- Data Article
- Open Access
Occurrence of ingression of Salmonella spp. in Betel leaf (Piper betle L.)
International Journal of Food Contamination volume 4, Article number: 6 (2017)
Salmonella spp. is one of the most common pathogens associated with fresh produce related foodborne illness. This study aimed to determine Salmonella spp. contamination level in betel leaf, internalization potential and possible decontamination process.
A total of 77% betel leaf sample collected from local market was found to be contaminated with Salmonella spp. Of all the Salmonella spp. isolated and identified, 28.5% belong to Salmonella enterica subsp. enterica serovar Enteritidis, 19.5% belong to Salmonella Typhimurium, 15.6% to Salmonella Paratyphi, 10.4% to Salmonella Schottmuelleri, 9.1% to Salmonella Gallinarum, 10.4% to Salmonella Choleraesuis and 6.5% belong to Salmonella Bongori. Internalized Salmonella spp. showed moderate resistance to commonly used antibiotics. Treatment with common surface food disinfectants could not remove Salmonella spp. completely from betel leaf indicating the possibility that the bacteria may be in internal tissue of the leaf. Assessment of internalization potential showed that Salmonella spp. isolated from inner part of betel leaf pose better internalization potential (6.7–7.4 logCFU/gm) comparing with ATCC (American Type Culture Collection) strains (0.86–0.6 logCFU/gm). The isolates also showed better survivability in internalized condition, biofilm formation ability and motility than ATCC strains. Prevalence and expression of invasion (sefA and invA) and type 3 secretion system (TTSS) associated genes (hila, avrA and sopE) were high in internalized Salmonella isolates. Commercial disinfectants as well as H2O2 were found to have poor efficacy (log reduction around 2 CFU/gm) against internalized Salmonella. Ozonated water showed better decontamination efficiency (log reduction around 3 CFU/gm) whereas ethanolic extract of Terminalia arjuna stem bark showed higher decontamination (log reduction around 4.5 CFU/gm) of internalized Salmonella.
Salmonella spp. can ingress into betel leaf and better decontamination treatment is needed to be established.
Foodborne illnesses with linkage to consumption of contaminated fresh products (such as betel leaf) is increasing and becoming a significant food safety issue worldwide nowadays (Gomes et al. 2009; Gorny 2006). Contamination can occur at any stage of production such as pre-harvest or post-harvest (Semenov et al. 2010; Goldberg et al. 2011; Bernstein 2011). Some recent studies reported internalization of bacteria into the plant part and subsequent translocation of bacteria to leaf and other aerial parts of the plant (Goldberg et al. 2011; Zhuang et al. 1995; Avila-Quezada et al. 2010; Hirneisen et al. 2012; Zheng et al. 2013; Bernstein et al. 2007a; Bernstein et al. 2007b). This event is alarming due to the fact that internalization of pathogenic bacteria into fresh produce pose high risk to the consumers as they are significantly resistant to external biocidal washing agents (Ibarra-Sanchez et al. 2004; Jablasone et al. 2005; Donkor et al. 2010). Though the mechanism of internalization of bacteria into plant parts are still poorly understood (Auty et al. 2005), both plant and bacteria related factors contribute to its internalization (Erickson et al. 2010; Gu et al. 2011).
Salmonella spp. is one of the most common pathogens associated with fresh produce related foodborne illness (Sivapalasingam et al. 2004; Lapidot et al. 2006). Recent reports clearly demonstrate that Salmonella not only survive passively, but also infect plants actively (Wiedemann et al., 2015; Schikora et al. 2012; Akhtyamova, 2013). Moreover, infection of plants depends on the active suppression of the host immune responses by Salmonella (Schikora et al. 2012). Most studies on Salmonella plant interactions suggested an epiphytic lifestyle of Salmonella on plants (Berger et al. 2010).
Betel leaf (Piper betle L.) is a masticatory with important socio-cultural and ceremonial use in south and southeast Asia. It is also an economically important export commodity. Betel leaf is consumed raw through chewing mainly by South-Asian populations living worldwide. Betel leaf pose significant nutritional values and medicinal properties and is traditionally known to be useful for the treatment of various diseases like bad breath, boils and abscesses, conjunctivitis, constipation, headache, hysteria, itches, mastitis, mastoiditis, leucorrhoea, otorrhoea, ringworm, swelling of gum, rheumatism, abrasion, cuts and injuries etc. as folk medicine (Khanra 1997). Further, the essential oil contained in the leaves possesses antibacterial, anti-protozoan and antifungal properties (Hoque et al. 2011). Betel leaf is a product that is regularly consumed fresh and raw, but is difficult to decontaminate, as a result, like other fresh produces, can be a common vehicle of transmission of enteropathogenic bacteria (Berger et al. 2010). It is mainly produced in Bangladesh and India and exported worldwide. Due to the contamination of betel leaf with Salmonella spp., export of betel leaf has been reduced and sometimes suspended (Montanari 2015). Contamination of fresh produce like betel leaf with Salmonella spp. pose great public health risk to the consumer. Hence, research on contamination level and pattern of Salmonella spp. and effective decontamination process is of great urgency.
The present study aims to determine contamination level and pattern and to evaluate potential decontamination methods to neutralize Salmonella spp. contamination in betel leaf.
Salmonella Enteritidis ATCC 13076, S. Typhimurium ATCC 13311 and S. Typhi ATCC 65154 were used as positive culture in this study. Some environmental isolates (n = 15) of Salmonella were also included in the study to observe differences in gene expression. All the isolates were collected form culture collection pool of Industrial Microbiology Laboratory, IFST, BCSIR, Dhaka, Bangladesh. Additionally, Salmonella spp. isolated from surface (n = 25) and internalized condition (n = 17) during this study were used.
In this experiment, a total of 100 samples was collected from different markets of Dhaka city, Bangladesh. Sterile polybags were used to collect the samples aseptically. Samples were collected as number of leaves (not weight). Twenty leaves were collected from each location. A total of ten sample was collected from each market. The sampling packs were marked properly and carried in ice box and transported to the laboratory within 3 h. Experiments were carried out within 1–8 h after collecting the samples. All the samples were kept at 4 °C until these were analyzed.
Identification and enumeration of Salmonella spp.
Detection and identification of Salmonella spp. was done according to ISO/DIS 6579-1. Briefly, 25 g leaf sample was stomached with 225 ml 1% peptone water and stomached sample was pre-enriched (Buffered peptone water) and enriched (tetrathionate broth and RV broth) and then selective media (XLD agar) was employed for specific detection according to the method. Isolates were further identified on the basis of biochemical tests (TSI agar/Urea agar/indole production/Voges-proskauer/Lysine decarboxylase). Enumeration of Salmonella spp. in betel leaf was done according to Husna et al. (2015). Briefly, samples were stomached in peptone water and serially diluted and plate on XLD agar plate by spread plate technique and incubated at 37 °C for 24 h. Salmonella spp. were counted and expressed as logCFU/g.
Treatment of betel leaf with food disinfectants
H2O2 (10%, v/v), sodium hypochlorite (Sigma, USA) (10%, w/v) and commercial disinfectant (collected from local market) (1 & 2) were used to treat betel leaves (collected from local market) contaminated with Salmonella spp. Briefly, the leaves (ten leave) were manually submerged into 200 ml solutions of the disinfectants for 30 min and rinsed with sterile water for a couple of times. Then the leaves were cut into pieces and Salmonella spp. load was determined as described above. Salmonella-free leaves were submerged for 5 min in solution with ~105 cfu/ml of the bacteria and then analyzed as the same procedure to serve as controls.
Detection of internalized Salmonella spp.
Internalized Salmonella spp. has been detected and enumerated according to Franz et al. (Franz et al. 2007). Briefly, the surface of the collected whole leaf was disinfected with serial washing using tap water, 80% ethanol for 10 s, 1%AgNO3 for 5 min, tap water and finally rinsing with deionized water. Then the leaves were cut into pieces and analyzed according to the method described earlier. Salmonella-free leaves were submerged for 5 min in solution with ~105 cfu/ml of the bacteria and washed with water, ethanol and AgNO3 as described above and analyzed for both surface and internalized Salmonella spp. This serves to eliminate the presence of Salmonella as control to assure the presence of no Salmonella spp. in surface after washing.
Leaf internalization of ATCC strains was performed according to Kroupitski et al. (2009). Briefly, ATCC Salmonella strains was grown overnight in Luria-Bertani (LB) medium and cells were collected and washed twice with sterile distilled water and resuspended in sterile distilled water. Intact betel leaves (which were previously tested to be Salmonella free) were submerged in 30 ml sterile distilled water in 50 ml sterile tube (one piece per tube) for 30 min. After that, sterile distilled water of the tube was replaced with 30 ml Salmonella suspension (~109 cfu/ml) and incubated for 2–3 h at 37 °C. After incubation, the leaves were washed twice with sterile distilled water to remove unattached bacteria. Internalized Salmonella spp. was enumerated as described earlier (Franz et al. 2007).
Survivability of internalized Salmonella spp.
Survivability of Salmonella spp. in internalized condition was determined according to Gorbatsevich et al. (2013). Betel leaf samples were sanitized (as described above) and cut into small pieces aseptically and inoculated with bacterial suspension with known cell concentration (LogCFU/ml) and incubated at 37 °C for 14 days. A portion (10 g) of the sample was analyzed each day to enumerate internalized Salmonella spp. as described earlier.
Antibiotic resistance of internalized Salmonella spp.
Antibiotic resistance pattern of the internalized Salmonella spp. were determined according to the method described by Kirby-Bauer (1966) on Mueller Hinton agar using commercial discs (Oxoid, UK). The following antibiotics with the disc strength were used: Ciprofloxacin (CIP, 5 μg), chloramphenicol (C, 30 μg), penicillin (P, 5 unit), tetracycline (TE, 30 μg), doxycycline (DO, 30 μg), neomycin (N, 30 μg), gentamycin (GN, 200 μg), ampicillin (AM, 10 μg), erythromycin (E, 15 μg) and nalidixic acid (NA, 30 μg). A control strain of E. coli ATCC 25922 was included in each plate. Antimicrobial breakpoints and interpretation were taken from the CLSI standards.
Motility and biofilm formation of Salmonella spp.
Motility of the isolates was determined according to the method of Sperandio et al. (2002). Isolates were grown overnight in LB broth at 37 °C and was spot inoculated in center of 0.4% (w/v) LB agar and incubated at 37 °C in static condition. Diameter of motility halos was measured to determine motility. Biofi1m formation assays were performed following the method of Fakruddin et al. (2014). Bacterial suspension was inoculated into 96 well polystyrene microtitre plates and incubated overnight at 30 °C. After incubation, wells were washed with PBS and stained with 0.1% safranin for 30 min at 30 °C. Adhered safranin was solubilized with dimethyl sulfoxide (DMSO) and absorbance of the wells were measured at 490 nm wavelength. Specific biofilm formation was then calculated.
Virulence gene presence and expression
Presence of six virulence associated gene in Salmonella spp. isolates has been determined. Isolates were grown in LB broth overnight at 37 °C and total RNA was extracted. Description and primer sequence of the genes are presented in Table 1. Virulence gene profile of leaf internalized Salmonella spp. was compared with that isolated from leaf surface and previously isolated environmental Salmonella strains. For determination of expression level of the virulence genes, total RNA was extracted from bacteria using Trizol reagent and cDNA was prepared using primescript RT reagent kit (TaKaRa Bio). Primers used for real time PCR are as follows: sefA (5’-GGCTTCGGTATCTGGTGGTGTG-3’ and 5’-GTCATTAATATTGGCTCCCTGAATA-3’), invA (5’-GCCTGCCGGAAGTATTGTTA-3’ and 5’-GGAGTTTCTCCCCCTCTTCA-3’), hilA (5’-ATTAAGGCGACAGAGCTGGA-3’ and 5’-GAATAGCAAACTCCCGACGA-3’), avrA (5’-GGAAACCGATCTCGAAATGA-3’ and 5’-TGCTGGTTCGAACAAAATCA-3’), sopE (5’-CAACACACTTTCACCGAGGAAG-3’ and 5’-GGTCTGGCTGGCGTATGC-3’) and spvC (5’-AATGAACTACGAAGTGGGCG-3’ and 5’-TCAAACGATAAAACGGTTCCTC-3’), 16 s (5’-TGTAGCGGTGAAATGCGTAG-3’ and 5’-CAAGGGCACAACCTCCAAG-3’). Transcripts were quantified by LightCycler (Roche Diagnostics) using SYBR Premix Ex Taq (TaKaRa Bio) in accordance with the manufacturer’s instructions. The expression levels of each gene were normalized, with the 16S rRNA gene as an internal control.
Decontamination of internalized Salmonella spp.
Decontamination with two commercial fruit and vegetable disinfection agent (anshin-yasai & Yokosan; hereby denoted as commercial disinfectant 1 & 2 respectively) was performed according to manufacturer’s instruction. Information listed on the product revealed that active ingredient of disinfectant-1 was calcium oxide and of disinfectant-2 was calcium bicarbonate. Decontamination with H2O2, sodium hypochlorite and ozonated water performed according to Bahreini et al. (2013). Ethanolic bark extract of Terminalia arjuna was prepared according to Mahbuba et al. (2012) and decontamination process was performed according to Orue et al. (2013). Briefly, selected chemicals and extracts were diluted with water at different concentrations. Artificially inoculated betel leaf were immersed in the suspension for 10 min. After that, the leaves were washed with sterile water, ethanol and AgNO3 (as described above) and presence and load of Salmonella spp. were determined as described previously.
All experiments were done twice and all samples performed at least in triplicate. Data were analyzed by SPSS 17.0 (SPSS Inc., Chicago, Ill, USA).
Prevalence of Salmonella spp. in betel leaf
A total of seventy seven (77) out of 100 samples were found to be contaminated with Salmonella spp. From the contaminated samples, 77 strains were isolated after pre-enrichment and enrichment and confirmed through biochemical and serological studies. The total percentages of occurrence were 77%. Betel leaf collected from all areas showed to be contaminated with Salmonella spp. (Fig. 1a). Prevalence observed in this study were 28.5%, 19.5%, 15.6%, 10.4%, 9.1%, 10.4% and 6.5% representing Salmonella Enteritidis, S. Typhimurium, S. Paratyphi, S. Schottmuelleri, S. Gallinarum, S. Choleraesuis and S. Bongori respectively (Fig. 1b).
Treatment of betel leaf with food disinfectants
Naturally contaminated betel leaves were washed with commercial food disinfectant 1 & 2, H2O2 and Sodium hypochlorite. Commercial disinfectant 1 and 2 showed 3.29 log and 3.87 log reduction respectively, while that of sodium hypochlorite and H2O2 showed a lower log reduction (2.37 log and 2.48 log respectively) (Table 2). Control leaves (surface inoculated Salmonella-free leaves treated with same treatments) were found to be negative for the presence of Salmonella spp. This result indicates that surface disinfection based treatment were not effective to decontaminate Salmonella spp. from betel leaf. Occurrence of internalized Salmonella spp. in betel leaf was also determined (Table 3). Surface decontamination can reduce Salmonella loads by 1.97 log and treatment with disinfectants after surface decontamination reduce Salmonella loads by 2.78 log, indicating that Salmonella spp. may be internalized in inner parts of the leaf.
Internalization potential of isolate and ATCC strain
Comparison of internalization potential of two Salmonella strains isolated from internalized condition in betel leaf with three (3) ATCC Salmonella strains showed that the isolates pose better internalization potential than the ATCC strains (Table 4). Salmonella isolates from internalized condition showed considerable internalization potential. Approx. 6.7 logCFU was found to be internalized in case of S. Typhimurium isolate and approx. 7.4 logCFU was internalized in case of S. Typhi isolate (Table 4). In contrast, ATCC isolates showed very little internalization (approx. 1.2 logCFU for S. Enteritidis ATCC 13076 and 1.6 logCFU for S. Typhi ATCC 65154) (Table 3). Control leaves were found to be free of any internalized Salmonella spp.
Antibiotic susceptibility and Survivability comparison of internalized Salmonella
Antibiotic susceptibility pattern on internalized Salmonella isolates (n = 17) was shown in Fig. 2 and it shows the isolates pose moderate antibiotic resistance. Comparison of survivability of Salmonella Typhi isolate and ATCC strains in internalized condition in betel leaf is shown in Fig. 3. All the isolates were able to internalize and wild isolates internalized in a greater degree but survivality within the tissue seems to be the same. No significant differences were observed. After 14 days incubation, 6.72 logCFU Salmonella spp. were viable in internalized condition (initial count at day 0 was 8.31 logCFU). In case of ATCC Salmonella strain, 5.23 logCFU Salmonella were viable after 14 days incubation (initial count 7.58 logCFU) (Fig. 3).
Motility and biofilm forming capability of the isolated Salmonella
Biofilm formation mediates survival of bacteria in internalized condition (Kroupitski et al. 2009) and motility mediates translocation in plant tissues (Warriner et al. 2003). Biofilm formation and motility of internalized Salmonella spp. isolated from betel leaf as well as of ATCC isolates was determined. Isolates showed better biofilm formation ability (SBF > 1) than the reference cultures (SBF < 1) (Table 5). Motility of the isolates were also higher (>40 mm) than that of reference cultures (<20 mm). These data coincide with the better survivability of the isolates in internalized condition than the ATCC cultures.
Virulence gene presence and expression
sefA and invA are reported to impart virulence in Salmonella spp. sefA and invA gene were present in 64.7% and 76.5% internalized Salmonella spp. isolate respectively in comparison to surface (72% & 60%) and environmental (63.6% & 68.2%) Salmonella spp. isolates. Other virulence associated genes such as hilA, avrA and sopE were present in 64.7%, 52.9% and 64.7% of internalized isolate respectively. These three genes were present in very low number of surface Salmonella isolates (4%, 4% & 16%, respectively) and environmental Salmonella isolates (18.2%, 18.2% & 13.6% respectively). However, prevalence of spvC gene in all type of isolate is very low (Fig. 4). The expression level of the virulence associated genes in internalized Salmonella spp. were much higher than that in surface and environmental isolates (Fig. 5). Elevated expression of sefA and invA in internalized Salmonella spp. suggest virulence potential of these isolates. Increased expression of T3SS related genes (such as hilA, avrA, sopE and sopC) indicates hyper-activation of T3SS in internalized isolates contributing better survival in internalized conditions.
Decontamination treatment of internalized Salmonella
Decontamination method of internalized Salmonella spp. has been performed and showed in Table 6. Commercial agents (1 & 2) have been found to have limited decontamination effect (around 1.2 log and 2 log reduction respectively) on internalized Salmonella spp. with increasing efficacy at elevated concentration. H2O2 showed almost similar efficacy compare with commercial agents (1.9 log reduction at 10% concentration). Washing leaves with internalized bacteria with ozonated water showed better neutralization effect (3 log reduction) than both commercial agents and H2O2. Betel leaves treated with Ethanolic bark extract of Terminalia arjuna reduced internalized Salmonella spp. significantly. There was a log reduction of 3.8 at 5% concentration, 4.8 log at 10% concentration and 4.6 log reduction at 15% concentration (Table 6).
A total of 100 betel leaf samples were collected from different regions, 77% of the samples, were found to be contaminated with Salmonella spp. Regional distribution of contaminated betel leaf and species distribution of Salmonella spp. was shown in Fig. 1. Several studies has also reported presence of Salmonella spp. in betel leaf earlier. Singla et al. (2009) and Singh et al. (2006) have reported Salmonella spp. in betel leaf of Indian origin and Husna et al. (2015) reported Salmonella spp. in betel leaf of Mymensingh region, Bangladesh and Salmonella count was around 5 log in their samples.
Contaminated betel leaves were washed with four surface disinfectants (anshin-yasai, yokosan, H2O2 and sodium hypochlorite) and results showed that these agents cannot fully decontaminate the betel leaf though reduced Salmonella spp. level. From these results, the possibility arises that Salmonella spp. were present not only in surface, but also in the internal parts of the betel leaf, hence imparting its resistance were to these surface disinfectants. Internalized Salmonella spp. in betel leaf samples were enumerated and result showed that a significant portion of total Salmonella spp. in the leaves are internalized.
Many previous researchers reported internalization of pathogenic bacteria, including Salmonella spp. into plant leaves. Goldberg et al. (2011) reported internalization of Salmonella Typhimurium in detached leaves of seven vegetables and fresh herbs. Hou et al. (2013) reported that bacteria such as Salmonella, E. coli O157:H7, Bacillus, Enterobacter, Pseudomonas and Pantoea can internalize into lettuce leaves naturally through wounds or via roots and stomata. Avila-Quezada et al. (2010) showed that Salmonella spp. can internalize and migrate into plant tissues such as seeds, fruits, leaves, roots and stems and survive for extended periods in internalized condition. Guo et al. (2002) reported that Salmonella spp. can enter fruits and other plant parts through abrasions. Guo et al. (2001) also reported short distance migration of Salmonella spp. into plant. Zheng et al. (2013) also reported that Salmonella spp. has the ability to internalize into tomato plants through roots, leaves and blossoms. Internalization of Salmonella spp. has also been reported in mangoes (Penteado et al. 2004), tomatoes (Buchanan et al. 1999), apple (Zhuang et al. 1995), lettuce (Reina et al. 2002), and sweet basil (Gorbatsevich et al. 2013). Internalization may occur naturally as reported in these studies, or may occur during washing (due to immersion) at post-harvest stages (Gomez-Lopez et al. 2013).
Internalization efficiency of reference Salmonella culture (S. Typhimurium ATCC 13311, S. Enteritidis ATCC 13076 and S. Typhi ATCC 65154) and S. Typhi and S. Typhimurium isolated from betel leaf (leaf with internalized Salmonella) has been compared and it was found that the isolates pose better internalization potential (6.7–7.4 logCFU/gm) when compared with the ATCC cultures (0.86–0.6 logCFU/gm). All the isolates were able to internalize and wild isolates internalized in a greater degree but survivality within the tissue seems to be the same. Salmonella spp. isolates from betel leaf showed better biofilm formation ability (SBF > 1) and motility (>40 mm) than ATCC cultures (SBF < 1 and motility <20 mm). Results indicate that the isolated internalized Salmonella spp. have moderate resistance to commonly used antibiotics (Fig. 2) but antibiotic resistance were lower compared to the reports of other previous researchers who reported higher resistance in Salmonella spp. isolated from different food and poultry samples of Bangladesh (Nipa et al. 2011; Mahbuba et al. 2012).
Internalized bacteria can evade disinfection, thus detailed study on the mechanism of internalization as well as on plant and environmental factors affecting internalization is needed to devise remediation methods ensuring safety of the fresh produces (Ge et al. 2013). Mechanism of internalization of bacteria in the plant has not been elucidated clearly till now. Generally, internalization is an active process dependent upon the plant and the pathogen (Hora et al. 2005). Bacteria can internalize through root during cultivation and through the stomata of leaf during pre-/post-harvest (Hoelzer et al. 2014). Bacterial internalization is influenced by the surface properties of the leaf, including morphology, chemical constituents and metabolic activities (Leveau 2009). Pathogenic bacteria can penetrate internal tissue of the plant through the roots (Solomon et al. 2002), and seeds (Islam et al. 2004) for further translocation and survival in the edible aerial plant tissues (Solomon et al. 2002). Some studies reported that bacterial strains varied widely in their endophytic colonization abilities, which could be related to the plant defense mechanisms that targeted bacterial extracellular components (Dong et al. 2003; Iniguez et al. 2005). Water used for the washing of the fruits can be contaminated by the pathogens while acting as the source of the internalization of the pathogens through the lenticels, stomata and the injured parts (Reina et al. 2002).
It has been reported previously that many virulence associated genes mediate internalization and persistence of Salmonella spp. in plant. sefA gene is involved in attachment with plant tissue while invA gene is involved in epithelial invasion of plant tissue. Of all the virulence genes, type III secretion system (TTSS) associated genes are most important for internalization of Salmonella (Schikora et al. 2012). hilA gene product is a central regulator of TTSS and also involved in epithelial invasion. avrA gene product is an effector protein of TTSS and mediate Salmonella internalization and persistence by suppressing the host inflammatory response. sopE gene product contributes invasion through generation of membrane deformations. spvC gene (located on virulence plasmid) product promotes rapid growth and survival of Salmonella spp. within host cells (Borges et al. 2013). Results showed that the prevalence of invasion (sefA and invA) and TTSS associated genes (hila, avrA and sopE) are high in internalized Salmonella isolates which indicates probable mechanisms of internalization of the isolates. It can be postulated that TTSS play central role in the internalization and persistence of Salmonella spp. in betel leaf. Prevalence of hilA and avrA gene was more in internalized S. Enteritidis, whereas prevalence of sopE gene is more prevalent in S. Typhimurium and prevalence of spvC gene was prevalent in S. Paratyphi and S. Gallinarum.
Decontamination efficiency of different food disinfectants at different concentrations against internalized Salmonella spp. has been evaluated. Commercial disinfectants (anshin-yasai and yokosan) as well as H2O2 are found to have poor efficacy (log reduction around 2 CFU/gm). Ozonated water showed better decontamination efficacy (log reduction around 3 CFU/gm). Singla et al. (2009) reported that treatment of betel leaf with 2% acetic acid reduced artificially surface-contaminated Salmonella spp. by 4 log. Singla (2011) showed combined treatment of 2% malic acid along with 2 ppm ozone significantly reduced Salmonella Typhimurium by 7 log in turnip and reduced Cronobacter sakazakii by 6.8 log in betel leaf. Husna et al. (2015) showed treatment of betel leaf with sorbitol and sodium benzoate can be effective to reduce Salmonella spp. in betel leaf though log reduction was very low compared to other studies. Hadjok et al. (2008) reported UV light (254 nm) combined with H2O2 can reduce contamination levels of human pathogens (Escherichia coli O157:H7, Pectobacterium carotovora, Pseudomonas fluorescens and Salmonella) on or within (internalized) fresh produces but reduction of internalized pathogen was around half of that for surface pathogens. Orue et al. (2013) reported that extracts from oregano and lime are as effective as chlorine based disinfectants for decontamination of Salmonella, Shigella and Escherichia coli O157:H7 on leafy vegetables. In our previous studies, we found ethanolic extract of Terminalia arjuna stem bark has anti-bacterial activity against Vibrio cholerae (Fakruddin et al. 2011) and Salmonella spp. (Mahbuba et al. 2012). In this study, ethanolic extract of Terminalia arjuna stem bark fared better reducing potential than the rest of the treatments (log reduction around 4.5 CFU/gm) (Table 6). Plant extract contains essential oil with antibacterial activity and could be useful for decontamination of internalized Salmonella spp.
Many reports exist describing internalization of bacteria in to plants through artificial inoculation experiments whereas report of incidence of natural internalization was still very few. Despite some limitations of this study such as lack of fluorescence microscopy and efficient method of isolation of nucleic acids directly from leaf, this study results indicate occurrence of natural ingression of Salmonella spp. in betel leaf. Future research is needed to further elucidate detailed mechanism of internalization of Salmonella spp. in betel leaf as well as other plant.
The present study provide indications of natural internalization of Salmonella spp. in betel leaf, though the mechanisms of internalization is yet to be elucidated. The internalization of pathogenic bacteria like Salmonella spp. is a public health concern because a small number of surviving cells can be potentially lethal. As Internalized Salmonella spp. in betel leaf evade surface disinfection, elucidation of internalization mechanisms and factors (plant, bacterial and environmental) affecting internalization into betel leaf is needed to ensure the safety of this economically important fresh produce. Efficient decontamination method has to be discovered to reduce the risk associated with internalized Salmonella in betel leaf.
American Type Culture Collection
Colony forming unit
Polymerase chain reaction
Specific biofilm formation
Triple sugar iron
Type 3 secretion system
Xylose lysine deoxycholate
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The authors acknowledge the help of Ms. Sumaiya Islam, Scientific Officer, Industrial microbiology laboratory, IFST, BCSIR in conducting this study.
No external funding received.
MF and MMA designed the study. MF, NH and RS performed all the experiments. MKI and MMA supervised the study. MF wrote the first draft of the manuscript and all authors read and approve the final manuscript.
The authors declare that they have no competing interests.
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