Probiotics for the control of parasites: an overview.

Probiotics are defined as live organisms, which confer benefits to the host. Their efficiency was demonstrated for the treatment of gastrointestinal disorders, respiratory infections, and allergic symptoms, but their use is mostly limited to bacterial and viral diseases. During the last decade, probiotics as means for the control of parasite infections were reported covering mainly intestinal diseases but also some nongut infections, that are all of human and veterinary importance. In most cases, evidence for a beneficial effect was obtained by studies using animal models. In a few cases, cellular interactions between probiotics and pathogens or relevant host cells were also investigated using in vitro culture systems. However, molecular mechanisms mediating the beneficial effects are as yet poorly understood. These studies indicate that probiotics might indeed provide a strain-specific protection against parasites, probably through multiple mechanisms. But more unravelling studies are needed to justify probiotic utilisation in therapeutics.

1. Introduction

Probiotics have been defined by WHO as “live organisms which when administered in adequate amounts confer a health benefit to the host” (http://www.who.int/foodsafety/publications/fs_management/probiotics2/en/). Importantly, a general probiotic statement on a genus or a species cannot be established, as two closely related strains can induce inverse effects. Therefore, a probiotic must always be fully characterised at a strain level [1]. A good probiotic strain should confer a beneficial property (immune stimulation, protection against pathogens, metabolism, etc), be nonpathogenic, resistant to low pH and acids, thereby persisting in the intestine, and able to adhere to the gut epithelium [2]. About 50 strains corresponding to 26 species fulfil these criteria. Most probiotic organisms are gram positive bacteria, isolated from the human gut microflora or various dairy products such as curd, lassi, and kulfi. However, probiotic beneficial effects have been more often demonstrated in model animals than by direct clinical evidences and depend largely on the dose ingested. Dose of at least five billion colony forming units per day for at least 5 days is recommended [2]. This minimum dose takes into account the survival capacity of the ingested probiotics in the gastrointestinal tract, where they are in competition with the resident bacteria [3]. Three main benefits are reported (Figure 1).

Figure 1

Schematic representation of the different routes by which probiotics may control a pathogen. (1) Probiotics can modulate their physicochemical environment (nutrients, mucus, receptors availability on epithelial cells, pH, tight junctions, and peristaltism). (2) Probiotics can produce biologically active molecules such as bacteriocins, antibiotics, or oxygen peroxide that possess antimicrobial properties. (3) Probiotics can induce immune modulation, either through interaction with dendritic cells that can, in turn, modulate the differentiation of naïve T cells into Th1, Th2, or Treg lymphocytes, leading to different cytokine induction and/or through a humoral immune response via IgA producing cells and their secretory IgA (sIgA).

Modulation of the intestinal environment, by probiotics having the capacity to control the proliferation of surrounding microorganisms and/or by competition for the occupancy of a common biotope (e.g., access to nutriments) [2]. For example, iron is a limiting nutriment: it is essential for most bacteria, and probiotics can compete for its availability. Lactobacillus can render iron unavailable for pathogenic microorganisms, either by binding ferric hydroxide on its surface [4] or by secreting siderophores that chelate and transport iron [3]. Some probiotics are also able to influence the composition and equilibrium of the gut microflora (For review, see [5]). For example, probiotic therapy using a mixture of probiotics (VSL#3) was shown to increase the total number of intestinal bacteria and to restore the diversity of the bacterial microbiota in patients [6]. Finally, probiotics can also control their biotic environment through regulation of intestinal motility and mucus secretion [2].

Secretion of active molecules (e.g. bacteriocins, antibiotics, free fatty acids, hydrogen peroxide) that can control growth and/or survival of surrounding microorganisms. Bacteriocins are secreted peptides or proteins that generally kill closely related bacteria by permeabilizing their membranes or by interfering with essential enzymes (For review, see [5]). Many of them are produced by Lactobacillus probiotic strains (lactacin B, lactacin F, nisin, etc.). Lactobacillus reuteri produces reuterin (3-hydroxypropionaldehyde), a broad-spectrum antibiotic, active against bacteria, yeast, fungi, protozoa, and viruses [7]. By lowering the local intestinal pH with lactic acid, probiotics can also modify the growth of acid-sensitive organisms [5].

Modulation of immunity, by stimulating the host immune response to a variety of pathogens. In the gut, probiotics interact with the epithelial cells, Peyer's patches M cells, and immune cells. These interactions result in an increase in the number of IgA producing cells accompanied by production of IgM and secretory IgA which are particularly important in mucosal immunity, contributing to the barrier against pathogenic organisms [8, 9]. In addition, probiotics can also affect dendritic cells, which are responsible for collection of antigens from gut and their presentation to naïve T cells, leading to their differentiation to T-helper (Th1, Th2) or T-regulatory lymphocytes. Probiotic molecules implicated in dendritic cell induction are poorly characterized, one exception being the S layer protein A of L. acidophilus NCFM that regulates maturation of dendritic cells and T cell functions [10]. Probiotics have also been shown to modulate cytokine release (TNF-α IFN-γ, IL-10, IL-12) [11]. These cytokines play a central role in maintaining the delicate balance between necessary and excessive defence mechanisms. For instance, polysaccharide A, synthesized by Bacillus fragilis NCTC 9343, protects against experimental colitis through an adequate induction of IL-10 production [12].

In conclusion, probiotics can kill or inhibit pathogens by strain-specific mechanisms relying on competition, molecule secretion, and/or immune induction. Most of the described interactions imply a prokaryotic pathogen that colonizes the same gut compartment. Recently, several studies have investigated whether probiotics could control the proliferation of eukaryotic pathogens, either in the gut as the probiotic, or in a different compartment (Figure 2, Table 1). This concept is supported by recent studies showing that gut commensal microflora can play a critical role in the completion of the life cycle of the intestinal parasitic nematode Trichuris muris and in the modulation of the host immune response [13] and can also provide indirect protective immunostimulation against the nongut parasite, Toxoplasma gondii [14]. In the following chapters, we will report the recent findings concerning the effects of probiotics on several parasites as illustrated in Table 1 and propose future directions to help to standardize probiotic tests on eukaryotic pathogens.

Figure 2

Schematic representation of the different eukaryotic pathogens (gut or nongut pathogens) for which probiotics have been tested. Not to scale. Approximate sizes: adult Ascaris up to 30 cm; Cryptosporidium oocyst 4 μm; Eimeria oocyst 10 μm; Giardia cyst 15 μm; adult Toxocara up to 20 cm; adult Trichinella 3 mm. Babesia 5 μm; Plasmodium 7 μm, adult Schistosoma 16 mm, and Trypanosoma trypomastigote 12 μm. Spo.: Sporozoite; Tro.: Trophozoite; Mer.: Merozoite; Cer.: Cercae; Ama.: Amastigote; Try.: Trypomastigote.

Table 1

List of probiotics tested on different eukaryotic pathogens. The first column illustrates the pathogens studied; the second one indicates the probiotics tested (and if known, their strain reference; n.s. non specified) and the corresponding references. The third column gives details of the level of the studies: clinical in patients (Human), in vivo in natural or experimental animal models (pig, mouse, calf, rat, chicken, gerbil), or at a cellular level (cyst differentiation and survival, trophozoites development, and invasion capacity). The fourth column specifies the administration conditions of the probiotic (A): a–d: before infection; a—0–3 days, b—3–7 days, c—7–15 days, d—more than 15 days, e—after infection, and f—concomitant administration and infection. The last column indicates the result (R) of the studies. Results are indicated in terms of reduction of parasitic load in comparison to control for in vivo studies or in term of reduction of viability/infectivity for in vitro assays, −: negative impact of probiotic, 0: no significant effect, +: 25–50% of reduction, ++: 50–75% of reduction, and +++: 75–100% of reduction. n.d.: not determined; ∗: clinical case.

Pathogen	Probiotic tested	Host	A	R
Ascaris suum	B. lactis (pig isolate) [53]	Pig	d	n.d.
Babesia microti	L. casei ATCC7469 [56, 58]	Mouse	a	+++
			b	+
Cryptosporidium parvum	L. reuteri 4000, 4020 [21]	Mouse	c	+++
	L. reuteri 4000, 4020 or L. acidophilus NCFM [22]	Mouse	c	++
	L. reuteri 4000, 4020 [23]	Mouse	c	++
	L. rhamnosus GG + L. casei shirota [24]	Human	e	∗
	VSL#3 or Actimel [25]	Neonatal rat	a	0
	B. brevis, E. faecium, P. alcaligenes [26]	Calf	f	0
	L. reuteri ATCC23272 or L. acidophilus NCFM [27, 28]	Cell culture		+
	B. breve ATCC15698 or B. longum ATCC15707 [28]	Cell culture		+++
	B. brevis, E. faecium and P. alcaligenes [29]	Cell culture		+++
Eimeria   tenella/acervulina	Primalac [45–47]	Chicken	d	++
	Mitomax [48]	Chicken	d	+
	Mitogrow [40]	Chicken	d	+
	L. acidophilus Lb33ac, L. salivarius Lb14c7 Lb16c6 [49]	Cell culture		++
Giardia lamblia	L. johnsonii LA1 [33]	Cell culture		+++
	L. johnsonii LA1 [34]	Gerbil	b	++
	L. casei MTCC1423 [35]	Mouse	b	+++
	E. faecium SF68 [36, 37]	Mouse	b	+++
Plasmodium chabaudi	L. casei ATCC7469 [59]	Mouse	c	+
Schistosoma mansoni	Z. mobilis [55]	Mouse	b	++
			e	−
Toxocara canis	E. faecalis CECT7121 [52]	Mouse	b	+++
Trichinella spiralis	L. casei ATCC7469 [50, 51]	Mouse	b	+
Trypanosoma cruzi	L. casei ATCC7469 [60]	Mouse	b	+++

B. breve: Bifidobacterium breve; B. brevis: Bacillus brevis; B. lactis: Bifidobacterium lactis; E. faecium: Enterococcus faecium; L. acidophilus: Lactobacillus acidophilus; L. casei : Lactobacillus casei; L. johnsonii: Lactobacillus johnsonii; L. paracasei: Lactobacillus paracasei; L. reuteri: Lactobacillus reuteri; L. rhamnosus: Lactobacillus rhamnosus; P. alcaligenes: Pseudomonas alcaligenes; S. boulardii: Saccharomyces boulardii; Z. mobilis: Zymomonas mobilis.

Sources of commercial probiotics: Actimel : Lactobacillus bulgaricus, Streptococcus thermophilius, and Lactobacillus casei DN-114 01; Mitogrow Imagilin Technology, consists of live Pediococcus acidilactici; Mitomax Imagilin Technology, consists of live Pediococcus acidilactici and Saccharomyces boulardii; Primalac contains primarily Lactobacillus acidophilus and Lactobacillus casei; VSL#3: four strains of lactobacilli (Lactobacillus plantarum, Lactobacillus casei, Lactobacillus acidophilus, and Lactobacillus bulgaricus), three strains of bifidobacteria (Bifidobacterium infantis, Bifidobacterium longum, and Bifidobacterium breve), and one strain of streptococcus (Streptococcus thermophilius).

2. Cryptosporidium

Cryptosporidium is an intestinal pathogen belonging to the Alveolata group that can cause devastating gastrointestinal infection in immunosuppressed humans. In the environment, Cryptosporidium is found as oocyst, the infective form, in water. After ingestion, the oocysts travel through the gut lumen to the small intestine, where they release the motile sporozoites that adhere and invade the epithelial gastrointestinal cells. The sporozoites focally disrupt the microvilli and penetrate the host cells to establish their intracellular niche, where they remain in an extracytoplasmic vacuole. After parasite replication and evasion, oocysts are generated and excreted in the faeces (for a review, see [15]) (Figure 2). Intestinal epithelial cells, infected by Cryptosporidium parvum, show impaired Na+ and H2O absorption as well as enhanced Cl− secretion, leading to diarrhea. Abnormalities in the barrier properties of the intestinal epithelium, caused in part by the disruption of intercellular junctional complexes, contribute also to diarrhea. Despite a real risk of waterborne outbreaks of cryptosporidiosis, there is no completely efficient therapy available. The most commonly used drugs, such as paromomycin and azithromycin or nitazoxanide, are only effective in combination with immune restoring agents [16]. Immunocompetent adult mice are capable of controling Cryptosporidium parvum infections, while IFN-γ knockout and severe combined immuno deficiency mice (SCID) are susceptible to this parasite [17, 18]. Besides immunity, the intestinal flora can also influence resistance to Cryptosporidium [19]: germ-free adult immunocompetent mice have an increased susceptibility to Cryptosporidium whereas SCID mice, colonized with a defined anaerobic flora (Altered Schaedler Flora), are able to resist infection [20].

Beneficial effects of probiotics upon cryptosporidiosis have been demonstrated: adult mice (female C57BL/6 immunosuppressed by the murine leukemia virus (strain LP-BM5), 3-4 weeks old) fed daily with L. reuteri strains 4000 and 4020 or L. acidophilus NCFM presented reduced oocyst shedding [21, 22]. This partial protection was not associated with an immune restoration (cytokines production). Daily ingestion of L. reuteri was also efficient to prevent C. parvum intestine colonization and tissue lesions in a host with a deficient immune system (gnotobiotic TCR-alpha deficient mice). Waters et al. suggested that protection was due to secretion of as yet unidentified antimicrobial products [23]. In human, a single case of resolution of prolonged cryptosporidiosis by a probiotic treatment was documented [24].

On the other hand, probiotics seem less efficient in neonatal animals [25]. No significant benefit could be observed using two different mixtures of probiotics, Actimel or VSL#3 probiotic mixture, although there was a tendency to a shorter duration of infection in probiotic-fed animals. Nevertheless, the authors concluded that one could not rule out some effect in other experimental conditions, such as a prolonged administration before infection and the use of alternative animal models with a mature gut flora and immune system. An absence of effect was also observed under field conditions in Holstein calves, born on a dairy farm where cryptosporidiosis was endemic. In spite of a daily ingestion of a bacterial mixture for 10 days after birth, the incidence of diarrhea and faecal shedding was similar in treated and nontreated animals [26]. One of the limitations of studies in farm animals is the simultaneous exposure to both probiotic and parasite from birth onwards.

Interestingly, in vitro studies demonstrated the inhibitory effects of cell-free supernatants of L. acidophilus NCFM and L. reuteri strain 23272 on C. parvum and C. hominis viability and infectivity [27, 28]. Similarly, cell-free supernatants of Bacillus brevis, Enterococcus faecium, and Pseudomonas alcaligenes reduce C. parvum oocyst persistence by inducing oocyst premature excystation [29]. The compounds at the basis of such an inhibition are under investigation.

3. Giardia

Giardia lamblia (also known as Giardia intestinalis or Giardia duodenalis) is an intestinal pathogenic protozoan parasite belonging to the Diplomonad group, that causes ~280 million symptomatic human infections per year [30]. This monoxenous waterborne parasite has the capacity to infect a wide range of hosts. In humans, as little as ten environmentally resistant cysts are sufficient to initiate an infection. The cysts liberate the motile and replicative forms known as trophozoïtes during their gastrointestinal transit. These forms proliferate in the gut lumen, where they adhere to the epithelium (Figure 2). This phase is associated with the symptoms of the disease: watery diarrhea, epigastric pain, nausea, vomiting, and weight loss usually appear 6–15 days after cyst ingestion, but half of the infections remain asymptomatic. Treatments are based on metronidazole and nitroimidazole, but infections may also resolve spontaneously. T cells, neutrophiles, macrophages as well as IgM, IgG, and IgA antibodies are major players of the immune response necessary for resolution of giardiasis. T-cell cytokines may also induce production and release of antigiardial defensins [31]. Some factors, such as common variable immunodeficiency (hypogammaglobulinemy) or altered gut microflora, appear to predispose to Giardia infection [29]. Although the clinical impact has been reported to be stronger in young children and undernourished or immunodeficient individuals, there is little insight into how Giardia spp. cause the disease since the trophozoites are not invasive and secrete unknown toxins [30].

The first proposal of the use of probiotics to control infections by Giardia came from the discovery that isogenic mice presented a variable susceptibility to Giardia infection depending on their intestinal flora [32]. Interestingly, resistance to Giardia infection could be transmitted from mouse to mouse by common housing and was abrogated by using antibiotics, such as neomycin, active against the resident anaerobic flora.

An important step towards the comprehension of the probiotic activity was the discovery that the culture supernatant of the probiotic strain LA1 of Lactobacillus johnsonii was capable of controlling G. lamblia growth in vitro [33]. In this study, six other Lactobacillus acidophilus strains were also tested but did not show any noticeable effects. L. johnsonii LA1 supernatant blocked G. lamblia development in G1 phase but was apparently unable to prevent the adhesion of G. lamblia to epithelial cells. Biochemical characterization of supernatants revealed the presence of unidentified heat-sensitive low molecular weight product(s) [33]. Daily addition of live bacteria to the drinking water of gerbils, seven days before oral infection by G. lamblia cysts, protected the animals [34]. A decrease in the production of cysts in the faeces, a reduction of the prepatent phase and global better health were also observed. This treatment showed protection against the diminished nutrient absorption as well as the histological changes of the intestinal mucosa normally associated with giardiasis. Increased splenocyte responses to T-cell and B-cell mitogens, as well as to Giardia antigens, suggested that, in addition to a potential effect of extracellular factors, L. johnsonii LA1 treatment reinforced the host immune response against Giardia.

Lactobacillus casei MTCC 1423 strain as well as Enterococcus faecium SF68 were also effective in eliminating Giardia infection from mice [35, 36]. Protection was associated with a diminution of atrophied villi and infiltrating cells in the small intestine of probiotic-treated mice [35] or with an enhancement of the immune response since a production of specific anti-Giardia intestinal IgA and IgG was noticed in treated mice [36]. Recently, in vivo experimentation on malnourished mice showed that daily pretreatment with L. casei MTCC1423 efficiently reduced both the severity and the duration of giardiasis, compared to nonprobiotic-fed malnourished mice [37].

Studies performed in human patients in 1995 indicated the beneficial effect of the administration of the probiotic yeast Saccharomyces boulardii (Reflos), not directly to prevent giardiasis but to help in the recovery from postinfection irritable bowel syndrome (PI-IBS, see Section 7), a complication appearing in some patients cured from the parasite by drug treatments [38]. This observation was supported by a later study showing that S. boulardii reduced the number of parasite cysts in faeces from patients treated by the combination of S. boulardii and the drug metronidazole versus patients treated by metronidazole only [39].

While these studies converge towards the existence of a beneficial effect provided by different types of probiotics in giardiasis, additional work needs to be realized to determine whether there is a direct effect on G. lamblia development in the host or just a reduction of the pathological effects, or, more likely, a combination of both.

4. Eimeria

Eimeria is an apicomplexan parasite responsible for coccidiosis in poultry, livestock, and small animals such as rabbits, dogs, and cats. Avian coccidiosis is a major parasitic disease in poultry, with a very high economical impact [40]. Birds become infected through ingestion of sporulated oocysts that subsequently excyst to form sporozoites in the lumen of the upper intestine. These sporozoites migrate to their preferred sites of development, different between the seven species of veterinary importance. They then invade villi enterocytes and undergo a first asexual multiplication, the schizogony, leading to the release of numerous merozoites that initiate a second schizogony by infecting new epithelial cells. Macro- and microgametes are finally produced, initiating the sexual phase that yields environmental resistant oocysts that are shed in the faeces [41] (Figure 2). Drugs (e.g., amprolium, halofuginone, or polyester ionophores such as monensin lasalocid) and live vaccines are the two main control measures to fight this disease. However, drug resistance has to be managed constantly, and no new drugs have been introduced for many years. Live vaccines against coccidiosis are highly effective, based on nonattenuated and attenuated strains. They show however a low margin of safety for the former and a risk of reversion to virulence as well as expensive large-scale production for the latter. No successful approaches to develop recombinant vaccines have been reported [42]. Alternative control methods are therefore needed [43]. Probiotics have been widely used in the poultry industry, because they help maintaining the normal intestinal microflora, improve feed intake and digestion, and are capable of stimulating the immune system [44]. Only a limited number of studies have addressed their protective effect against the Eimeria species responsible for avian coccidiosis [45-49].

The administration of Primalac, a commercially available Lactobacillus-based preparation, to chicken from birth to three weeks is able to stimulate intestinal intraepithelial lymphocytes and significantly decrease (up to 75% reduction) the number of E. acervulina oocysts in the treated chickens [45]. Moreover, in birds fed on a vitamin A deficient diet, Primalac was shown to enhance birds immunity, even if, in this case, oocyst shedding was less reduced than in the previous study (up to 26%) [46]. A third series of experiments with the same general protocol but with a doubled infective dose showed a small but significant elevation of cytokine levels (γ-IFN and IL-2) together with a reduction in oocyst shedding in Primalac-treated versus control chicken, but no differences in the anti-Eimeria antibody level [47]. It was concluded that the protection level may depend upon the challenge dose but is mediated by immune stimulation as attested by elevation of the cytokines levels [47].

Other commercially available probiotic preparations (Mitomax, a combination of Pediococcus acidilactici and Saccharomyces boulardii, and Mitogrow, Pediococcus acidilactici only) were tested in chickens subsequently infected with E. tenella and E. acervulina using the experimental procedures described by Dalloul et al. [40, 48]. While Mitomax caused a 10–38% reduction in the number of shed oocysts, accompanied with an elevated level of anti-Eimeria antibodies [48], Mitogrow caused an elevation of anti-Eimeria antibodies and no significant reduction in the number of E. acervulina shed oocysts [40].

Thus, although the results converge towards the existence of a protective, though partial effect, by these different probiotic preparations against avian coccidiosis, the mechanisms involved remain currently elusive, with variable data concerning the reduction in oocyst shedding, the levels of cytokines, and anti-Eimeria antibodies.

Tierney et al. investigated the interactions between chicken-derived Lactobacillus strains and Eimeria [49]. Three Lactobacillus strains were isolated from different parts of chicken gastrointestinal tract and were tested for their capacity to prevent E. tenella invasion in vitro in a MDBK (Madin-Darby bovine kidney) cell model. All strains inhibited the invasion significantly, possibly through steric interference or competitive exclusion. The potential effect of their secreted extracellular factors was further investigated by testing Lactobacillus culture supernatants. One supernatant produced by the caecum-derived isolate Lactobacillus salivarius Lb16c6 displayed a significant activity that was marginally affected by a 30 min treatment at 100°C. The molecular principle responsible for this inhibitory effect is, however, not yet discovered.

5. Worms

In the course of their work showing that immunostimulants can induce nonspecific resistance against parasites, Bautista-Garfias et al. evaluated the capacity of viable or dead probiotic Lactobacillus casei to induce resistance against Trichinella spiralis in mice [50]. This nematode is responsible for trichinellosis, one of the most widespread and clinically important diseases in the world. Humans can be infected by eating infected food. Worms mature in the intestine of an intermediate host, such as pig, enter the blood and the lymphatic system and encyst in striated muscles. The migration of larvae causes host tissue damages and inflammatory reactions with complications, which may lead to death. The efficiency of treatments based on mebendazole or albendazole is variable. Both viable and dead L. casei ATCC7469 were administrated orally to NIH mice and induced a protective response with a significant reduction of both adult worms (58 and 44%, resp.) and larvae per gram of muscle (up to 70%). Treatment with culture supernatant of L. casei was less efficient but still showed a significant effect (32% reduction of adult worms). The authors attribute the protective effect to the production of IL-2, γ-IFN, and nitric oxide [50, 51].

Toxocara canis is an intestinal ascarid that infects primarily dogs. Humans and rodents are paratenic hosts that become infected by ingesting eggs, either on contaminated food or by geophagy. Ingested eggs hatch and spread out throughout the body, leading to symptoms associated with human toxocariasis (visceral or occular larva migrans or covert toxocariasis). Basualdo et al. reported the spectacular effect of E. faecalis CECT 7121 on T. canis larvae development in N:NIH-Swiss mice: a 90% reduction of the number of larvae in liver and lungs was measured 48 h after infection with embryonated eggs [52].

Similarly, Ascaris suum, which normally infects pigs, can also be transmitted to humans, where the migrating larvae produce liver lesions and eosinophilic pneumonitis. Probiotic treatment of sows during pregnancy and of their piglets after birth with Bifidobacterium lactis (a pig isolate) attenuate the inhibition of glucose absorption in the small intestine induced by A. suum infection, a sign associated with the parasite expulsion from the jejunum [53]. Probiotic-treated pigs still expulse A. suum normally from the intestine. Treatment appears thus to counteract a negative aspect of the response to infection related to nutrient uptake without affecting the protective immune response [53, 54].

Schistosoma mansoni, a blood-dwelling trematode worm, is the primary causative agent of bilharziosis. Human infection is initiated during water exposure to the free-swimming fork-tailed cercariae. After maturation in skin, larvae migrate through the skin, blood, lungs, and liver and finally reach the mesenteric venous plexus. Some of the eggs deposited by the female adults pass through the venule walls, cross the intestinal mucosa, and are evacuated with the fecal material. Eggs then infect their intermediate snail host, Biomphalaria glabrata. Zymomonas mobilis, a bacterium mainly known for its bioethanol-producing capabilities and originally isolated from alcoholic beverages, was reported to provide over 60% protection from the infection of S. mansoni, in mice, when orally administrated as a curative treatment (7 days after infection with cercaria) [55]. The degree of protection was determined 60 days after infection, by the number of worms recovered from the murine liver by perfusion. As far as histopathology was concerned, lesions (granulomas) in the liver and the intestine were numerous and similar in the treated and nontreated groups. Eggs were also abundant in the intestine, particularly in the jejunum-ileum part. On the contrary, the administration of Z. mobilis as a prophylactic way (7 days before infestation) did not significantly protect from infection, and worse, the combination of prophylactic and curative treatments exacerbated the symptoms.

6. Other Parasites

For other eukaryotic pathogens, the effects of probiotics have mainly been reported by one research group that demonstrated the potential effect of L. casei ATCC 7469 in the protection of nongut parasites, such as Babesia, Plasmodium, or Trypanosoma (Bautista and coworkers in Mexico).

Oral or intraperitoneal treatments of L. casei ATCC 7469 in Babesia microti (Gray strain) infected mice significantly reduced parasitemia, potentially through a stimulation of the innate immune system [56]. The protective response was improved when the lactobacilli were administered 3 days before or on the same day of parasite infection versus 7 days before. Since in B. bovis infections, the early innate response has been attributed to early appearance of IL-12 and γ-IFN transcripts in the spleen [57], it has been suggested that L. casei could enhance this protective response. The molecular mechanism is currently under investigation, through the testing of low and high molecular components isolated from lactobacilli for their capacity to induce early protective immune response against B. microti [58].

L. casei ATCC 7469 also conferred a protective effect against the malaria parasite Plasmodium chabaudi AS in NIH mice [59]. L. casei enhanced a nonspecific resistance to P. chabaudi, with longer prepatent periods (5 days versus 4 days in control mice), shorter patent periods (8 days versus 11 days in control mice), accompanied by a reduction in parasitemia and viability of parasites recovered from the spleen of treated mice. Nitric oxide concentration was increased (500% to 900%) in serum of L. casei-treated mice and was proposed to confer a protective effect upon the plasmodial infection.

The same probiotic strain also showed a protective effect against Trypanosoma cruzi (Ninoa strain), the agent of Chagas disease in NIH mice [60]. Oral or intraperitoneal doses of lactobacilli 7 days before parasite infection showed a significantly reduced parasitemia over the next 50 days. Whether the host immune response, known to be stimulated by L. casei [61] and capable of controling T. cruzi infections [62], was responsible for this protective effect is still discussed.

Finally, a beneficial effect of administration of the probiotic yeast Saccharomyces boulardii (Ultra-levure) in association with antibiotics was reported in acute amoebiasis due to Entamoeba histolytica, with significant decrease of the duration of symptoms (diarrhea, fever, abdominal pain) and presence of cysts in stools [63].

7. Postinfective Irritable Bowel Syndrome

Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder in which abdominal pain is associated with defecation or alterations in bowel habits in the absence of an organic cause [64]. The pathophysiology of IBS remains elusive but it is generally accepted that symptoms originate from a gut dysfunction and include altered motility in response to stimuli and sensory perception [65, 66]. Low-grade inflammation and immune activation are one proposed mechanism of IBS pathogenesis. The strongest recognized environmental risk factor for IBS development is bacterial gastroenteritis. Postinfective IBS (PI-IBS) patients display similar dysfunctions to those of IBS patients. As gastroenteritis disrupts intestinal microbiota, it has been proposed that correction of gut dysfunctions by commensal microbiota could offer therapeutic potential in PI-IBS patients [65, 67, 68]. Intestinal parasites, such as Blastocystis hominis, Cryptosporidium parvum, Giardia lamblia, Entamoeba histolytica, or the nematode Trichinella spiralis can cause IBS-like symptoms and may also play a possible role in the IBS etiology [66, 69, 70]. The potential of probiotics to treat IBS-like symptoms associated with parasite infection has been little evaluated. Reliable studies come from the T. spiralis model in NIH Swiss mice, which shows similarities to PI-IBS [65]. Adult worms and larvae induce functional alterations (inflammatory response, increased bowel motility, growth of smooth muscle, and modification of mucus production), which persist at least 3 weeks after parasite expulsion. None of the tested probiotics administrated orally (Lactobacillus paracasei NCC2461, L. johnsonii NCC533 (LA1), Bifidobacterium longum NCC2705, and B. lactis NCC362) interfered with parasite eviction. However, a strain specific effect was measured on the persistent muscle hypercontractibility observed in this model after recovery from infection: only L. paracasei attenuates postinfective hypercontractibility. The beneficial effect is correlated with a modulation of the immunologic response to the parasite and/or a direct or indirect effect of L. paracasei on muscle hypercontractibility. The protective activity is also present in L. paracasei-culture supernatant and is heat labile, indicating that it is probably a secreted metabolite. L. paracasei effects were further investigated using an elegant NMR-based metabolomic approach [71]. T. spiralis-infected mice showed altered metabolic profiles, which were related to intestinal hypercontractibility, muscular hypertrophy, and disrupted jejunal functions. L. paracasei treatment normalized the muscular activity and the disturbed energy metabolism. The authors concluded that L. paracasei treatment may be beneficial in patients with PI-IBS.

In a gnotobiotic T-Cell receptor-deficient mice model, C. parvum induces a persistent infection as well as IBS-like lesions in the caecum. When these mice were pre-colonized by L. reuteri and then challenged with C. parvum, fewer parasites were detected, and associated hyperplasic and inflammatory lesions were diminished [23, 70].

Although clinical evidences of efficacy begin to emerge, the overall impact of probiotics for PI-IBS treatments stays highly debated. This is mainly due to the difficulty to compare the studies because of differences in experiment design, probiotic dose and strains, and responsible agent [67, 68, 72–74].

8. Probiotic Treatments, an Emerging Therapeutic Strategy in Parasitic Diseases?

The above studies converge towards a beneficial effect of probiotics to control parasitic infections and point towards a strain-specific probiotic effect. As yet, little is known on the cellular or molecular mechanisms sustaining these effects. So far, the experimental studies on Cryptosporidium, Giardia, or Eimeria are the only ones that support a probiotic action via the secretion of an active principle that can inhibit parasite development, although the molecular nature of these components remains unknown. Probiotics have been also proposed to influence gut microflora and development of immune response. The underlying mechanisms are however not clear, involving stimulation of different subsets of immune system cells to produce cytokines, which in turn play a role in the induction and regulation of the immune response, and to enhance intestinal IgA immune responses and increase intestinal mucin production (for a review, see [75]). L. johnsonii LA1, Lactobacillus strain GG, or Bifidobacterium lactis Bb12 have all been shown to modulate IgA immune responses [75], whereas L. rhamnosus GG increased intestinal mucin production [76]. These actions may boost intestinal clearance of parasites such as Giardia and could explain the in vivo protection conferred by some probiotics [31]. Similarly, IL-10 and secretory IgA response, important actors in an efficient anti-Cryptosporidium immune response, have been shown to be induced by some probiotic strains [77]. Even if a direct link between probiotic administration, immune effectors induction, and parasite elimination has not been yet clearly established, it seems highly probable.

Proposing probiotics as alternatives to classical treatments, such as drugs or vaccines, against parasites appears unreasonable; a complementary therapeutic approach to reduce risks of infestation or to sustain classical treatments seems more realistic. For the moment, studies of probiotic effects on parasites are still in their infancy, and further investigations are needed to move forward in this direction. Several important points also need to be addressed.

The probiotics used have to be precisely characterized at a strain level.

Efforts need to be made to standardize protocols in each model (administration, dose, time, etc.). Absence of probiotic effect on cryptosporidiosis was indeed observed for short probiotic pretreatments (2 days) or concomitant contact with probiotic and pathogen [25, 26] in contrast to longer pretreatments (13 days [21, 22]). But long-term immune stimulation does not increase the effect. In a healthy subject, a great activation of the immune system cannot be conveniently obtained, because constant antigen stimulation could produce negative effects on the host, including autoimmunity [9].

More studies need to be realised, combining a larger number of pathogens as well as their corresponding host/animal models, with a greater variety of probiotics (either individually or in combination).

Another factor of variability that has to be taken into account is the gut microflora of the experimental animal models. While it is obvious that the animal genetic background is important, the environmental factors, such as hygiene conditions, feed quality, and stress, can also affect the established microflora, influencing the results of the studies [78]. To overcome such intrinsic variations, models with identical genetic background (inbred strain) and a controlled microflora, which are subject to the same feeding, are needed. Simplified models such as gnotobiotic animals (mice with a defined microflora) are invaluable tools for exploring effects of gut microorganisms as probiotics on the host [5]. It would also be interesting to monitor the establishment of the probiotics in the gut and its influence on the established microflora.

In depth understanding of the molecular mechanisms sustaining probiotic action is required to properly design future probiotic treatments. As probiotics can kill pathogens through secretion, inhibit their adhesion or invasion, inactivate toxins, or compete for nutriments, most studies focused on intestinal pathogens with the hypothesis of a local probiotic efficiency. But in vivo studies on nongut pathogens (Plasmodium, Trypanosoma, Babesia, etc.) support a remote effect provided by probiotics probably through a nonspecific immune stimulation. In all cases, a lot of effort needs to go in the elucidation of the mode of action of the promising organisms.

9. Conclusion

The concept that probiotics could control the development of eukaryotic pathogens is emerging. Therapeutic approaches with probiotics could help to reduce the risks of infestation by specific parasites or complement classical anti-parasite treatments. A better understanding of molecular mechanisms underlying the beneficial effects of probiotic on the parasite infection is essential to validate the approach. Further deeper investigations are thus needed using more defined protocols (specific probiotics and experimental models), as well as extended clinical investigations. Gnotobiotics, whose genotype and microbial status can be clearly defined and whose diet and environmental conditions can be easily controlled, could be invaluable tools to go forward in this direction.