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本文引用的文献

1
Reciprocal oxylipin-mediated cross-talk in the Aspergillus-seed pathosystem.曲霉菌-种子病理系统中互作的氧脂介导的串扰。
Mol Microbiol. 2008 Jan;67(2):378-91. doi: 10.1111/j.1365-2958.2007.06045.x.
2
Improved protocols for functional analysis in the pathogenic fungus Aspergillus flavus.致病性真菌黄曲霉功能分析的改进方案。
BMC Microbiol. 2007 Nov 26;7:104. doi: 10.1186/1471-2180-7-104.
3
Role of oxylipins and other lipid mediators in fungal pathogenesis.氧脂素和其他脂质介质在真菌致病机制中的作用。
Future Microbiol. 2006 Aug;1(2):219-27. doi: 10.2217/17460913.1.2.219.
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Aspergillus flavus: human pathogen, allergen and mycotoxin producer.黄曲霉:人类病原体、过敏原及霉菌毒素产生菌。
Microbiology (Reading). 2007 Jun;153(Pt 6):1677-1692. doi: 10.1099/mic.0.2007/007641-0.
5
Oxylipins as developmental and host-fungal communication signals.氧化脂质作为发育和宿主-真菌通讯信号。
Trends Microbiol. 2007 Mar;15(3):109-18. doi: 10.1016/j.tim.2007.01.005. Epub 2007 Feb 2.
6
Understanding the genetics of regulation of aflatoxin production and Aspergillus flavus development.了解黄曲霉毒素产生及黄曲霉生长调控的遗传学机制。
Mycopathologia. 2006 Sep;162(3):155-66. doi: 10.1007/s11046-006-0050-9.
7
Quorum sensing in dimorphic fungi: farnesol and beyond.双态真菌中的群体感应:法尼醇及其他。
Appl Environ Microbiol. 2006 Jun;72(6):3805-13. doi: 10.1128/AEM.02765-05.
8
Feedback control of morphogenesis in fungi by aromatic alcohols.芳香醇对真菌形态发生的反馈控制
Genes Dev. 2006 May 1;20(9):1150-61. doi: 10.1101/gad.1411806. Epub 2006 Apr 17.
9
Talking to themselves: autoregulation and quorum sensing in fungi.自言自语:真菌中的自我调节与群体感应
Eukaryot Cell. 2006 Apr;5(4):613-9. doi: 10.1128/EC.5.4.613-619.2006.
10
Lipoxygenases: occurrence, functions and catalysis.脂氧合酶:存在、功能与催化作用
J Plant Physiol. 2006 Feb;163(3):348-57. doi: 10.1016/j.jplph.2005.11.006. Epub 2005 Dec 28.

黄曲霉中由密度依赖性和脂氧合酶活性控制的形态转变。

Morphological transitions governed by density dependence and lipoxygenase activity in Aspergillus flavus.

作者信息

Horowitz Brown S, Zarnowski R, Sharpee W C, Keller N P

机构信息

Department of Medical Microbiology and Immunology and Department of Plant Pathology, UW-Madison, 1550 Linden Dr., Madison, WI 53706, USA.

出版信息

Appl Environ Microbiol. 2008 Sep;74(18):5674-85. doi: 10.1128/AEM.00565-08. Epub 2008 Jul 25.

DOI:10.1128/AEM.00565-08
PMID:18658287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2547031/
Abstract

Aspergillus flavus differentiates to produce asexual dispersing spores (conidia) or overwintering survival structures called sclerotia. Results described here show that these two processes are oppositely regulated by density-dependent mechanisms and that increasing the cell density (from 10(1) to 10(7) cells/plate) results in the lowest numbers of sclerotial and the highest numbers of conidial. Extract from spent medium of low-cell-density cultures induced a high-sclerotium-number phenotype, whereas high-cell-density extract increased conidiation. Density-dependent development is also modified by changes in lipid availability. Exogenous linoleic acid increased sclerotial production at intermediate cell densities (10(4) and 10(5) cells/plate), whereas oleic and linolenic acids inhibited sclerotium formation. Deletion of Aflox encoding a lipoxygenase (LOX) greatly diminished density-dependent development of both sclerotia and conidia, resulting in an overall increase in the number of sclerotia and a decrease in the number of conidia at high cell densities (>10(5) cells/plate). Aflox mutants showed decreased linoleic acid LOX activity. Taken together, these results suggest that there is a quorum-sensing mechanism in which a factor(s) produced in dense cultures, perhaps a LOX-derived metabolite, activates conidium formation, while a factor(s) produced in low-density cultures stimulates sclerotium formation.

摘要

黄曲霉分化产生无性传播孢子(分生孢子)或越冬存活结构即菌核。此处描述的结果表明,这两个过程受密度依赖性机制的反向调控,并且增加细胞密度(从每平板10¹个细胞到10⁷个细胞)会导致菌核数量最少而分生孢子数量最多。低细胞密度培养物的用过培养基提取物诱导出高菌核数表型,而高细胞密度提取物则增加分生孢子形成。脂质可用性的变化也会改变密度依赖性发育。外源性亚油酸在中等细胞密度(每平板10⁴和10⁵个细胞)时增加菌核产生,而油酸和亚麻酸则抑制菌核形成。编码脂氧合酶(LOX)的Aflox缺失极大地减少了菌核和分生孢子的密度依赖性发育,导致在高细胞密度(>每平板10⁵个细胞)时菌核数量总体增加而分生孢子数量减少。Aflox突变体显示亚油酸LOX活性降低。综上所述,这些结果表明存在一种群体感应机制,其中在高密度培养物中产生的一种或多种因子,可能是一种源自LOX的代谢产物,激活分生孢子形成,而在低密度培养物中产生的一种或多种因子刺激菌核形成。