Abstract

This study was conducted to investigate the effect of soybean meal (SM) and soluble starch (SS) on biogenic amine production and microbial diversity using in vitro ruminal fermentation. Treatments comprised of incubation of 2 g of mixture (expressed as 10 parts) containing different ratios of SM to SS as: 0:0, 10:0, 7:3, 5:5, 3:7, or 0:10. In vitro ruminal fermentation parameters were determined at 0, 12, 24, and 48 h of incubation while the biogenic amine and microbial diversity were determined at 48 h of incubation. Treatment with highest proportion of SM had higher (p<0.05) gas production than those with higher proportions of SS. Samples with higher proportion of SS resulted in lower pH than those with higher proportion of SM after 48 h of incubation. The largest change in NH3-N concentration from 0 to 48 h was observed on all SM while the smallest was observed on exclusive SS. Similarly, exclusive SS had the lowest NH3-N concentration among all groups after 24 h of incubation. Increasing methane (CH4) concentrations were observed with time, and CH4 concentrations were higher (p<0.05) with greater proportions of SM than SS. Balanced proportion of SM and SS had the highest (p<0.05) total volatile fatty acid (TVFA) while propionate was found highest in higher proportion of SS. Moreover, biogenic amine (BA) was higher (p<0.05) in samples containing greater proportions of SM. Histamines, amine index and total amines were highest in exclusive SM followed in sequence mixtures with increasing proportion of SS (and lowered proportion of SM) at 48 h of incubation. Nine dominant bands were identified by denaturing gradient gel electrophoresis (DGGE) and their identity ranged from 87% to 100% which were mostly isolated from rumen and feces. Bands R2 (uncultured bacterium clone RB-5E1) and R4 (uncultured rumen bacterium clone L7A_C10) bands were found in samples with higher proportions of SM while R3 (uncultured Firmicutes bacterium clone NI_52), R7 (Selenomonas sp. MCB2), R8 (Selenomonas ruminantium gene) and R9 (Selenomonas ruminantium strain LongY6) were found in samples with higher proportions of SS. Different feed ratios affect rumen fermentation in terms of pH, NH3-N, CH4, BA, volatile fatty acid and other metabolite concentrations and microbial diversity. Balanced protein and carbohydrate ratios are needed for rumen fermentation.

Highlights

  • This study was conducted to determine the effects of SM and soluble starch (SS) on biogenic amine (BA) and microbial diversity using in vitro ruminal fermentation

  • The NH3-N concentration (Chaney and Marbach (1962), volatile fatty acid (VFA) and other metabolites (high performance liquid chromatography (HPLC), Agilent Technologies 1200 series, Tokyo, Japan) (Tabaru et al (1988) and Han et al (2005) and expected CH4 production was calculated from the relationship between CH4 and short chain fatty acids (Demeyer and Van Nevel, 1975)

  • Total gas production increased as incubation time increased

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Summary

INTRODUCTION

Rumen bacteria require sources of nitrogen, minerals, vitamins, and growth factors for their growth; nitrogen and energy are required in the largest quantities and must be simultaneously available to stimulate rapid growth of bacteria. Both dietary and ruminal microbes are the sources of amines in ruminants. A close relationship between ruminal and histamine profiles in preacidotic stages induced by high concentrate diet fed to cattle was reported (Motoi et al, 1984), but the effects of various ratios and synchronization of protein and carbohydrates on rumen fermentation and their effects on rumen microbial diversity and BA production were not thoroughly investigated. This study was conducted to determine the effects of SM and soluble starch (SS) on BA and microbial diversity using in vitro ruminal fermentation

MATERIALS AND METHODS
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