- Open Access
Seasonal changes in microbial community composition in river water studied using 454-pyrosequencing
© Kaevska et al. 2016
- Received: 24 April 2015
- Accepted: 23 March 2016
- Published: 5 April 2016
The aims of this study were to determine the microbial community in five rivers in the proximity of a city in the Czech Republic using 454-pyrosequencing, as well as to assess seasonal variability over the course of 1 year and to identify the factors influencing the structure of bacterial communities. Samples from five rivers around the city of Brno were obtained during four seasons and analysed using 454 pyrosequencing of the 16S rRNA gene. The core composition of bacterial communities consisted of Actinobacteria, Bacteroidetes, Proteobacteria, Firmicutes, Fusobacteria, TM7 and others. Our approach enabled us to more closely study the correlation between the abundance of different families and environmental factors. Overall, Actinobacteria negatively correlated with phosphorus, sulphate, dissolved particle and chloride levels. In contrast, Proteobacteria positively correlated with sulphate, dissolved particle, chloride, dissolved oxygen and nitrite levels. Future work should focus on the dynamics of bacterial communities present in river water and their relation to the overall stability of the water ecosystem.
- River water
- Microbial community
- Environmental factors
The community composition of water microorganisms in natural water bodies is important for the mineralisation of organic matter and circulation of important elements in aquatic environments. Culture-independent methods enable a more complex and detailed view of the structure of bacterial communities in nature. With the development of next-generation sequencing, there have been a large number of studies dedicated to unravelling the structure as well as the function of microorganisms in all kinds of environments. Drinking water and biofilms from water distribution systems have been the subject of such studies (Douterelo et al. 2014; Hwang et al. 2012). There is also a large number of studies focused on waste water (Hu et al. 2012; Ye and Zhang 2013), as well as microbial communities in sea water or estuaries (Gilbert et al. 2012; Zhang et al. 2014). However, only a limited number of studies have focused on the spatio-temporal changes of bacterial communities and their correlation with physical and chemical factors in the environment.
Although there are many studies focused on microbial ecology in different types of water, bacterial communities in urban rivers are not well documented. The majority of studies have focused on indicator bacteria of faecal pollution (Murray et al. 2001). The impact of the chemical and physical properties of water on the structure of bacterial communities has been studied in rivers in China (Liu et al. 2013; Zhang et al. 2012). In Europe, Winter et al. (2007) studied the longitudinal changes in bacterial community composition in the Danube River. The authors found a positive correlation between bacterial richness and concentration of P-PO4. However, the bacterial community composition was determined by denaturating gradient gel electrophoresis which did not reveal much information about the species present.
The aims of the present study were to determine the microbial community in five different rivers in the proximity of a city in the Czech Republic using 454-pyrosequencing, as well as to assess their seasonal variability over the course of a year and to identify the factors influencing the structure of bacterial communities.
Sample collection and processing
Physical and chemical parameters of water
All of the water samples were subjected to physical and chemical analyses according to accredited methods in a specialised laboratory for water analysis in the company Povodi Moravy a.s. Brno. All the methods performed were according to the ČSN EN ISO/IEC 17025:2005 norms. Analysed parameters included; temperature, pH, oxygen saturation, total oxygen, chlorides, sulphates, nitrates, nitrites, turbidity, total phosphorus, total nitrogen dissolved particles and dissolved oxygen.
DNA isolation and PCR
DNA was isolated from the pellet using the commercially available PowerSoil DNA isolation kit, MoBio (USA). PCR was performed using universal bacterial primers for amplification of the V2/V3 regions of the 16S RNA gene (Nossa et al. 2010). The primers were flanked with standard MID sequences and tags needed for the pyrosequencing. The PCR reaction was prepared using the HotStarTaq Master Mix Kit following the manufacturer´s instructions (Qiagen), with cycling conditions as follows; 95 °C for 15 min followed by 30 cycles of incubation at 94 °C for 40 s, 55 °C for 55 s and 72 °C for 60 s, and a final extension step at 72 °C for 5 min. PCR products were visualised using electrophoresis on 1.5 % agarose gels and purified from the gel using the QIAquick Gel Extraction Kit (Qiagen).
Amplicon library preparation and high-throughput sequencing was performed using the 454 GS Junior from Roche, using the chemistry recommended by the manufacturer (Roche). Sequences were analysed using the QIIME software (Caporaso et al. 2010). Quality trimming criteria included no mismatch in MID sequences and a maximum of 1 mismatch in primer sequences. The obtained sequences with qual score higher than 20 were shortened to the same length of 350 bp and classified with RDP Seqmatch (Cole et al. 2014) with an operational taxonomic unit (OTU) discrimination level set to 97 %.
Correlations of bacterial occurrence with measured parameters were calculated using Spearman’s rank correlation coefficient. Correlations were visualised using a cluster heatmap generated using MATLAB version 2013a (MathWorks).
Environmental characteristics of the water
Environmental characteristics of the samples from five rivers in the four seasons throughout the year
Oxygen saturation (%)
Dissolved particles (mg/L)
Dissolved oxygen (mg/L)
Microbial community composition
Diversity indexes in the examined samples sorted by season
We have studied the bacterial community composition at five sampling points around the city of Brno during four seasons. Fifteen environmental factors were also measured at each sampling point and the variance of bacterial families was correlated with the fluctuations in these parameters. A similar study was performed by Zhang et al. (2012) in river water in China; however, the authors used denaturating gradient gel electrophoresis (DGGE) to study the bacterial community composition. Although DGGE and pyrosequencing may target different taxonomical units (Vaz-Moreira et al. 2011), pyrosequencing of the 16S rRNA gene is a powerful tool with higher capacity than DGGE and enables in-depth study of community composition.
The microbial diversity indices are shown in Table 2. Chao 1 and Shannon values are similar to those obtained by other authors in river water (Zhang et al. 2012). Our results showed the highest diversity in the autumn season, although the diversity during the rest of the year was relatively steady.
Similarly to other studies, we found the bacterial composition to be characteristic for a season rather than a given locality (Gilbert et al. 2012; Zhang et al. 2012, 2014), although we found sampling site 5 to have a different composition (Fig. 2). This may be due to the fact that the sampling site lay downstream of a populated area, at a point where the river is wide.
Our approach enabled us to obtain detailed insight into bacterial community structure and thus we could correlate specific genera with certain environmental factors. More specifically, we performed correlation analyses on the phyla and also on families belonging to Proteobacteria and Actinobacteria. Similar statistical analyses regarding the influence of environmental factors on microbial communities were performed on samples from a subtropical river (Liu et al. 2013), although the authors used DGGE and could not precisely specify the bacterial genera present. However, the authors found a strong correlation between temperature and variation in bacterial community composition. Another study performed by Zhang et al. (2014) presents further evidence that temperature is the main force driving changes in bacterial composition. We also observed changes in the phyla composition between seasons (Fig. 3), which we studied more closely in Proteobacteria, where we observed specific families to be strongly negatively correlated with temperature (Fig. 4). However, another study suggests that other factors, such as salinity or depth could be more important in determining variability (Fortunato et al. 2012). The composition of nutrients is also important for bacterial composition as different organisms are adapted to different conditions. We analysed the correlation between bacterial communities and eleven water factors. All of these had a certain influence on the community composition, although we could not specify which factor exerted the highest influence. Environmental factors were also analysed in relation to bacterial richness along the Danube River; phosphates and chlorides were found to be the most important in this regard (Winter et al. 2007).
In conclusion, we have analysed the bacterial community composition at five different sites and have determined the correlation with different environmental factors. We have identified a few factors that influenced the composition of bacterial communities in rivers. Fluctuations in the bacterial communities across seasons, and at different temperatures, as well as at different phosphorus and chloride levels were noted. However, we have not focused on the levels of pollution in the water or its effects on the bacterial community composition. Future work should address the dynamics of bacterial communities and their relation to the overall health or pollution levels of the water ecosystem.
MK participated in the design of the study and interpretation of results and drafted the manuscript, PV participated in the data acquisition and performed the analyses of the sequences, KS performed the statistical analyses and participated in their interpretation, IS participated in the design of the study, and interpretation of data. All authors read and approved the final manuscript.
The results of the project LO1218 were obtained with financial support from the Ministry of Education, Youth and Sports (MEYS) of the Czech Republic under the NPU I program. The study was supported by the Ministry of Agriculture of the Czech Republic (RVO0516).
The authors declare that they have no competing interests.
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