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实时荧光定量 PCR 法监测瘤胃中厌氧真菌生物量和种群大小。

Real-time PCR assays for monitoring anaerobic fungal biomass and population size in the rumen.

机构信息

Graduate School of Bioresources, Mie University, 1577 Kurimamachiya-cho, Tsu, Mie 514-8507, Japan.

出版信息

Curr Microbiol. 2011 Apr;62(4):1147-51. doi: 10.1007/s00284-010-9843-7. Epub 2010 Dec 14.

Abstract

The relationship between copy numbers of internal transcribed spacer 1 (ITS1) and biomass or zoospore count of anaerobic fungi was studied to develop a quantitative real-time PCR-based monitoring method for fungal biomass or population in the rumen. Nine fungal strains were used to determine the relationship between ITS1 copy number and fungal biomass. Rumen fluid from three sheep and a cow were used to determine the relationship between ITS1 copy number and fungal population. ITS1 copy number was determined by real-time PCR with a specific primer set for anaerobic fungi. Freeze-dried fungal cells were weighed for fungal biomass. Zoospore counts were determined by the roll-tube method. A positive correlation was observed between both ITS1 copy number and dry weight and ITS1 copy number and zoospore counts, suggesting that the use of ITS1 copy numbers is effective for estimating fungal biomass and population density. On the basis of ITS1 copy numbers, fluctuations in the fungal population in sheep rumen showed that although the values varied among individual animals, the fungal population tended to decrease after feeding. In the present study, a culture-independent method was established that will provide a powerful tool for understanding the ecology of anaerobic fungi in the rumen.

摘要

本研究旨在探讨内转录间隔区 1(ITS1)的拷贝数与厌氧真菌生物量或游动孢子计数之间的关系,从而开发一种基于实时定量 PCR 的瘤胃真菌生物量或种群监测方法。使用 9 株真菌菌株来确定 ITS1 拷贝数与真菌生物量之间的关系。使用来自 3 只绵羊和 1 头牛的瘤胃液来确定 ITS1 拷贝数与真菌种群之间的关系。使用针对厌氧真菌的特定引物组通过实时 PCR 测定 ITS1 拷贝数。通过称重冻干真菌细胞来确定真菌生物量。通过滚管法确定游动孢子计数。ITS1 拷贝数与干重和 ITS1 拷贝数与游动孢子计数之间均存在正相关关系,这表明使用 ITS1 拷贝数可以有效地估计真菌生物量和种群密度。基于 ITS1 拷贝数,绵羊瘤胃中真菌种群的波动表明,尽管个体动物之间的值存在差异,但在进食后真菌种群往往会减少。在本研究中,建立了一种无需培养的方法,这将为理解瘤胃中厌氧真菌的生态学提供有力工具。

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