Abstract

Lactobacilli are probiotics with Aflatoxin (AF) detoxification ability, found in fermented products, GIT of animals and environment. Purpose of this study was to investigate the ability of broiler isolates of Lactobacillus against Aflatoxin B1 (AFB1). For this purpose, 5 isolates of Lactobacillus from broiler gut were incubated with 100 ppb AFB1 in aqueous environment and effect of different parameters (cell fractions, time, temperature, pH) on detoxification was determined by HPLC. The ameliorative effect of Lactobacillus salivarius (LS) against AFB1 was studied in broiler. The results revealed that LS (CR. 4) showed the best results (in vitro) as compared to other isolates (L. salivarius (CR. 3, CR, 4), L. agilis (CE. 2.1, CE. 3.1) and L. crispatus (CE. 28). Cell debris of CR. 4 showed significantly higher detoxification (P<0.05). Maximum amount of AFB1 was detoxified at 30°C (97%), pH 4.0 (99%) and 6 h (99.97%). In vivo study showed that AFB1 decreased weight gain (1,269 ± 0.04 gm/ bird), feed consumed (2,161 ± 0.08 gm/ bird), serum total protein (2.42 ± 0.34 gm/ dl), serum albumin (0.5 ± 0.2 2 gm/dl) and antibody titer (4.2 ± 0.83). Liver function enzymes were found (alanine transaminase (ALT): 32 ± 10.7 U/L) and aspartate transaminase (AST): 314.8 ± 27 U/L) elevated in AFB1 fed broilers. Treatment with 1% LS not only decreased the toxic effects of AFB1 (group D) but also improved the overall health of broilers due to its probiotic effects (p<0.05) as compared to control negative (group A). The detoxification ability of LS was better than commercial binder (CB) (0.2% Protmyc). It was concluded that detoxification of AFB1 by Lactobacillus was strain, temperature, pH and time dependent. LS has detoxification ability against AFB1 in vivo.

Highlights

  • Aflatoxins (AFs) are highly toxic secondary metabolites produced by A. flavus and A. parasiticus (Faria et al, 2017)

  • Five Lactobacillus isolates (Table 1) were investigated for their activity against Aflatoxin B1 (AFB1).When incubated with AFB1 (50 PPB), whole viable cells of CR. 4 removed maximum amount of AFB1 (92.3%) as compared to CE.28 (89.4%), CE. 2.1 (86.6%), CE. 3.1 (81.2%) and CR. 3 (74.6%)

  • Different temperatures were observed for their effect on detoxification potential of isolates

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Summary

Introduction

Aflatoxins (AFs) are highly toxic secondary metabolites produced by A. flavus and A. parasiticus (Faria et al, 2017). Among different molecules AFs, Aflatoxin B1 (AFB1) is highly toxic (B1>G1>B2>G2). It is a serious health hazard for birds, animals and human, as it is hepatotoxic, mutagenic, carcinogenic, teratogen and immunosuppressant (Kosztik et al, 2020). AFs enters body through ingestion, inhalation and skin penetration. Inside body it is activated by cytochrome P450enzyme system in liver to produce a highly reactive intermediate, AFB1-8,9-epoxide. This highly reactive radical binds to nucleophile sites in DNA forming 8,9-dihydro-8(N7guanyl)-9-hydroxy-AFB1 adduct. It is a critical step in the initiation of AFB1-induced carcinogenesis (Guo et al, 2020)

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