alexa Allovahlkampfia spelaea is a Potential Environmental Host for Pathogenic Bacteria | Open Access Journals
ISSN: 2155-9597
Journal of Bacteriology & Parasitology
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Allovahlkampfia spelaea is a Potential Environmental Host for Pathogenic Bacteria

Mona Embarek Mohamed1*, Enas Abdelhameed Huseein2, Haiam Mohamed Farrag2,5, Fatma Abdel Aziz Mostafa3,5 and Alaa Thabet Hassan4
1Department of Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt
2Department of Parasitology, Faculty of Medicine, Assiut University, Assiut, Egypt
3Department of Botany and Microbiology, Faculty of Science, Cairo University, Giza, Egypt
4Department of Chest Diseases, Assiut University Hospitals, Assiut, Egypt
5Faculty of Applied Medical Science, Shaqra University, Kingdom of Saudi Arabia
Corresponding Author : Mona Embarek Mohamed
Department of Microbiology and Immunology
Faculty of Medicine, Assiut University
71515 Assiut, Egypt
Tel: +20-882413500/2411899
Fax: +20882333327
E-mail: [email protected]
Received: November 19, 2015 Accepted: December 28, 2015 Published: January 04, 2016
Citation:Mohamed ME, Huseein EA, Farrag HM, Mostafa FAA, Hassan AT (2016) Allovahlkampfia spelaea is a Potential Environmental Host for Pathogenic Bacteria. J Bacteriol Parasitol 7:255. doi:10.4172/2155-9597.1000255
Copyright: © 2016 Mohamed ME, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Allovahlkampfia spelaea was identified for the first time in 2009. As a free living amoeba, it has been suggested to be a protective host for some bacterial pathogens against harsh environmental conditions and can transmit them to vulnerable hosts. We aimed in this study to test the interactions between Allovahlkampfia spelaea and some waterborne and foodborne bacteria and unravel if the tested bacteria can survive and multiply inside amoeba. We used a keratitis isolate of Allovahlkampfia spelaea grown in PYG medium containing proteose peptone, yeast extracts, and glucose. We examined amoeba interactions with Methicillin resistant Staphylococcus aureus, Escherichia coli 1, Klebsiella pneumoniae, Enterobacter aerogenes, Citrobacter cloaca, Proteus mirabilis, Raoultella terrigena, Raoultella ornitholytica, Aeromonas hydrophila and Pseudomonas aeruginosa using the co-culture assays. Amoebal survival rate with different bacterial strains were determined. With the exception of Proteus mirabilis that showed decreased survival rates inside amoebal cells, other bacterial isolates could survive and multiply inside Allovahlkampfia spelaea that was associated with decreased survival rates of the amoeba. Particularly, Pseudomonas aeruginosa, Aeromonas hydrophila and MRSA exhibited significantly increased multiplication rates inside amoeba. Our study demonstrated that Allovahlkampfia spelaea may act as a replicative host for pathogenic bacteria with environmental and clinical implications.

Allovahlkampfia spelaea ; Amoeba-bacteria interactions; Co-culture experiments; Gram negative bacteria; Intracellular survival
Allovahlkampfia spelaea (A. spelaea ) belongs to the genus Allovahlkampfia in the family Vahlkampfiidae , class Heterolobosea , and Phylum Percolozoa [1] that was identified for the first time in 2009 [2]. A. spelaea is a free living amoeba (FLA) and has been found to be associated with keratitis as evident in a research conducted by Tolba et al. [3]. FLA is ubiquitous in nature [4] and some of them produce serious human infections [5]. Amoeba in nature may have contact with other microorganisms including bacteria. Amoebae are the dominant bacterial consumers, contributing to recycling of nutrients and maintaining the structure of the microbial community [6]. Most FLA genera are characterized by a biphasic life cycle consisting of a vegetative trophozoite stage and a physiologically static cyst stage [2]. Cysts are highly resistant and remain viable (and infective) for several years which facilitates spreading and colonization of new ecological niches [7]. On the other hand, bacteria have developed several antipredator strategies including cell size reduction, modified cell morphology, modification of cell wall characteristics, high-speed motility, biofilm or microcolony formation, and production of exopolymers or toxins [8]. In this case, amoebae may act as a protective host for some bacterial pathogens against harsh environmental conditions that normally kill. The role of FLA in survival and protection of pathogenic bacteria is increasingly recognized [9]. The amoebae aid in bacterial transmission to susceptible hosts thus constitutes a problem to the ecosystem health [5]. Additionally, bacteria become more resistant to disinfectants [6,9,10]. Many microorganisms are known to be hosted by FLA including; Acinetobacter spp., Aeromonas spp., Enterobacter spp., Escherichia coli (E. coli ), Klebsiella pneumonia (Kl. pneumonia ), Pseudomonas aeruginosa (Ps. aeruginosa ), Salmonella spp., and Staphylococcus aureus (Staph. aureus ) [11]. The hypothesis in our study was that A. spelaea may play a role for survival and multiplication of bacterial pathogens.
Materials and Methods
Molecular characterization of A. spelaea that was conducted at the Department of Medical Genomics, Graduate School of Frontier Sciences, The University of Tokyo, Japan.
Culture and molecular characterization of A. spelaea
A. spelaea used in this study was obtained from a patient with keratitis. A. spelaea was isolated on 1.5% non-nutrient agar made with Page’s saline (PAS) and seeded with E. coli kept at 30°C for 7 days. Cultures were examined using inverted microscope for presence of FLA and subcultured every 10 to 14 days by inverting a slice on a new agar plate as described previously [12]. The morphology of the trophozoite and cysts (non-stained and Giemsa’s Stained) were identified using light microscope and inverted microscope according to Smirnov and Goodkov [13]. Molecular characterization of A. spelaea by polymerase chain reaction (PCR) of the 18S ribosomal RNA and sequencing was performed using primers described previously [12,14-16].
Bacterial cultures and antibiotic susceptibility tests
Bacterial strains used in this study were isolated from cases with lower respiratory tract and urinary tract infections. The tested strains were Methicillin-resistant Staph. aureus (MRSA), Enterobacteriaceae [E. coli 1, Kl. pneumoniae, Enterobacter aerogenes (E. aerogenes ), Citrobacter cloaca (C. cloacae ), Proteus mirabilis (Pr mirabilis ), Raoultella terrigena (R. terrigena ), Raoultella ornitholytica (R. ornitholytica )], and other Gram negative bacteria; Aeromonas hydrophila (A. hydrophila ) and Ps. aeruginosa . Gram negative bacteria were identified up to the species level by API 20E system (BioMérieux, France) while detection of MRSA based on colonial morphology, Gram staining, and standard biochemical reactions according to the Bergey's Manual of Systematic Bacteriology [17]. Our Gram negative bacteria were all sensitive to imipenem and meropenem (Oxoid, England) while MRSA were sensitive to linezolid. Susceptibility tests were performed using the disk diffusion method as recommended by the Clinical and Laboratory Standards Institute (CLSI) guidelines [18]. Bacteria were cultured in brain heart infusion broth overnight at 37°C without shaking prior to experimentation and were used at the stationary growth phase.
Co-culture experiments
A. spelaea was grown without shaking in 15 ml PYG medium (0.75 %, w/v, proteose peptone; 0.75 %, w/v, yeast extract; 1.5%, w/v, glucose) in tissue culture flasks at 30°C, as described previously [19]. The medium being refreshed 17-20h prior to all experimentation. This resulted in more than 95% of the amoebae in the trophozoite form. Supernatants from A. spelaea cultures were centrifuged at 2800×g for 30 min. New pellets were resuspended in PYG before being processed to recover cultivable bacteria. Co-culture experiments were performed with a slight modification to a previous method [20]. A. spelaea was incubated in a concentration of 1×106 amoebae/mL PYG medium/well in 24 well plates until confluent. The cells were washed once with PAS. Next, Different bacterial strains were added in a concentration of 1×107 colony forming units (c.f.u)/well/mL PYG giving a multiplicity of infection (MOI) of 10. PH was adjusted to 7.2 and the plates were incubated for 1 h at 30°C to permit bacterial uptake. To kill residual extracellular bacteria, medium was replaced with PYG supplemented with 16 mg/L imipenem, a concentration greater than the highest MIC observed for all Gram-negative strains and linezolid in concentration of 1.5 μg/ml was used for MRSA. Plates were incubated for 1 h at 30°C. Antibiotics were removed by washing three-times with PAS. At the final wash, the discarded supernatants were also plated onto nutrient agar plates to determine bacterial presence and 100 μl fresh PAS were added to wells. The microtiter plates were incubated again at 30°C (designated time 0 h). The wells were processed at 0 h, 8 h, 24 h, 48 h, and 72 h. To count the extracellular bacteria, PAS was carefully aspirated and sampled. To determine the number of intracellular bacteria, 100 μl of fresh PAS were added to the wells and the surface of each well bottom was scraped to remove adherent cells. Finally, amoebae were lysed by adding sodium dodecyl sulphate (SDS) in 0.5% final concentration to each well for 20 min, and the number of bacteria was enumerated by plating on nutrient agar plates [21]. A. spelaea viability was monitored using the eosin dye exclusion assay using light and inverted microscope according to Wang and Ahearn [22].
Statistical analysis
The SPSS program version 20.0 was used for the statistical analysis of data. Data were presented as number and percentage, or mean ± SD as appropriate. ANOVA test was used before data were transformed (Log10), p value <0.05 was considered statistically significant.
Results and Discussion
As newly discovered in 2009 in the karst caves of Slovenia, data on A. spelaea (Figure 1) and their interactions with bacteria are lacking. For identification and characterization of A. spelaea , we depended upon 18S rRNA gene sequencing that revealed our strain to be A. spelaea strain SK1. Being a member of FLA, the role of A. spelaea in survival and multiplication of pathogenic bacteria should be considered. So, we aimed in this study to investigate survival and/or multiplication of the tested bacteria inside amoeba cells. Our bacterial strains were isolated from cases of urinary and respiratory tract infections and the majority of them are known to be natural contaminants of the water and food systems.
Co-culture of A. spelaea and bacteria
In our co-culture system, we followed the survival of bacteria inside A. spelaea at 30°C. Bacteria alone were incubated with various concentrations of SDS, and it was found that 0.5% SDS had no effect on bacterial viability.
Bacterial survival and multiplication inside A. spelaea
Figure 2 shows the intracellular bacterial counts in the presence of A. spelaea . With the exception of Pr. mirabilis that showed low counts throughout the experiment, our results showed that pathogenic bacteria survived and multiplied within the amoeba host. In particular, Ps. aeruginosa and A. hydrophila where the cell counts exceeded 5 log cycles at time 0h with highly significant differences versus other bacterial strains (P <0.001 for both) and increased significantly in number to reach >8 and >7 log cycle at time 24h of co-incubation, respectively in comparison to other isolates (p <0.001 for both). The high multiplication rate of A. hydrophila inside FLA in our study has been demonstrated before [23,24]. Ps. aeruginosa is an environmental Gram-negative bacillus that colonizes hospital water systems and causes nosocomial infections [25]. Additionally, Ps. aeruginosa - amoeba co-infections have been described in keratitis patients [26]. Our A. spelaea was isolated from a patient with keratitis, so the interactions between A. spelaea and Ps. aeruginosa are of special concern in those patients. The isolation of FLA naturally infected with Ps. aeruginosa [6,27-30] demonstrated the role of amoebae and their cysts as vectors for these intracellular bacteria [31]. Our results showed the intracellular multiplication of Ps. aeruginosa as supported previously [21,32,33]. In contrast to our findings, another report [34] supported the extracellular multiplication mode of Ps. aeruginosa with better growth outside than inside eukaryotic cells. In our work, MRSA intracellular counts were >4 log cycle at time 0h that significantly differed from other bacteria (p<0.001) and increased by >1 log cycle at time 24 h of co-incubation that differed from Ps. aeruginosa and A. hydrophila (p<0.001) but showed no significant differences (p>0.05) against the Enterobacteriaceae group. Huws et al. [35] demonstrated the proliferation of epidemic strains of MRSA inside FLA. Our Enterobacteriaceae group started with ~ 1 log cycle growth at time 0 h that increased up to 4 log cycle for C. cloacae and E. coli 1, and >2 log cycle for Kl. pneumoniae , E. aerogenes , R. terrigena , and R. ornitholytica . Previous data demonstrated that Enterobacteriaceae can survive and multiply within amoeba host [24, 36-40] which is consistent with our findings. At 48h co-incubation, the intracellular counts for all bacteria in our study decreased onwards. The decrease after 2-3 days of incubation, has been reported previously [20,41] which may be attributed to the limited intracellular life of bacteria, or the presence of viable not cultivable cells [42]. In our work, the intracellular viable count of Pr. mirabilis showed significantly the highest levels at time 0h (p=0.045, 0.021, 0.01, and 0.005 versus time 8h, 24h, 48h, and 72h, respectively). As the comparative counts of Pr. mirabilis in the presence of amoebae were lower, then, this was evidence of predation by A. spelaea .
Extracellular bacterial counts
The extracellular bacterial counts in our work, as shown in figure 2, occurred as a result of intracellular multiplication and subsequent release of vesicles containing live bacteria as reported [9,43]. They were characterized by gradual increase from time 0h to 8h co-incubation (p≤ 0.001) until significantly maximum extracellular counts at time 24h co-incubation (p<0.001). Then bacterial counts decreased significantly to very low or undetected levels at 72h co-incubation (p>0.05 versus time 0h). Significant maximum extracellular viable counts at 24h co-incubation were detected for bacteria that showed the highest growth intracellulary; Ps. aeruginosa and A. hydrophila (p<0.001 for both versus other bacteria tested). Pr. mirabilis extracellular counts reached very low levels with insignificant differences between time 8h co-incubation until the end of experiment (p>0.05). There are varying accounts in the literature on the types of interaction between bacteria and FLA with different types of endocytosis and intracellular behaviors including intracellular lysis of bacteria, followed by its digestion by amoebae or intracellular survival and multiplication of bacteria leading to amoebal lysis which may be dependent on virulence of bacteria [44]. As shown in our work, the non-invasive bacteria are taken up by amoeba as a food source (in our case Pr. mirabilis ), while the invasive bacteria are able to reside and multiply inside amoebae without being killed (in our case the other bacteria) [36], where they use amoebae as a transmission vehicle and develop resistance against other phagocytic cells in host tissues [5,45]. Nevertheless, the precise mechanisms of intracellular survival of our tested bacteria remain unclear and have to be determined. Although a previous report has demonstrated the ability of bacteria to inhibit the fusion of lysosomes with phagosomes as a critical step in the intracellular survival inside Acanthamoeba castellanii (A. castellanii ) [46], so, our bacterial strains may use similar mechanisms to evade the amoeba-cell defenses. Other reports [35,41,47] that demonstrated the multiplication of Staph. aureus within FLA, suggested that Staph. aureus possess no specific mechanism for evading digestion but have post-ingestion defenses such as a thicker cell wall, or an antioxidant yellow carotenoid. Pickup et al. [47] stated that Kl. pneumonae has the ability to resist phagocytosis and digestion as a result of polysaccharide capsule. The ability of many bacterial pathogens to survive intracellularly in A. spelaea may be a key step in the evolution of those bacteria to produce human and animal infections.
The survival rate of A. spelaea in the presence of bacteria
Number of viable A. spelaea in absence of bacteria increased from 1×106 cell/mL (100%) on time 0h to ~ 0.96×107 cells/mL (110%) and 1.88×107 (119%) cells/mL on 24h and 48h, respectively, and then survived to ~ 0.8×106 cell/mL (82%) at 72h (Figure 3). Growth of cocultivated A. spelaea , except with Pr. mirabilis , was inhibited with varying degrees. The statistical analysis showed highly significant differences in survival rates of alone-cultivated compared to the cocultivated A. spelaea (p<0.001 for 24h and 48h, and p<0.002 for 72h except for R. ornitholytica and E. aerogenes where p=0.097 for both). A. spelaea growth at 24h co-incubation was highly significantly affected by Ps. aeruginosa and A. hydrophila where p were <0.008 and <0.01 versus other bacterial strains, respectively. In this context, it is well known that the invasive property of Ps. aeruginosa target the amoeba with their toxins that cause cell lysis [34,48]. A. spelaea growth was significantly enhanced by Pr. mirabilis (p<0.002, <0.003, and <0.003 for 24h, 48h, and 72h co-incubation versus other bacterial strains, respectively). The decrease in survival rates of A. spelaea when co-incubated with our bacterial strains suggests that amoebal lysis occurred as a result of bacterial multiplication. Nevertheless, bacterial growth did not result in total killing of the amoebal cells that survived until end of the experiment at 72 h, which suggests the adaptation of our bacteria to the intracellular environment without causing total protozoal lysis as reported previously [20]. Our results are in accordance with previously published data [6,39,49-51] that detected decreased amoebal survival in presence of pathogenic bacteria.
The predation/survival/intracellular replication data for our bacteria differed in some instances from some work on bacteria and FLA interactions already published [7,52] that revealed a dose-dependent proliferative response of FLA when co-incubated with bacteria like E. coli , Staph. aureus, C cloacae , and Ps. aeruginosa . We attribute this discrepancy between our results and previous data to the use of A. spelaea isolate that has not been investigated before, different bacterial strains used, different MOI, or different co-culture conditions as yet reported [20]. The predatory activity of FLA is known to be influenced by several factors including the type and amount of surrounding bacteria [53,54]. As obvious in our findings, A. spelaea may act as a bacterial predator, or as a reservoir for bacteria, with environmental and clinical implications. Our results although may not reflect all possible modality of interactions as a single amoebal host have been employed, demonstrated that many pathogenic bacteria are able to interact with A. spelaea , even species which were not expected to have an intracellular life cycle. A. spelaea effect on health ecosystem has two problems. First, A. spelaea serve as reservoirs for pathogenic bacteria. Second, A. spelaea species can themselves cause disease in humans or animals. In the environment, the interactions of bacteria and A.spelaea are expected to be much more complex than reported here, as different bacterial prey are present in different niches that can be colonized by competing bacterial and protozoan predators. Deciphering the mechanisms of bacteria-protozoa interaction will assist in a better understanding of A. spelaea and bacterial lifestyle.
Conflict of Interest
The authors declare that they have no conflict of interest.
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