Abstract

High-throughput sequencing is commonly used to study soil microbial communities. However, different primers targeting different 16S rRNA hypervariable regions often generate different microbial communities and result in different values of diversity and community structure. This study determined the consequences of using two bacterial primers (338f/806r, targeting the V3–V4 region, and 520f/802r, targeting the V4 region) to assess bacterial communities in the soils of different land uses along a latitudinal gradient. The results showed that the variations in the soil bacterial diversity in different land uses were more evident based on the former pair. The statistical results showed that land use had no significant impact on soil bacterial diversity when primer pair 520f/802r was used. In contrast, when primer pair 338f/806r was used, the cropland and orchard soils had significantly higher operational taxonomic units (OTUs) and Shannon diversity index values than those of the shrubland and grassland soils. Similarly, the soil bacterial diversity generated by primer pair 338f/806r was significantly impacted by mean annual precipitation, soil total phosphorus (TP), soil total nitrogen (TN), and soil available phosphorus (AVP), while the soil bacterial diversity generated by primer pair 520f/802r showed no significant correlations with most of these environmental factors. Multiple regression models indicated that soil pH and soil organic carbon (SOC) shaped the soil bacterial community structure on the Loess Plateau regardless of what primer pair was used. Climatic conditions mainly affected the diversity of rare bacteria. Abundant bacteria are more sensitive than rare bacteria to environmental changes. Very little of the variation in the rare bacterial community was explained by environmental factors or geographic distance, suggesting that the communities of rare bacteria are unpredictable. The distributions of the abundant taxa were mainly determined by variations in environmental factors.

Highlights

  • Soil harbors many highly taxonomically and metabolically diverse microorganisms, which drive multiple ecological functions, such as nutrient cycling, climate regulation, carbon sequestration, soil health, and ecosystem stability

  • The primer pairs had no significant effects on detecting soil bacterial diversity

  • The variations in the observed number of operational taxonomic units (OTUs) and Shannon diversity index were more evident for the 338f/806r primer pair than the 520f/802r primer pair, suggesting that the 338f/806r pair can clearly reflect the variations in the bacterial diversity

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Summary

Introduction

Soil harbors many highly taxonomically and metabolically diverse microorganisms, which drive multiple ecological functions, such as nutrient cycling, climate regulation, carbon sequestration, soil health, and ecosystem stability. Most studies associated with soil microbial communities have focused on highly abundant species rather than rare species. Communities of rare microorganisms exhibit high genetic and functional diversity and may regulate biogeochemical cycling and ecosystem stability [1]. Low-abundance microorganisms have greater metabolic capacity and grow faster in soils [1]. Rare microorganisms reduce sulfate content in peat soils [2]. In a long-term fertilization experiment, a rare soil bacterial community, rather than a dominant soil bacterial community, controlled multiple ecosystem functions [3].

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