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Revista mexicana de ciencias pecuarias

versão On-line ISSN 2448-6698versão impressa ISSN 2007-1124

Rev. mex. de cienc. pecuarias vol.15 no.1 Mérida Jan./Mar. 2024  Epub 12-Abr-2024

https://doi.org/10.22319/rmcp.v15i1.6379 

Articles

Microsilages elephant grass BRS Capiaçu added with commercial microbial consortium on different days of regrowth

Allan Stênio da Silva Santosa 

Daniel Louçana da Costa Araújoa 

Ivone Rodrigues da Silvaa  * 

Matheus Sousa Araújoa 

Arnaud Azevêdo Alvesa 

Henrique Nunes Parenteb 

Maria Elizabete de Oliveiraa 

João Batista Lopesa 

a Federal University of Piaui, Teresina, Piauí, Brazil.

b Federal University of Maranhão, Chapadinha, Maranhão, Brazil.


Abstract

This study aimed to evaluate whether bacterial inoculation improves the fermentative, microbiological, and chemical characteristics of silages of the elephant grass cv. BRS Capiaçu on different regrowth days. The experimental design was completely randomized and set up in a 3x2 factorial arrangement (three regrowth days, with and without inoculant), with four replications. There was a significant interaction between the regrowth days and inoculant on the pH, ammoniacal nitrogen (N-NH3), and effluent losses (EL) of the silages. Inoculation decreased the EL with the advance of regrowth days and increased the dry matter recovery index compared to the silages without inoculant. The population of molds and yeasts decreased when inoculation was adopted to the forage harvested after 85 d. There was a significant interaction between the dry matter (DM), crude protein (CP) and neutral detergent fiber corrected for ash and protein (NDFap) contents of the silages. Inoculation in the grass harvested after 85 d increased the DM contents of the silage. The highest CP contents were observed in the silages after 85 d. The NDFap contents of the grasses harvested after 110 and 135 d were higher than those of the grass harvested after 85 d. The NDFap contents of the silages without inoculant increased with the harvest age. The BRS Capiaçu forage silage harvested at 110 d demonstrated favorable performance for silage production. However, the influence of inoculant use was low for the characteristics evaluated.

Keywords Biological inputs; Pennisetum purpureum; Quality

Resumen

Este estudio tuvo como objetivo evaluar si la inoculación bacteriana mejora las características fermentativas, microbiológicas y químicas de los ensilados del pasto elefante cv. BRS Capiaçu en diferentes días de rebrote. El diseño experimental fue completamente al azar y se estableció en un arreglo factorial 3x2 (tres días de rebrote, con y sin inoculante), con cuatro repeticiones. Hubo una interacción significativa entre los días de rebrote y el inoculante sobre el pH, el nitrógeno amoniacal (N-NH3) y las pérdidas por efluentes (PE) de los ensilados. La inoculación disminuyó la PE con el avance de los días de rebrote y aumentó la tasa de recuperación de materia seca en comparación con los ensilados sin inoculante. La población de mohos y levaduras disminuyó cuando se adoptó la inoculación al forraje cosechado después de 85 d. Hubo una interacción significativa entre la materia seca (MS), la proteína cruda (PC) y la fibra detergente neutro corregida por los contenidos de cenizas y proteína (FDNcp) de los ensilados. La inoculación en el pasto cosechado después de 85 días aumentó el contenido de MS del ensilado. Los mayores contenidos de PC se observaron en los ensilados después de 85 días. Los contenidos de FDNcp de los pastos cosechados después de 110 y 135 días fueron mayores que el del pasto cosechado después de 85 días. El contenido de FDNcp de los ensilados sin inoculante aumentó con la edad de cosecha. El ensilado de forraje de BRS Capiaçu cosechado a los 110 días demostró un desempeño favorable para la producción de ensilado. Sin embargo, la influencia del uso de inoculantes fue baja para las características evaluadas.

Palabras clave Insumos biológicos; Pennisetum purpureum; Calidad

Introduction

Elephant grass (Pennisetum purpureum Schum) stands out among the tropical grasses used for silage due to its high production capacity, nutritive value, adaptability to the local edaphoclimatic conditions, number of varieties, easy cultivation, and high acceptability by animals 1.

The low soluble solids and dry matter contents associated with the high buffering power of this grass negatively influence the fermentation process during ensilage and cause losses that compromise silage quality2. From this perspective, new cultivars have been developed to improve the characteristics of elephant grass, e.g., the cultivar BRS Capiaçu.

Released in 2016 by Embrapa Gado de Leite, the cultivar BRS Capiaçu has stood out due to its high dry matter yield (72t ha-1 yr-1), producing about 30 % more forage mass (300t MV ha-1 yr-1), showing more soluble carbohydrates and crude protein contents in relation to other elephant grass cultivars, and being a less expensive alternative than maize as a perennial crop that does not require annual seed purchase3,4,5.

Biological inputs are widely used as bacterial inoculants in the ensilage of elephant grass to improve the population of lactic acid bacteria, which decrease the pH and intensify fermentation, thus reducing losses caused by undesirable microorganisms and increasing the nutrient quality of silages6,7,8.

Furthermore, the harvest age of elephant grass during ensilage influences the development of microbial populations since the low moisture content and the high concentration of soluble carbohydrates are necessary for the development of lactic acid bacteria9,10. Therefore, balancing forage production and quality is essential to producing BRS Capiaçu grass silages.

As a forage recently released on the market, studies on the cultivar BRS Capiaçu, especially for its use as silage, are still required to provide appropriate conditions for fermentation. In this scenario, this study aimed to identify whether bacterial inoculation improves the fermentative, microbiological, and chemical characteristics of the silage of the elephant grass (Pennisetum purpureum Schum.) cultivar BRS Capiaçu on different regrowth days.

Material and methods

Treatments and ensilage management

The experiment was conducted in Teresina, Piauí, Brazil (latitude: 5o 2’28.41 S, longitude: 42o 47’0.08 W, at an elevation of 67 m asl.) from March 2019 to March 2021. The elephant grass (Pennisetum purpureum Schum) used in the experiment was subjected to manual uniformization at a mean height of 10 cm from the ground, followed by fertilization with 50 kg of N ha-1, 60 kg of K2O ha-1, and 60 kg of P2O5 supplied as urea, potassium chloride, and single superphosphate, respectively. Except for phosphate fertilization, all other nutrients were resupplied after 47 d according to soil analysis and the recommendations of Embrapa (2008). The grass was irrigated daily using a micro-sprinkler system from March to June 2019.

A completely randomized design was set up in a 2x3 factorial arrangement. The treatments corresponded to the bacterial inoculant combinations and the grass regrowth days, identified as follows: Factor 1) Bacterial inoculation when ensilage: presence and absence of inoculant; Factor 2) Days of grass regrowth: 85, 110, and 135 d. Based on this arrangement, six treatments were generated, and each was evaluated with four replications, totaling twenty-four experimental units.

The forage was harvested after 85, 110 and 135 d of regrowth from an area of 60 m2 already established, delimiting 20 m2 for each evaluated age. The plants were cut manually, with a cleaver, at a height of 10 cm from the ground and chopped into fragments of 1 to 2 cm, in a stationary shredder. After this process, chopped forage was manually homogenized with the silage additive according to each treatment and placed in plastic trays.

The lyophilized bacterial inoculant SILOTRATO® was applied during the ensilage of the BRS Capiaçu grass following the recommendations of the manufacturer (two grams per ton of green mass), such as ensuring product quality until the expiration date, exclusive use for animal feed and non-toxicity. The bacterial inoculant was composed of various homofermentative lactic acid bacteria, facultative homofermentative bacteria, and facultative heterofermentative bacteria, and 5 % of an enzyme complex with a count limit of 1010 CFU.g-1, according to each harvest age and control treatment (without inoculant application).

Cylindrical experimental silos made of polyvinyl chloride (PVC) were used in the assays, each measuring 50 cm in length and 10 cm in width. Each silo received 1.3 kg of dry sand, which was separated from the forage by a shading screen to allow quantifying the effluent produced.

After complete homogenization, the grass was deposited in the silos and compacted with the aid of a wooden piston by adopting a density of 600 kg m-3 of natural matter per silo. After being filled, the silos were closed with tap covers containing Bunsen valves, sealed with adhesive tape, and weighed. Then, the silos were stored at ambient temperature and opened 83 d after ensilage.

Fermentative losses and dry matter recovery index

The dry matter losses through gas and effluent and the dry matter recovery index (DMRI) were quantified by the weight difference according to the equations described by Schmidt et al11. The gas losses were obtained according to Equation 1:

PG =[PsChf-PsCha/(MVFE×MSFE)]×100 (1)

where: PG= gas losses, PsChf= filled silo weight at the beginning of ensilage (kg), PsCha= filled silo weight at the end of ensilage (kg), MVFE = ensiled forage fresh matter (kg), MSFE= ensiled forage dry matter (%) discounting the weight of the sand added to the silo.

The effluent losses were obtained by Equation 2:

EL (kg/t of MV)=[PVf-Ts-PVi-Ts]/MFi×100 (2)

where: EL= effluent losses, PVf= empty silo weight + sand weight at the end of ensilage (kg), Ts= silo tare, PVi= empty silo weight + sand weight at the beginning of ensilage (kg), MFi= forage mass at the beginning of ensilage (kg).

The dry matter recovery rate was estimated using Equation 3:

DMRI%=(MFf×MSf)/(MFi×MSi)×100 (3)

where: DMRI= dry matter recovery index (%), MFf= forage matter at the end of ensilage (kg), MSf= dry matter at the end of ensilage (%DM), MFi= forage matter at the beginning of ensilage (kg), MSi = forage dry matter content at the beginning of ensilage (%DM).

pH and ammoniacal nitrogen

Before ensilage, the chemical composition of the BRS Capiacu grass was analyzed at each harvest age (Table 1).

Table 1 Chemical composition of the BRS Capiaçu grass at different harvest ages 

Item Regrowth ages (days)
85 110 135
DM 16.8 21.9 26.0
OM 91.0 92.1 91.9
ASH 9.0 7.9 8.1
CP 6.1 5.4 3.9
EE 1.3 1.3 1.6
NDFap 72.9 71.8 71.0
ADF 52.8 56.5 51.6
NFC 10.7 14.6 15.4
HEM 20.1 15.3 19.4

DM= dry matter, OM= organic matter, ASH= ashes; CP= crude protein, EE= ether extract, NDFap= neutral detergent fiber corrected for ash and protein, ADF= acid detergent fiber, NFC= non-fiber carbohydrates, HEM= hemicellulose.

When the silos were opened, the samples were separated and split into three aliquots, the first of which was used fresh soon after homogenization to determine the pH according to Silva and Queiroz12. The ammoniacal nitrogen (N-NH3) was determined according to Ferreira et al13 based on the silage extract.

Chemical composition

After thawing, the second aliquot was pre-dried in a forced-air oven at 55 °C and ground to pass through a 1 mm sieve in a Wiley knife mill. The subsamples were analyzed for dry matter (DM; method 934.01), ash (method 942.05), crude protein (CP; method 978.04), and ether extract (EE; method 920.39) according to AOAC14. Neutral detergent fiber corrected for ash and protein (NDFap), acid detergent fiber (ADF) and hemicellulose were determined by the sequential method according to the procedures described by Van Soest et al15 adapted for autoclave (0.5 atm/1h) using TNT bags with a porosity of 100 µm16.

Microbiological profile

The third aliquot was used to evaluate the microbiological profile of the silages by quantifying the microbial populations of Lactobacillus sp., Clostridium sp., filamentous fungi, and yeasts. The entire microorganism analysis was performed in a laminar flow cabinet.

The microbial populations in the silage were quantified by preparing an aqueous suspension with a fresh silage sample (25g) in 225 mL of peptone water, which was manually homogenized for three minutes. After homogenization, decimal dilutions were prepared in sterile tubes containing 9 mL of the solution and then sown in duplicate in sterile Petri dishes at dilutions of 10-1, 10-2, and 10-3. The count of Lactobacillus was performed by adding 20 mL of MRS agar to the plates (Lactobacillus MRS agar). After homogenization and solidification of the culture medium, 10 mL of the same agar was added to form the overlayer. The dishes were then incubated at 35 ± 2 °C for 72 h in a bacteriological incubator.

The bacterial count of the genus Clostridium was performed by adding 20 mL of Clostridium perfringens agar and a 0.85 % egg yolk/saline emulsion at a proportion of 1:1 in the Petri dishes. Then, the inoculation was performed with 0.1 mL of the corresponding dilutions. Subsequently, 10 mL of the same agar was added to form the overlayer. Finally, the dishes were incubated at 35 ± 2 °C in anaerobiosis for 48 h in a bacteriological incubator. The filamentous fungi and yeasts were counted by adding 20 mL of Potato Dextrose Agar (PDA) with 10 % tartaric acid in the Petri dishes. After the culture medium solidified, 0.1 mL of the corresponding dilutions was added to the dishes, which were then incubated at 37 ± 2 °C for 120 h in a bacteriological incubator. The microorganisms were counted after incubation, and the results were expressed as log CFU g-1(17.

Statistical analysis

The data referring to fermentative losses, chemical composition, and the microbiological profile were analyzed using the least squares method, by the GLM procedure, and by performing the analysis of variance and the SNK means comparison test through the PROC NLIN procedure of the SAS software (Statistical Analysis System, version 9.0) at a significance level of 0.05.

The statistical model used was as follows:

Yijk=µ+αi+βj+(α*βij)+eijk   (4)

where:

Yijk= dependent variable,

µ= overall mean,

αi= inoculation effect (fixed effect; i = presence and absence when ensilage), βj = effect of the grass regrowth days (fixed effect; j = 85, 110, and 135 d),

α*βij= effect of the interaction between the bacterial inoculant and the grass regrowth days,

eijk= random error associated with each observation.

Results

There was a significant interaction (P<0.05) between the regrowth days and inoculation on the fermentative characteristics of pH, ammoniacal nitrogen (N-NH3), and effluent losses (EL) of the BRS Capiaçu grass silage (Table 2). The silage harvested after 85 d showed the lowest (P<0.05) pH (3.5), which increased to 3.79 when the inoculant was applied, an effect observed only for the silage of the forage harvested at the shortest age (85 d). The silage harvested after 135 d showed the lowest (P<0.05) N-NH3 content (1.50 %) in relation to the forages harvested after 85 and 135 d.

No difference was observed in the N-NH3 values of the silages regarding inoculation (P>0.05), with a mean of 1.95 % N-NH3. Regarding the losses of ensiled mass, the effluent losses (EL) of the BRS Capiaçu grass silages were, on average, 145.53 kg t-1. However, when the inoculant was applied to the forage harvested at 135 d, the effluent losses decreased.

Table 2 Fermentative characteristics of BRS Capiaçu grass silages at different harvest ages and bacterial inoculation 

Item Inoculant Harvest ages (days) Mean SEM P-value
85 110 135 Inoculant Harvest age Inoculant x harvest age
pH With 3.79Ab 4.23Aa 4.26Aa 4.10 0.07 0.4002 <0.0001 0.0095
Without 3.50Bc 4.49Aa 4.13Ab 4.04
Mean 3.65 4.20 4.36
NH3-N, % TN With 1.97Aa 2.17Aa 1.72Aa 1.95 0.08 0.5128 0.0005 0.0327
Without 2.50Aa 2.10Aa 1.50Ab 2.03
Mean 2.23 2.13 1.61
Effluent losses, kg t-1 With 165.14Aa 154.46Ab 93.58Bc 137.73 5.42 0.1753 <0.0001 0.0014
Without 150.95Aa 150.44Aa 135.19Aa 145.53
Mean 158.04 152.45 114.39
Gas losses, % of DM With 2.48 0.41 0.44 1.11A 0.18 0.8266 0.0025 0.5000
Without 1.83 0.85 0.40 1.03A
Mean 2.16a 0.63b 0.42b
Dry matter recovery, % of DM With 73.99 89.12 87.29 83.47A 2.18 0.5732 <0.0001 0.1143
Without 75.14 83.60 89.09 82.61A
Mean 74.57b 86.36a 88.19a

SEM= standard error of the mean.

Means followed by the same lowercase letter in the row and uppercase letter in the column do not differ by the SNK test at a 5% significance level.

The gas losses (PG) were higher (P<0.05) in the BRS Capiaçu grass silage harvested after 85 d (2.16 %), whereas inoculation did not reduce (P>0.05) this parameter. The highest DMRI (P>0.05) was obtained in the silages of the forages harvested after 110 and 135 d, 15.08 % higher than the DMRI of the forage harvested after 85 d (Table 2).

The population of lactic acid bacteria (LAB) was higher (P<0.05) in the silage of the BRS Capiaçu grass forage harvested after 85 and 110 d (5.9 log10 CFU g-1). However, inoculation did not decrease (>0.05) the population of LAB (Table 3).

There was significant interaction (P<0.05) of the regrowth days and inoculation on the population of molds and yeasts of the BRS Capiaçu grass silage. The population of molds and yeasts was, on average, 4.0 log10 CFU g-1. However, when the inoculant was applied to the forage, the concentration of molds and yeasts was observed between the ages of 85 and 135 d, while in the treatments without application of inoculants, no significant differences (P>0.05) were observed between the assessed ages. No populations of Clostridium spp. were detected (Table 3).

There was significant interaction (P<0.05) of the regrowth days and inoculation on the dry matter (DM), ash, crude protein (CP) and neutral detergent fiber corrected for ash and protein (NDFap) of the BRS Capiaçu grass silages. The DM content of the silages increased (P<0.05) with the harvest age, ranging from 29.36 % in the silage of the forage harvested after 85 d to 34.15 % in the forage harvested after 135 d. Inoculation increased (P<0.05) the DM content of the forage harvested after 85 d from 27.33 % to 29.36 % (Table 4).

Table 3 Microbiological profile of BRS Capiaçu grass silages at different harvest ages and bacterial inoculation 

Item (log10 CFU g-1) Inoculant Harvest ages (days) Mean SEM P-value
85 110 135 Inoculant Harvest age Inoculant x harvest age
Lactic acid bacteria With 6.0 5.4 3.8 5.1A 0.25 0.2575 0.0005 0.8815
Without 6.2 5.9 4.8 5.5A
Mean 6.1a 5.7a 4.0b
Molds and yeasts With 3.4Ab 3.8Aab 4.6Aa 3.9 0.21 0.8008 0.5663 0.0137
Without 5.0Aa 3.7Aa 3.3Aa 4.0
Mean 4.2 3.7 4.0

SEM= standard error of the mean.

Means followed by the same lowercase letter in the row and uppercase letter in the column do not differ by the SNK test at a 5% significance level.

Table 4 Chemical composition of BRS Capiaçu grass silages at different harvest ages and bacterial inoculation 

Item (%) Inoculant Harvest ages (days) Mean SEM P-value
85 110 135 Inoculant Harvest age Inoculant x harvest age
DM With 29.36Ac 30.55Ab 34.15Aa 31.35 0.38 0.5097 <0.0001 0.0223
Without 27.33Bc 31.67Ab 34.21Aa 31.07
Mean 28.35 31.11 34.21
Ash With 8.66Aa 6.97Bb 7.56Ab 7.73 0.12 0.0088 <0.0001 0.0053
Without 8.97Aa 8.29Ab 7.39Ac 8.21
Mean 8.81 7.63 7.47
CP With 5.21Aa 3.54Bb 3.32Ab 4.02 0.14 0.0297 <0.0001 <0.0001
Without 5.37Aa 4.61Ab 2.91Bc 4.28
Mean 5.26 4.08 3.12
EE With 1.32 0.89 0.79 1.00B 0.04 0.0497 <0.0001 0.1510
Without 1.29 1.01 1.02 1.11A
Mean 1.30ª 0.95b 0.90b
NDFap With 68.59Ab 72.08Aa 71.91Aa 70.86 0.42 0.1345 <0.0001 0.0214
Without 68.83Ac 70.70Ab 71.96Aa 70.49
Mean 68.71 71.39 71.93
ADF With 47.67 49.20 49.94 48.94A 0.20 0.0406 <0.0001 0.8647
Without 46.64 48.62 49.25 48.17B
Mean 47.15b 48.91a 49.60a

DM= dry matter, CP= crude protein, EE= ether extract, NDFap= neutral detergent fiber corrected for ash and protein, ADF= acid detergent fiber,

SEM= standard error of the mean.

Means followed by the same lowercase letter in the row and uppercase letter in the column do not differ by the SNK test at a 5% significance level.

The highest ash, CP, and EE contents (P<0.05) were observed in the silage of the BRS Capiaçu grass harvested after 85 d. In contrast, inoculation of the forage harvested after 110 d resulted in the lowest (P<0.05) ash content (6.97 % vs 8.29 %). Inoculation resulted in the lowest (P<0.05) EE content in the silage (1.0 %) in relation to the silage without inoculation (1.11 %). Inoculation resulted in equivalence (P>0.05) in the CP content of the silages of the forages harvested after 110 and 135 d (3.43 %), although lower (P<0.05) than the silage of the forage harvested after 85 d (5.21 %). The CP content of the forage without inoculation decreased (P<0.05) with the advance of regrowth days (Table 4).

The NDFap contents of BRS Capiaçu grass forage silage harvested at 110 and 135 d (88.45 % and 72 %) were higher (P<0.05) than those of forage silage harvested at 85 d (84.81 % and 68.59 %). The NDFap contents of uninoculated silages increased (P<0.05) with harvest age (Table 4).

The ADF contents were lower (P<0.05) in the silage of the forage harvested after 85 d. Inoculant application resulted in the highest (P<0.05) ADF conten t in the silage (48.94 %) in relation to the absence of inoculant (48.17 %) (Table 4).

Discussion

The conservation of forage in the ensiling process is based on the principle of conservation in an anaerobic environment, where the absence of oxygen in the silo predisposes to the increase of lactic acid bacteria (LAB), which emit pH and prevent the development of undesirable microorganisms that harm the quality of the silage18.

The application or not of inoculant did not influence the population of molds and yeasts in the forage silage. The silages of the forages harvested at younger ages (85 and 110 d) showed a greater population of LAB, favoring the fermentation of the forage harvested after 85 d due to its lowest pH. According to Kung et al19, the possible explanations for flaws in the use of LAB-based inoculants include the intense competition of the epiphytic flora and soluble carbohydrates, excess oxygen, and problems during inoculation.

The low pH of the silages (<4.5) favored the absence of Clostridium spp. in this study. According to Pahlow et al20, these bacteria demand high pH values for their development. The presence of undesirable microorganisms is mainly associated with flaws during fermentation.

The absence of Clostridium ssp. in the silages of the present study, responsible for proteolysis during ensilage, contributed to the low N-NH3 concentrations obtained in the silages. Furthermore, the fact that the pH values of the silages were below 4.5 increases the fermentation efficiency and reduces protein hydrolysis in non-protein nitrogen compounds 21. Similar results were obtained for the silage of the elephant grass cv. Roxo with bacterial inoculation22.

The low PG values can be attributed to the absence of Clostridium spp. bacteria in the silages of the present study, the main ones responsible for CO2 production and other acids. Inoculation was unfavorable in reducing the pH due to the reduced losses observed in this study. In all silages, the dry matter contents (DM) increased from as the age regrowth days increased. According to Van Soest23, the increase in DM is mainly due to the high effluent losses resulting from the low DM contents before ensilage, which was observed in the present study. With regard to inoculant application, an increase in DM content was observed only at 85 d of cutting age, treatment with the lowest DM content.

Microbial inoculation reduced the proteolytic activity of the silages, resulting in a rapid pH reduction since proteolytic bacteria develop better in silages with higher pH values. Therefore, the high pH value in the forages harvested after 110 and 135 d (4.20 and 4.36) favored CP reduction compared to the silages harvested after 85 d, which showed the highest CP and the lowest pH (3.65). The BRS Capiaçu grass silages showed CP contents lower than the 7 % minimum proposed by Church24 as necessary to sustain microbial activity in the rumen, indicating the need for protein supplementation in order to meet the nutrient requirements of ruminants.

Inoculation in the BRS Capiaçu grass forage resulted in the lowest EE content in relation to the silage without the inoculant. However, these silages showed less than 8 % of EE, which is recommended by McGuffey and Schingoethe25 to prevent reductions in food consumption and limited ruminant performance. However, the low EE proportion impacts the energy value of silages, considering the calorific value of lipids in relation to other organic compounds.

According to Wilson26, tropical grasses require support structures represented by the cell wall. Therefore, the older the plant age, the greater the proportion of cell wall components and the lower the cell content. These statements left the results of the BRS Capiaçu silages harvested after 85 d, which showed the lowest contents of fibrous constituents (NDFap and ADF) and the highest contents of non-fiber constituents (CP and EE) compared to the regrowth days of 110 and 135 d.

Inoculation in the BRS Capiaçu grass forage resulted in the highest ADF content in relation to the non-inoculated sample. A similar behavior was observed by others7,27, who mention increased ADF contents (48.35 % and 46.86 %) in silages of the elephant grass cultivars Napier and Cameron with bacterial inoculant. Inoculation in the silages of the BRS Capiaçu grass may have increased the cellulose contents through the absence of activity in the enzymatic complex of the inoculant, solubilizing cell wall constituents28, and increasing the ADF contents.

Conclusions and implications

The BRS Capiaçu forage silage harvested at 110 d demonstrated favorable performance for silage production. However, the influence of inoculant use was low for the characteristics evaluated. These results indicate that the BRS Capiaçu cultivar naturally can have good ensiling capacity and the use of inoculants can be ineffective as it depends on several factors, such as forage management, concentration of epiphytic bacteria and the inoculant, in addition to environmental conditions. Therefore, to more comprehensively evaluate the potential of using inoculants, it is necessary to use specific inoculants in the BRS Capiaçu cultivar. These investigations can provide valuable insights into the effectiveness and economic viability of using inoculants to optimize the fermentation and quality of BRS Capiaçu silage harvested at different ages.

Acknowledgments

Thanks to the Postgraduate Program in Tropical Animal Science of the Federal University of Teresina, Piauí, Brazil, the National Council for Scientific and Technological Development (CNPq, Brasília, DF, Brazil), and the Federal Institute of Maranhão (Caxias, Maranhão, Brazil).

Literature cited

1. Cardoso AM, Araujo SAC, Rocha NS, Domingues FN, Azevedo JC, Pantoja LA. Elephant grass silage with the addition of crambe bran conjugated to different specific mass. Acta Scientiarum. Anim Sci 2016;38:375-382. [ Links ]

2. Retore M, Alves JP, Junior MAPO, Mendes SS. Qualidade da silagem do capim-elefante BRS Capiaçu. Dourados, MS: Embrapa Agropecuária Oeste; 2020. [ Links ]

3. Pereira AV, Lédo FJS, Machado JC. BRS Kurum. Capiaçu - New elefhant grass cultivars for grazing and cut-and-carry system. Crop Breed Applied Biotech 2017; 17:59-62. [ Links ]

4. Monção FP, Costa MAMS, Rigueira JPS, Sales ECJ, Leal DB, Silva MFP, et al. Productivity and nutritional value of BRS capiaçu grass (Pennisetum purpureum) managed at four regrowth ages in a semiarid region. Trop Anim Health Prod 2020; 52:235-241. [ Links ]

5. Pereira AV, Oliveira JC, Ledo FJS, Diniz FH, Xavier DF, Lanes JJSN, et al. BRS Capiaçu e BRS Kurumi: Cultivo e uso. Brasília, DF: Embrapa, 2021. [ Links ]

6. Desta ST, Yuan X, Li J, Shao T. Ensiling characteristics, structural and nonstructural carbohydrate composition and enzymatic digestibility of Napier grass ensiled with additives. Biores Technol 2016;221:447-454. [ Links ]

7. Costa R, Silva RC, Souza ED, Vieira EM, Nascimento TSS, Alencar AP. Bagaço de cana-de-açúcar (Saccharum officinarum L.) na ensilagem do capim-elefante (Pennisetum purpureum Schum) com ou sem inoculante bacteriano. Rev Acta Kariri-Pesquisa e Desenvolvimento 2017;2:29-36. [ Links ]

8. Shah AA, Xianjun Y, Zhihao D, Junfeng L, São T. Microbiological and chemical profiles of elephant grass inoculated with and without Lactobacillus plantarum and Pediococcus acidilactici. Archives Microbiol 2018;200:311-328. [ Links ]

9. Cândido MJD, Gomide CAM, Alexandrino E, Gomide JA, Pereira WE. Morfofisiologia do dossel de Panicum maximum cv. Mombaça sob lotação intermitente com três períodos de descanso. Rev Brasileira Zoot 2005;34:406-415. [ Links ]

10. Zanine AM, Santos EM, Ferreira DJ, Gomes-Pereira O. Populações microbianas e componentes nutricionais nos órgãos do capim-tanzânia antes e após a ensilagem. Semina: Ciênc Agrár 2007;28:143-150. [ Links ]

11. Schmidt P. Perdas fermentativas na ensilagem, parâmetros digestivos e desempenho de bovinos de corte alimentados com rações contendo silagens de cana-de-açúcar (tese de doutorado). Piracicaba, SP: Universidade de São Paulo; 2006. [ Links ]

12. Silva DJ, Queiroz AC. Análise de alimentos: métodos químicos e biológicos. 3a ed. Viçosa, MG: UFV; 2002. [ Links ]

13. Ferreira DA, Gonçalves LC, Molina LR, Castro-Neto AC, Tomich TR. Características de fermentação da silagem de cana-de-açúcar tratada com ureia, zeólita, inoculante bacteriano e inoculante bacteriano/enzimático. Arquivo Brasileiro Med Vet Zoot 2007;59:423-433. [ Links ]

14. AOAC - Official methods of analysis. 12th ed. Washington, DC. Association of Official Analytical Chemists. 1990. [ Links ]

15. Van-Soest PJ, Robertson JB, Lewis BA. Methods for dietary fiber, neutral detergent fiber, and nonstarch polyssacharides in relation to animal nutrition. J Dairy Sci 1991;74:3583-3597. [ Links ]

16. Valente TNP, Detmann E, Filho SCV, Queiroz AC, Sampaio CB, Gomes DI. Avaliação dos teores de fibra em detergente neutro em forragens, concentrados e fezes bovinas moídas em diferentes tamanhos e em sacos de diferentes tecidos. Rev Brasileira Zoot 2011;40:1148-1154. [ Links ]

17. Silva N, Junqueira VCA, Silveira NFA. Manual de métodos de análise microbiológica de alimentos. Varela, SP; 1997. [ Links ]

18. Machado FS, Rodriguez NM, Rodrigues JAS, Ribas, MN, Teixeira AM, Ribeiro Júnior GO, et al. Qualidade da silagem de híbridos de sorgo em diferentes estádios de maturação. Arquivo Brasileiro Med Vet Zoot 2012; 64:711-720. [ Links ]

19. Kung Jr L, Stokes MR, Lin CJ. Silage aditives. In: American Society of Agronomy, Silage Science and Technology. Madison, WI; 2003:305-360. [ Links ]

20. Pahlow G, Muck RE, Driehuis F, Oude-Elferink SJWH, Spoelstra SF. Microbiology of ensiling. In: American Society of Agronomy, Silage Science and Technology. Madison, WI; 2003:31-93. [ Links ]

21. McDonald P, Henderson AR, Heron SJE. The biochemistry of silage. 2ª ed. Marlow: Chalcomb Publications; 1991. [ Links ]

22. Bernardes TF, Souza NSS, Silva JSLP, Santos IAP, Faturi C, Domingues F. Uso de inoculante bacteriano e melaço na ensilagem de capim-elefante. Rev Ciênc Agrá, Amazonian J Agr Environ Sci 2013;56:173-178. [ Links ]

23. Van Soest P. Nutritional ecology of the ruminant. New York, EUA: Cor-nell University Press; 1994. [ Links ]

24. Church DC. The ruminal animal digestive physiology and nutrition. New Jarsey: Prentice Hall, 1988. [ Links ]

25. McGuffey RK, Schingoethe DJ. Feeding value of a high oil variety of sunflowers as silage to lactating dairy cows. J Dairy Sci 1980;63:1109-1113. [ Links ]

26. Wilson JR. Cell wall characteristics in relation to forage digestion by ruminants: review. J Agr Sci 1994;122:173-182. [ Links ]

27. Rodrigues PHM, Lopes TFT, Andrade SJT, Melotti L, Lucci CS, Lima FR. et al. Adição de inoculantes microbianos sobre a composição química e perfil fermentativo da silagem de capim-elefante (Pennisetum purpureum Schum.). Acta Scientiarum. Anim Sci 2003;25:397-402. [ Links ]

28. Coan RM, Vieira PF, Silveira RN, Reis RA, Malheiros EB, Pedreira, MS. Inoculante enzimático-bacteriano, composição química e parâmetros fermentativos das silagens dos capins Tanzânia e Mombaça. Rev Brasileira Zoot 2005;34:416-424. [ Links ]

Received: January 05, 2023; Accepted: September 18, 2023

*Corresponding author: ivonezootecnista@gmail.com

Conflicts of Interest

The authors have no conflicts of interest to declare.

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