Therapeutic enhancement of newly derived bacteriocins against Giardia lamblia

•L. acidophilus bacteriocin showed in vitro activity against G. lamblia trophozoites.•Bacteriocin induced severe morphological changes using electron microscopy.•Oral bacteriocin for 5 days was sufficient to induce massive parasite reduction.•L. acidophilus bacteriocin induced amelioration of intest...

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Veröffentlicht in:Experimental parasitology 2014-11, Vol.146, p.52-63
Hauptverfasser: Amer, Eglal I., Mossallam, Shereen F., Mahrous, Hoda
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Mahrous, Hoda
description •L. acidophilus bacteriocin showed in vitro activity against G. lamblia trophozoites.•Bacteriocin induced severe morphological changes using electron microscopy.•Oral bacteriocin for 5 days was sufficient to induce massive parasite reduction.•L. acidophilus bacteriocin induced amelioration of intestinal pathology.•Bacteriocin holds great promise as an alternative therapy for giardiasis. Trials for identifying efficient anti-giardial agents are still ongoing. Nowadays, bacteriocins have attracted the attention as potential antimicrobial compounds. For the first time, the current study evaluated the therapeutic efficacy of bacteriocins derived from newly isolated Egyptian strains of probiotics Lactobacilli; L. acidophilus (P106) and L. plantarum (P164) against Giardia lamblia. Bacteriocins' efficacy was evaluated both in vitro; by growth inhibition and adherence assays, and in vivo; through estimation of parasite density, intestinal histopathological examination and ultrastructural analysis of Giardia trophozoites. In vivo bacteriocins' clinical safety was assessed. In vitro results proved that 50 µg of L. acidophilus bacteriocin induced reduction of the mean Giardia lamblia trophozoites by 58.3 ± 4.04%, while at lower concentrations of 10 and 20 µg of both L. acidophilus and L. plantarum, non significant reduction of the mean parasite density was achieved. In vitro trophozoites adherence was susceptible to the tested bacteriocins at all studied concentrations with variable degrees, while the highest adherence reduction was demonstrated using 50 µg of L acidophilus bacteriocin. In vivo, oral inoculation of 50 µg/mouse L. acidophilus bacteriocin for 5 successive days resulted in a noteworthy decline of the intestinal parasite density, along with amelioration of intestinal pathology of infected mice. Ultrastructural examination proved thatfive doses of L. acidophilus bacteriocin showed marked changes in cellular architecture of the trophozoites with evident disorganization of the cell membrane, adhesive disc and cytoplasmic components. This is the first reported study of the safe anti-giardial efficacy of L. acidophilus (P106) derived bacteriocin, hence highlighting its great promise as a potential therapeutic safe alternative to existing commercial drugs.
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Trials for identifying efficient anti-giardial agents are still ongoing. Nowadays, bacteriocins have attracted the attention as potential antimicrobial compounds. For the first time, the current study evaluated the therapeutic efficacy of bacteriocins derived from newly isolated Egyptian strains of probiotics Lactobacilli; L. acidophilus (P106) and L. plantarum (P164) against Giardia lamblia. Bacteriocins' efficacy was evaluated both in vitro; by growth inhibition and adherence assays, and in vivo; through estimation of parasite density, intestinal histopathological examination and ultrastructural analysis of Giardia trophozoites. In vivo bacteriocins' clinical safety was assessed. In vitro results proved that 50 µg of L. acidophilus bacteriocin induced reduction of the mean Giardia lamblia trophozoites by 58.3 ± 4.04%, while at lower concentrations of 10 and 20 µg of both L. acidophilus and L. plantarum, non significant reduction of the mean parasite density was achieved. In vitro trophozoites adherence was susceptible to the tested bacteriocins at all studied concentrations with variable degrees, while the highest adherence reduction was demonstrated using 50 µg of L acidophilus bacteriocin. In vivo, oral inoculation of 50 µg/mouse L. acidophilus bacteriocin for 5 successive days resulted in a noteworthy decline of the intestinal parasite density, along with amelioration of intestinal pathology of infected mice. Ultrastructural examination proved thatfive doses of L. acidophilus bacteriocin showed marked changes in cellular architecture of the trophozoites with evident disorganization of the cell membrane, adhesive disc and cytoplasmic components. 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Trials for identifying efficient anti-giardial agents are still ongoing. Nowadays, bacteriocins have attracted the attention as potential antimicrobial compounds. For the first time, the current study evaluated the therapeutic efficacy of bacteriocins derived from newly isolated Egyptian strains of probiotics Lactobacilli; L. acidophilus (P106) and L. plantarum (P164) against Giardia lamblia. Bacteriocins' efficacy was evaluated both in vitro; by growth inhibition and adherence assays, and in vivo; through estimation of parasite density, intestinal histopathological examination and ultrastructural analysis of Giardia trophozoites. In vivo bacteriocins' clinical safety was assessed. In vitro results proved that 50 µg of L. acidophilus bacteriocin induced reduction of the mean Giardia lamblia trophozoites by 58.3 ± 4.04%, while at lower concentrations of 10 and 20 µg of both L. acidophilus and L. plantarum, non significant reduction of the mean parasite density was achieved. In vitro trophozoites adherence was susceptible to the tested bacteriocins at all studied concentrations with variable degrees, while the highest adherence reduction was demonstrated using 50 µg of L acidophilus bacteriocin. In vivo, oral inoculation of 50 µg/mouse L. acidophilus bacteriocin for 5 successive days resulted in a noteworthy decline of the intestinal parasite density, along with amelioration of intestinal pathology of infected mice. Ultrastructural examination proved thatfive doses of L. acidophilus bacteriocin showed marked changes in cellular architecture of the trophozoites with evident disorganization of the cell membrane, adhesive disc and cytoplasmic components. 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Mossallam, Shereen F. ; Mahrous, Hoda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-2884277154c384ef6a1f90cba0dc2e90884aa7c92ea756e68e58ca84de46922e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Bacteriocin</topic><topic>Bacteriocins - isolation &amp; purification</topic><topic>Bacteriocins - pharmacology</topic><topic>Bacteriocins - therapeutic use</topic><topic>Cell Adhesion - drug effects</topic><topic>Female</topic><topic>Giardia lamblia</topic><topic>Giardia lamblia - drug effects</topic><topic>Giardia lamblia - growth &amp; development</topic><topic>Giardia lamblia - ultrastructure</topic><topic>Giardiasis - drug therapy</topic><topic>Humans</topic><topic>In vitro</topic><topic>In vivo</topic><topic>Intestinal Mucosa - parasitology</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestine, Small - parasitology</topic><topic>Intestine, Small - pathology</topic><topic>Lactobacillus acidophilus</topic><topic>Lactobacillus acidophilus - chemistry</topic><topic>Lactobacillus plantarum</topic><topic>Lactobacillus plantarum - chemistry</topic><topic>Male</topic><topic>Mice</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microscopy, Electron, Transmission</topic><topic>Probiotics - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amer, Eglal I.</creatorcontrib><creatorcontrib>Mossallam, Shereen F.</creatorcontrib><creatorcontrib>Mahrous, Hoda</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amer, Eglal I.</au><au>Mossallam, Shereen F.</au><au>Mahrous, Hoda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Therapeutic enhancement of newly derived bacteriocins against Giardia lamblia</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>2014-11</date><risdate>2014</risdate><volume>146</volume><spage>52</spage><epage>63</epage><pages>52-63</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><abstract>•L. acidophilus bacteriocin showed in vitro activity against G. lamblia trophozoites.•Bacteriocin induced severe morphological changes using electron microscopy.•Oral bacteriocin for 5 days was sufficient to induce massive parasite reduction.•L. acidophilus bacteriocin induced amelioration of intestinal pathology.•Bacteriocin holds great promise as an alternative therapy for giardiasis. Trials for identifying efficient anti-giardial agents are still ongoing. Nowadays, bacteriocins have attracted the attention as potential antimicrobial compounds. For the first time, the current study evaluated the therapeutic efficacy of bacteriocins derived from newly isolated Egyptian strains of probiotics Lactobacilli; L. acidophilus (P106) and L. plantarum (P164) against Giardia lamblia. Bacteriocins' efficacy was evaluated both in vitro; by growth inhibition and adherence assays, and in vivo; through estimation of parasite density, intestinal histopathological examination and ultrastructural analysis of Giardia trophozoites. In vivo bacteriocins' clinical safety was assessed. In vitro results proved that 50 µg of L. acidophilus bacteriocin induced reduction of the mean Giardia lamblia trophozoites by 58.3 ± 4.04%, while at lower concentrations of 10 and 20 µg of both L. acidophilus and L. plantarum, non significant reduction of the mean parasite density was achieved. In vitro trophozoites adherence was susceptible to the tested bacteriocins at all studied concentrations with variable degrees, while the highest adherence reduction was demonstrated using 50 µg of L acidophilus bacteriocin. In vivo, oral inoculation of 50 µg/mouse L. acidophilus bacteriocin for 5 successive days resulted in a noteworthy decline of the intestinal parasite density, along with amelioration of intestinal pathology of infected mice. Ultrastructural examination proved thatfive doses of L. acidophilus bacteriocin showed marked changes in cellular architecture of the trophozoites with evident disorganization of the cell membrane, adhesive disc and cytoplasmic components. This is the first reported study of the safe anti-giardial efficacy of L. acidophilus (P106) derived bacteriocin, hence highlighting its great promise as a potential therapeutic safe alternative to existing commercial drugs.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25300763</pmid><doi>10.1016/j.exppara.2014.09.005</doi><tpages>12</tpages></addata></record>
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subjects Animals
Bacteriocin
Bacteriocins - isolation & purification
Bacteriocins - pharmacology
Bacteriocins - therapeutic use
Cell Adhesion - drug effects
Female
Giardia lamblia
Giardia lamblia - drug effects
Giardia lamblia - growth & development
Giardia lamblia - ultrastructure
Giardiasis - drug therapy
Humans
In vitro
In vivo
Intestinal Mucosa - parasitology
Intestinal Mucosa - pathology
Intestine, Small - parasitology
Intestine, Small - pathology
Lactobacillus acidophilus
Lactobacillus acidophilus - chemistry
Lactobacillus plantarum
Lactobacillus plantarum - chemistry
Male
Mice
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Probiotics - chemistry
title Therapeutic enhancement of newly derived bacteriocins against Giardia lamblia
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