Review
- cAMP receptor proteins in mycobacteria
-
Jeong-Il Oh, Yuna Oh, Yupin Hwang
-
J. Microbiol. 2026;64(10):e2607013. Published online October 31, 2026
-
DOI: https://doi.org/10.71150/jm.2607013
-
-
Abstract
PDF
-
Cyclic adenosine monophosphate (cAMP) signaling is a major regulatory system in mycobacteria, and the cAMP receptor protein (CRP) serves as its principal transcriptional effector. In Mycobacterium tuberculosis, CRP controls a broad regulon associated with metabolic adaptation, respiration, cell envelope-associated processes, dormancy-related resuscitation, and virulence. Structural and biophysical studies have demonstrated that mycobacterial CRPs differ from the classical Escherichia coli paradigm: apo-CRP adopts restrained or asymmetric conformations, whereas cAMP binding promotes a more symmetric, DNA-binding-competent state and enhances the specificity of CRP-DNA interactions. In Mycobacterium smegmatis, the major paralog Crp1 (MSMEG_6189) regulates metabolic and respiratory adaptation, oxidative stress defense, and isoniazid susceptibility, whereas Crp2 (MSMEG_0539) appears to play a more limited or subsidiary role. Recent findings further reveal that CRP activity is modulated by lysine acetylation, cooperative promoter recruitment with the virulence-associated response regulator PhoP, and respiratory inhibition-induced increases in intracellular cAMP, thereby linking metabolic and respiratory status to adaptive and virulence-associated gene regulation. This review summarizes the structure, allosteric regulation, regulon, and physiological functions of mycobacterial CRPs, highlighting their role as central integrators of cAMP signaling, respiratory and metabolic state, persistence-associated physiology, and antibiotic susceptibility.
Review
- Reverse Zoonotic Transmission of SARS-CoV-2 and Monkeypox Virus: A Comprehensive Review
-
Chiranjib Chakraborty, Manojit Bhattacharya, Md Aminul Islam, Hatem Zayed, Elijah Ige Ohimain, Sang-Soo Lee, Prosun Bhattacharya, Kuldeep Dhama
-
J. Microbiol. 2024;62(5):337-354. Published online May 23, 2024
-
DOI: https://doi.org/10.1007/s12275-024-00138-9
-
-
1,499
View
-
16
Download
-
7
Web of Science
-
7
Crossref
-
Abstract
PDF
-
Reverse zoonosis reveals the process of transmission of a pathogen through the human-animal interface and the spillback of the zoonotic pathogen. In this article, we methodically demonstrate various aspects of reverse zoonosis, with a comprehensive discussion of SARS-CoV-2 and MPXV reverse zoonosis. First, different components of reverse zoonosis, such as humans, different pathogens, and numerous animals (poultry, livestock, pets, wild animals, and zoo animals), have been demonstrated. Second, it explains the present status of reverse zoonosis with different pathogens during previous occurrences of various outbreaks, epidemics, and pandemics. Here, we present 25 examples from literature. Third, using several examples, we comprehensively illustrate the present status of the reverse zoonosis of SARS-CoV-2 and MPXV. Here, we have provided 17 examples of SARS-CoV-2 reverse zoonosis and two examples of MPXV reverse zoonosis. Fourth, we have described two significant aspects of reverse zoonosis: understanding the fundamental aspects of spillback and awareness. These two aspects are required to prevent reverse zoonosis from the current infection with two significant viruses. Finally, the One Health approach was discussed vividly, where we urge scientists from different areas to work collaboratively to solve the issue of reverse zoonosis.
-
Citations
Citations to this article as recorded by

- Environmental degradation as a recipe for emerging viral diseases: implications for global health
Shuaibu Abdullahi Hudu, Abdulgafar Olayiwola Jimoh, Syafinaz Amin-Nordin, Sharifah Syed Hassan
One Health Outlook.2026;[Epub] CrossRef - Phylogenetic analyses of the spread of Clade I MPOX in African and non-African nations
Chiranjib Chakraborty, Manojit Bhattacharya, Arpita Das, Ali S. Abdelhameed
Virus Genes.2025; 61(3): 265. CrossRef - Efficient and modular reverse genetics system for rapid generation of recombinant severe acute respiratory syndrome coronavirus 2
Sojung Bae, Jinjong Myoung
Journal of Microbiology.2025; 63(7): e2504015. CrossRef - Real-time malaria detection in the Amazon rainforest via drone-collected eDNA and portable qPCR
Yin Cheong Aden Ip, Luca Montemartini, Jia Jin Marc Chang, Andrea Desiderato, Nicolás D. Franco-Sierra, Christian Geckeler, Mailyn Adriana Gonzalez Herrera, Michele Gregorini, Meret Jucker, Steffen Kirchgeorg, Martina Lüthi, Elvira Mächler, Frederik Bendi
One Health.2025; 21: 101167. CrossRef - One digital health through wearables: a viewpoint on human–pet integration towards Healthcare 5.0
Mostafa Haghi, Samira Abani, Soheil Khooyooz, Anice Jahanjoo, Samaneh Rashidibajgan, Nima TaheriNejad, Thomas M. Deserno, Holger Volk
Frontiers in Digital Health.2025;[Epub] CrossRef - Development of a multiplex real-time PCR for the simultaneous detection of monkeypox virus clades I, II, and goatpox virus
Yongqiang Lin, Zijing Guo, Jinsong Chen, Xianwen Zhang, Long Zhou, Yanmin Li, Zhidong Zhang
Frontiers in Veterinary Science.2024;[Epub] CrossRef - Differential Impact of Spike Protein Mutations on SARS-CoV-2 Infectivity and Immune Evasion: Insights from Delta and Kappa Variants
Tae-Hun Kim, Sojung Bae, Jinjong Myoung
Journal of Microbiology and Biotechnology.2024; 34(12): 2506. CrossRef
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
-
-
1,946
View
-
43
Download
-
8
Web of Science
-
8
Crossref
-
Abstract
PDF
-
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.
-
Citations
Citations to this article as recorded by

- Clinical characteristics of two companion canines with severe fever with thrombocytopenia syndrome virus (Bandavirus dabieense) in Seoul, Republic of Korea
Hye-Ryung Byun, Seong-Ryeong Ji, Jeong-Yeon Hwang, So-Yoon Lee, Joon-Seok Chae
Veterinary Research Communications.2026;[Epub] CrossRef - Targeting the lethal weakness of SFTSV: Latest advances in antiviral strategies and immune prevention
Ruiqi Weng, Hao Wu, Yutong Xu, Zhiyi Wang, Siyi Gu, Keda Chen
iScience.2026; 29(4): 115154. CrossRef - Vaccine value profile for severe fever with thrombocytopenia syndrome (SFTS)
Laura Skrip, Arata Hidano, Yong Poovorawan, Sarawut Khongwichit, Hirofumi Kato, Sebastian Kapell, Motoharu Abe, Sung-mok Jung, Mark Jit, Kye-Hyung Kim, Jongyoun Yi, Taiga Miyazaki, Takeshi Kawaguchi, Tamaki Okabayashi, Joon-Seok Chae, Koya Ariyoshi, W. Jo
Vaccine.2026; 82: 128596. CrossRef - Efficacy of severe fever with thrombocytopenia syndrome vaccines in animal models: a systematic review and meta-analysis
Eric Sibomana, Eurade Ntakiyisumba, Fabrice Hirwa, Maryum Tanveer, Noutlady Inthavong, Jaime C. Cabarles, John Hwa Lee, Gayeon Won
Frontiers in Microbiology.2026;[Epub] CrossRef - The immunogenicity and protection efficacy evaluation of mRNA vaccine candidate for severe fever with thrombocytopenia syndrome in mice
Da-Eun Jeong, Jack Yoon, Baek Kim, Jun-Gu Kang, Abdallah M. Samy
PLOS Neglected Tropical Diseases.2025; 19(4): e0012999. CrossRef - Efficient and modular reverse genetics system for rapid generation of recombinant severe acute respiratory syndrome coronavirus 2
Sojung Bae, Jinjong Myoung
Journal of Microbiology.2025; 63(7): e2504015. CrossRef - Current status of severe fever with thrombocytopenia syndrome in China (Review)
Hao Sun, Quanman Hu, Saiwei Lu, Yanyan Yang, Li Zhang, Jinzhao Long, Yuefei Jin, Haiyan Yang, Shuaiyin Chen, Guangcai Duan
International Journal of Molecular Medicine.2025; 56(5): 1. CrossRef - Domain-Specific Impacts of Spike Protein Mutations on Infectivity and Antibody Escape in SARS-CoV-2 Omicron BA.1
Tae-Hun Kim, Sojung Bae, Jinjong Myoung
Journal of Microbiology and Biotechnology.2025;[Epub] CrossRef
Article
- Microbial co-occurrence network in the rhizosphere microbiome: its association with physicochemical properties and soybean yield at a regional scale
-
Sarbjeet Niraula , Meaghan Rose , Woo-Suk Chang
-
J. Microbiol. 2022;60(10):986-997. Published online September 27, 2022
-
DOI: https://doi.org/10.1007/s12275-022-2363-x
-
-
1,096
View
-
3
Download
-
17
Web of Science
-
16
Crossref
-
Abstract
PDF
-
Microbial communities in the rhizosphere play a crucial role
in determining plant growth and crop yield. A few studies
have been performed to evaluate the diversity and co-occurrence
patterns of rhizosphere microbiomes in soybean (Glycine
max) at a regional scale. Here, we used a culture-independent
method
to compare the bacterial communities of the
soybean rhizosphere between Nebraska (NE), a high-yield
state, and Oklahoma (OK), a low-yield state. It is well known
that the rhizosphere microbiome is a subset of microbes that
ultimately get colonized by microbial communities from the
surrounding bulk soil. Therefore, we hypothesized that differences
in the soybean yield are attributed to the variations in
the rhizosphere microbes at taxonomic, functional, and community
levels. In addition, soil physicochemical properties
were also evaluated from each sampling site for comparative
study. Our result showed that distinct clusters were formed
between NE and OK in terms of their soil physicochemical
property. Among 3 primary nutrients (i.e., nitrogen, phosphorus,
and potassium), potassium is more positively correlated
with the high-yield state NE samples. We also attempted
to identify keystone communities that significantly affected the
soybean yield using co-occurrence network patterns. Network
analysis revealed that communities formed distinct clusters
in which members of modules having significantly positive
correlations with the soybean yield were more abundant in
NE than OK. In addition, we identified the most influential
bacteria for the soybean yield in the identified modules. For
instance, included are class Anaerolineae, family Micromonosporaceae,
genus Plantomyces, and genus Nitrospira in the
most complex module (ME9) and genus Rhizobium in ME23.
This research would help to further identify a way to increase
soybean yield in low-yield states in the U.S. as well as worldwide
by reconstructing the microbial communities in the
rhizosphere.
-
Citations
Citations to this article as recorded by

- Interaction of soil microbial communities with soil nutrients, enzymes activity, and allelopathic compounds in flue-cured tobacco continuous monocropping field
Yihong Pan, Tiyuan Xia, Qiulian Peng, Kun Huang, Lijuan Zhou, Guohuan Xiong
Physiological and Molecular Plant Pathology.2026; 141: 103032. CrossRef - Research Progress on Rhizosphere Microbiota for Controlling Soil-Borne Diseases: Mechanisms, Applications, and Challenges
Yong Liu, Xiaofang Sun, Jia Lai, Shugu Wei, Yuzhen Sheng, Yinchao Zhang, Qianfang Zhang, Pengsheng Ye, Ling Huang, Hualan Zeng
Microorganisms.2026; 14(4): 900. CrossRef - Gradient Potassium Application Differentially Regulates Rhizosphere Bacterial and Fungal Communities in Cherry Tomato (Solanum lycopersicum var. cerasiforme)
Chenpeng Gao, Guigui Wan, Ruifeng Cheng, Quansheng Li, Qinglu Fan, Jinxia Cui, Linnan Wu
Plants.2026; 15(10): 1545. CrossRef - Role of rhizosphere specific microbiome in enhancing soybean productivity across contrasting soil and crop management systems
Prem Ranjan, Diptimayhee Das, Vindhya Bundela, Aketi Ramesh, Rakesh Kumar Verma, Raghavendra Nargund, Urmila Manandhar, Rhae Drijber, Rakesh K. Upadhyay, Mahaveer Prasad Sharma
Frontiers in Plant Science.2026;[Epub] CrossRef - Paddy soils with contrasting rice yields harbor distinct microbial networks and candidate key microbes
Do-Hyun Kim, Sang Yoon Kim, Yeomyeong Lee, Sohee Yoon, Hyerin An, Yu-Na Jeon, Jaekyeong Song, Sujin Kim, Jung Seon Kim, Gyeongjun Cho
Applied Soil Ecology.2026; 225: 107166. CrossRef - Cover crops legacy modulates soybean rhizosphere microbiome across phenological stages
Caio César Gomes Freitas, Carolinne Rosa de Carvalho, Rafael Lima Oliveira, Nariane de Andrade, Danilo Ferreira da Silva, Mísia Souza Vieira, Victor Lucas Vieira Prudêncio Araújo, João Henrique dos Santos Ferreira, José Roberto Portugal, Carlos Alexandre
Applied Soil Ecology.2026; 225: 107220. CrossRef - Plant–Microbiome Interactions for Rhizosphere Health: A Three‐Step Framework for Crop Resilience
Wei Qiu, Xiufeng Tang, Qirong Shen, Jun Yuan
Plant, Cell & Environment.2026;[Epub] CrossRef - Soybean productivity can be enhanced by understanding rhizosphere microbiota: evidence from metagenomics analysis from diverse agroecosystems
Honglei Ren, Huilong Hong, Bire Zha, Sobhi F. Lamlom, Hongmei Qiu, Yongqiang Cao, Rujian Sun, Haorang Wang, Junkui Ma, Hengbin Zhang, Liping Sun, Qing Yang, Changjun Zhou, Xiulin Liu, Xueyang Wang, Chunlei Zhang, Fengyi Zhang, Kezhen Zhao, Rongqiang Yuan,
Microbiome.2025;[Epub] CrossRef - Impact of Bacterial Pustule Disease Occurrence on Bacterial and Fungal Communities Within Vegetable Soybean Plants
Choosak Khaengraeng, Wuttichai Mhuantong, Usawadee Chaiprom, Sawita Suwannarat, Nattakorn Kuncharoen, Nutjarin Haewou, Warapon Bunkoed, Tiyakhon Chatnaparat
Plant Pathology.2025; 74(5): 1228. CrossRef - A molecular conveyor belt-associated protein controls the rotational direction of the bacterial type 9 secretion system
Abhishek Trivedi, Jacob A. Miratsky, Emma C. Henderson, Abhishek Singharoy, Abhishek Shrivastava, Clay Fuqua
mBio.2025;[Epub] CrossRef - Discontinuation of glacial meltwater input reshapes the diversity and stability of eukaryotic planktonic microbial communities in glacial lakes
Xiaodong Li, Qianggong Zhang, Peng Zhang, Qing Yang, Zijian Lu, Yanan Zhou, Meiqi Huang, Guangli Mu, Zhao Xue, Linyuan Lu, Yindong Tong
Environmental Research.2025; 286: 122785. CrossRef - Rice-microbiome-metabolite crosstalk: Deciphering the defence signatures of traditional rice landraces against blast (Magnaporthe oryzae)
R. Karan, M.K. Prasannakumar, N. Vamsidharreddy, J. Harish, H.B. Mahesh, C. Manjunatha, K.N. Pallavi, Pramesh Devanna, Selva babu Selvamani, Aditya Narayan Sarangi
Plant Stress.2025; 18: 101084. CrossRef - The rhizosphere microbiome of 51 potato cultivars with diverse plant growth characteristics
Benoit Renaud Martins, Viviane Radl, Krzysztof Treder, Dorota Michałowska, Karin Pritsch, Michael Schloter
FEMS Microbiology Ecology.2024;[Epub] CrossRef - Response of Soil Microorganisms and Phenolic to Pseudostelariae heterophylla Cultivation in Different Soil Types
Yingying Liu, Dan Wu, Yongjun Kan, Li Zhao, Chang Jiang, Wensheng Pang, Juan Hu, Meilan Zhou
Eurasian Soil Science.2024; 57(3): 446. CrossRef - Analysis of the rhizosphere bacterial diversity of Angelica dahurica var. formosana from different experimental sites and varieties (strains)
Meiyan Jiang, Fei Yao, Yunshu Yang, Yang Zhou, Kai Hou, Yinyin Chen, Dongju Feng, Wei Wu
PeerJ.2023; 11: e15997. CrossRef - Long-term fertilization coupled with rhizobium inoculation promotes soybean yield and alters soil bacterial community composition
Wanling Wei, Dawei Guan, Mingchao Ma, Xin Jiang, Fenliang Fan, Fangang Meng, Li Li, Baisuo Zhao, Yubin Zhao, Fengming Cao, Huijun Chen, Jun Li
Frontiers in Microbiology.2023;[Epub] CrossRef
Review
- 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
-
-
955
View
-
0
Download
-
7
Crossref
-
Abstract
PDF
-
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

-
Dissecting the homeodomain
MAT
locus and engineering novel tripolar and bipolar mating systems in
Cryptococcus amylolentus
Liping Xiong, Vikas Yadav, Sheng Sun, Joseph Heitman, Marcio Rodrigues
mBio.2026;[Epub] CrossRef - 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 of
Lentinula edodes
by Synthetic Pheromones
Byeongsuk Ha, Sinil Kim, Minseek Kim, Hyeon-Su Ro
Mycobiology.2018; 46(4): 407. CrossRef
Review
- Histone deacetylase-mediated morphological transition in Candida albicans
-
Jueun Kim , Ji-Eun Lee , Jung-Shin Lee
-
J. Microbiol. 2015;53(12):805-811. Published online December 2, 2015
-
DOI: https://doi.org/10.1007/s12275-015-5488-3
-
-
1,041
View
-
1
Download
-
28
Crossref
-
Abstract
PDF
-
Candida albicans is the most common opportunistic fungal
pathogen, which switches its morphology from single-cell
yeast to filament through the various signaling pathways responding
to diverse environmental cues. Various transcriptional
factors such as Nrg1, Efg1, Brg1, Ssn6, and Tup1 are
the key components of these signaling pathways. Since C.
albicans can regulate its transcriptional gene expressions using
common eukaryotic regulatory systems, its morphological
transition by these signaling pathways could be linked
to the epigenetic regulation by chromatin structure modifiers.
Histone proteins, which are critical components of eukaryotic
chromatin structure, can regulate the eukaryotic chromatin
structure through their own modifications such as acetylation,
methylation, phosphorylation and ubiquitylation. Recent
studies revealed that various histone modifications, especially
histone acetylation and deacetylation, participate in morphological
transition of C. albicans collaborating with well-known
transcription factors in the signaling pathways. Here, we review
recent studies about chromatin-mediated morphological
transition of C. albicans focusing on the interaction between
transcription factors in the signaling pathways and histone
deacetylases.
-
Citations
Citations to this article as recorded by

- The Rpd3 histone deacetylase is a critical regulator of temperature-mediated morphogenesis and virulence in the human fungal pathogen Histoplasma
Nebat Ali, Mark Voorhies, Rosa A. Rodriguez, Anita Sil, Jessica Brown
PLOS Biology.2026; 24(3): e3003341. CrossRef - F2F-202, a Selective Histone Deacetylase 6 (HDAC6) Inhibitor, Behaves as an Arrow with Multiple Tips against Azole-Resistant C. albicans: Modulation of Yeast-to-Hyphae Transition, Trailing Effect, and Oxidative Stress
Simona Barone, Baptiste Mateu, Marialuisa Piccolo, Anna Guadagni, Carlo Irace, Francesca Lembo, Vincenzo Summa, Elisabetta Buommino, Margherita Brindisi
ACS Infectious Diseases.2026; 12(6): 2101. CrossRef - Dual‐Targeting, Hybrid Antifungal Agents Targeting Candida albicans—An Overview
Sarmistha Pal, Sriparna Pusti, Iftakhar Hussain Ansari, Sanchita Pradhan, Hritabrata Bhattacharya, Shuvradip Das
Chemical Biology & Drug Design.2026;[Epub] CrossRef - Regulation of Ergosterol Biosynthesis in Pathogenic Fungi: Opportunities for Therapeutic Development
Lingyun Song, Sha Wang, Hang Zou, Xiaokang Yi, Shihan Jia, Rongpeng Li, Jinxing Song
Microorganisms.2025; 13(4): 862. CrossRef - Is a Fungal Apocalypse Inevitable or Just a Hallucination? An Overview of the Antifungal Armamentarium Used in the Fight against Pathogenic Fungi
Doaa M. Hanafy, David J. Leaver
ACS Medicinal Chemistry Letters.2025; 16(3): 379. CrossRef - Protein lysine acetylation regulates oral microorganisms
Yuanchao Yang, Hailun He, Bingshi Liu, Zhuoyue Li, Jiaman Sun, Zhili Zhao, Yan Yang
Frontiers in Cellular and Infection Microbiology.2025;[Epub] CrossRef - Genome-wide identification of the lysine deacetylases gene and its dynamic expression profile during adversity stress and infestation in Arthrinium phaeospermum
Sijia Liu, Ziqi Ye, Jia Song, Yutong Liu, Shujiang Li
World Journal of Microbiology and Biotechnology.2025;[Epub] CrossRef -
Histone deacetylase Sir2 promotes the systemic
Candida albicans
infection by facilitating its immune escape via remodeling the cell wall and maintaining the metabolic activity
Chen Yang, Guanglin Li, Qiyue Zhang, Wenhui Bai, Qingiqng Li, Peipei Zhang, Jiye Zhang, Antonio Di Pietro
mBio.2024;[Epub] CrossRef - Curcumin Epigenetically Represses Histone Acetylation of Echinocandin B Producing Emericella rugulosa
Vandana Kumari, Vinay Kumar, Manisha Kaushal, Antresh Kumar
Physiologia.2023; 3(2): 221. CrossRef - Comparative acetylomic analysis reveals differentially acetylated proteins regulating fungal metabolism in hypovirus‐infected chestnut blight fungus
Ru Li, Fengyue Chen, Shuangcai Li, Luying Yuan, Lijiu Zhao, Shigen Tian, Baoshan Chen
Molecular Plant Pathology.2023; 24(9): 1126. CrossRef - Discovery of BRD4–HDAC Dual Inhibitors with Improved Fungal Selectivity and Potent Synergistic Antifungal Activity against Fluconazole-Resistant Candida albicans
Zhuang Li, Yahui Huang, Jie Tu, Wanzhen Yang, Na Liu, Wei Wang, Chunquan Sheng
Journal of Medicinal Chemistry.2023; 66(8): 5950. CrossRef - BET–HDAC Dual Inhibitors for Combinational Treatment of Breast Cancer and Concurrent Candidiasis
Yahui Huang, Na Liu, Zhizhi Pan, Zhuang Li, Chunquan Sheng
Journal of Medicinal Chemistry.2023; 66(2): 1239. CrossRef - Effects of Hst3p inhibition in Candida albicans: a genome-wide H3K56 acetylation analysis
Marisa Conte, Daniela Eletto, Martina Pannetta, Anna M. Petrone, Maria C. Monti, Chiara Cassiano, Giorgio Giurato, Francesca Rizzo, Peter Tessarz, Antonello Petrella, Alessandra Tosco, Amalia Porta
Frontiers in Cellular and Infection Microbiology.2022;[Epub] CrossRef - Contributions of a Histone Deacetylase (SirT2/Hst2) to Beauveria bassiana Growth, Development, and Virulence
Qing Cai, Li Tian, Jia-Tao Xie, Dao-Hong Jiang, Nemat O. Keyhani
Journal of Fungi.2022; 8(3): 236. CrossRef - Potential antifungal targets based on histones post-translational modifications against invasive aspergillosis
Yiman Li, Zhihui Song, Ente Wang, Liming Dong, Jie Bai, Dong Wang, Jinyan Zhu, Chao Zhang
Frontiers in Microbiology.2022;[Epub] CrossRef - A fungal sirtuin modulates development and virulence in the insect pathogen, Beauveria bassiana
Qing Cai, Li Tian, Jia‐Tao Xie, Qiu‐Ying Huang, Ming‐Guang Feng, Nemat O. Keyhani
Environmental Microbiology.2021; 23(9): 5164. CrossRef -
Genetic Analysis of Sirtuin Deacetylases in Hyphal Growth of
Candida albicans
Guolei Zhao, Laura N. Rusche, Aaron P. Mitchell
mSphere.2021;[Epub] CrossRef - Discovery of Novel Fungal Lanosterol 14α-Demethylase (CYP51)/Histone Deacetylase Dual Inhibitors to Treat Azole-Resistant Candidiasis
Guiyan Han, Na Liu, Chenglan Li, Jie Tu, Zhuang Li, Chunquan Sheng
Journal of Medicinal Chemistry.2020; 63(10): 5341. CrossRef - Protein Acetylation/Deacetylation: A Potential Strategy for Fungal Infection Control
Junzhu Chen, Qiong Liu, Lingbing Zeng, Xiaotian Huang
Frontiers in Microbiology.2020;[Epub] CrossRef - Investigating Common Pathogenic Mechanisms between Homo sapiens and Different Strains of Candida albicans for Drug Design: Systems Biology Approach via Two-Sided NGS Data Identification
Shan-Ju Yeh, Chun-Chieh Yeh, Chung-Yu Lan, Bor-Sen Chen
Toxins.2019; 11(2): 119. CrossRef - Diverse roles of Tup1p and Cyc8p transcription regulators in the development of distinct types of yeast populations
Libuše Váchová, Zdena Palková
Current Genetics.2019; 65(1): 147. CrossRef - Chromatin Profiling of the Repetitive and Nonrepetitive Genomes of the Human Fungal Pathogen Candida albicans
Robert Jordan Price, Esther Weindling, Judith Berman, Alessia Buscaino, Antonio Di Pietro
mBio.2019;[Epub] CrossRef - Emerging New Targets for the Treatment of Resistant Fungal Infections
Na Liu, Jie Tu, Guoqiang Dong, Yan Wang, Chunquan Sheng
Journal of Medicinal Chemistry.2018; 61(13): 5484. CrossRef - Evidence for Mitochondrial Genome Methylation in the Yeast Candida albicans: A Potential Novel Epigenetic Mechanism Affecting Adaptation and Pathogenicity?
Thais F. Bartelli, Danielle C. F. Bruno, Marcelo R. S. Briones
Frontiers in Genetics.2018;[Epub] CrossRef - Plant Homeodomain Genes Play Important Roles in Cryptococcal Yeast-Hypha Transition
Yunfang Meng, Yumeng Fan, Wanqing Liao, Xiaorong Lin, Emma R. Master
Applied and Environmental Microbiology.2018;[Epub] CrossRef - Disruption of gul-1 decreased the culture viscosity and improved protein secretion in the filamentous fungus Neurospora crassa
Liangcai Lin, Zhiyong Sun, Jingen Li, Yong Chen, Qian Liu, Wenliang Sun, Chaoguang Tian
Microbial Cell Factories.2018;[Epub] CrossRef - The Candida albicans HIR histone chaperone regulates the yeast-to-hyphae transition by controlling the sensitivity to morphogenesis signals
Sabrina Jenull, Michael Tscherner, Megha Gulati, Clarissa J. Nobile, Neeraj Chauhan, Karl Kuchler
Scientific Reports.2017;[Epub] CrossRef - Histone Deacetylases and Their Inhibition in Candida Species
Cécile Garnaud, Morgane Champleboux, Danièle Maubon, Muriel Cornet, Jérôme Govin
Frontiers in Microbiology.2016;[Epub] CrossRef
Research Support, Non-U.S. Gov't
- Negative regulation of the vacuole-mediated resistance to K+ stress by a novel C2H2 zinc finger transcription factor encoded by aslA in Aspergillus nidulans
-
Dong Soo Park , Yeong Man Yu , Yong Jin Kim , Pil Jae Maeng
-
J. Microbiol. 2015;53(2):100-110. Published online January 28, 2015
-
DOI: https://doi.org/10.1007/s12275-015-4701-8
-
-
1,016
View
-
0
Download
-
22
Crossref
-
Abstract
PDF
-
In fungi and plants, vacuoles function as a storage and sequestration
vessel for a wide variety of ions and are responsible
for cytosolic ion homeostasis and responses to ionic
shock. In the filamentous fungus Aspergillus nidulans, however,
little is known about the molecular genetic mechanisms
of vacuolar biogenesis and function. In the present study,
we analyzed the function of the aslA gene (AN5583) encoding
a novel C2H2-type zinc finger transcription factor (TF)
in relation to K+ stress resistance, vacuolar morphology, and
vacuolar transporters. The mutant lacking aslA showed increased
mycelial growth and decreased branching at high
K+ concentrations. Deletion of aslA also caused elevated K+
stress-inducible expression of the genes, nhxA (AN2288),
vnxA (AN6986), and vcxA (AN0471), encoding putative endosomal
and vacuolar cation/H+ exchangers, as well as cpyA
and vpsA genes encoding the proteins involved in vacuolar
biogenesis. Interestingly, vacuolar fragmentation induced by
K+ stress was alleviated by aslA deletion, resulting in persistence
of unfragmented vacuoles. In the presence of bafilomycin,
an inhibitor of vacuolar H+-ATPase, the mutant phenotype
was suppressed in terms of growth rates and vacuolar
morphology. These results together suggest that the C2H2-
type zinc finger TF AslA attenuates the K+ stress-inducible
expression of the genes encoding the ion pumps involved in
vacuolar sequestration of K+ ions powered by vacuolar H+-
ATPase, as well as the proteins that function in vacuolar
biogenesis.
-
Citations
Citations to this article as recorded by

-
Cytological and morphological responses of the ectomycorrhizal fungus
Rhizopogon roseolus
to saline conditions
Septyani Amini, Rena Rifki Safitri, Tadanori Aimi, Norihiro Shimomura
Mycologia.2026; 118(2): 260. CrossRef - Distinct vacuolar responses to salinity stress in the hyphal cell of salt-tolerant and salt-sensitive strains of Rhizopogon roseolus
Septyani Amini, Tadanori Aimi, Norihiro Shimomura
Fungal Biology.2026; 130(4): 101759. CrossRef -
The hyphae-specific C
2
H
2
transcription factor HscA regulates development, stress response, and mycotoxin production in
Aspergillus
species
Ye-Eun Son, Kyu-Hyun Kim, He-Jin Cho, Jae-Hyuk Yu, Hee-Soo Park, Aaron P. Mitchell
mSphere.2025;[Epub] CrossRef - Molecular circuit between Aspergillus nidulans transcription factors MsnA and VelB to coordinate fungal stress and developmental responses
Emmanouil Bastakis, Jennifer Gerke, Seyma Özkan, Rebekka Harting, Tanja Lienard, Christoph Sasse, Emmanouil S. Xylakis, Merle Aden, Anja Strohdiek, Gabriele Heinrich, Verena Grosse, Gerhard H. Braus, Zachary A. Lewis
PLOS Genetics.2025; 21(7): e1011578. CrossRef - Genome-Wide Mapping Reveals an Extensive AtfA Regulatory Influence on Development, Metabolism, and Stress Preparedness in Aspergillus nidulans
Márton Miskei, Sandugash Ibragimova, Beatrix Kocsis, Tibor Nagy, Hee-Soo Park, Tamás Emri, Jae-Hyuk Yu, Éva Leiter, István Pócsi
Cells.2025; 14(24): 1965. CrossRef - The Zinc Finger Protein Zfp2 Regulates Cell–Cell Fusion and Virulence in Cryptococcus neoformans
Cheng-Li Fan, Lin Li, Ji-Chong Shi, Tong-Bao Liu
Journal of Fungi.2025; 11(12): 868. CrossRef - The pleiotropic phenotype of FlbA of Aspergillus niger is explained in part by the activity of seven of its downstream-regulated transcription factors
Xiaoyi Chen, Juan P. Moran Torres, Peter Jan Vonk, J. Mirjam A. Damen, Karli R. Reiding, Jan Dijksterhuis, Luis G. Lugones, Han A.B. Wösten
Fungal Genetics and Biology.2024; 172: 103894. CrossRef - Survival Factor A (SvfA) Contributes to Aspergillus nidulans Pathogenicity
Joo-Yeon Lim, Ye-Eun Jung, Hye-Eun Hwang, Cheol-Hee Kim, Nese Basaran-Akgul, Sri Harshini Goli, Steven P. Templeton, Hee-Moon Park
Journal of Fungi.2023; 9(2): 143. CrossRef - A C2H2 Zinc Finger Protein PlCZF1 Is Necessary for Oospore Development and Virulence in Peronophythora litchii
Honghui Zhu, Junjian Situ, Tianfang Guan, Ziyuan Dou, Guanghui Kong, Zide Jiang, Pinggen Xi
International Journal of Molecular Sciences.2022; 23(5): 2733. CrossRef - 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 - Characterization of BbKlf1 as a novel transcription factor vital for asexual and infection cycles of Beauveria bassiana
Rehab Abdelmonem Mohamed, Chong‐Tao Guo, Si‐Yuan Xu, Sheng‐Hua Ying, Ming‐Guang Feng
Environmental Microbiology Reports.2022; 14(5): 719. 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 - Mannitol-1-phosphate dehydrogenase, MpdA, is required for mannitol production in vegetative cells and involved in hyphal branching, heat resistance of conidia and sexual development in Aspergillus nidulans
Joo-Yeon Lim, Seung-Hyun Jang, Hee-Moon Park
Current Genetics.2021; 67(4): 613. CrossRef - The putative C2H2 transcription factor RocA is a novel regulator of development and secondary metabolism in Aspergillus nidulans
Dong Chan Won, Yong Jin Kim, Da Hye Kim, Hee-Moon Park, Pil Jae Maeng
Journal of Microbiology.2020; 58(7): 574. CrossRef - Survival factor SvfA plays multiple roles in differentiation and is essential for completion of sexual development in Aspergillus nidulans
Joo-Yeon Lim, Eun-Hye Kang, Yun-Hee Park, Jun-Ho Kook, Hee-Moon Park
Scientific Reports.2020;[Epub] CrossRef - Fungal oxylipins direct programmed developmental switches in filamentous fungi
Mengyao Niu, Breanne N. Steffan, Gregory J. Fischer, Nandhitha Venkatesh, Nicholas L. Raffa, Molly A. Wettstein, Jin Woo Bok, Claudio Greco, Can Zhao, Erwin Berthier, Ernst Oliw, David Beebe, Michael Bromley, Nancy P. Keller
Nature Communications.2020;[Epub] CrossRef - The Cys2His2 zinc finger protein Zfp1 regulates sexual reproduction and virulence in Cryptococcus neoformans
Cheng-Li Fan, Lian-Tao Han, Su-Ting Jiang, An-Ni Chang, Ze-Yang Zhou, Tong-Bao Liu
Fungal Genetics and Biology.2019; 124: 59. CrossRef - Global gene expression changes reflecting pleiotropic effects of Irpex lacteus induced by low‐intensity electromagnetic field
Ling Sun, Xinyi Li, Haile Ma, Ronghai He, Prince O. Donkor
Bioelectromagnetics.2019; 40(2): 104. CrossRef - Transcription Factors Controlling Primary and Secondary Metabolism in Filamentous Fungi: The β-Lactam Paradigm
Carlos García-Estrada, Rebeca Domínguez-Santos, Katarina Kosalková, Juan-Francisco Martín
Fermentation.2018; 4(2): 47. CrossRef - Differential Control of Asexual Development and Sterigmatocystin Biosynthesis by a Novel Regulator in Aspergillus nidulans
Yong Jin Kim, Yeong Man Yu, Pil Jae Maeng
Scientific Reports.2017;[Epub] CrossRef - The signal peptide peptidase SppA is involved in sterol regulatory element‐binding protein cleavage and hypoxia adaptation in Aspergillus nidulans
Chinbayar Bat‐Ochir, Jun‐Yong Kwak, Sun‐Ki Koh, Mee‐Hyang Jeon, Dawoon Chung, Yin‐Won Lee, Suhn‐Kee Chae
Molecular Microbiology.2016; 100(4): 635. CrossRef - ZNF1 Encodes a Putative C2H2 Zinc-Finger Protein Essential for Appressorium Differentiation by the Rice Blast Fungus Magnaporthe oryzae
Xiaofeng Yue, Yawei Que, Lin Xu, Shuzhen Deng, Youliang Peng, Nicholas J. Talbot, Zhengyi Wang
Molecular Plant-Microbe Interactions®.2016; 29(1): 22. CrossRef
Research Support, Non-U.S. Gov't
- 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
-
-
947
View
-
0
Download
-
16
Crossref
-
Abstract
PDF
-
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

- AoMbp1 interacts with AoSwi6 and regulates hyphal development, stress tolerance, trap morphogenesis, and pathogenicity in Arthrobotrys oligospora
Na Bai, Hui Yuan, Guiqiu Luo, Yi Chen, Meihua Xie, Jinkui Yang
Pesticide Biochemistry and Physiology.2026; 218: 106930. CrossRef - The analysis of transcriptomics reveals the function of TrPLD3 in the pathogenicity of Trichothecium roseum infecting apples
Xiao Li, Qianqian Zhang, Qili Liu, Xiaobin Xu, Jinzhu Li, Dandan Zhu, Yuanyuan Zong, Huali Xue, Yang Bi
Postharvest Biology and Technology.2025; 227: 113628. CrossRef - Genome-Wide Mapping Reveals an Extensive AtfA Regulatory Influence on Development, Metabolism, and Stress Preparedness in Aspergillus nidulans
Márton Miskei, Sandugash Ibragimova, Beatrix Kocsis, Tibor Nagy, Hee-Soo Park, Tamás Emri, Jae-Hyuk Yu, Éva Leiter, István Pócsi
Cells.2025; 14(24): 1965. CrossRef - 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