6): 3833. CrossRef - Influential factors on the composition of the conventionally raised broiler gastrointestinal microbiomes
K.M. Feye, M.F.A. Baxter, G. Tellez-Isaias, M.H. Kogut, S.C. Ricke
Poultry Science.2020; 99(2): 653. CrossRef - Genome reconstruction of a novel carbohydrate digesting bacterium from the chicken caecal microflora
Ankit T. Hinsu, Ramesh J. Pandit, Shriram H. Patel, Androniki Psifidi, Fiona M. Tomley, Subrata K. Das, Damer P. Blake, Chaitanya G. Joshi
Meta Gene.2019; 20: 100543. CrossRef - Functioning of the Intestinal Ecosystem: From New Technologies in Microbial Research to Practical Poultry Feeding – A Review
Zenon Zduńczyk
Annals of Animal Science.2019; 19(2): 239. CrossRef - Faecalibacterium diversity in dairy cow milk
Keith W. Savin, Jody Zawadzki, Martin J. Auldist, Jianghui Wang, Doris Ram, Simone Rochfort, Benjamin G. Cocks, Christopher Staley
PLOS ONE.2019; 14(8): e0221055. CrossRef - Olfactory Communication via Microbiota: What Is Known in Birds?
Öncü Maraci, Kathrin Engel, Barbara A. Caspers
Genes.2018; 9(8): 387. CrossRef
Reviews
- MINIREVIEW] Transcriptional control of sexual development in Cryptococcus neoformans
-
Matthew E. Mead , Christina M. Hull
-
J. Microbiol. 2016;54(5):339-346. Published online April 20, 2016
-
DOI: https://doi.org/10.1007/s12275-016-6080-1
-
-
43
View
-
0
Download
-
6
Crossref
-
Abstract
-
Developmental processes are essential for the normal life cycles
of many pathogenic fungi, and they can facilitate survival
in challenging environments, including the human host. Sexual
development of the human fungal pathogen Cryptococcus neoformans
not only produces infectious particles (spores) but has
also enabled the evolution of new disease-related traits such as
drug resistance. Transcription factor networks are essential
to the development and pathogenesis of C. neoformans, and a
variety of sequence-specific DNA-binding proteins control
both key developmental transitions and virulence by regulating
the expression of their target genes. In this review we discuss
the roles of known transcription factors that harbor important
connections to both development and virulence. Recent studies
of these transcription factors have identified a common
theme in which metabolic, stress, and other responses that are
required for sexual development appear to have been co-opted
for survival in the human host, thus facilitating pathogenesis.
Future work elucidating the connection between development
and pathogenesis will provide vital insights into the evolution
of complex traits in eukaryotes as well as mechanisms that
may be used to combat fungal pathogens.
-
Citations
Citations to this article as recorded by

- Effect of a Mating Type Gene Editing in Lentinula edodes Using RNP/Nanoparticle Complex
Minseek Kim, Minji Oh, Ji-Hoon Im, Eun-Ji Lee, Hojin Ryu, Hyeon-Su Ro, Youn-Lee Oh
Journal of Fungi.2024; 10(12): 866. CrossRef - Current Perspectives on Uniparental Mitochondrial Inheritance in Cryptococcus neoformans
Amber R. Matha, Xiaorong Lin
Pathogens.2020; 9(9): 743. CrossRef - Investigation of Mating Pheromone–Pheromone Receptor Specificity in Lentinula edodes
Sinil Kim, Byeongsuk Ha, Minseek Kim, Hyeon-Su Ro
Genes.2020; 11(5): 506. CrossRef - The Evolution of Sexual Reproduction and the Mating-Type Locus: Links to Pathogenesis of Cryptococcus Human Pathogenic Fungi
Sheng Sun, Marco A. Coelho, Márcia David-Palma, Shelby J. Priest, Joseph Heitman
Annual Review of Genetics.2019; 53(1): 417. CrossRef -
Pathways of Pathogenicity: Transcriptional Stages of Germination in the Fatal Fungal Pathogen
Rhizopus delemar
Poppy C. S. Sephton-Clark, Jose F. Muñoz, Elizabeth R. Ballou, Christina A. Cuomo, Kerstin Voelz, Aaron P. Mitchell
mSphere.2018;[Epub] CrossRef - Activation of the Mating Pheromone Response Pathway ofLentinula edodesby Synthetic Pheromones
Byeongsuk Ha, Sinil Kim, Minseek Kim, Hyeon-Su Ro
Mycobiology.2018; 46(4): 407. CrossRef
- REVIEW] Developmental regulators in Aspergillus fumigatus
-
Hee-Soo Park , Jae-Hyuk Yu
-
J. Microbiol. 2016;54(3):223-231. Published online February 27, 2016
-
DOI: https://doi.org/10.1007/s12275-016-5619-5
-
-
49
View
-
0
Download
-
51
Crossref
-
Abstract
-
The filamentous fungus Aspergillus fumigatus is the most prevalent
airborne fungal pathogen causing severe and usually
fatal invasive aspergillosis in immunocompromised patients.
This fungus produces a large number of small hydrophobic
asexual spores called conidia as the primary means of reproduction,
cell survival, propagation, and infectivity. The initiation,
progression, and completion of asexual development
(conidiation) is controlled by various regulators that govern
expression of thousands of genes associated with formation
of the asexual developmental structure conidiophore, and
biogenesis of conidia. In this review, we summarize key regulators
that directly or indirectly govern conidiation in this
important pathogenic fungus. Better understanding these
developmental regulators may provide insights into the improvement
in controlling both beneficial and detrimental
aspects of various Aspergillus species.
-
Citations
Citations to this article as recorded by

-
Pleiotropic functions of SscA on the asexual spore of the human pathogenic fungus
Aspergillus fumigatus
Ye-Eun Son, Jiwoo Han, Kyung-Tae Lee, Hee-Soo Park
Mycology.2024; 15(2): 238. CrossRef - Regulation of Conidiation and Aflatoxin B1 Biosynthesis by a Blue Light Sensor LreA in Aspergillus flavus
Kunzhi Jia, Yipu Jia, Qianhua Zeng, Zhaoqi Yan, Shihua Wang
Journal of Fungi.2024; 10(9): 650. CrossRef - Comprehensive Insights into the Remarkable Function and Regulatory Mechanism of FluG during Asexual Development in Beauveria bassiana
Fang Li, Juefeng Zhang, Haiying Zhong, Kaili Yu, Jianming Chen
International Journal of Molecular Sciences.2024; 25(11): 6261. CrossRef - Genome-wide patterns of noncoding and protein-coding sequence variation in the major fungal pathogen Aspergillus fumigatus
Alec Brown, Jacob L Steenwyk, Antonis Rokas, J Comeron
G3: Genes, Genomes, Genetics.2024;[Epub] CrossRef - Cellular communication and fusion regulate cell fusion, trap morphogenesis, conidiation, and secondary metabolism in Arthrobotrys oligospora
Wenjie Wang, Yankun Liu, Shipeng Duan, Na Bai, Meichen Zhu, Jinkui Yang
Microbiological Research.2024; 278: 127516. CrossRef - The Cryptochrome CryA Regulates Lipid Droplet Accumulation, Conidiation, and Trap Formation via Responses to Light in Arthrobotrys oligospora
Yanmei Shen, Xuewei Yang, Meichen Zhu, Shipeng Duan, Qianqian Liu, Jinkui Yang
Journal of Fungi.2024; 10(9): 626. CrossRef - The CfKOB1 gene related to cell apoptosis is required for pathogenicity and involved in mycovirus-induced hypovirulence in Colletotrichum fructicola
Jun Zi Zhu, Ping Li, Zhuo Zhang, Xiao Gang Li, Jie Zhong
International Journal of Biological Macromolecules.2024; 271: 132437. CrossRef - Functional and Quality Assessment of a Spore Harvester for Entomopathogenic Fungi for Biopesticide Production
Fidel Diego-Nava, Carlos Granados-Echegoyen, Jaime Ruíz-Vega, Teodulfo Aquino-Bolaños, Rafael Pérez-Pacheco, Alejo Díaz-Ramos, Nancy Alonso-Hernández, Fabián Arroyo-Balán, Mónica Beatriz López-Hernández
AgriEngineering.2023; 5(2): 801. CrossRef - Verticillium dahliae Asp1 regulates the transition from vegetative growth to asexual reproduction by modulating microtubule dynamic organization
Juan Tian, Mengli Pu, Bin Chen, Guangda Wang, Chunli Li, Xiaxia Zhang, Yanjun Yu, Zhi Wang, Zhaosheng Kong
Environmental Microbiology.2023; 25(3): 738. CrossRef - Antifungal Activity of Plant Secondary Metabolites on Candida albicans: An Updated Review
Andleeb Khan, Sivakumar Sivagurunathan Moni, M. Ali, Syam Mohan, Huma Jan, Saiema Rasool, Mohammad A Kamal, Saeed Alshahrani, Maryam Halawi, Hassan A Alhazmi
Current Molecular Pharmacology.2023; 16(1): 15. CrossRef - Chitin Biosynthesis in Aspergillus Species
Veronica S. Brauer, André M. Pessoni, Mateus S. Freitas, Marinaldo P. Cavalcanti-Neto, Laure N. A. Ries, Fausto Almeida
Journal of Fungi.2023; 9(1): 89. CrossRef - Transcription factor CreA is involved in the inverse regulation of biofilm formation and asexual development through distinct pathways in Aspergillus fumigatus
Shuai Liu, Xiaoyan Lu, Mengyao Dai, Shizhu Zhang
Molecular Microbiology.2023; 120(6): 830. CrossRef - A new butenolide with antifungal activity from solid co-cultivation of Irpex lacteus and Nigrospora oryzae
Ya-Mei Wu, Xue-Qiong Yang, Jing-Xin Chen, Ting Wang, Tai-Ran Li, Fan-Rong Liao, Run-Tong Liu, Ya-Bin Yang, Zhong-Tao Ding
Natural Product Research.2023; 37(13): 2243. CrossRef - A Network of Sporogenesis-Responsive Genes Regulates the Growth, Asexual Sporogenesis, Pathogenesis and Fusaric Acid Production of Fusarium oxysporum f. sp. cubense
Songmao Lu, Huobing Deng, Yaqi Lin, Meimei Huang, Haixia You, Yan Zhang, Weijian Zhuang, Guodong Lu, Yingzi Yun
Journal of Fungi.2023; 10(1): 1. CrossRef - Light regulates the degradation of the regulatory protein VE-1 in the fungus Neurospora crassa
María del Mar Gil-Sánchez, Sara Cea-Sánchez, Eva M. Luque, David Cánovas, Luis M. Corrochano
BMC Biology.2022;[Epub] CrossRef - The C-22 sterol desaturase Erg5 is responsible for ergosterol biosynthesis and conidiation in Aspergillus fumigatus
Nanbiao Long, Guowei Zhong
Journal of Microbiology.2022; 60(6): 620. CrossRef - Comparative Transcriptomic Analyses Reveal the Regulatory Mechanism of Nutrient Limitation-Induced Sporulation of Antrodia cinnamomea in Submerged Fermentation
Huaxiang Li, Dan Ji, Zhishan Luo, Yilin Ren, Zhenming Lu, Zhenquan Yang, Zhenghong Xu
Foods.2022; 11(17): 2715. CrossRef - Azole‐resistant Aspergillus fumigatus as an emerging worldwide pathogen
Sofia Marisel Rivelli Zea, Takahito Toyotome
Microbiology and Immunology.2022; 66(3): 135. CrossRef - Transcriptional Regulation by the Velvet Protein VE-1 during Asexual Development in the Fungus Neurospora crassa
Sara Cea-Sánchez, María Corrochano-Luque, Gabriel Gutiérrez, N. Louise Glass, David Cánovas, Luis M. Corrochano, Reinhard Fischer
mBio.2022;[Epub] CrossRef - The secondary metabolite regulator, BbSmr1, is a central regulator of conidiation via the BrlA‐AbaA‐WetA pathway in Beauveria bassiana
Jin‐Feng Chen, Yu Liu, Gui‐Rong Tang, Dan Jin, Xi Chen, Yan Pei, Yan‐Hua Fan
Environmental Microbiology.2021; 23(2): 810. CrossRef - BbWor1, a Regulator of Morphological Transition, Is Involved in Conidium-Hypha Switching, Blastospore Propagation, and Virulence in Beauveria bassiana
Lei Qiu, Tong-Sheng Zhang, Ji-Zheng Song, Jing Zhang, Ze Li, Juan-Juan Wang, Christina A. Cuomo
Microbiology Spectrum.2021;[Epub] CrossRef - The putative sensor histidine kinase VadJ coordinates development and sterigmatocystin production in Aspergillus nidulans
Yanxia Zhao, Mi-Kyung Lee, Jieyin Lim, Heungyun Moon, Hee-Soo Park, Weifa Zheng, Jae-Hyuk Yu
Journal of Microbiology.2021; 59(8): 746. CrossRef - Novel Biological Functions of the NsdC Transcription Factor in Aspergillus fumigatus
Patrícia Alves de Castro, Clara Valero, Jéssica Chiaratto, Ana Cristina Colabardini, Lakhansing Pardeshi, Lilian Pereira Silva, Fausto Almeida, Marina Campos Rocha, Roberto Nascimento Silva, Iran Malavazi, Wenyue Du, Paul S. Dyer, Matthias Brock, Flávio V
mBio.2021;[Epub] CrossRef -
The Heterotrimeric Transcription Factor CCAAT-Binding Complex and Ca
2+
-CrzA Signaling Reversely Regulate the Transition between Fungal Hyphal Growth and Asexual Reproduction
Yiran Ren, Chi Zhang, Ziqing Chen, Ling Lu, Reinhard Fischer
mBio.2021;[Epub] CrossRef - The fungal‐specific histone acetyltransferase Rtt109 regulates development, DNA damage response, and virulence in Aspergillus fumigatus
Yuanwei Zhang, Jialu Fan, Jing Ye, Ling Lu
Molecular Microbiology.2021; 115(6): 1191. CrossRef - Deep convolutional neural network: a novel approach for the detection of Aspergillus fungi via stereomicroscopy
Haozhong Ma, Jinshan Yang, Xiaolu Chen, Xinyu Jiang, Yimin Su, Shanlei Qiao, Guowei Zhong
Journal of Microbiology.2021; 59(6): 563. CrossRef - The Arf-GAP AoGlo3 regulates conidiation, endocytosis, and pathogenicity in the nematode-trapping fungus Arthrobotrys oligospora
Yuxin Ma, Xuewei Yang, Meihua Xie, Guosheng Zhang, Le Yang, Na Bai, Yining Zhao, Dongni Li, Ke-Qin Zhang, Jinkui Yang
Fungal Genetics and Biology.2020; 138: 103352. CrossRef - The Autophagy-Related Gene Aolatg4 Regulates Hyphal Growth, Sporulation, Autophagosome Formation, and Pathogenicity in Arthrobotrys oligospora
Duanxu Zhou, Meihua Xie, Na Bai, Le Yang, Ke-Qin Zhang, Jinkui Yang
Frontiers in Microbiology.2020;[Epub] CrossRef -
Molecular Mechanisms of Conidial Germination in
Aspergillus
spp
Tim J. H. Baltussen, Jan Zoll, Paul E. Verweij, Willem J. G. Melchers
Microbiology and Molecular Biology Reviews.2020;[Epub] CrossRef - Reducing Aspergillus fumigatus Virulence through Targeted Dysregulation of the Conidiation Pathway
James I. P. Stewart, Vinicius M. Fava, Joshua D. Kerkaert, Adithya S. Subramanian, Fabrice N. Gravelat, Melanie Lehoux, P. Lynne Howell, Robert A. Cramer, Donald C. Sheppard, James W. Kronstad
mBio.2020;[Epub] CrossRef - Velvet activated McrA plays a key role in cellular and metabolic development in Aspergillus nidulans
Mi-Kyung Lee, Ye-Eun Son, Hee-Soo Park, Ahmad Alshannaq, Kap-Hoon Han, Jae-Hyuk Yu
Scientific Reports.2020;[Epub] CrossRef - The Transcriptional Regulator HbxA Governs Development, Secondary Metabolism, and Virulence in Aspergillus fumigatus
Timothy Satterlee, Binita Nepal, Sophie Lorber, Olivier Puel, Ana M. Calvo, Irina S. Druzhinina
Applied and Environmental Microbiology.2020;[Epub] CrossRef -
The Cell Wall Integrity Pathway Contributes to the Early Stages of
Aspergillus fumigatus
Asexual Development
Marina Campos Rocha, João Henrique Tadini Marilhano Fabri, Isabelle Taira Simões, Rafael Silva-Rocha, Daisuke Hagiwara, Anderson Ferreira da Cunha, Gustavo Henrique Goldman, David Cánovas, Iran Malavazi, Irina S. Druzhinina
Applied and Environmental Microbiology.2020;[Epub] CrossRef -
In vitro and in vivo characterization of two nonsporulating Aspergillus fumigatus clinical isolates from immunocompetent patients
Zheng Zhang, Yuan Jiang, Jun Chen, Peiying Chen, Qingtao Kong, Ling Lu, Hong Sang
Medical Mycology.2020; 58(4): 543. CrossRef - The brlA Gene Deletion Reveals That Patulin Biosynthesis Is Not Related to Conidiation in Penicillium expansum
Chrystian Zetina-Serrano, Ophélie Rocher, Claire Naylies, Yannick Lippi, Isabelle P. Oswald, Sophie Lorber, Olivier Puel
International Journal of Molecular Sciences.2020; 21(18): 6660. CrossRef - Recurrent Loss of abaA, a Master Regulator of Asexual Development in Filamentous Fungi, Correlates with Changes in Genomic and Morphological Traits
Matthew E Mead, Alexander T Borowsky, Bastian Joehnk, Jacob L Steenwyk, Xing-Xing Shen, Anita Sil, Antonis Rokas, Jason E Stajich
Genome Biology and Evolution.2020; 12(7): 1119. CrossRef - The histone acetyltransferase GcnE regulates conidiation and biofilm formation in Aspergillus fumigatus
Chi-Jan Lin, Yi-Hsuan Hou, Ying-Lien Chen
Medical Mycology.2019;[Epub] CrossRef - Aspergillus fumigatus phosphoethanolamine transferase gene gpi7 is required for proper transportation of the cell wall GPI-anchored proteins and polarized growth
Haomiao Ouyang, Ting Du, Hui Zhou, Iain B. H. Wilson, Jinghua Yang, Jean-Paul Latgé, Cheng Jin
Scientific Reports.2019;[Epub] CrossRef - Identification of a Novel Transcription Factor TP05746 Involved in Regulating the Production of Plant-Biomass-Degrading Enzymes in Talaromyces pinophilus
Ting Zhang, Lu-Sheng Liao, Cheng-Xi Li, Gui-Yan Liao, Xiong Lin, Xue-Mei Luo, Shuai Zhao, Jia-Xun Feng
Frontiers in Microbiology.2019;[Epub] CrossRef - The Velvet Proteins VosA and VelB Play Different Roles in Conidiation, Trap Formation, and Pathogenicity in the Nematode-Trapping Fungus Arthrobotrys oligospora
Guosheng Zhang, Yaqing Zheng, Yuxin Ma, Le Yang, Meihua Xie, Duanxu Zhou, Xuemei Niu, Ke-Qin Zhang, Jinkui Yang
Frontiers in Microbiology.2019;[Epub] CrossRef - An LaeA- and BrlA-Dependent Cellular Network Governs Tissue-Specific Secondary Metabolism in the Human Pathogen Aspergillus fumigatus
Abigail L. Lind, Fang Yun Lim, Alexandra A. Soukup, Nancy P. Keller, Antonis Rokas, Aaron P. Mitchell
mSphere.2018;[Epub] CrossRef - MybA, a new player driving survival of the conidium of the human pathogen Aspergillus fumigatus
Özlem Sarikaya Bayram, Jean Paul Latgé, Özgür Bayram
Current Genetics.2018; 64(1): 141. CrossRef - C-terminus Proteolysis and Palmitoylation Cooperate for Optimal Plasma Membrane Localization of RasA in Aspergillus fumigatus
Qusai Al Abdallah, Adela Martin-Vicente, Ana Camila Oliveira Souza, Wenbo Ge, Jarrod R. Fortwendel
Frontiers in Microbiology.2018;[Epub] CrossRef - Aspergillus fumigatus -induced early inflammatory response in pulmonary microvascular endothelial cells: Role of p38 MAPK and inhibition by silibinin
Jun Song, Weihua Pan, Yue Sun, Jing Han, Weimin Shi, Wanqing Liao
International Immunopharmacology.2017; 49: 195. CrossRef - Comparative Transcriptomic and Proteomic Analyses Reveal a FluG‐Mediated Signaling Pathway Relating to Asexual Sporulation of Antrodia camphorata
Hua‐Xiang Li, Zhen‐Ming Lu, Qing Zhu, Jin‐Song Gong, Yan Geng, Jin‐Song Shi, Zheng‐Hong Xu, Yan‐He Ma
PROTEOMICS.2017;[Epub] CrossRef - Human fungal pathogens: Why should we learn?
Jeong-Yoon Kim
Journal of Microbiology.2016; 54(3): 145. CrossRef - Aspergillus fumigatus spore proteomics and genetics reveal that VeA represses DefA-mediated DNA damage response
Kwang-Soo Shin, Hee-Soo Park, Young Kim, In-Beom Heo, Young Hwan Kim, Jae-Hyuk Yu
Journal of Proteomics.2016; 148: 26. CrossRef - Utilization of a Conidia-Deficient Mutant to Study Sexual Development in Fusarium graminearum
Hokyoung Son, Jae Yun Lim, Yoonji Lee, Yin-Won Lee, Sung-Hwan Yun
PLOS ONE.2016; 11(5): e0155671. CrossRef - Putative methyltransferase LaeA and transcription factor CreA are necessary for proper asexual development and controlling secondary metabolic gene cluster expression
Xiujun Zhang, Yingying Zhu, Longfei Bao, Liwei Gao, Guangshan Yao, Yanan Li, Zhifeng Yang, Zhonghai Li, Yaohua Zhong, Fuli Li, Heng Yin, Yinbo Qu, Yuqi Qin
Fungal Genetics and Biology.2016; 94: 32. CrossRef - How to invade a susceptible host: cellular aspects of aspergillosis
Sven Krappmann
Current Opinion in Microbiology.2016; 34: 136. CrossRef - Negative regulation and developmental competence in Aspergillus
Mi-Kyung Lee, Nak-Jung Kwon, Im-Soon Lee, Seunho Jung, Sun-Chang Kim, Jae-Hyuk Yu
Scientific Reports.2016;[Epub] CrossRef
Research Support, U.S. Gov't, Non-P.H.S.
- Structure and Function of the Mating-type Locus in the Homothallic Ascomycete, Didymella zeae-maydis
-
Sung-Hwan Yun , Olen C. Yoder , B. Gillian Turgeon
-
J. Microbiol. 2013;51(6):814-820. Published online December 19, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3465-2
-
-
48
View
-
0
Download
-
12
Crossref
-
Abstract
-
Homothallic Didymella zeae-maydis undergoes sexual reproduction
by selfing. Sequence analysis of the mating type
(MAT) locus from this fungus revealed that MAT carries
both MAT1-1-1 and MAT1-2-1 genes found in heterothallic
Dothideomycetes, separated by ~1.0 kb of noncoding DNA.
To understand the mechanistic basis of homothallism in D.
zeae-maydis, each of the MAT genes was deleted and the effects
on selfing and on ability to cross in a heterothallic manner
were determined. The strain carrying an intact MAT1-1-1
but defective MAT1-2-1 gene (MAT1-1-1;ΔMAT1-2-1) was
self-sterile, however strains carrying an intact MAT1-2-1 but
defective MAT1-1-1 gene (ΔMAT1-1-1;MAT1-2-1), when
selfed, showed delayed production of a few ascospores.
Attempts to cross the two MAT deletion strains yielded fewer
ΔMAT1-1-1;MAT1-2-1 than MAT1-1-1;ΔMAT1-2-1 progeny
and very few ascospores overall compared to WT selfs. This
study demonstrates that, as in the other homothallic Dothideomycetes,
both MAT genes are required for full fertility,
but that, in contrast to other cases, the presence of a single
MAT1-2-1 gene can induce homothallism, albeit inefficiently,
in D. zeae-maydis.
-
Citations
Citations to this article as recorded by

- Structure and number of mating pheromone genes is closely linked to sexual reproductive strategy in Huntiella
Andi M. Wilson, Michael J. Wingfield, Brenda D. Wingfield
BMC Genomics.2023;[Epub] CrossRef - The Role of Chromatin and Transcriptional Control in the Formation of Sexual Fruiting Bodies in Fungi
Minou Nowrousian
Microbiology and Molecular Biology Reviews.2022;[Epub] CrossRef - First Characterisation of the Phoma Species Complex on Maize Leaves in Central Europe
Lucia Ramos Romero, Dagmar Tacke, Birger Koopmann, Andreas von Tiedemann
Pathogens.2021; 10(9): 1216. CrossRef - Integrative Activity of Mating Loci, Environmentally Responsive Genes, and Secondary Metabolism Pathways during Sexual Development of Chaetomium globosum
Zheng Wang, Francesc López-Giráldez, Junrui Wang, Frances Trail, Jeffrey P. Townsend, Alexander Idnurm
mBio.2019;[Epub] CrossRef - Transition from heterothallism to homothallism is hypothesised to have facilitated speciation among emerging Botryosphaeriaceae wheat-pathogens
Elisha Thynne, Megan C. McDonald, Peter S. Solomon
Fungal Genetics and Biology.2017; 109: 36. CrossRef - Molecular manipulation of the mating-type system and development of a new approach for characterizing pathogen virulence in Pyrenophora tritici-repentis
Gazala Ameen, Gayan Kariyawasam, Gongjun Shi, Timothy L. Friesen, Justin D. Faris, Shaukat Ali, Jack B. Rasmussen, Zhaohui Liu
Fungal Genetics and Biology.2017; 109: 16. CrossRef - Genetic Dissection of Sexual Reproduction in a Primary Homothallic Basidiomycete
Márcia David-Palma, José Paulo Sampaio, Paula Gonçalves, Joseph Heitman
PLOS Genetics.2016; 12(6): e1006110. CrossRef - Mating-Type Gene Structure and Spatial Distribution ofDidymella tanacetiin Pyrethrum Fields
Tamieka L. Pearce, Jason B. Scott, Frank S. Hay, Sarah J. Pethybridge
Phytopathology®.2016; 106(12): 1521. CrossRef -
Fungal Sex: The
Ascomycota
Richard J. Bennett, B. Gillian Turgeon, Joseph Heitman
Microbiology Spectrum.2016;[Epub] CrossRef - Characterization and distribution of mating-type genes of the turfgrass pathogen Sclerotinia homoeocarpa on a global scale
Alexander I. Putman, Lane P. Tredway, Ignazio Carbone
Fungal Genetics and Biology.2015; 81: 25. CrossRef - Unisexual versus bisexual mating in Cryptococcus neoformans: Consequences and biological impacts
Ci Fu, Sheng Sun, R.B. Billmyre, Kevin C. Roach, Joseph Heitman
Fungal Genetics and Biology.2015; 78: 65. CrossRef - Pondering Mating: Pneumocystis jirovecii, the Human Lung Pathogen, Selfs without Mating Type Switching, in Contrast to Its Close Relative Schizosaccharomyces pombe
Patrik Inderbitzin, B. Gillian Turgeon
mBio.2015;[Epub] CrossRef
Research Support, Non-U.S. Gov'ts
- 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
-
J. Microbiol. 2013;51(6):800-806. Published online December 19, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3100-2
-
-
50
View
-
0
Download
-
13
Crossref
-
Abstract
-
The nsdD gene encoding a GATA type transcription factor
positively controls sexual development in Aspergillus nidulans.
According to microarray data, 20 genes that were upregulated
by deleting nsdD during various life cycle stages were
randomly selected and deleted for functional analysis. None
of the mutants showed apparent changes in growth or development
compared with those of the wild-type except the
AN3154 gene that encodes a putative APSES transcription
factor and is an ortholog of Saccharomyces cerevisiae swi4.
Deleting AN3154 resulted in retarded growth and development,
and the gene was named rgdA (retared growth and
development). The rgdA deletion mutant developed a reduced
number of conidia even under favorable conditions for asexual
development. The retarded growth and development was
partially suppressed by the veA1 mutation. The conidial heads
of the mutant aborted, showing reduced and irregular shaped
phialides. Fruiting body development was delayed compared
with that in the wild-type. The mutant did not respond to
various nutritional or environmental factors that affected the
development patterns. The rgdA gene was expressed at low
levels throughout the life cycle and was not significantly affected
by several regulators of sexual and asexual development
such as nsdD, veA, stuA, or brlA. However, the rgdA gene
affected brlA and abaA expression, which function as key
regulators of asexual sporulation, suggesting that rgdA functions
upstream of those genes.
-
Citations
Citations to this article as recorded by

- Putative APSES family transcription factor mbp1 plays an essential role in regulating cell wall synthesis in the agaricomycete Pleurotus ostreatus
Hayase Kojima, Moriyuki Kawauchi, Yuitsu Otsuka, Kim Schiphof, Kenya Tsuji, Akira Yoshimi, Chihiro Tanaka, Shigekazu Yano, Takehito Nakazawa, Yoichi Honda
Fungal Genetics and Biology.2024; 175: 103936. CrossRef - Regulators of the Asexual Life Cycle of Aspergillus nidulans
Ye-Eun Son, Jae-Hyuk Yu, Hee-Soo Park
Cells.2023; 12(11): 1544. CrossRef - Characterization of the mbsA Gene Encoding a Putative APSES Transcription Factor in Aspergillus fumigatus
Yong-Ho Choi, Sang-Cheol Jun, Min-Woo Lee, Jae-Hyuk Yu, Kwang-Soo Shin
International Journal of Molecular Sciences.2021; 22(7): 3777. CrossRef - The Putative APSES Transcription Factor RgdA Governs Growth, Development, Toxigenesis, and Virulence in Aspergillus fumigatus
Sang-Cheol Jun, Yong-Ho Choi, Min-Woo Lee, Jae-Hyuk Yu, Kwang-Soo Shin, Aaron P. Mitchell
mSphere.2020;[Epub] CrossRef - Analogous and Diverse Functions of APSES-Type Transcription Factors in the Morphogenesis of the Entomopathogenic Fungus Metarhizium rileyi
Caiyan Xin, Jinping Zhang, Siji Nian, Guangxi Wang, Zhongkang Wang, Zhangyong Song, Guangwei Ren, Ning-Yi Zhou
Applied and Environmental Microbiology.2020;[Epub] CrossRef - Distribution, evolution and expression ofGATA-TFsprovide new insights into their functions in light response and fruiting body development ofTolypocladium guangdongense
Chenghua Zhang, Gangzheng Wang, Wangqiu Deng, Taihui Li
PeerJ.2020; 8: e9784. CrossRef - Characterization of the APSES-family transcriptional regulators of Histoplasma capsulatum
Larissa V G Longo, Stephanie C Ray, Rosana Puccia, Chad A Rappleye
FEMS Yeast Research.2018;[Epub] CrossRef - Essential APSES Transcription Factors for Mycotoxin Synthesis, Fungal Development, and Pathogenicity in Aspergillus flavus
Guangshan Yao, Feng Zhang, Xinyi Nie, Xiuna Wang, Jun Yuan, Zhenhong Zhuang, Shihua Wang
Frontiers in Microbiology.2017;[Epub] CrossRef - Characterizing the nuclear proteome of Paracoccidioides spp.
Lucas Nojosa Oliveira, Luciana Casaletti, Sônia Nair Báo, Clayton Luiz Borges, Patrícia de Sousa Lima, Célia Maria de Almeida Soares
Fungal Biology.2016; 120(10): 1209. CrossRef - Isolation and Characterization of Two Methyltransferase Genes, AfuvipB and AfuvipC in Aspergillus fumigatus
Mohammed A. Abdo Elgabbar, Kap-Hoon Han
The Korean Journal of Mycology.2015; 43(1): 33. CrossRef - Depletion of ε-COP in the COPI Vesicular Coat Reduces Cleistothecium Production inAspergillus nidulans
Eun-Hye Kang, Eun-Jung Song, Jun Ho Kook, Hwan-Hee Lee, Bo-Ri Jeong, Hee-Moon Park
Mycobiology.2015; 43(1): 31. CrossRef - FgFlbD regulates hyphal differentiation required for sexual and asexual reproduction in the ascomycete fungus Fusarium graminearum
Hokyoung Son, Myung-Gu Kim, Suhn-Kee Chae, Yin-Won Lee
Journal of Microbiology.2014; 52(11): 930. CrossRef - Transcriptional regulation of fksA, a β-1,3-glucan synthase gene, by the APSES protein StuA during Aspergillus nidulans development
Bum-Chan Park, Yun-Hee Park, Soohyun Yi, Yu Kyung Choi, Eun-Hye Kang, Hee-Moon Park
Journal of Microbiology.2014; 52(11): 940. CrossRef
- 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
-
-
27
View
-
0
Download
-
3
Scopus
-
Abstract
-
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.
- Incidence of Wolbachia and Cardinium Endosymbionts in the Osmia Community in Korea
-
Gilsang Jeong , Kyeongyong Lee , Jiyoung Choi , Seokjo Hwang , Byeongdo Park , Wontae Kim , Youngcheol Choi , Ingyun Park , Jonggill Kim
-
J. Microbiol. 2009;47(1):28-32. Published online February 20, 2009
-
DOI: https://doi.org/10.1007/s12275-009-0198-3
-
-
43
View
-
0
Download
-
12
Scopus
-
Abstract
-
Sex ratio distorting endosymbionts induce reproductive anomalies in their arthropod hosts. They have recently been paid much attention as firstly texts of evolution of host-symbiont relationships and secondly potential biological control agents to control arthropod pests. Among such organisms, Wolbachia and Cardinium bacteria are well characterized. This study aims at probing such bacteria in the Osmia community to evaluate their potential utilization to control arthropod pests. Among 17 PCR tested species, Osmia cornifrons and a parasitic fly are infected with Wolbachia and a mite species is infected with Cardinium. Phylogenetic tree analyses suggest that horizontal transfer of the bacteria occurred between phylogenetically distant hosts.
- Screening of Growth- or Development-related Genes by Using Genomic Library with Inducible Promoter in Aspergillus nidulans
-
Bang-Yong Lee , Sang-Yong Han , Han Gil Choi , Jee Hyun Kim , Kap-Hoon Han , Dong-Min Han
-
J. Microbiol. 2005;43(6):523-528.
-
DOI: https://doi.org/2295 [pii]
-
-
Abstract
-
Using the genomic library constructed at the downstream of the niiA promoter, which induces the over-expression of an inserted DNA fragment, we have attempted to screen the genes affecting growth or development by over-expression. The wild-type strain was transformed using the AMA-niiA(p) library and cultured on 1.2 M sorbitol media, in which asexual sporulation is induced, but sexual development is repressed. Over 100,000 strains transformed to pyrG+ were analyzed with regard to any changes in phenotype. Consequently, seven strains were isolated for further analyses. These strains were designated NOT [niiA(p) over-expression transformants] stains. Four of the strains were of the inducible type, and the remaining strains were of the multi-copy suppression type. Two of the inducible-type strains, NOT1 and NOT40, harbored genes which had been inserted in reverse direction, suggesting that the mutant phenotypes had been derived from an excess amount of anti-sense mRNA. Domain analyses of the deduced polypeptides from the DNA fragments rescued from the transformants revealed that NOT1, NOT40 and NOT6 harbored a LisH motif, a forkhead domain, and a Zn(II)2Cys6 binuclear zinc cluster, respectively.
- Fungal-sporulation suppressing substances produced by pseudomonas aeruginosa KMCS-1
-
Min, Bu Yong , Shim, Jae Young , Kim, Kun Woo , Lee, Jong Kyu , Yoon, Kwon Sang
-
J. Microbiol. 1996;34(3):284-288.
-
-
-
Abstract
-
Among the bacteria isolated form compost piles of cattle excretion in a pasture located at the suburbs of Chunchon city, Pseudomonas aeruginosa KMCS-1 was selected for the test of antifungal substances produced. Six fractions were separated by silica gel column chromatography, and then the antifungal activity of each fraction was assayed against Escherichia coli, Bacillus subtilis, Candida albicans, Rhizopus sp., Aspergillus nidulans, Coprinus cinereus, and Pyricularia oryzae by paper disc method. Two fractions showed significant suppressive activities against A. nidulans, C. cinereus, and P. oryzae; however, their mycelial growth was not affected by neither of these fractions. Inhibitory activities of these fractions to sporulation was assayed at the concentration of 50. 25, 12. 5, and 6.25 ㎍/ml and the average inhibition rates against sporulation of A. nidulans, C. cinereus, and P. oryzae were 94.0, 98.3, and 77.9%, respectively. Further purification and analysis of active substances are now being conducted.
- Quantitative Analysis of Expressed Genes in Aspergillus Oryzae by Sequencing 3'-directed cDNA Clones
-
Hwang, Hyun Ah , Lee, Dong Whan , Kim, Jong Hwa , Lee, Tae Kyoo , Yang, Moon Sik , Chae, Keon Sang
-
J. Microbiol. 1998;36(2):111-117.
-
-
-
Abstract
-
Sequence analysis of randomly selected 3'-directed cKNA clones has been known to be one of the most powerful methods of examining the genes highly expressed in a tissue or cell type. We constructed a 3'-directed cDNA libraty from Aspergillus oryzae mycelia, and sequenced 345 randomly selected 3'-directed cDNA clones. Determined nucleotide sequences, not shorter than 30nt, were compared with one other to generate gene signatures (GSs) and were then compared with GenBank entries to analyze sequence similarity to known genes. A GS for the most highly expressed gene appeared six times, one GS five times, five GSs four times, five GSs three times and 22 GSs twice. In total, 324 clones yielded 268 GSs consisting of 34 redundant GSs appeaning at least twice and 234 solitary ones. Forty-three GSs showed similarities ranging from 60% to 99% with known sequences from Genbank. A considerable number of A. oryzae GSs mateched those obtained from the sexual structures of A. nidulans suggests that A. oryzae may not be phylogentically distant from A. nidulans and that A. oryzae may have a sexual life cycle from the ancient period.
- Microscopic Examination of the Suppressive Action of Antifungal Substances from Pseudomonas aeruginosa on Asexual Sporulation of Fungi
-
Yoon, Kwon S. , Min, Bu Y. , Choi, Hyoung T. , Lee, Jong K. , Kim, Kun W.
-
J. Microbiol. 1999;37(1):27-34.
-
-
-
Abstract
-
Two fractions with unusual antifungal activity that suppress asexual sporulation of several fungi were obtained from culture filtrate of Pseudomonas aeruginosa and were partially purified through the repeated silicagel flash column chromatographies. The sporulation-suppressive actions of these fractions in Aspergillus nidulans, Rhizopus stolonifer, and Coprinus cinereus, were analyzed by light and electron microscopes. The germination ability of the spores produced in the presence of these fractions were also checked to determine the persistent effects of these antifungal substances on the next generation. Light microscopic observation of developing sporangia of R. stolonifer grown in the presence of both fractions revealed that the significant number of sporangia failed to reach maturity, and frequently, uncontrolled growths of hyphae and rhizoids from the sporangiophores were found. In A. nidulans addition of these fractions appeared to cause different classes of morphological abnormality in conidia development, which included aborted formation of conidiogenous cells from the apex of conidiophores and enhanced hyphal growths either at the tip or middle of the conidiophores. Germination abilities of spores obtained from the cultures grown in the presence of antifungal fractions were 40∼60% in Aspergillus, 50∼80% in Coprinus (thallic spores), and 30∼40% in Rhizopus compared to those of normal spores.