Species Richness, rRNA Gene Abundance, and Seasonal Dynamics of Airborne Plant-Pathogenic Oomycetes

被引:11
作者
Lang-Yona, Naama [1 ]
Pickersgill, Daniel A. [1 ,2 ]
Maurus, Isabel [1 ]
Teschner, David [1 ,2 ]
Wehking, Joern [1 ,2 ]
Thines, Eckhard [3 ]
Poeschl, Ulrich [1 ]
Despres, Viviane R. [2 ]
Froehlich-Nowoiskyl, Janine [1 ]
机构
[1] Max Planck Inst Chem, Multiphase Chem Dept, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Mol Phys, Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Inst Microbiol & Wine Res, Mainz, Germany
关键词
airborne Oomycetes; Peronosporomycetes; plant pathogen; seasonal distribution; Sanger sequencing; qPCR analysis; meteorological parameter; DOWNY MILDEW; PHYTOPHTHORA-CINNAMOMI; GLOBAL ATMOSPHERE; WARNING SYSTEM; LATE BLIGHT; FUNGAL; PHYLOGENY; DISEASE; QUANTIFICATION; OOSPORES;
D O I
10.3389/fmicb.2018.02673
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oomycetes, also named Peronosporomycetes, are one of the most important and widespread groups of plant pathogens, leading to significant losses in the global agricultural productivity. They have been studied extensively in ground water, soil, and host plants, but their atmospheric transport vector is not well characterized. In this study, the occurrence of airborne Oomycetes was investigated by Sanger sequencing and quantitative PCR of coarse and fine aerosol particle samples (57 filter pairs) collected over a 1-year period (2006-2007) and full seasonal cycle in Mainz, Germany. In coarse particulate matter, we found 55 different hypothetical species (OTUs), of which 54 were plant pathogens and 29 belonged to the genus Peronospora (downy mildews). In fine particulate matter (< 3 mu m), only one species of Hyaloperonospora was found in one sample. Principal coordinate analysis of the species composition revealed three community clusters with a dependence on ambient temperature. The abundance of Oomycetes rRNA genes was low in winter and enhanced during spring, summer, and fall, with a dominance of Phytophthora, reaching a maximum concentration of similar to 1.6 x 10(6) rRNA genes per cubic meter of sampled air in summer. The presence and high concentration of rRNA genes in air suggests that atmospheric transport, which can lead to secondary infection, may be more important than currently estimated. This illustrates the need for more current and detailed datasets, as potential seasonal shifts due to changing meteorological conditions may influence the composition of airborne Oomycetes. An insight into the dynamics of airborne plant pathogens and their major drivers should be useful for improved forecasting and management of related plant diseases.
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页数:11
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共 86 条
[1]   Comparison of decision methods to initiate fungicide applications against Cercospora blight of carrot [J].
Abraham, V ;
Kushalappa, AC ;
Carisse, O ;
Bourgeois, G ;
Auclair, P .
PHYTOPROTECTION, 1995, 76 (03) :91-99
[2]   Biology and systematics of heterokont and haptophyte algae [J].
Andersen, RA .
AMERICAN JOURNAL OF BOTANY, 2004, 91 (10) :1508-1522
[3]  
[Anonymous], 2001, Aerobiologia, DOI DOI 10.1023/A:1010849522964
[4]  
[Anonymous], 2012, Technical Report No. 597
[5]   Diversity of peronosporomycete (oomycete) communities associated with the rhizosphere of different plant species [J].
Arcate, JM ;
Karp, MA ;
Nelson, EB .
MICROBIAL ECOLOGY, 2006, 51 (01) :36-50
[6]   LONG-RANGE TRANSPORT OF TOBACCO BLUE MOLD SPORES [J].
AYLOR, DE ;
TAYLOR, GS ;
RAYNOR, GS .
AGRICULTURAL METEOROLOGY, 1982, 27 (3-4) :217-232
[7]   A kingdom-level phylogeny of eukaryotes based on combined protein data [J].
Baldauf, SL ;
Roger, AJ ;
Wenk-Siefert, I ;
Doolittle, WF .
SCIENCE, 2000, 290 (5493) :972-977
[8]  
BEAKES G W., 2015, eLS, P1, DOI DOI 10.1002/9780470015902.A0001984
[9]   Crop-destroying fungal and oomycete pathogens challenge food security [J].
Bebber, Daniel P. ;
Gurr, Sarah J. .
FUNGAL GENETICS AND BIOLOGY, 2015, 74 :62-64
[10]   Quantification of disease progression of several microbial pathogens on Arabidopsis thaliana using real-time fluorescence PCR [J].
Brouwer, M ;
Lievens, B ;
Van Hemelrijck, W ;
Van den Ackerveken, G ;
Cammue, BPA ;
Thomma, BPHJ .
FEMS MICROBIOLOGY LETTERS, 2003, 228 (02) :241-248