» Articles » PMID: 11010882

PCR Primers That Amplify Fungal RRNA Genes from Environmental Samples

Overview
Date 2000 Sep 30
PMID 11010882
Citations 150
Authors
Affiliations
Soon will be listed here.
Abstract

Two PCR primer pairs were designed to amplify rRNA genes (rDNA) from all four major phyla of fungi: Ascomycota, Basidiomycota, Chytridomycota, and Zygomycota. PCRs performed with these primers showed that both pairs amplify DNA from organisms representing the major taxonomic groups of fungi but not from nonfungal sources. To test the ability of the primers to amplify fungal rDNA from environment samples, clone libraries from two avocado grove soils were constructed and analyzed. These soils possess different abilities to inhibit avocado root rot caused by Phythophthora cinnamomi. Analysis of the two rDNA clone libraries revealed differences in the two fungal communities. It also revealed a markedly different depiction of the soil fungal community than that generated by a culture-based analysis, confirming the value of rDNA-based approaches for identifying organisms that may not readily grow on agar media. Additional evidence of the usefulness of the primers was obtained by identifying fungi associated with avocado leaves. In both the soil and leaf analyses, no nonfungal rDNA sequences were identified, illustrating the selectivity of these PCR primers. This work demonstrates the ability of two newly developed PCR primer sets to amplify fungal rDNA from soil and plant tissue, thereby providing unique tools to examine this vast and mostly undescribed community of organisms.

Citing Articles

Vegetation-soil-microbiota dynamics across a 50-year reconstructed grassland chronosequence on the Loess Plateau of China.

Ma Y, Shen Y, Jin L, Tian Y, Ma H, Lan J PeerJ. 2024; 12:e18723.

PMID: 39717049 PMC: 11665427. DOI: 10.7717/peerj.18723.


Seasonal Variations of Sediment Fungal Community of a Shallow Lake in North China.

Yi Y, Yin S Microorganisms. 2024; 12(11).

PMID: 39597517 PMC: 11596378. DOI: 10.3390/microorganisms12112127.


Screening and application of functional autochthonous starter culture from cured meat, which can reduce nitrite content.

Zhang Q, Shen J, Meng G, Wang H, Liu C, Zhu C Int Microbiol. 2024; .

PMID: 39400630 DOI: 10.1007/s10123-024-00606-7.


Changes in sediment greenhouse gases production dynamics in an estuarine wetland following invasion by .

Jiang Y, Shao Y, Huang J, Du Y, Wen Y, Tang H Front Microbiol. 2024; 15:1420924.

PMID: 39070262 PMC: 11275515. DOI: 10.3389/fmicb.2024.1420924.


Microbial Diversity Associated with the Cabernet Sauvignon Carposphere (Fruit Surface) from Eight Vineyards in Henan Province, China.

Zhang J, Zhu C, Zhao Z, Liu C Foods. 2024; 13(11).

PMID: 38890855 PMC: 11172321. DOI: 10.3390/foods13111626.


References
1.
Simon L, Lalonde M, Bruns T . Specific amplification of 18S fungal ribosomal genes from vesicular-arbuscular endomycorrhizal fungi colonizing roots. Appl Environ Microbiol. 1992; 58(1):291-5. PMC: 195206. DOI: 10.1128/aem.58.1.291-295.1992. View

2.
Borneman J, Skroch P, OSullivan K, Palus J, Rumjanek N, Jansen J . Molecular microbial diversity of an agricultural soil in Wisconsin. Appl Environ Microbiol. 1996; 62(6):1935-43. PMC: 167971. DOI: 10.1128/aem.62.6.1935-1943.1996. View

3.
Farrelly V, Rainey F, Stackebrandt E . Effect of genome size and rrn gene copy number on PCR amplification of 16S rRNA genes from a mixture of bacterial species. Appl Environ Microbiol. 1995; 61(7):2798-801. PMC: 167554. DOI: 10.1128/aem.61.7.2798-2801.1995. View

4.
Kappe R, Fauser C, Okeke C, Maiwald M . Universal fungus-specific primer systems and group-specific hybridization oligonucleotides for 18S rDNA. Mycoses. 1996; 39(1-2):25-30. DOI: 10.1111/j.1439-0507.1996.tb00079.x. View

5.
Barns S, Fundyga R, Jeffries M, Pace N . Remarkable archaeal diversity detected in a Yellowstone National Park hot spring environment. Proc Natl Acad Sci U S A. 1994; 91(5):1609-13. PMC: 43212. DOI: 10.1073/pnas.91.5.1609. View