Oxygen limitation induces acid tolerance and impacts simulated gastro-intestinal transit in Listeria monocytogenes J0161
© Sewell et al.; licensee BioMed Central. 2015
Received: 4 December 2014
Accepted: 19 March 2015
Published: 10 April 2015
Listeria monocytogenes is a food-borne pathogen and the causative agent of listeriosis, a severe infection to those with a pre-disposition. Infections often arise through consumption of contaminated foods, where high intrinsic resistance to food processing practises permit survival and growth. Several practises, including refrigeration, acidification and oxygen limitation are ineffective in controlling L. monocytogenes, therefore foods which do not undergo thermal processing, e.g. ready-to-eat products, are considered high risk.
While the responses to several food processing practises have been investigated, there are few reports on the responses of L. monocytogenes to oxygen limitation. Therefore the aim of this study was to investigate the effects of oxygen limitation on stress response andsurvival capacity during simulated gastro-intestinal transit.
Anaerobiosis induced an acid tolerance response, causing cells to be more resistant to organic and inorganic acids than aerobically grown counterparts (p < 0.05).
Using a gastro-intestinal transit model it was found that anaerobic growth induced an acid tolerance response which enhanced resistance to pH 2.5 simulated gastric juice (SGJ) compared to aerobically grown cells (p < 0.05). This response was most pronounced in exponential phase cells. However, exposure of stationary phase cells to pH 3.5 SGJ enhanced bile tolerance, suggesting a link between acid and bile tolerance.
The responses of L. monocytogenes to oxygen limitation are not extensively studied. These findings provide an initial insight into the effects of anaerobiosis on stress response and survival potential in L. monocytogenes. While it appears anaerobiosis may impact these, further work is required to confirm these findings are not strain specific.
KeywordsListeria monocytogenes Gastro-intestinal transit Acid tolerance response Anaerobiosis Adaptation
Listeria monocytogenes is a Gram positive food-borne pathogen associated with human disease/illness, ranging from mild gastroenteritis to potentially fatal invasive listeriosis [1,2]. Transmission of L. monocytogenes typically occurs through consumption of contaminated foodstuffs where ready-to-eat (RTE) foods are often compromised .
As RTE foods are not subjected to further control measures post processing/pre consumption food manufacturers adopt the use of modified atmosphere packaging (MAP) in an attempt to control the growth of pathogenic or spoilage organisms present in RTE foodstuffs . The application of MAP utilises oxygen (O2), nitrogen (N2) and carbon dioxide (CO2) in an attempt to inhibit the growth of micro-organisms by decreasing O2 availability and increasing CO2 levels within food packaging .
Several RTE products have been implicated in listeriosis outbreaks, including dairy products, vegetables, meat and poultry products; many of which are packaged under modified atmosphere . One such outbreak was caused by L. monocytogenes J0161 in 2000, where 30 cases of listeriosis were linked to the consumption of RTE deli turkey , often stored under MAP.
MAP success in pathogen control is dependent upon several factors including micro-organisms present, CO2 concentration, storage temperature and food type . While MAP has proven success in controlling the growth of strictly aerobic micro-organisms, studies have found that the growth and survival of facultative anaerobes, such as L. monocytogenes, may be enhanced by its application . Additionally, Francis et al.  demonstrated that the glutamate decarboxylase system, a key acid-tolerance response (ATR) component, was important for listerial survival in MAP products. Given the importance of low pH in the human immune system, conditions inducing an ATR may impact virulence . Therefore, it was the aim of this study to assess the extent by which oxygen limiting conditions induce the ATR and influence simulated gastro-intestinal survival in an outbreak strain of L. monocytogenes J0161.
Cultures of L. monocytogenes strain J0161 were grown to mid-exponential (OD600 0.3 – 0.5) or stationary phase in Brain Heart Infusion (BHI) broth under aerobic or anaerobic conditions. Anaerobic conditions were achieved using an anaerobic cabinet (Don Whitley, Yorkshire, UK) and monitored using anaerobic indicator strips (Oxoid, UK). For acid tolerance assays exponential phase cells were directly subjected to 5 M HCl (volume sufficient to reduce the medium to pH 3) or 2% organic acids (citric, acetic, lactic acid) in BHI. At intervals samples were removed, diluted in buffered peptone water (BPW) and plated onto BHI agar using a spiral plater (Don Whitley, Yorkshire, UK). Plates were incubated for 24–48 hours under aerobic conditions and log reductions calculated relative to time-point zero.
To model gastro-intestinal transit, SGJ was prepared as previously described  and adjusted to pH 1.7 or 2.5. Cells were assessed for their capacity to survive ‘short’ and ‘long’ gastric transit as described by Barbosa et al. . Sixteen ml of pH adjusted SGJ was added to 4 ml of culture and incubated at 37°C for 60 minutes (short transit) or 120 minutes (long transit). After this time SGJ was neutralised to approximately pH 7.2 by addition of NaOH and 0.1x total volume of a 3% w/v bile salt solution, giving a final concentration of 0.3% w/v (as found in vivo). Following addition of bile salts cells were incubated for a further 60 minutes (short transit) or 120 minutes (long transit). Throughout simulated gastric transit, samples were removed at 30 minute intervals, dilutions made in BPW, plated using a spiral plater and incubated for 24–48 hours at 37°C. All experiments included growth controls (PBS) subjected to PBS throughout sampling, neutralised simulated gastric juice controls (SGJ) subjected to SGJ during the first phase of simulated gastric transit and bile salt only controls (bile) subjected to PBS during the first phase of simulated gastric transit followed by 0.3% w/v bile salts.
Anaerobiosis induced acid tolerance occurred during exposure to both organic and inorganic acids (Figure 1). Previously published literature has reported increased expression of glutamate decarboxylase (GAD) during anaerobic growth in L. monocytogenes. Given the well-established role of GAD in acid tolerance it is possible that GAD induction through anaerobic growth may initiate an acid tolerance response. This hypothesis is supported by the findings presented in this study where cells grown under anaerobic conditions displayed increased resistance to all acid types tested compared to their aerobically grown counterparts.
To establish systemic infection L. monocytogenes cells must overcome several barriers before reaching the intestinal epithelial cells for adhesion, invasion and subsequent infection. The first of these is survival within acidic gastric juice. The pH of the human stomach varies from pH 1–3 in healthy individuals to pH 3.5-4.5 in susceptible populations, such as the elderly, following food consumption , a pH range known to initiate an ATR in L. monocytogenes . After the stomach, cells must survive exposure to the 1 litre of bile secreted daily by the liver if they are to establish systemic infection . Therefore, it was deemed relevant to assess the extent by which the anaerobiosis induced ATR permitted survival of L. monocytogenes J0161 cells during simulated gastric transit at pH 2.5 and at pH 3.5, how this transit is impacted by growth phase, and the effect of ATR has on bile tolerance in L. monocytogenes J0161.
As with exponential phase cells, those grown to stationary phase were readily able to survive exposure to pH 3.5 SGJ (Figure 3A and C). However, they were able to survive bile salt exposure. Interestingly, mild acid stress of stationary phase cells induced a cross protection to bile salt relative to bile control cells. Pre-exposure to pH 3.5 SGJ resulted in significantly greater recovery of cells during the ‘intestinal’ phase of transit (p < 0.05). The extent of this cross protection was pre-condition dependent, those grown aerobically possessing greater bile salt tolerance than those grown anaerobically (p < 0.05), suggesting a possible link between acid adaptation and Listeria persistence during gastric transit.
In summary, this report demonstrates the induction of an anaerobiosis induced ATR in L. monocytogenes J0161. When applying these findings to a novel simulated gastro-intestinal transit model it appears that this response may aid transit of L. monocytogenes through the low pH of the stomach. Previous studies have investigated the effects of oxygen limitation on L. monocytogenes virulence [18,19]. In these studies oxygen limitation was found to enhance invasive and infective potentials respectively. While this has been largely attributed to increased expression and secretion of adhesion proteins , here we provide evidence to suggest that oxygen limitation enhances resistance to gastric juice, thus increasing the likelihood of invasive infection . Furthermore, cells were found to possess growth phase dependent bile tolerance which was impacted by pre-exposure to low pH; a finding which may explain the ability of L. monocytogenes to persist in the presence of bile in vivo.
While this study was carried out using a single strain, the isolate originated from a human listeriosis case which was part of a large-scale outbreak culminating in 29 human infections and four deaths  and so can be considered an important model organism when investigating Listeria pathogenesis.
Simulated gastric juice
Acid tolerance response
Buffered peptone water
Phosphate buffered saline
DS acknowledges the financial support provided by the University of Northampton, UK through their Postgraduate Studentship scheme. The authors also thank Professor Martin Wiedmann, Cornell University, USA for supply of L. monocytogenes J0161.
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