Transcriptional analysis of the conidiation pattern shift of the entomopathogenic fungus Metarhizium acridum in response to different nutrients
© The Author(s). 2016
Received: 19 April 2016
Accepted: 27 July 2016
Published: 9 August 2016
Most fungi, including entomopathogenic fungi, have two different conidiation patterns, normal and microcycle conidiation, under different culture conditions, eg, in media containing different nutrients. However, the mechanisms underlying the conidiation pattern shift are poorly understood.
In this study, Metarhizium acridum undergoing microcycle conidiation on sucrose yeast extract agar (SYA) medium shifted to normal conidiation when the medium was supplemented with sucrose, nitrate, or phosphate. By linking changes in nutrients with the conidiation pattern shift and transcriptional changes, we obtained conidiation pattern shift libraries by Solexa/Illumina deep-sequencing technology. A comparative analysis demonstrated that the expression of 137 genes was up-regulated during the shift to normal conidiation, while the expression of 436 genes was up-regulated at the microcycle conidiation stage. A comparison of subtractive libraries revealed that 83, 216, and 168 genes were related to sucrose-induced, nitrate-induced, and phosphate-induced conidiation pattern shifts, respectively. The expression of 217 genes whose expression was specific to microcycle conidiation was further analyzed by the gene expression profiling via multigene concatemers method using mRNA isolated from M. acridum grown on SYA and the four normal conidiation media. The expression of 142 genes was confirmed to be up-regulated on standard SYA medium. Of these 142 genes, 101 encode hypothetical proteins or proteins of unknown function, and only 41 genes encode proteins with putative functions. Of these 41 genes, 18 are related to cell growth, 10 are related to cell proliferation, three are related to the cell cycle, three are related to cell differentiation, two are related to cell wall synthesis, two are related to cell division, and seven have other functions. These results indicate that the conidiation pattern shift in M. acridum mainly results from changes in cell growth and proliferation.
The results indicate that M. acridum shifts conidiation pattern from microcycle conidiation to normal conidiation when there is increased sucrose, nitrate, or phosphate in the medium during microcycle conidiation. The regulation of conidiation patterning is a complex process involving the cell cycle and metabolism of M. acridum. This study provides essential information about the molecular mechanism of the induction of the conidiation pattern shift by single nutrients.
KeywordsConidiation pattern shift Normal and microcycle conidia Metarhizium acridum Pathway analysis
Conidia (spores) are the beginning and end of the differentiation process in the lifecycle of fungi [1, 2], and they play important roles in reproduction and survival . Most filamentous fungi have two conidiation patterns: normal and microcycle conidiation . Normal conidiation is the most common reproductive mode of filamentous fungi , and microcycle conidiation is a survival mechanism under stress conditions, whereby the normal lifecycle is bypassed [3, 5–8]. To date, microcycle conidiation has been described in more than 100 fungal species [3, 5, 7], and it has been divided into four basic categories based on the morphological characteristics of conidia .
The conidiation patterns can be shifted from normal to microcycle conidiation under various conditions, such as high and/or low temperature [6, 10, 11], high and/or low pH [12, 13], high salt concentration , and the presence of certain nutrients [7, 10, 15, 16]. Nutrients are the most common factors that affect fungal conidiation patterns. In Colletotrichum gloeosporioides, microcycle conidiation occurs in substrate-limited liquid cultures . In Beauveria bassiana, microcycle conidiation is observed in the absence of a carbon source in the basal medium . In Aspergillus flavus, exogenous putrescine inhibits microcycle conidiation and induces mycelial development . In Neurospora intermedia, microcycle conidiation occurs under low sugar and nitrogen conditions . The culture conditions for normal and microcycle conidiation are different, and even a subtle change in culture conditions can cause a substantially different conidiation pattern. The conidiation pattern shift in response to nutrients may be regulated by some sensors and pathways . However, the molecular mechanisms of the conidiation pattern shift in response to nutrients have not been elucidated.
The conidia of entomopathogenic fungi are formulated as myco-insecticides [21–23]. Metarhizium acridum is a model system for entomopathogenic fungi, and it is widely used for locust control in Africa, Asia, and Australia [24–26]. The entomopathogenic fungus M. acridum displays two conidiation patterns: normal conidiation on 1/4 strength Sabouraud’s dextrose agar medium (1/4 SDAY), but microcycle conidiation on sucrose yeast extract (SYA) medium . In the present study, the effects of single nutrients on the conidiation pattern of M. acridum were investigated by the addition of 7.5 % sucrose (sucrose-rich (SR) medium), 0.75 % nitrate (nitrate-rich (NR) medium) or 0.25 % phosphate (phosphate-rich (PR) medium) to the microcycle conidiation medium (SYA). The results showed that normal conidiation occurred on 1/4 SDAY and the three nutrient-rich media, and conidiophores and normal conidiation occurred 21 h post-inoculation (hpi), while microcycle conidia were produced on SYA medium during this period. The transcripts of M. acridum derived from SYA medium, the three nutrient-rich media, and 1/4 SDAY medium were compared. The genes involved in the conidiation pattern shift and the genes involved in the regulation of the conidiation pattern shift in the three nutrient-rich media were identified. Then, the mechanisms of the conidiation pattern shift of M. acridum in response to different nutrients were explored.
Conidiation pattern shift of M. acridum in response to different nutrients
Characterization of a digital gene expression (DGE) database
Major characteristics of all the DGE libraries
Value for conidiation library
Total no. of tags
No. of distinct tags
Total no. of tags
No. of distinct tags
Unambiguous tag-mapped genes
No. of genes
% of reference genes
DEGs of M. acridum during normal and microcycle conidiation
Among the 436 genes whose expression was up-regulated during microcycle conidiation, there were 16 transcription factors, including five zinc finger protein (ZFP) transcription factors, one basic leucine zipper domain (bZIP) family transcription factor, and one helix-loop-helix (HLH) transcription factors, five mitogen-activated protein (MAP) kinases, 15 absorption- and transportation-related genes, including three carbohydrate and water reabsorption genes, six RNA transport proteins, five stress-related genes, including two cytochrome P450 genes, two peroxidase genes, and one glutathione-disulfide reductase gene, and 13 nutrient and energy metabolism-related genes, including four glycolysis-related genes, three TCA-cycle-related genes, and six phosphorylation-related genes (Additional file 5). A GO analysis revealed that these genes are mainly involved in catalytic activity, transporter activity, and binding function processes (Additional file 1: Table S1). These genes are mainly involved in amino acid metabolism, microbial metabolism in diverse environments, carbohydrate metabolism, cell growth and death, energy metabolism, lipid metabolism, xenobiotics biodegradation and metabolism, metabolism of terpenoids and polyketides, nucleotide metabolism, replication and repair, signal transduction, translation, transcription, biosynthesis of secondary metabolites, glycan biosynthesis and metabolism, transport and catabolism, and metabolism of cofactors and vitamins pathways (Additional file 4). Many genes whose expression was up-regulated during microcycle conidiation encode proteins that function in cell division, cell proliferation, cell wall formation, and cytoskeletal rearrangement, including a tyrosine-protein phosphatase , a transcriptional coactivator , a zinc knuckle domain protein , a serine-type carboxypeptidase , sedoheptulose-1, 7-bisphosphatase , a catalase [34, 35], cytochrome P450 , a mannan endo-1, 6-α-mannosidase-like protein [37, 38], an actin-associated protein , and a HLH transcription factor , suggesting that these up-regulated genes play a role in microcycle conidiation. Interestingly, members of the normal conidiation FluG pathway, including snaD, GNAT, fluG, pkaA , fadA , and gasA , were up-regulated during microcycle conidiation (Additional file 5).
These results indicate that genes related to both normal and microcycle conidiation are mainly involved in amino acid metabolism, cell growth and death, energy metabolism, lipid metabolism, metabolism of terpenoids and polyketides, translation pathways, and other pathways (Additional file 4). These pathways participate in cell proliferation, cell development, cell cycle, and cytoskeletal rearrangement processes. The common pathways in the conidiation pattern shift indicate that normal and microcycle conidiation have similar developmental processes and can be regulated through some common pathways, eg, the FluG pathway. However, compared with normal conidiation, microcycle conidiation involved two more pathways, more genes in 10 pathways (Additional file 4), and higher gene expression in common pathways, such as the FluG pathway. These genes and pathways might be related to the shift between normal and microcycle conidiation.
Genes involved in the conidiation pattern shift related to different nutrients
With respect to the nitrate-rich medium, 216 specifically expressed genes were screened in the target libraries. Of these, the expression of 203 genes was up-regulated, and the expression of 13 genes was down-regulated (Additional file 8). Among these, there were seven transcription factors, including four zinc finger transcription factors and one GATA-binding transcription factor, three stress-related genes, including two cytochrome P450 genes and one dioxygenase, 41 metabolism-related genes, including three binding proteins and one protein tyrosine phosphatase, and five genes involved in the cell cycle process. A pathway analysis found that these genes are mainly involved in amino acid metabolism, carbohydrate metabolism, cell growth and death, lipid metabolism, xenobiotics biodegradation and metabolism, nucleotide metabolism, transport and catabolism pathways, and microbial metabolism in diverse environments pathways (Additional file 7). A GO analysis found that most of the genes had roles in catalytic activity, protein kinase activity, transporter activity, transferase activity, hydrolase activity, and adenyl ribonucleotide binding. The results showed that at a high nitrate level, the expression of catalytic-, hydrolase-, transferase-, and ribonucleotide-binding-related genes was up-regulated. A reasonable explanation is that nitrogen affects cell morphology by controlling amino acid metabolism.
For the phosphate-rich medium, 168 specifically expressed genes were filtered in the target libraries. Of these, the expression of 151 genes was up-regulated, and the expression of 17 genes was down-regulated (Additional file 9). Among these, there were five transcription factors, including three zinc finger transcription factors, seven stress-related genes, including two cytochrome P450 genes and three dioxygenases, 24 metabolism-related genes, including two TCA-cycle-related genes, one phosphorylation-related gene, five binding proteins, and three phosphatases, and two cell cycle genes. A pathway analysis found that the genes are mainly involved in amino acid metabolism, carbohydrate metabolism, cell growth and death, lipid metabolism, xenobiotics biodegradation and metabolism, transport and catabolism, and microbial metabolism in diverse environment pathways (Additional file 7). A GO analysis found that most of the genes are involved in catalytic activity, nucleic acid binding, protein kinase activity, transferase activity, adenyl ribonucleotide binding, ATPase activity, and peptidase activity. The results showed that phosphate might affect cell division, proliferation, and differentiation by controlling the formation of ATP and affecting the cytoskeleton.
Carbon, nitrogen, and phosphorus are basic components of the cell. They are constituents of nucleic acids, sugar-phosphate backbones, and phospholipid bilayers, and they are required for cell division and membrane formation . However, the conidiation pattern shifts in response to these nutrients were controlled by different genes, some of which played roles in the same pathway. MAP kinase , the origin recognition complex subunit , and a serine/threonine protein kinase  are located in the cell growth and death pathway, and they played roles in the conidiation pattern shift in response to sucrose, nitrate, and phosphate, respectively. The conidiation pattern shift in response to nutrients involved different pathways. Exo-beta-D-glucosaminidase is involved in the sucrose-induced conidiation pattern shift, and it has an effect on hyphal growth at low sugar concentrations . Acyltransferase is involved in the nitrate-induced conidiation pattern shift, and it participates in the composition of the membrane at high nitrogen concentrations . L-asparaginase is involved in the phosphate-induced conidiation pattern shift, and it has an effect on growth under certain phosphate concentrations [50, 51]. These results indicate that carbon, nitrogen, and phosphorus influence the fungal conidiation pattern by perturbing the cell cycle, nutrient metabolism, and related pathways of M. acridum.
DEGs involved in conidiation were confirmed by the gene expression profiling via multigene concatemers (MgC-GEP) method
Functions of some microcycle conidiation-relate genes screened by Gene Expression profiling via Multigene Concatemers
glycosyl hydrolase, family 18, putative
isoamyl alcohol oxidase, putative
C6 transcription factor
transcription factor ATF2
cytochrome P450 3A17
amino acid transporter, putative
LysM domain-containing protein
zinc knuckle domain protein
glycerophosphoryl diester phosphodiesterase family protein
ERV2 protein-like protein
putative ZIP zinc transporter
histone acetyltransferase Spt10
integral membrane protein
late sexual development protein
sister chromatid cohesion protein Ctf8, putative
histone acetyltransferase Spt10
integral membrane protein
exosome complex exonuclease Rrp
putative transcriptional coactivator HFI1
HLH transcription factor (Hpa3), putative
Ser/Thr protein phosphatase
high mobility group protein
alcohol dehydrogenase, putative
cell wall synthesis
dihydrodipicolinate synthase, putative
checkpoint protein kinase, putative
putative xylanase 3
tyrosine-protein phosphatase CDC14
serine/threonine-protein kinase hal4
integral membrane protein
related to heme synthesis
related to sucrose uptake
inhibition of hyphal extension
related to metabolism
LysR family regulatory protein, putative
related to metabolism
NADP-dependent alcohol dehydrogenase C
Most fungi have two different conidiation patterns, and the mechanisms of normal conidiation have been well studied in most industrial and model species [1, 2]. In Aspergillus nidulans, snaD encodes a spindle pole body protein, which is a positive factor in the conidiation process, by promoting the nucleation of tip cells and cell division . In Neurospora crassa, GNAT negatively regulates conidiation through a cAMP-dependent pathway on solid media, and deletion of GNAT leads to decreased aerial hyphal height and premature conidiation . In M. acridum, FKS is involved in cell wall integrity and conidiation . However, the mechanisms of the conidiation pattern shift are not clear.
Previous research found that M. acridum produces microcycle conidia on insect cadavers, while producing normal conidia on PDAY medium , suggesting that microcycle conidia maybe produced under nutritive stress. In the present study, microcycle conidiation of M. acridum was shifted to normal conidiation after adding single nutrients to SYA medium. This phenotypic change is similar to the conidiation pattern shift in B. bassiana  and A. flavus . Our results revealed that nutrients can cause the conidiation pattern shift in M. acridum. However, the underlying mechanisms are far from clear.
To understand the mechanism of the conidiation pattern shift, we used a statistical comparison analysis to obtain 1040 DEGs that are involved in the conidiation pattern shift. These genes are involved in catalytic activity, cellular transport, cell cycle, developmental processes, signal transduction, stress responses, and metabolic processes. The results indicated that a very complex molecular network is involved in the conidiation pattern shift.
The conidiation pattern shift can be induced in some fungi by different nutrients [7, 14, 56]. Therefore, some genes that are regulated by nutrients might be involved in the conidiation pattern shift. The glucose level-sensing gene snf3  and the nitrogen-starvation gene glnA  were detected in our conidiation pattern shift-related gene library. The results indicate that exogenous nutrients affected the conidiation pattern shift by controlling the expression of nutrient-related genes. Our research identified pathways and molecular mechanisms for the conidiation pattern shift that are regulated by a single nutrient.
Previous studies have indicated that microcycle conidiation can produce more spores in a shorter time compared with normal conidiation [59, 60]. Moreover, the spores formed by microcycle conidiation are more uniform in size compared with those formed by normal conidiation [27, 61]. This means that the conidiation pattern shift may be associated with cell growth, cell division, cytoskeletal rearrangement, and energy metabolism. snaD and GNAT are likely to be involved in this process. In A. nidulans, snaD affects conidiation by promoting the nucleation of tip cells and cell division . In N. crassa, GNAT induces the conidiation pattern shift by reducing intracellular cAMP levels . Our results indicate that the conidiation pattern shift of M. acridum is consistent with those of industrial and model species. pcvA , gasA , fadA , GNAT  and pkaA  were reported to be specific, negative regulators of conidiation, but their transcription levels were higher during microcycle conidiation than normal conidiation. It may be that: (1) these genes are related to nutrient starvation, and on nutrient-rich media, their function is inhibited by nutrients, which results in normal conidiation; and (2) the transcription levels of these genes may be related to spore production.
In summary, there are differences in the morphological and genetic features between the two conidiation patterns. However, little information has been reported about the process of the conidiation pattern shift. The present study used Solexa/Illumina deep-sequencing technology to show that a large number of DEGs are associated with the conidiation pattern shift in M. acridum in the presence of single nutrients. Further studies could confirm these DEGs using transgenic technology to enhance the yields of biopesticides. This study also provides a template for future investigations of the conidiation pattern shift in fungi, and it offers hints about the molecular mechanism of conidiation regulation by different nutrients.
Our results indicate that the conidiation pattern shift is a complex biological process in which the cell cycle and metabolism of M. acridum are perturbed by sucrose, nitrate, and phosphate. This research provides essential information about the molecular mechanism of the conidiation pattern shift that is induced by single nutrients.
Fungal strain and culture conditions
The M. acridum strain CQMa102 used in this study is a locust-specific strain that was isolated by the Genetic Engineering Research Center of Chongqing University and used in a previous study . Conidia were harvested after the fungus was cultured on 1/4 SDAY medium (SDAY, 1 % dextrose, 0.25 % mycological peptone, 2 % agar and 0.5 % yeast extract, w/v) at 28 °C for 12–15 d.
SYA medium was used for microcycle conidiation under previously described conditions . Sucrose-, nitrate-, and phosphate-rich media, which were used for normal conidiation, had the same composition as SYA medium, except the amount of sucrose, nitrate and phosphate increased to 75, 7.5, and 2.5 g/L, respectively.
Library preparation and sequencing
After incubation for 21 h at 28 °C, the fungal cell mass was harvested by centrifugation and washed with sterile double-distilled H2O. Total RNA was extracted from the fungal cell mass using Trizol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. Oligo(dT) magnetic beads were used to purify mRNA from 6 μg of total RNA, and an oligo(dT) primer was used to synthesize first- and second-strand cDNAs. Sequencing was performed on a High-Seq2000 platform (Illumina, San Diego, CA, USA). Sequence analysis was conducted as described previously .
Screening of DEGs
Based on the five DGE databases, a statistical comparison was performed to identify DEGs between the libraries using the rigorous algorithm with a false discovery rate (FDR) < 0.001 and an absolute value for the log2 ratio > 1 . To screen for genes involved in the shift between microcycle and normal conidiation, we constructed four subtractive libraries: an SYA vs. SR media library, an SYA vs. NR media library, an SYA vs. PR media library, and an SYA vs. 1/4 SDAY media library.
To identify genes involved in the regulation of the conidiation pattern shift in response to single nutrients, three subtractive libraries based on the in silico analysis were constructed to screen for genes that are specifically expressed in the conidiation pattern shift in response to sucrose, nitrate, or phosphate. To screen for genes that are specifically expressed in the conidiation pattern shift in response to sucrose, the genes expressed in the 1/4 SDAY, NR, and PR media libraries were removed from the SYA vs. SR media subtractive library, and the remaining genes were the sucrose-regulated genes that are involved in the conidiation pattern shift. Nitrate- and phosphate-regulated genes involved in the conidiation pattern shift were also identified using this method.
GO functional and pathway enrichment analysis
GO is a gene functional classification system with three ontologies: molecular function, cellular component, and biological process. In gene expression profiling analysis, a GO enrichment analysis of functional significance uses a hypergeometric test to map all DEGs to terms in the GO database (http://www.geneontology.org/), looking for significantly enriched GO terms in the DEGs compared to the genome background.
Pathway enrichment analysis identifies significantly enriched metabolic pathways or signal transduction pathways in DEGs by comparison with the whole genome background. The formula is the same as that used in the GO analysis; a pathway with a Q value ≤ 0.05 was defined as having a significant enrichment of DEGs. DEGs that are involved in most major biochemical, metabolism, and signal transduction pathways could be identified through the pathway of significant enrichment.
Verification of the DEGs by expression profiling via multigene concatemers
To verify the DEGs, 217 genes were randomly chosen from the 436 genes whose expression was up-regulated during microcycle conidiation, and gapdh (GenBank accession number: EFY84384), a gene encoding glyceraldehyde 3-phosphate dehydrogenase, was used as an internal control. Primer design was performed according to a previous method . All the primers used in this study are listed in Additional file 11. The expression levels of the selected genes were analyzed in all five media (1/4 SDAY, SYA, SR, NR, and PR) using the MgC-GEP method , with minor modifications. For each sample, reverse transcription reaction mixtures were followed by polymerase chain reaction (PCR) amplification with 1 μM of a specific forward primer and 1 μM of a specific reverse primer. The PCR conditions consisted of an initial denaturation at 95 °C for 5 min, followed by five cycles of 94 °C for 30 s, 68 °C for 30 s, 72 °C for 30 s, and ending in a single extension cycle of 72 °C for 5 min. All of the 218 PCR products were mixed and concentrated to 200 μl, and then extracted using the QIAquick Gel Extraction kit (Qiagen, Valencia, CA, USA). The extraction products were further amplified by PCR with 1 μM of a universal forward primer and 1 μM of a universal reverse primer. The amplification conditions were as follows: an initial denaturation at 95 °C for 5 min, followed by 28 cycles of 94 °C for 30 s, 53 °C for 30 s, and 72 °C for 30 s, and ending in a single extension cycle of 72 °C for 5 min. The PCR products were extracted with the QIAquick Gel extraction kit and used for quantitative gene expression analysis as described previously .
ABC, ATP-binding cassette; ATP, Adenosine triphosphate; bZIP, basic leucine zipper domain; cAMP, cyclic adenosine monophosphate; DGE, digital gene expression; GO, Gene Ontology; HLH, helix-loop-helix; hpi, hours post-inoculation; KEGG, Kyoto Encyclopedia of Genes and Genomes; MAP, mitogen-activated protein; MFS, major facilitator superfamily; MgC-GEP, gene expression profiling via multigene concatemers; NR, nitrate-rich medium; PR, phosphate-rich medium; SDAY, Sabouraud’s dextrose agar medium; SR, sucrose-rich medium; SYA, sucrose yeast extract agar medium; TCA, tricarboxylic acid; ZFP, zinc finger protein
We would like to thank the anonymous reviewers for the helpful comments.
This work was supported by the Natural Science Foundation of China (Grant Number: 31272090).
Availability of data and materials
The sequences reported in this paper have been deposited as raw reads in the GenBank SRA database (accession number.: SRR3382569, SRR3382603, SRR3382605, SRR3382606 and SRR3382607).
YX conceived and designed the study. ZW prepared the RNA samples for RNAseq and performed the qPCRs. ZW, KJ and YX analysed data. ZW, KJ and YX drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All procedures were performed within the research guidelines of the Chongqing University, China and did not require approval of an ethics committee.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Nielsen J. Modelling the growth of filamentous fungi. Adv Biochem Eng Biotechnol. 1992;46:187–223.PubMedGoogle Scholar
- Papagianni M. Fungal morphology and metabolite production in submerged mycelial processes. Biotechnol Adv. 2004;22:189–259.View ArticlePubMedGoogle Scholar
- Hanlin R. Microcycle conidiation — A review. Mycoscience. 1994;35:113–23.View ArticleGoogle Scholar
- Park HS, Yu JH. Genetic control of asexual sporulation in filamentous fungi. Curr Opin Microbiol. 2012;15:669–77.View ArticlePubMedGoogle Scholar
- Ahearn DG, Price D, Simmons RB, Mavo A, Zhang ST, Crow SA. Microcycle conidiation and medusa head conidiophores of aspergilli on indoor construction materials and air filters from hospitals. Mycologia. 2007;99:1–6.View ArticleGoogle Scholar
- Anderson JG, Smith JE. The production of conidiophores and conidia by newly germinated conidia of Aspergillus niger (microcycle conidiation). J Gen Microbiol. 1971;69:185–97.View ArticlePubMedGoogle Scholar
- Lapaire CL, Dunkle LD. Microcycle conidiation in Cercospora zeae-maydis. Phytopathology. 2003;93:193–9.View ArticlePubMedGoogle Scholar
- Maheshwari R. Microconidia of Neurospora crassa. Fungal Genet Biol. 1999;26:1–18.View ArticlePubMedGoogle Scholar
- Jung B, Kim S, Lee J. Microcyle conidiation in filamentous fungi. Mycology. 2014;42(1):1–5.View ArticleGoogle Scholar
- Sekiguchi J, Gaucher GM, Costerton JW. Microcycle conidiation in Penicillium urticae: an ultrastructural investigation of conidiogenesis. Can J Microbiol. 1975;21:2069–83.View ArticlePubMedGoogle Scholar
- Mieslerova B, Lebeda A. Influence of temperature and light conditions on germination, growth and conidiation of Oidium neolycopersici. J Phytopathol. 2010;158:616–27.Google Scholar
- Pažout J, Schröder P. Microcycle conidiation in submerged cultures of Penicillium cyclopium attained without temperature changes. J Gen Microbiol. 1988;134:2685–92.PubMedGoogle Scholar
- Liu Q, Xiao CL. Influence of nutrient and environmental factors on conidial germination of Potebniamyces pyri. Phytopathology. 2005;95:572–80.View ArticlePubMedGoogle Scholar
- Vezina C, Singh K, Sehgal SN. Sporulation of filamentous fungi in submerged culture. Mycologia. 1965;57:722–36.View ArticleGoogle Scholar
- Bosch A, Yantorno O. Microcycle conidiation in the entomopathogenic fungus Beauveria bassiana bals. (vuill.). Process Biochem. 1999;34:707–16.View ArticleGoogle Scholar
- Rangel D, Braga G, Anderson A, Roberts D. Influence of growth environment on tolerance to uv-b radiation, germination speed, and morphology of Metarhizium anisopliae var. acridum conidia. J Invertebr Pathol. 2005;90:55–8.View ArticlePubMedGoogle Scholar
- Cascino JJ, Harris RF, Smith CS, Andrews JH. Spore yield and microcycle conidiation of Colletotrichum gloeosporioides in liquid culture. Appl Environ Microbiol. 1990;56:2303–10.PubMedPubMed CentralGoogle Scholar
- Khurana N, Saxena RK, Gupta R, Rajam MV. Polyamines as modulators of microcycle conidiation in Aspergillus flavus. Microbiology. 1996;142:517–23.View ArticlePubMedGoogle Scholar
- Pandit A, Maheshwari R. Life-history of Neurospora intermedia in a sugar cane field. J Bioscience. 1996;21:57–79.View ArticleGoogle Scholar
- Osherov N, May GS. The molecular mechanisms of conidial germination. FEMS Microbiol Lett. 2001;199:153–60.View ArticlePubMedGoogle Scholar
- Furlong MJ, Pell JK. Interactions between the fungal entomopathogen Zoophthora radicans Brefeld (Entomophthorales) and two hymenopteran parasitoids attacking the diamondback moth, Plutella xylostella L. J Invertebr Pathol. 1996;68:15–21.View ArticlePubMedGoogle Scholar
- Lord JC. Response of the wasp Cephalonomia tarsalis (Hymenoptera : Bethylidae) to Beauveria bassiana (Hyphomycetes : Moniliales) as free conidia or infection in its host, the sawtoothed grain beetle, Oryzaephilus surinamensis (Coleoptera : Silvanidae). Bio Control. 2001;21:300–4.View ArticleGoogle Scholar
- Nielsen C, Skovgard H, Steenberg T. Effect of Metarhizium anisopliae (Deuteromycotina : Hyphomycetes) on survival and reproduction of the filth fly parasitoid, Spalangia cameroni (Hymenoptera : Pteromalidae). Environ Entomol. 2005;34:133–9.View ArticleGoogle Scholar
- Hunter DM, Milner RJ, Spurgin PA. Aerial treatment of the Australian plague locust, Chortoicetes terminifera (Orthoptera: Acrididae) with Metarhizium anisopliae (Deuteromycotina: Hyphomycetes). Bull Entomol Res. 2001;91:93–9.PubMedGoogle Scholar
- Peng GX, Wang ZK, Yin YP, Zeng DY, Xia YX. Field trials of Metarhizium anisopliae var. acridum (Ascomycota : Hypocreales) against oriental migratory locusts, Locusta migratoria manilensis (Meyen) in Northern China. Crop Prot. 2008;27:1244–50.View ArticleGoogle Scholar
- Li Z, Alves S, Roberts D, Fan M, Delalibera I, Tang J, et al. Biological control of insects in Brazil and China: history, current programs and reasons for their successes using entomopathogenic fungi. Biocontrol Sci Techn. 2010;20:117–36.View ArticleGoogle Scholar
- Zhang SZ, Peng GX, Xia YX. Microcycle conidiation and the conidial properties in the entomopathogenic fungus Metarhizium acridum on agar medium. Biocontrol Sci Techn. 2010;20:809–19.View ArticleGoogle Scholar
- Gao Q, Jin K, Ying SH, Zhang YJ, Xiao GH, Shang YF, et al. Genome sequencing and comparative transcriptomics of the model entomopathogenic fungi Metarhizium anisopliae and M. acridum. PLoS Genet. 2011;7:e1001264.View ArticlePubMedPubMed CentralGoogle Scholar
- Saito RM, Perreault A, Peach B, Satterlee JS, van den Heuvel S. The CDC-14 phosphatase controls developmental cell-cycle arrest in C. elegans. Nat Cell Biol. 2004;6:777–83.View ArticlePubMedGoogle Scholar
- Huang SM, Schonthal AH, Stallcup MR. Enhancement of p53-dependent gene activation by the transcriptional coactivator Zac1. Oncogene. 2001;20:2134–43.View ArticlePubMedGoogle Scholar
- Loudet O, Michael TP, Burger BT, Le Mette C, Mockler TC, Weigel D, et al. A zinc knuckle protein that negatively controls morning-specific growth in Arabidopsis thaliana. P Natl Acad Sci USA. 2008;105:17193–8.View ArticleGoogle Scholar
- Morita H, Tomita S, Maeda H, Okamoto A, Yamagata Y, Kusumoto K, et al. Serine-type carboxypeptidase KexA of Aspergillus oryzae has broader substrate specificity than Saccharomyces cerevisiae Kex1 and is required for normal hyphal growth and conidiation. Appl Environ Microbiol. 2012;78:8154–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Miyagawa Y, Tamoi M, Shigeoka S. Overexpression of a cyanobacterial fructose-1,6-/sedoheptulose-1,7-bisphosphatase in tobacco enhances photosynthesis and growth. Nat Biotechnol. 2001;19:965–9.View ArticlePubMedGoogle Scholar
- Hansberg W, Salas-Lizana R, Dominguez L. Fungal catalases: function, phylogenetic origin and structure. Arch Biochem Biophys. 2012;525:170–80.View ArticlePubMedGoogle Scholar
- Shibuya K, Paris S, Ando T, Nakayama H, Hatori T, Latge JP. Catalases of Aspergillus fumigatus and inflammation in aspergillosis. Nihon Ishinkin Gakkai Zasshi. 2006;47:249–55.View ArticlePubMedGoogle Scholar
- Gonzalez FJ. Role of cytochromes P450 in chemical toxicity and oxidative stress: studies with CYP2E1. Mutat Res. 2005;569:101–10.View ArticlePubMedGoogle Scholar
- Kitagaki H, Wu H, Shimoi H, Ito K. Two homologous genes, DCW1 (YKL046c) and DFG5, are essential for cell growth and encode glycosylphosphatidylinositol (GPI)-anchored membrane proteins required for cell wall biogenesis in Saccharomyces cerevisiae. Mol Microbiol. 2002;46:1011–22.View ArticlePubMedGoogle Scholar
- Montijn RC, van Rinsum J, van Schagen FA, Klis FM. Glucomannoproteins in the cell wall of Saccharomyces cerevisiae contain a novel type of carbohydrate side chain. J Biol Chem. 1994;269:19338–42.PubMedGoogle Scholar
- Freeman NL, Lila T, Mintzer KA, Chen Z, Pahk AJ, Ren R, et al. A conserved proline-rich region of the Saccharomyces cerevisiae cyclase-associated protein binds SH3 domains and modulates cytoskeletal localization. Mol Cell Biol. 1996;16:548–56.View ArticlePubMedPubMed CentralGoogle Scholar
- Sauve S, Naud JF, Lavigne P. The mechanism of discrimination between cognate and non-specific DNA by dimeric b/HLH/LZ transcription factors. J Mol Biol. 2007;365:1163–75.View ArticlePubMedGoogle Scholar
- Roze LV, Beaudry RM, Keller NP, Linz JE. Regulation of aflatoxin synthesis by FadA/cAMP/protein kinase A signaling in Aspergillus parasiticus. Mycopathologia. 2004;158:219–32.View ArticlePubMedGoogle Scholar
- Brodhagen M, Keller NP. Signalling pathways connecting mycotoxin production and sporulation. Mol Plant Pathol. 2006;7:285–301.View ArticlePubMedGoogle Scholar
- Roncal T, Ugalde U. Conidiation induction in Penicillium. Res Microbiol. 2003;154:539–46.View ArticlePubMedGoogle Scholar
- Yuan H, Liu D. Signaling components involved in plant responses to phosphate starvation. J Integr Plant Biol. 2008;50:849–59.View ArticlePubMedGoogle Scholar
- Kronstad J, De Maria A, Funnell D, Laidlaw RD, Lee N, Ramesh MMDM. Signaling via cAMP in fungi: interconnections with mitogen-activated protein kinase pathways. Arch Microbiol. 1998;170:395–404.View ArticlePubMedGoogle Scholar
- Springer J, Kneissl M, Putter V, Grummt F. Identification and characterization of MmORC4 and MmORC5, two subunits of the mouse origin of replication recognition complex. Chromosoma. 1999;108:243–9.View ArticlePubMedGoogle Scholar
- Ruizperez VL, Murillo FJ, Torresmartinez S. PkpA, a Novel Phycomyces-Blakesleeanus serine/threonine protein kinase. Curr Genet. 1995;28:309–16.View ArticleGoogle Scholar
- Pera LM, Baigorí MD, Callieri D. Influence of environmental conditions on hyphal morphology in pellets of Aspergillus niger: role of β-N-acetyl-D-glucosaminidase. Curr Microbiol. 1999;39:65–7.View ArticlePubMedGoogle Scholar
- Kamisaka Y, Yokochi T, Nakahara T, Suzuki O. Characterization of the diacylglycerol acyltransferase activity in the membrane-fraction from a fungus. Lipids. 1993;28:583–7.View ArticleGoogle Scholar
- Geckil H, Gencer S. Production of L-asparaginase in Enterobacter aerogenes expressing Vitreoscilla hemoglobin for efficient oxygen uptake. Appl Microbiol Biot. 2004;63:691–7.View ArticleGoogle Scholar
- Qin M, Zhao FS. L-asparaginase release from Escherichia coli cells with aqueous two-phase micellar systems. Appl Biochem Biotech. 2003;110:11–21.View ArticleGoogle Scholar
- Jin K, Zheng X, Xia Y. Gene expression profiling via multigene concatemers. PLoS One. 2011;6:e15711.View ArticlePubMedPubMed CentralGoogle Scholar
- Liu B, Morris NR. A spindle pole body-associated protein, SNAD, affects septation and conidiation in Aspergillus nidulans. Mol Gen Genet. 2000;263:375–87.View ArticlePubMedGoogle Scholar
- Kays AM, Rowley PS, Baasiri RA, Borkovich KA. Regulation of conidiation and adenylyl cyclase levels by the Galpha protein GNA-3 in Neurospora crassa. Mol Cell Biol. 2000;20:7693–705.View ArticlePubMedPubMed CentralGoogle Scholar
- Yang M, Jin K, Xia YX. MaFKS, a beta-1,3-glucan synthase, is involved in cell wall integrity, hyperosmotic pressure tolerance and conidiation in Metarhizium acridum. Curr Genet. 2011;57:253–60.View ArticlePubMedGoogle Scholar
- Slade SJ, Harris RF, Smith CS, Andrews JH. Microcycle conidiation and spore-carrying capacity of Colletotrichum gloeosporioides on solid media. Appl Environ Microb. 1987;53:2106–10.Google Scholar
- Ebbole DJ. Carbon catabolite repression of gene expression and conidiation in Neurospora crassa. Fungal Genet Biol. 1998;25:15–21.View ArticlePubMedGoogle Scholar
- Fisher SH. Regulation of nitrogen metabolism in Bacillus subtilis: vive la difference! Mol Microbiol. 1999;32:223–32.View ArticlePubMedGoogle Scholar
- Khurana N, Saxena RK, Gupta R, Kuhad RC. Light-independent conidiation in Trichoderma spp. a novel approach to microcycle conidiation. World J Microb Biot. 1993;9:353–6.View ArticleGoogle Scholar
- Maheshwari R. Microcycle conidiation and its genetic-basis in Neurospora crassa. J Gen Microbiol. 1991;137:2103–15.View ArticlePubMedGoogle Scholar
- Huo Z, Yang X, Raza W, Huang Q, Xu Y, Shen Q. Investigation of factors influencing spore germination of Paenibacillus polymyxa ACCC10252 and SQR-21. Appl Microbiol Biotechnol. 2010;87:527–36.View ArticlePubMedGoogle Scholar
- Xu X, Yang J, An Y, Pan Y, Liu G. Over-expression of pcvA involved in vesicle-vacuolar fusion affects the conidiation and penicillin production in Penicillium chrysogenum. Biotechnol Lett. 2012;34:519–26.View ArticlePubMedGoogle Scholar
- Zuber S, Hynes MJ, Andrianopoulos A. G-protein signaling mediates asexual development at 25 degrees C but has no effect on yeast-like growth at 37 degrees C in the dimorphic fungus Penicillium marneffei. Eukaryot Cell. 2002;1:440–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang S, Xia Y. Identification of genes preferentially expressed during microcycle conidiation of Metarhizium anisopliae using suppression subtractive hybridization. FEMS Microbiol Lett. 2008;286:71–7.View ArticlePubMedGoogle Scholar
- Audic S, Claverie JM. The significance of digital gene expression profiles. Genome Res. 1997;7:986–95.PubMedGoogle Scholar
- Dünkler A, Jorde S, Wendland J. An Ashbya gossypii cts2 mutant deficient in a sporulation-specific chitinase can be complemented by Candida albicans CHT4. Microbiol Res. 2008;163:701–10.View ArticlePubMedGoogle Scholar
- Yamashita N, Motoyoshi T, Nishimura A. Molecular cloning of the isoamyl alcohol oxidase-encoding gene (mreA) from Aspergillus oryzae. J Biosci Bioeng. 2000;89:522–7.View ArticlePubMedGoogle Scholar
- Laity JH, Lee BM, Wright PE. Zinc finger proteins: new insights into structural and functional diversity. Curr Opin Struct Biol. 2001;11:39–46.View ArticlePubMedGoogle Scholar
- Gołda A, Szyniarowski P, Ostrowska K, Kozik A, Rapała-Kozik M. Thiamine binding and metabolism in germinating seeds of selected cereals and legumes. Plant Physiol Biochem. 2004;42:187–95.View ArticlePubMedGoogle Scholar
- Bhoumik A, Lopez-Bergami P, Ronai Z. ATF2 on the double-activating transcription factor and DNA damage response protein. Pigment Cell Res. 2007;20:498–506.View ArticlePubMedPubMed CentralGoogle Scholar
- Jeney A, Béki E, Keszthelyi A, Leslie JF, Hornok L. Cloning and characterization of Fpmtr1, an amino acid transporter gene of Fusarium proliferatum (Gibberella intermedia). J Basic Microbiol. 2007;47:16–24.View ArticlePubMedGoogle Scholar
- Giefing-Kröll C, Jelencsics KE, Reipert S, Nagy E. Absence of pneumococcal PcsB is associated with overexpression of LysM domain-containing proteins. Microbiology. 2011;157:1897–909.View ArticlePubMedGoogle Scholar
- Pistorius S, Goergens H, Engel C, Plaschke J, Krueger S, Hoehl R, et al. N-Acetyltransferase (NAT) 2 acetylator status and age of tumour onset in patients with sporadic and familial, microsatellite stable (MSS) colorectal cancer. Int J Colorectal Dis. 2007;22:137–43.View ArticlePubMedGoogle Scholar
- Arias CA, Panesso D, McGrath DM, Qin X, Mojica MF, Miller C, et al. Genetic basis for in vivo daptomycin resistance in enterococci. N Engl J Med. 2011;365:892–900.View ArticlePubMedPubMed CentralGoogle Scholar
- Sevier CS. Erv2 and quiescin sulfhydryl oxidases: Erv-domain enzymes associated with the secretory pathway. Antioxid Redox Sign. 2012;16:800–8.View ArticleGoogle Scholar
- Feng L, Wang K, Li Y, Tan Y, Kong J, Li H, et al. Overexpression of SBPase enhances photosynthesis against high temperature stress in transgenic rice plants. Plant Cell Rep. 2007;26:1635–46.View ArticlePubMedGoogle Scholar
- Mathews WR, Wang F, Eide DJ, Doren MV. Drosophila fear of intimacy encodes a Zrt/IRT-like protein (ZIP) family zinc transporter functionally related to mammalian ZIP proteins. J Biol Chem. 2005;280:787–95.View ArticlePubMedGoogle Scholar
- Carrozza MJ, Utley RT, Workman JL, Cote J. The diverse functions of histone acetyltransferase complexes. Trends Genet. 2003;19:321–9.View ArticlePubMedGoogle Scholar
- Nakayama K, Nakayama N, Davidson B, Sheu JJ, Jinawath N, Santillan A, et al. A BTB/POZ protein, NAC-1, is related to tumor recurrence and is essential for tumor growth and survival. Proc Natl Acad Sci. 2006;103:18739–44.View ArticlePubMedPubMed CentralGoogle Scholar
- Abramyan J, Feng CW, Koopman P. Cloning and expression of candidate sexual development genes in the cane toad (Bufo marinus). Dev Dyn. 2009;238:2430–41.View ArticlePubMedGoogle Scholar
- Hagemann C, Weigelin B, Schommer S, Schulze M, Al-Jomah N, Anacker J, et al. The cohesin-interacting protein, precocious dissociation of sisters 5A/sister chromatid cohesion protein 112, is up-regulated in human astrocytic tumors. Int J Mol Med. 2011;27:39–51.PubMedGoogle Scholar
- Ahn JD, Morishita R, Kaneda Y, Lee SJ, Kwon KY, Choi SY, et al. Inhibitory effects of novel AP-1 decoy oligodeoxynucleotides on vascular smooth muscle cell proliferation in vitro and neointimal formation in vivo. Circ Res. 2002;90:1325–32.View ArticlePubMedGoogle Scholar
- Chekanova JA, Shaw RJ, Wills MA, Belostotsky DA. Poly(A) tail-dependent exonuclease AtRrp41p from Arabidopsis thaliana rescues 5.8 S rRNA processing and mRNA decay defects of the yeast ski6 mutant and is found in an exosome-sized complex in plant and yeast cells. J Biol Chem. 2000;275:33158–66.View ArticlePubMedGoogle Scholar
- Zuo Z, Urban G, Scammell JG, Dean NM, McLean TK, Aragon I, et al. Ser/Thr protein phosphatase type 5 (PP5) is a negative regulator of glucocorticoid receptor‐mediated growth arrest. Biochemistry. 1999;38:8849–57.View ArticlePubMedGoogle Scholar
- Passalacqua M, Patrone M, Picotti GB, Del Rio M, Sparatore B, Melloni E, et al. Stimulated astrocytes release high-mobility group 1 protein, an inducer of LAN-5 neuroblastoma cell differentiation. Neuroscience. 1998;82:1021–8.View ArticlePubMedGoogle Scholar
- Guizzetti M, Costa LG. Inhibition of muscarinic receptor-stimulated glial cell proliferation by ethanol. J Neurochem. 1996;67:2236–45.View ArticlePubMedGoogle Scholar
- Kunzelmann K. Ion channels and cancer. J Membr Biol. 2005;205:159–73.View ArticlePubMedGoogle Scholar
- Boughton BA, Dobson RC, Gerrard JA, Hutton CA. Conformationally constrained diketopimelic acid analogues as inhibitors of dihydrodipicolinate synthase. Bioorg Med Chem Lett. 2008;18:460–3.View ArticlePubMedGoogle Scholar
- Kershaw MJ, Thornton CR, Wakley GE, Talbot NJ. Four conserved intramolecular disulphide linkages are required for secretion and cell wall localization of a hydrophobin during fungal morphogenesis. Mol Microbiol. 2005;56:117–25.View ArticlePubMedGoogle Scholar
- Xiao Z, Xue J, Sowin TJ, Zhang H. Differential roles of checkpoint kinase 1, checkpoint kinase 2, and mitogen-activated protein kinase-activated protein kinase 2 in mediating DNA damage-induced cell cycle arrest: implications for cancertherapy. Mol Cancer Ther. 2006;5:1935–43.View ArticlePubMedGoogle Scholar
- Jouany JP, Medina B, Bertin G, Julliand V. Effect of live yeast culture supplementation on hindgut microbial communities and their polysaccharidase and glycoside hydrolase activities in horses fed a high-fiber or high-starch diet. J Anim Sci. 2009;87:2844–52.View ArticlePubMedGoogle Scholar
- de Cárcer G, Pérez de Castro I, Malumbres M. Targeting cell cycle kinases for cancer therapy. Curr Med Chem. 2007;14:969–85.View ArticlePubMedGoogle Scholar
- Schneiter R, Toulmay A. The role of lipids in the biogenesis of integral membrane proteins. Appl Microbiol Biotechnol. 2007;73:1224–32.View ArticlePubMedGoogle Scholar
- Jover R, Hoffmann F, Scheffler-Koch V, Lindberg RL. Limited heme synthesis in porphobilinogen deaminase-deficient mice impairs transcriptional activation of specific cytochrome P450 genes by phenobarbital. Eur J Biochem. 2000;267:7128–37.View ArticlePubMedGoogle Scholar
- Chan MT, Yu SM. The 39 untranslated region of a rice alpha-amylase gene functions as a sugar-dependent mRNA stability determinant. Proc Natl Acad Sci. 1998;95:6543–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Vierheilig H, Alt-Hug M, Wiemken A, Boller T. Hyphal in vitro growth of the arbuscular mycorrhizal fungus Glomus mosseae is affected by chitinase but not by β-1,3-glucanase. Mycorrhiza. 2001;11:279–82.View ArticlePubMedGoogle Scholar
- Van der Meer JR, Frijters AC, Leveau JH, Eggen RI, Zehnder AJ, de Vos WM. Characterization of the Pseudomonas sp. strain P51 gene tcbR, a LysR-type transcriptional activator of the tcbCDEF chlorocatechol oxidative operon, and analyses of the regulatory region. J Bacteriol. 1991;173:3700–8.PubMedPubMed CentralGoogle Scholar
- Iaaska VK, Iaaska BE. Electrophoretic analysis of substrate specificity of wheat alcohol dehydrogenases. Biokhimiia. 1978;43:2011–5.PubMedGoogle Scholar
- Shimizu M, Goto M, Hanai M, Shimizu T, Izawa N, Kanamoto H, et al. Selectable tolerance to herbicides by mutated acetolactate synthase gees integrated into the chloroplast genome of tobacco. Plant Physiol. 2008;147:1976–83.View ArticlePubMedPubMed CentralGoogle Scholar