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Brazilian Journal of Poultry Science

Print version ISSN 1516-635XOn-line version ISSN 1806-9061

Rev. Bras. Cienc. Avic. vol.10 no.3 Campinas July/Sept. 2008

https://doi.org/10.1590/S1516-635X2008000300007 

Genomic variants of bacteriophages against Salmonella enterica serovar Enteritidis with potential application in the poultry industry

 

 

Robeson JI; Retamales JI; Borie CII

ILaboratorio de Bacteriología Instituto de Biología, Pontificia Universidad Católica de Valparaíso, Valparaíso
IILaboratorio de Microbiología, Facultad de Ciencias Veterinarias y Pecuarias, Universidad de Chile, Santiago

Mail Address

 

 


ABSTRACT

Salmonella enterica serovar Enteritidis (SE) is a prevalent gastrointestinal pathogen worldwide, threatening both animal and human health. In the latter, disease is associated to the consumption of SE-contaminated products from the poultry industry. The control of SE infection is largely based on the use of antibiotics and vaccines, but the use of lytic bacteriophages is re-emerging as an additional strategy for SE control. In fact, a number of recent reports point to the adequacy of bacteriophage as an efficient prophylactic or therapeutic countermeasure to SE infections. However, less attention has been focused on the basic biology of these bacteriophages. Here we report on three bacteriophages (f18, IF1 and EST2) that share a common viral particle morphology but are genomic variants as judged by their EcoRI DNA restriction patterns. Furthermore, they differ in their lytic capability towards SE, being EST2 the most efficient. They show a very narrow host range, efficiently infecting only SE strains. In terms of stability in various suspension media, including distilled water, all three bacteriophages remained viable, without noticeable decay in titer for at least 15 days at 25ºC. These results suggest the suitability of the tested bacteriophages as SE-controlling agents in the poultry industry.

Keywords: Bacteriophages, Biocontrol, Salmonella Enteritidis.


 

 

INTRODUCTION

During the last decades in Chile and worldwide, Salmonella enterica serovar Enteritidis (SE) has emerged as one of the most prevalent pathogens in humans and animals. They cause intestinal disorders that are mainly associated with the consumption of poultry products contaminated with SE (Darwin & Millar, 1999; Fica et al., 2001; Gard-Petter, 2001; Seo et al., 2002; De Avila et al., 2003).

The main mechanisms for the control this pathogen are based on the use of antibiotics, vaccines, and probiotics, but the emergence of multi-resistant SE strains requires the adoption of new measures, independent from traditional chemotherapies. This has led to the reemergence of the use of bacteriophages as therapeutic or prophylactic agents as an alternative for the treatment of SE infections (Matsuzaki et al., 2005).

Recent studies indicate the use of lytic bacteriophages as a method to control and detect different bacterial agents, such as Escherichia coli O157:H7, Mycobacterium, Campylobacter, Listeria, Staphylococcus, and Pseudomonas (Abdul-Hassan et al., 1990; Goodridge et al., 2003; Siquiera et al., 2003; Wagenaar et al., 2005).

The use of bacteriophages for the control of SE has been reported in association with processed fruits (Leverentz et al., 2001) and during Cheddar cheese manufacturing (Modi et al., 2001). Higgins et al. (2005) also studied their effect on broiler carcasses, and found a significant reduction of SE infection. Bacteriophages active against SE were successfully used to decrease SE infection levels in broilers (Sklar & Joerger, 2001; Fiorentin et al., 2005; Toro et al., 2005; Andreatti Filho et al., 2007, Atterbury et al., 2007). In this context, a group of bacteriophages isolated in Chile by Santander & Robeson (2002), which ability to control SE infection was first studied using Caenorhabditis elegans (Santander & Robeson, 2004), was recently tested for its capacity to successfully control SE infection in broilers (Borie et al., 2008a) and White Leghorn chickens (Borie et al., 2008b). However, these studies do not detail the genomic architecture of the mentioned bacteriophages or their biological activity in vitro. In fact, only the reports of Santander & Robeson (2002) and of Fiorentin et al. (2004) establish analysis criteria based on restriction patterns using EcoR1 and RAPD, respectively. In addition, there is no information as to stability of the viral particles in suspension media for field application.

In this study, we defined the genomic variants of a group of bacteriophages with similar morphology. These variants present different lytic capacity against Enteritidis serovar in in vitro experiments. Bacteriophage suspension conditions for field application were established. It was shown that they remain stable for 15 days.

 

MATERIALS AND METHODS

Bacteriophage isolation

Samples from broiler fecal matter, residual waters of confined animal facilities (horses, ducks, geese, chickens, cattle), municipal sewage waters, and poultry products were collected. Samples were homogenized or diluted in saline solutions, and processed to enrich phages using the method of Santander & Robeson (2002). To a 100 mL flash containing LB broth (Miller, 1972) supplemented with rifampicin (Rif, 100µg/ml) and nalidixic acid (Nal, 100 µg/ml) 0.5ml of an exponential-growth culture of a SE strain resistant to both antibiotics and 1ml of sample were added. The flask was incubated in an orbital shaker at 37ºC and 250 rpm for 18 to 24h. Phages were amplified by seeding in order to obtain lysis macroplaques with double agar layer technique using the same SE strain as marker strain (Davis et al., 1980).

Phage purification, amplification, and titering

The obtained phages were purified by collecting plate forming units (pfu) by understreaking double agar layers. Large-scale bacteriophage amplification was carried out according to the technique detailed in Sambrook et al. (1989). Bacteriophages were titered using dilution in BSG buffer (Gerhardt et al., 1981) and seeding on LB agar plates.

Viral genome analysis

Phage DNA was isolated according to Kaiser et al. (1989), with modifications (proteinase K instead of pronase). The purified DNA was then digested with EcoR1 restriction enzyme (Gibco, BRL), and fragments were separated by electrophoresis in agarose gel at 0.7% in TAE buffer, which was stained with ethidium bromide to allow fragment visualization under UV light (Sambrook et al., 1989). The obtained fragments were then compared to the molecular weight standard of DNA fragments of the lambda bacteriophage digested with HindIII (Fermentas, Lithuania).

Electron microscopy of viral particles

Viral particle morphology was observed by transmission electron microscopy, according to the techniques standardized by Hayat (1989). Phages were fixed in 0.1 M glutaraldehyde in sodium cacodylate buffer (pH 7.2). Osmium tetraoxide at 1% was added to the fixed samples, which were dehydrated in graded series of ethanol. Samples were then negatively stained with uranyl acetate at 4%. Viral particles were observed under electron microscope at 80 kV with 85,000x magnification.

Host range

Cross-streak seeding was carried out, corroborated by macroplaque essays, to determine the lytic activity presented by selected phages on bacterial strains commonly found in poultry.

"In vitro" phage lytic activity against SE

An exponential-growth phase SE culture was added to 20ml LB broth (10g triptone; 5g NaCl, 5g yeast extract; 1L distilled water). When culture reached an OD600 nm 0.25, phages were added at 0.1 multiplicity of infection (MOI), and bacterial reduction was observed every 20 minutes in a spectrophotometer (Spectronic 21D) by measuring OD600 nm at 37ºC. Each bacteriophage was tested in triplicate.

Frequency of phage-resistant SE variants

An exponential-growth phase SE culture was infected with phages at 1 MOI, and incubated in a shaker at 37ºC for 1h at 250rpm. The infected culture was then serially diluted in BSG, and plated on LB agar supplemented with Rif and Nal. After incubation for 24h at 37ºC, the number of mutants/ml was determined.

Phage titer stability

In order to test bacteriophage stability, dilutions of the three genetically different phages (1x103pfu/ml.) were incubated at 25ºC, and titer variation in time was determined by seeding in double LB agar plates, using SE as marker strain. The following media tested: BSG buffer (control), BMG (BSG buffer replacing NaCl by 1mM MgSO4,), distilled water, and peptone water (buffer of the probiotic product for poultry Broilac, Brazil).

 

RESULTS AND DISCUSSION

The bacteriophages analyzed in the present study, designated as f18, IF1, and EST2, were selected due their capacity to produce lysis plaques in a SE overlay culture. Bacteriophages from circular lysis plaques with translucent borders were amplified, purified, and examined under electron microscopy.

Viral particle morphology of the three studied bacteriophages (Figure 1) corresponds to B1 morphotype (i.e., are similar to Lambda bacteriophage), with a circular head and tail relatively longer than the head. In addition, they present a basal plaque, although the presence of adherent fibers is not clear. Therefore, the observed morphological characteristics suggest the presence of bacteriophages of the Order Caudovirales, which includes the genera Siphoviridae and Myoviridae. (ICTV, 2007). The examined bacteriophages, due to the morphology of the viral particles, are similar to the bacteriophage F 10 described by Atterbury et al. (2007).

 

 

The examination of the genome of the bacteriophages determined that their molecular mass was similar do the lambda bacteriophage DNA (49 Kpb) and that they present a characteristic pattern when treated with the enzyme EcoR1. The susceptibility of the genomes to EcoR1 and DNase (data not shown) indicate that they correspond to a bicatenary DNA. These results of this analysis are shown in Figure 2, A and B, and indicate that this is a homogenous phage group with some genomic variants. This is consistent with the selection of bacteriophages using a single SE strain. However, it is not clear if these bacteriophages, under the perspective of genomic architecture, are different from those reported by Fiorentin et al. (2004), who used RAPD for viral DNA analysis. Further data on the genomic sequence of these different bacteriophages are required to establish possible homologies. This information is essential to design genetic modification strategies aiming at improving the lytic capacity of SE-controlling bacteriophages.

 

 

The host range of these phage genomic variants may explain the specificity of these biological control agents (Table 1). The lytic activity is similar among the studied phages and it affects only the Enteritidis serovar of the genus Salmonella. The remaining tested strains, which are usually present in poultry, are resistant to the action of phages f18, IF1, and EST2. It must be noted that the studied bacteriophages do not affect bacterial strains present in the intestinal flora of broilers, and therefore, would not result in dysbiosis, which may be caused by the use of antibiotics.

 

 

The main difference among the three studied phage genomic variants is the time required to promote SE lysis in vitro, as demonstrated by the decrease in OD(600 nm.). These results are shown in Figure 3. The phage genomic variants called EST2 and f18 were more efficient to decrease OD(600 nm.) from 0,65 (which was used as control, corresponding to SE growth in the absence of bacteriophages) to 0,05 at the end of the incubation period. Phage EST2 reached these results 60 min post-infection, whereas f18 required the entire incubation period of 3h. The genomic variant IF1 only decreased OD(600 nm.) to 0.02, as compared to the control. Therefore, the phage genomic variants EST2 and f18 may be good biological agents for SE control. The results obtained in the present study are more favorable as compared to those of Attebury et al. (2007), who reported a less intense lytic activity of the bacteriophages they tested.

 

 

A relevant aspect in the context of the application of bacteriophages as agents to control bacterial infections is the selection of resistant mutant bacteria, which could be a negative aspect of the use of such biocontrol agents. In this sense, it must be mentioned that phage-resistant SE mutant strains were detected at a level of 10-4 mutants*ml-1 (Figure 4). Santander & Robeson (2007) in SE, and Park et al. (2000) in Pseudomonas plecoglossicida, found that this resistance to bacteriophages is due to a change in the bacterium surface, specifically to the loss of an important bacterial LPS site that is used by the phage to recognize and to adhere to the bacterium: the O-Polysaccharide (O-PS). However, this O-PS loss also results in the loss of the bacterial virulence, infective capacity, and capacity to kill the nematode Caenorhbditis elegans (Santander & Robeson, 2007). Therefore, in the case of the bacteriophages tested in the present study, the emergence of resistant SE mutants does not hinder the use of those biocontrol agents. In addition, these bacteriophage-resistant SE mutants could be used as seeds for the selection of new bacteriophages against SE.

 

 

Suspension media and phage application are essential to ensure the efficacy of these agents in the control of SE in poultry houses, and therefore titer stability in different suspension media must be determined before its massive and industrial prophylactic application. In order to ensure the success of bacteriophages as SE-control agents in poultry production, different suspension media were tested in vitro. The results indicated that the studied media presented excellent conditions to maintain stable phage titers (Figure 5). However, the use of magnesium-supplemented phosphate buffer is recommended over BSG buffer, which contains NaCl and may irritate birds' eyes if the phage solution is sprayed. Distilled water may cause titer variation, and therefore, lytic activity variation if pH or dissolved salts are not duly controlled. Also, under the context of prophylaxis, the studied bacteriophages maintained their titers in suspension media containing probiotic bacterial strains, opening the possibility of developing phage-enriched probiotic products for the control of SE in poultry production.

 

CONCLUSION

Genomic variants of bacteriophages belonging to the same morphotype were determined. These variants had different lytic activity against SE, and variants EST2 and f18 could potentially be used as agents for the control of SE infections. In addition, the use of phosphate buffer supplemented with 1mM Mg++ and 0.01% gelatin for the field application of bacteriophages is recommended.

 

ACKNOWLEDGMENTS

The authors thank Comisión Nacional de Investigación Científica y Tecnológica de Chile (CONICYT) for the funding granted to one of the authors (CB) thorugh project FONDECYT 1060569, which allowed the development of this research study.

 

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Mail Address:
James Robeson
Instituto de Biología
Pontificia Universidad Católica de Valparaíso
Av. Brasil 2950
Valparaíso, Chile
E-mail: jrobeson@ucv.cl

Arrived: March/2008
Approved: August/2008

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