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Communication

Effect of Storage Period on the Fermentation Profile and Bacterial Community of Silage Prepared with Alfalfa, Whole-Plant Corn and Their Mixture

1
College of Animal Science and Technology, Hainan University, Haikou 570228, China
2
College of Grassland Science and Technology, China Agricultural University, Beijing 100193, China
3
Department of Crop and Soil Science, Oregon State University, Corvallis, OR 97331, USA
*
Author to whom correspondence should be addressed.
Fermentation 2022, 8(10), 486; https://doi.org/10.3390/fermentation8100486
Submission received: 31 August 2022 / Revised: 16 September 2022 / Accepted: 23 September 2022 / Published: 26 September 2022
(This article belongs to the Section Industrial Fermentation)

Abstract

:
This study aimed to investigate the impact of storage time on the bacterial community and fermentation profile of silage prepared with alfalfa, whole-plant corn, and their mixture. Fresh alfalfa and whole-plant corn were chopped and combined in fresh weight ratios of 1:0 (alfalfa, control), 0.8:0.2 (M1), 0.6:0.4 (M2), and 0:1 (corn). Three silos of each treatment were analyzed after 30, 60, and 90 d of storage. With storage time, pH, acetic acid, propionic acid, butyric acid, and ammonia nitrogen levels increased in alfalfa silage (p < 0.01), whereas lactic acid level decreased (p < 0.01). Compared to alfalfa silage, M1, M2, and corn silages were better fermented and more stable during storage. The dominant bacteria in M1, M2, and corn silages shifted significantly from L. plantarum, L. buchneri, and L. brevis to L. acetotolerans and L. buchneri during 30 to 60–90 d of storage, and storage time decreased the bacterial diversity of these silages. In conclusion, storage time significantly decreased the fermentation quality of alfalfa silage and remarkably optimized the bacterial community structure of well-fermented M1, M2, and corn silages. Alfalfa should be ensiled with at least 20% whole-plant corn to improve silage fermentation quality and storage stability.

1. Introduction

Ensiling is a forage preservation method whereby, under anaerobic conditions, lactic acid bacteria (LAB) produce organic acids from sugars present in the fresh material. The net result is a reduction in pH which prevents the growth and proliferation of spoilage microorganisms [1,2].
According to biochemical and microbiological events, ensiling can be grouped into four stages of different intensity and length, consisting of the initial aerobic stage, the fermentation stage, the stable stage during storage, and the feed-out stage [3]. In each of these stages, changes in chemical characteristics and microbial community occur to varying degrees, depending on forage properties, ensiling management, and conservation period [4,5]. The research on the dynamics of the microbial community and the fermentation parameters during storage has focused mainly on ensiled alfalfa [6,7,8,9], whole-plant corn [10,11,12,13,14], corn grain [15], wheat [16], sorghum [11,17], oat [18], rice straw [19], sugarcane (top) [20,21], total mixed ration [22], and alfalfa-based mixture [23,24]. To date, there is little information regarding the effect of storage period on the microbial community and fermentation parameters of silage prepared with alfalfa, whole-plant corn, and their mixture.
Our previous work evaluated the influence of mixing ratio on individual bacteria of co-ensiling alfalfa with whole-plant corn in the early stage of fermentation [25], but did not further explore the influence on bacterial composition and diversity changes that occur during storage. Therefore, this work was undertaken to investigate the effect of storage period on the bacterial community and fermentation profile of silage prepared with alfalfa, whole-plant corn, and their mixture.

2. Materials and Methods

2.1. Ensiling

Alfalfa (eight plots, each 100 m2) and corn (ten plots, each 50 m2) were grown at the Yanchi research station (37°78′ N, 107°40′ E) in northwest China’s Ningxia Hui Autonomous Region. The experimental design and experiment flow diagram was presented in Figure 1. In brief, the alfalfa was from the third cutting harvested at the early flowering period. The whole-plant corn was harvested at the 1/3 milk line period. Both forages were chopped to 2 cm and randomly grouped into 36 piles (400 g for each). Chopped alfalfa and corn were combined in fresh weight (FW) ratios of 1:0 (alfalfa, control), 0.8:0.2 (M1), 0.6:0.4 (M2), and 0:1 (corn). The 200 g of forages mass was placed into a plastic bag silo (20 cm × 30 cm) and was evacuated by a sealer (DS2300, Shenzhen Dingsheng Electric Appliance Co., Ltd., Shenzhen, China). Three silos of each treatment were opened for silage parameters evaluation after 30, 60, and 90 d of storage at 26–29 °C.

2.2. Analyses

A 20 g subsample from each silo was homogenized in 180 mL of distilled water and pH was determined immediately. The extract was centrifuged at 10,000× g for 5 min at 4 °C and passed through a 0.22 μm filter. The filtrate was analyzed by high performance liquid chromatography system (LC-20A, SHIMADZU, Shimadzu, Japan) for lactic acid (LA), acetic acid (AA), propionic acid (PA), and butyric acid (BA), as described by Wang et al. (2020) [25]. Ammonia nitrogen (NH3-N) was determined by the phenol method [26] and expressed on a total nitrogen (TN) basis.
A second subsample of approximately 100 g was placed in an air dry oven for 72 h at 65 °C to determine dry matter (DM), followed by grinding to pass through a 1 mm screen. Dry matter loss (DM loss) was calculated in accordance with Wang et al. (2020) [25]. Water soluble carbohydrates (WSC) were determined by the method of Murphy (1958) [27]. Crude protein (CP) was determined according to AOAC (2001) [28] and converted to TN by a coefficient of 6.25. Silage bacterial community was analyzed by the next generation sequencing technique according to Wang et al. (2019) [29], using a universal primer pair of 806-R (5′-GGACTACHVGGGTWTCTAAT-3′) and 338-F (5′-ACTCCTACGGGAGGCAGCAG-3′).

2.3. Statistical Analysis

Statistical analysis was performed using SAS (Version 9.1, SAS Institute Inc., Cary, CA, USA). The impact of treatment, storage period, and the interaction of treatment and storage period on fermentation and chemical parameters was analyzed in a 4 × 3 factorial arrangement using the general linear model:
Yijk = μ + αi + βj + αβij + εijk
where Yijk is the observed value, μ is the overall mean, αi is the treatment impact (i = alfalfa, M1, M2, and corn), βj is the storage period impact (j = 30, 60, and 90 d), αβij is the treatment and storage period interaction impact and εijk is the error. Means were compared using Duncan’s multiple range test, using a significant level of p < 0.05.

3. Results

3.1. Fermentation Profile of Silage during Storage

Chemical composition of ensiling materials was previously reported by Wang et al. (2020). Briefly, DM and WSC concentrations in fresh forages were 205.67 g/kg FW and 60.42 g/kg DM (alfalfa), 222.09 g/kg FW and 86.83 g/kg DM (M1), 239.26 g/kg FW and 93.39 g/kg DM (M2), and 280.27 g/kg FW and 146.35 g/kg DM (corn). The CP concentrations in fresh alfalfa, M1, M2, and corn were 205.49, 172.01, 147.38, and 81.92 g/kg DM, respectively.
Dynamics of fermentation and chemical parameters of silage during storage are provided in Table 1 and Table 2. Significant effects (p < 0.01) were observed for treatment, storage period, and their interaction on silage pH, LA, PA, and BA (Table 1). With storage time, pH, AA, PA, BA, and NH3-N levels in alfalfa silage increased (p < 0.01), whereas the LA level decreased (p < 0.01). With more corn in the mixture, silage pH, AA, PA, BA, and NH3-N values reduced (p < 0.01), irrespective of storage time. As shown in Table 2, DM loss level gradually increased but WSC concentration progressively decreased in all silages as ensiling progressed.

3.2. Bacterial Community of Silage during Storage

Bacterial community dynamic changes of silage at the phylum, genus, and species levels are illustrated in Figure 2A–C, respectively. After 30 d of storage, Firmicutes relative abundance decreased and Proteobacteria abundance increased as corn proportion increased (Figure 2A). With fermentation time, Firmicutes abundance was enriched and Proteobacteria abundance was reduced in M1, M2, and corn silages. Bacterial community of alfalfa silage stored for 30 d consisted mainly of Lactobacillus (72.68%), Weissella (14.91%), and Pediococcus (7.9%) and was relatively stable thereafter (Figure 2B). In contrast, Lactobacillus population increased and Pediococcus, Weissella, and Leuconostoc population decreased in M1, M2, and corn silages during storage. Moreover, Lactobacillus population increased and Pediococcus and Weissella populations decreased as the proportion of corn increased from 20% to 100% in each of these three storage periods. During alfalfa silage storage, L. curvatus abundance slightly decreased and L. brevis abundance moderately increased (Figure 2C). In contrast, L. plantarum was overtaken by L. acetotolerans in M1, M2, and corn silages during storage. After 30 d of storage, L. plantarum, L. farciminis, and L. acetotolerans population enriched, whereas L. curvatus, W. cibaria, and P. parvulus population dropped in silage with more corn. In contrast, L. acetotolerans accumulated and L. curvatus, L. brevis, L. plantarum, and W. cibaria richness reduced in silage stored for 60 or 90 d as corn proportion increased.

4. Discussion

4.1. Fermentation Profile of Silage during Storage

Few changes occur during storage stage when silage pH is sufficiently low and anaerobic conditions are maintained [30]. A low pH (3.6–4.5) is one of the key characteristics of well-preserved silage [31]. In the current work, alfalfa silage stored for 30 d was poorly fermented, indicated by a moderately high pH (4.61) and high level of AA (29.33 g/kg DM), PA (23.98 g/kg DM), BA (9.77 g/kg DM), and NH3-N (99.01 g/kg TN). Furthermore, alfalfa silage was anaerobically unstable and fermentation quality progressively dropped during storage. Li et al. (2020) also reported that LA concentration of alfalfa silage decreased and AA, BA, and NH3-N levels increased during 28–56 d of fermentation [8]. Fresh alfalfa is high in buffering capacity and low in DM and WSC [25,29], which hinders fast initial acidification in the early period of ensiling [1]. As a result, clostridial fermentation developed, accompanied by a high concentration of BA [8,32]. In this work, inclusion of corn improved silage fermentation in a proportion-dependent manner, confirming the results of previous studies [5,25]. Compared to alfalfa silage, M1, M2, and corn silages were better fermented with the pH falling into the range of 3.6–4.5 and more stable during storage.

4.2. Bacterial Community of Silage during Storage

The LAB closely related to silage fermentation are mainly composed of Pedicoccus, Enterococcus, Streptococcus, Lactococcus, Lactobacillus, Weissella, and Leuconostoc [1,2,33]. These bacteria are grouped into homo-fermentative LAB and hetero-fermentative LAB based on fermentation pattern [33]. Both homo-fermentation and hetero-fermentation can occur simultaneously during silage fermentation. In the current work, L. curvatus richness in alfalfa silage decreased and L. brevis richness increased during storage. These changes were accompanied by an increase in AA production and a reduction in LA production, suggesting the transition from homo-fermentation to hetero-fermentation during storage. These results are similar to those of Guo et al. (2018), who reported that L. plantarum population declined and Weissella population increased in alfalfa silage during 30–90 d of storage [6]. Based on 1 mole of fructose for the substrate, homo-fermentative LAB can yield 2 moles of LA and hetero-fermentative LAB produce 1/3 mole of LA and 1/3 mole of AA or ethanol [1]. It is usually believed that homo-fermentative lactobacilli, such as L. curvatus and L. plantarum, predominate in well-fermented silage until the end of fermentation, when they are overtaken by hetero-fermentative LAB, such as L. buchneri and L. brevis [30]. Beck (1972) explained that these transitions were attributable to the high tolerance of hetero-fermenters to AA [34]. The current work showed that L. acetotolerans predominated in the bacterial community of corn silage with AA concentration increasing from 17.56 to 23.58 g/kg DM during 60–90 d of storage. This agrees with the results of Xu et al. (2021) [14]. Some research has shown, however, that L. acetotolerans, a homo-fermentative LAB, was detected from fermented vinegar and is tolerant to a high concentration of AA [35,36]. In addition, its physiological characteristics are different from the other homo-fermenters belonging to Lactobacillus [35]. In the near future, it is suggested to isolate this species from corn silage and to apply it to alfalfa ensiling for improving silage fermentation quality.

5. Conclusions

In conclusion, storage time significantly lowered the fermentation quality of alfalfa silage, and remarkably decreased the bacterial diversity and optimized the bacterial community structure of well-fermented M1, M2, and corn silages. Alfalfa should be ensiled with at least 20% whole-plant corn to improve the silage fermentation quality and storage stability in practical production. In the following work, it is recommended that the lactic acid bacteria species L. acetotolerans should be isolated from corn silage and applied to alfalfa ensiling.

Author Contributions

Conceptualization, K.M. and M.W.; methodology, K.M.; software, K.M.; validation, Z.Y., D.B.H. and M.W.; formal analysis, K.M.; investigation, M.W.; resources, Z.Y. and M.W.; data curation, K.M.; writing—original draft preparation, K.M.; writing—review and editing, S.H., D.B.H. and M.W.; visualization, M.W.; supervision, Z.Y. and M.W.; project administration, M.W.; funding acquisition, M.W. and S.H. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the Scientific Research Fund Project of Hainan University (KYQD-ZR22014 and KYQD-ZR22013).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available upon request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. The experimental design and experiment flow diagram.
Figure 1. The experimental design and experiment flow diagram.
Fermentation 08 00486 g001
Figure 2. Dynamics of bacterial community of silage during storage at the phylum (A), genus (B) and species (C) levels (n = 3). M1 and M2, alfalfa and corn mixed with ratio of 0.8:0.2 and 0.6:0.4 on a fresh weight basis.
Figure 2. Dynamics of bacterial community of silage during storage at the phylum (A), genus (B) and species (C) levels (n = 3). M1 and M2, alfalfa and corn mixed with ratio of 0.8:0.2 and 0.6:0.4 on a fresh weight basis.
Fermentation 08 00486 g002
Table 1. Dynamics of fermentation profile of silage during storage (n = 3).
Table 1. Dynamics of fermentation profile of silage during storage (n = 3).
Storage Period (d) 3 p Value 5
Item 1Treatment 2306090SEM 4TST × S
pHAlfalfa4.61 aC4.76 aB4.83 aA0.07<0.001<0.001<0.001
M14.06 bB4.13 bAB4.19 bA
M23.90 cA3.87 cB3.86 cB
Corn3.61 dB3.62 dAB3.65 dA
LA (g/kg DM)Alfalfa68.78 bA53.28 cB47.04 cB4.05<0.0010.002<0.001
M1111.03 aA97.44 bAB83.89 aB
M2120.26 aA115.34 aA83.32 aB
Corn78.48 bA74.72 bAB63.12 bB
AA (g/kg DM)Alfalfa29.33 aB52.65 aA56.49 aA2.34<0.001<0.0010.101
M117.29 bC29.37 bB37.22 bA
M219.59 bB30.81 bA37.95 bA
Corn13.28 bB17.56 cB23.58 cA
PA (g/kg DM)Alfalfa23.98 aB44.43 aA44.71 aA2.51<0.001<0.0010.006
M115.83 bC33.48 bB41.88 aA
M212.42 bC29.77 bB41.93 aA
Corn3.50 cC8.79 cB14.01 bA
BA (g/kg DM)Alfalfa9.77 aB12.73 aA13.49 aA0.89<0.0010.001<0.001
M10.00 b0.00 b0.00 b
M20.00 b0.00 b0.00 b
Corn0.00 b0.00 b0.00 b
NH3-N (g/kg TN)Alfalfa99.01 aB110.42 aA120.16 aA4.44<0.001<0.0010.239
M173.64 bB76.19 bB87.16 bA
M250.74 cB54.33 cAB61.43 cA
Corn38.68 dB42.60 dAB48.90 dA
1 LA, lactic acid; AA, acetic acid; PA, propionic acid; BA, butyric acid; DM, dry matter; NH3-N, ammonia nitrogen; TN, total nitrogen. 2 M1 and M2, alfalfa and corn mixed with ratio of 0.8:0.2 and 0.6:0.4 on a fresh weight basis. 3 Means with different superscripts in the same row A–C or column a–d indicate a significant difference (p < 0.05). 4 SEM, standard error of the mean. 5 T, treatment; S, storage period; T × S, interaction of treatment and storage period.
Table 2. Dynamics of chemical composition of silage during storage (n = 3).
Table 2. Dynamics of chemical composition of silage during storage (n = 3).
Storage Period (d) 3 p Value 5
Item 1Treatment 2306090SEM 4TST × S
DM (g/kg FW)Alfalfa207.04 dA201.22 dB200.44 dB5.07<0.0010.0240.796
M1228.33 c226.59 c224.61 c
M2241.16 b238.14 b240.10 b
Corn286.89 a284.69 a282.46 a
DM loss (g/kg FW)Alfalfa19.37 aC40.67 aB61.94 aA2.86<0.001<0.0010.177
M117.50 bC38.58 abB58.72 abA
M217.33 bC36.39 bcB57.32 bA
Corn16.15 cC35.53 cB56.71 bA
WSC (g/kg DM)Alfalfa14.62 dA12.20 dB9.49 dC3.31<0.001<0.0010.449
M132.16 cA24.83 cB24.41 cB
M242.76 b41.13 b39.52 b
Corn68.80 aA64.40 aAB59.46 aB
CP (g/kg DM)Alfalfa190.47 aB200.08 aA202.81 aA7.91<0.001<0.0010.002
M1164.59 bB171.53 bA171.12 bA
M2139.29 c138.14 c140.77 c
Corn70.83 d72.83 d72.64 d
1 DM, dry matter; DM loss, dry matter loss; FM, fresh weight; WSC, water soluble carbohydrates; CP, crude protein. 2 M1 and M2, alfalfa and corn mixed with ratio of 0.8:0.2 and 0.6:0.4 on a fresh weight basis. 3 Means with different superscripts in the same row A–C or column a–d indicate a significant difference (p < 0.05). 4 SEM, standard error of the mean. 5 T, treatment; S, storage period; T × S, interaction of treatment and storage period.
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MDPI and ACS Style

Mao, K.; Yu, Z.; Huang, S.; Wang, M.; Hannaway, D.B. Effect of Storage Period on the Fermentation Profile and Bacterial Community of Silage Prepared with Alfalfa, Whole-Plant Corn and Their Mixture. Fermentation 2022, 8, 486. https://doi.org/10.3390/fermentation8100486

AMA Style

Mao K, Yu Z, Huang S, Wang M, Hannaway DB. Effect of Storage Period on the Fermentation Profile and Bacterial Community of Silage Prepared with Alfalfa, Whole-Plant Corn and Their Mixture. Fermentation. 2022; 8(10):486. https://doi.org/10.3390/fermentation8100486

Chicago/Turabian Style

Mao, Kai, Zhu Yu, Shuai Huang, Musen Wang, and David B. Hannaway. 2022. "Effect of Storage Period on the Fermentation Profile and Bacterial Community of Silage Prepared with Alfalfa, Whole-Plant Corn and Their Mixture" Fermentation 8, no. 10: 486. https://doi.org/10.3390/fermentation8100486

APA Style

Mao, K., Yu, Z., Huang, S., Wang, M., & Hannaway, D. B. (2022). Effect of Storage Period on the Fermentation Profile and Bacterial Community of Silage Prepared with Alfalfa, Whole-Plant Corn and Their Mixture. Fermentation, 8(10), 486. https://doi.org/10.3390/fermentation8100486

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