Next Article in Journal
Rationally Designed Synthetic Haptens to Generate Anti-Ciguatoxin Monoclonal Antibodies, and Development of a Practical Sandwich ELISA to Detect Ciguatoxins
Previous Article in Journal
Aflatoxin B1 Conversion by Black Soldier Fly (Hermetia illucens) Larval Enzyme Extracts
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Toxins
Volume 11
Issue 9
10.3390/toxins11090534
toxins-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Impact of the Lipopolysaccharide Chemotype of Salmonella Enterica Serovar Typhimurium on Virulence in Gnotobiotic Piglets

by
Alla Splichalova
1,
Zdislava Splichalova
1,
Daniela Karasova
2,
Ivan Rychlik
2,
Paolo Trevisi
3,
Marek Sinkora
1 and
Igor Splichal
1,*
1
Laboratory of Gnotobiology, Institute of Microbiology, Czech Academy of Sciences, 549 22 Novy Hradek, Czech Republic
2
Department of Immunology, Veterinary Research Institute, 621 00 Brno, Czech Republic
3
Department of Agricultural and Food Sciences, University of Bologna, 40127 Bologna, Italy
*
Author to whom correspondence should be addressed.
Toxins 2019, 11(9), 534; https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11090534
Submission received: 5 August 2019 / Revised: 6 September 2019 / Accepted: 11 September 2019 / Published: 13 September 2019
(This article belongs to the Section Bacterial Toxins)
Browse Figures
Versions Notes

Abstract

:
Salmonella Typhimurium is an enteric pathogen that causes acute and chronic infections in humans and animals. One-week-old germ-free piglets were orally colonized/infected with the Salmonella Typhimurium LT2 strain or its isogenic rough ΔrfaL, ΔrfaG or ΔrfaC mutants with exactly defined lipopolysaccharide (LPS) defects. After 24 h, the piglets were euthanized and the colonization of the small intestine, translocations into the mesenteric lymph nodes, liver, spleen, lungs, and bacteremia, along with changes in the ileum histology, and transcription levels of the tight junction proteins claudin-1, claudin-2, and occludin were all assessed. Additionally, transcription levels of IL-8, TNF-α, and IL-10 in the terminal ileum, and their local and systemic protein levels were evaluated. Wild-type Salmonella Typhimurium showed the highest translocation, histopathological changes, upregulation of claudins and downregulation of occludin, transcription of the cytokines, intestinal IL-8 and TNF-α levels, and systemic TNF-α and IL-10 levels. Depending on the extent of the incompleteness of the LPS, the levels of the respective elements decreased, or no changes were observed at all in the piglets colonized/infected with Δrfa mutants. Intestinal IL-10 and systemic IL-8 levels were not detected in any piglet groups. This study provided foundational data on the gnotobiotic piglet response to colonization/infection with the exactly defined rough Salmonella Typhimurium LT2 isogenic mutants.
Keywords:
lipopolysaccharide; Salmonella Typhimurium; Δrfa mutant; cytokines; tight junction proteins; gnotobiotic; germ-free piglet
Key Contribution: Defects in the LPS of Salmonella Typhimurium reduced its virulence for germ-free piglets. The absence of O-antigen resulted in residual virulence but the absence of an outer core of LPS resulted in complete avirulence.

1. Introduction

Members of the genus Salmonella are enteric pathogens that cause acute and chronic infections in a broad range of hosts [1]. Salmonella enterica serovar Typhimurium (Salmonella Typhimurium) belongs among the most frequent non-typhoid Salmonella serovars that cause gastroenteritis in both humans and pigs [2,3]. While it can cause self-limited gastroenteritis in healthy individuals, infection with Salmonella Typhimurium can progress to a life-threatening systemic illness in immunocompromised patients [4,5].
Lipopolysaccharide (LPS) is a prominent virulence factor of Gram-negative bacteria and is the most abundant component of their cell walls. It forms a selectivity permeable barrier that restricts the entry of molecules into the bacterial cell [6] and it is composed of the lipid A, the core oligosaccharide, and the O-antigen consisting of repeating sugar units [7]. LPS can be released either from damaged Gram-negative bacteria cell wall or via outer membrane vesicles [8]. It triggers the host innate immune response during infection through recognition of the lipid A (endotoxin) by Toll-like receptor 4 complex. This initiates a signal cascade leading to production of cytokines that are crucial for clearance of infection [7]. Endotoxemia can be manifested from imperceptible dysregulation of bioactive substances [9] to life-endangering multiple organ failure induced by exaggerated levels of inflammatory mediators [10]. A completely synthesized LPS is known as the S-form (smooth). LPS may also be present in incomplete forms as semi-rough (SR) and rough (R) in the order of decreasing completion of the core oligosaccharide [11]. Constructions and experimental use of defined Salmonella enterica LPS mutants as safe oral vaccine candidates in conventional mice [12] and pigs [13] were reported. In these experiments, attention was paid to the induction of specific immunity. The innate immune response, however (a first sentinel of immune defense), was studied with partially characterized rough Salmonella enterica mutants only [14,15].
This study aimed to determine the role of specific parts of LPS, such as O-antigen, and the outer and inner core in the innate immune response and pathological changes in the gnotobiotic piglet ileum without bacterial interferences of non-defined conventional microbiota. For this purpose, we used Salmonella Typhimurium mutants with decreasing completeness of the LPS, in the direction of wild-type > ΔrfaL > ΔrfaG > ΔrfaC. We have shown previously that these mutations attenuated strains of serovars Typhimurium and Enteritidis for chickens. Moreover, these mutants differentially interacted with porcine leukocytes and exhibited differential protein secretion in vitro [16,17,18,19]. We were therefore interested in the interaction of the Δrfa mutants with an extremely sensitive model represented by germ-free piglets.
Pigs are used as an animal model in biomedical research studies due to their closely related anatomy, genetics, and physiology to humans [20], and represent a suitable animal model of human infectious diseases [21]. Moreover, the sensitivity of the pig to LPS is similar to that of humans [22] in contrast to rodents that are much more resistant [23]. Gnotobiotic animals with lowered colonization resistance [24] make it possible to study host interactions with less virulent microbes that could be suppressed in the presence of a balanced microbiota [25,26]. Colostrum-free piglets, deprived of maternal immunoglobulins and cells [27] and reared in a microbiologically controlled (gnotobiotic) isolator, can be used as a model of immunocompromised infants [28]. Salmonella Typhimurium strain LT2 [29] is known as “laboratory strain”. It induced a weak inflammatory response in the intestine of one-week-old conventional piglets [30], but it caused a strong response in germ-free piglets [31].
We hypothesized that the virulence of different rough mutants would decrease with decreasing completeness of the LPS, as found in the Δrfa mutants of Salmonella Typhimurium strain X 9241 in conventional BALB/c mice [12]. However, Salmonella Typhimurium causes in conventional mice illness similar to typhoid fever in contrast to gastroenteritis in humans and pigs [32]. To test our hypothesis, we orally colonized/infected one-week-old hysterectomy-derived colostrum-deprived germ-free piglets with the Salmonella Typhimurium LT2 strain or its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants for 24 h.

2. Results

2.1. Clinical Signs

All piglets survived for the experimental period of 24 h. The germ-free piglets inoculated with wild-type Salmonella Typhimurium developed diarrhea 10 h post-infection, and their feces changed from pale brown and pasty, to yellow and watery. They also suffered from fever, anorexia, somnolence, tachycardia, tachypnea, and tremor. The piglets infected with the ΔrfaL mutant showed similar signs. Weaker and delayed signs were expressed in the ΔrfaG-infected group. The piglets inoculated with the ΔrfaC Salmonella Typhimurium mutant less expressed clinical signs of salmonellosis than the ΔrfaG piglets.

2.2. Salmonella Colonization of the Small Intestine and Its Translocation

Wild-type Salmonella Typhimurium colonized the small intestine at the highest degree, with a median count greater than 1010 CFU/g in the ileum (Figure 1A). ΔrfaL and ΔrfaG mutants colonized the intestine at a lower density with medians around 108 CFU/g, and this decrease was statistically significant in ΔrfaL but not in the ΔrfaG mutant. Colonization ability of the ΔrfaC mutant was 6-log lower in comparison to the wild-type Salmonella Typhimurium, and 4-log lower as compared to the ΔrfaG mutant. Wild-type Salmonella Typhimurium was found in all tested organs of all piglets—mesenteric lymph nodes (Figure 1B), liver (Figure 1C), spleen (Figure 1D), and lungs (Figure 1E), and caused bacteremia (Figure 1F). Salmonella Typhimurium counts in mesenteric lymph nodes (MLN) (Figure 1B) are directly proportional to the completeness of the LPS. Translocations of ΔrfaG, and ΔrfaC mutants, but not ΔrfaL, were significantly lowered. Three out of 8 ΔrfaG and 2 out of 6 ΔrfaC, respectively, were found in the MLN of these groups. The liver translocation (Figure 1C) was detected in all WT-infected piglets, but only in 6, 5, and 0 out of 8 piglets infected with the ΔrfaL, ΔrfaG, and ΔrfaC mutants, respectively. Similarly, the wild-type Salmonella Typhimurium infected the spleen of all piglets (Figure 1D), while ΔrfaL, ΔrfaG, and ΔrfaC mutants were detected in only 6, 5 and 2 out of 8 infected piglets, respectively. All the mutants displayed low levels of lung translocation (Figure 1E).

2.3. Histopathological Changes in the Ileum

The ileum of the germ-free piglets showed long villi containing abundant vacuolated enterocytes and no signs of inflammation (Figure 2 A,B). In contrast, the ileum of the piglets infected with wild-type Salmonella Typhimurium (Figure 2C,D) was affected by acute inflammation characterized by villus atrophy, submucosal edema, vessel dilation, exudate in the lumen, the presence of neutrophils in the lamina propria, hyperemia, erosion of the epithelial layer, and peritonitis, as it is summarized in the histological score (Figure 2K). The majority of these changes, expressed at lower levels, were also found in the ΔrfaL group (Figure 2E,F,K). Hemorrhage was absent in the WT and other groups. Inflammatory changes in the ΔrfaG (Figure 2G,H) and ΔrfaC (Figure 2I,J) groups were indiscernible—with only negligible villus atrophy, vessel dilation, neutrophils in the lamina propria, and submucosal edema. Using our scoring system, the total histological score for WT, ΔrfaL, ΔrfaG, and ΔrfaC groups were evaluated as 8.2, 5.8, 1.9, and 1.9, respectively (Figure 2K).

2.4. Expression of Tight Junction Proteins Claudin-1, Claudin-2, and Occludin in the Ileum

The transcription of claudin-1 increased after the infection of the germ-free piglets with the wild-type Salmonella Typhimurium and the ΔrfaL mutant (Figure 3A). Statistical differences were observed between the WT, and the germ-free, ΔrfaG, and ΔrfaC groups. Claudin-2 transcription was increased in the WT group, and statistical differences were found between this group and the ΔrfaC group, but not other piglets (Figure 3B). Occludin (Figure 3C) showed the opposite trend than the claudins (Figure 3A,B), i.e., its transcription in the ileum of wild-type and ΔrfaL Salmonella Typhimurium-infected piglets was statistically significantly lower than in germ-free piglets. Comparable relations to other groups were found in the ΔrfaL mutant–infected piglets. However, no statistical differences were found between WT or ΔrfaL groups, or between the ΔrfaG or ΔrfaC groups.

2.5. Transcriptions of IL-8, TNF-α, and IL-10 in the Ileum, and Their Local and Systemic Levels

Wild-type Salmonella Typhimurium induced transcriptions of IL-8 (Figure 4A), TNF-α (Figure 4B), and IL-10 (Figure 4C) in the ileum, as compared to the control germ-free piglets. Only in the case of IL-8 was this induction statistically significant. IL-8 (Figure 4D) and TNF-α (Figure 4E) levels were significantly induced by wild-type Salmonella Typhimurium, and its ΔrfaL mutant, in the ileum. No IL-10 levels in the ileum (Figure 4F) or IL-8 levels in plasma (Figure 4G) were found. TNF-α in plasma (Figure 4H) was induced by wild-type Salmonella Typhimurium and was statistically different from other groups. Similarly, IL-10 was increased in plasma (Figure 4I) and was statistically different in the ΔrfaC and germ-free groups, but not in the ΔrfaL and ΔrfaG groups.

3. Discussion

Salmonella translocates beyond the intestinal barrier to the mesenteric lymph nodes (MLN) via lymphatic vessels, while less virulent strains can be trapped and destroyed [33]. Highly virulent Salmonella can spread via lymph vessels to the liver, spleen and other organs, or it can reach these sites via the blood [34]. Salmonella Typhimurium strain LT2 is avirulent for conventional piglets [30], but the germ-free piglets infected with this strain die 36–48 hrs after the infection (unpublished results). While wild-type Salmonella Typhimurium LT2 translocated to all observed organs and caused bacteremia in our experiments, its Δrfa mutants with incompletely synthetized LPS showed lowered or neglected translocation and did not cause bacteremia. These findings corresponded to the findings in conventional mice [12].
Wild-type Salmonella Typhimurium LT2 and the ΔrfaL mutant induced devastating histopathological changes in the ileum of the full-term gnotobiotic piglets, but with no hemorrhages, unlike the previous study performed in preterm hysterectomy-derived gnotobiotic piglets [28]. The mutants with more incomplete LPS chains (ΔrfaG and ΔrfaC) showed a reduced detrimental effect, as did other rough Salmonella strains of different serovars [14,33].
The intestinal epithelium, the single cell layer of epithelial cells in the gastrointestinal tract, is important for both nutrient uptake and protection of the host against bacterial translocation. The barrier function is dependent on tight junction proteins such as claudins and occludin, which join adjacent enterocytes in the apical region. This barrier can be disturbed with enteric infections [35]. Claudin-1 belongs to the group of barrier-forming claudins, and claudin-2 to the pore-forming claudins [36]. The increase in claudin-1 transcription in the ileum of the wild-type Salmonella Typhimurium-infected gnotobiotic piglets probably indicates the body’s attempt to seal the intestinal barrier to protect the piglets against excessive loss of electrolytes via diarrhea. The scope of claudin-1 induction gradually decreased in piglets infected with Δrfa mutants, with the decreasing completeness of their lipopolysaccharide chains in the direction of ΔrfaL > ΔrfaG > ΔrfaC, corroborating with decreasing severity of the infection as evaluated by clinical signs. In contrast to our finding, the conventional piglet ileum infected with Salmonella Infantis showed decreased claudin-1 protein [37]. This discrepancy should be explained by the attempt to seal the intestinal barrier from the beginning of infection, but by manifestation of its devastating effect five days post infection. Claudin-2 was increased in the ST group too. We suppose that these changes of claudin-2 with seemingly opposite function than claudin-1 [36] complete the attempt to maintain the functionality of damaged intestinal barrier. In contrast, transcription of occludin decreased in wild-type Salmonella Typhimurium and ΔrfaL mutant-infected piglets. Although occludin is also a tight junction protein and is related to the transfer of large biomolecules and cells [38], its function is much less understood than that of the claudins [36]. We were unaware of a precise mechanism of action by Salmonella Typhimurium that resulted in occludin’s expression opposite to that reported for claudins, but Salmonella Typhimurium alters the tight junctions in the epithelial barrier that result in increased bacterial translocation and induction of neutrophil transepithelial migration [39]. Similarly, neutrophil recruitment into inflamed intestine was found in Salmonella Typhimurium-induced colitis in streptomycin-treated C57Bl/6 mice [40]. Our newly obtained data are in agreement with previous findings in preterm gnotobiotic piglets colonized with probiotic Lactobacillus rhamnosus GG, and challenged with virulent Salmonella Typhimurium [41]. Other authors found that the expression of occludin protein in the conventional Salmonella Infantis-infected piglets was not influenced five days after challenge [37].
Inflammatory changes are governed by inflammatory mediators, mainly by cytokines. Salmonella Typhimurium can disrupt tight junctions, either by direct contact with epithelium or via cytokine induction [42]. To monitor piglet response to Salmonella Typhimurium challenge, we used three cytokines with different activities—chemotactic cytokine (chemokine) interleukin IL-8, a pro-inflammatory cytokine TNF-α, and a regulatory cytokine IL-10 [43]. IL-8 attracts neutrophils into inflammatory site [44], TNF-α is a pluripotent cytokine that is a potent mediator of inflammation inducible by LPS [45], and IL-10 regulates immune response to prevent an excessive inflammatory reaction [46]. Gene transcripts of all three cytokines increased in the terminal ileum of the piglets infected with wild-type Salmonella Typhimurium. Expression of these cytokines was also partially induced by the ΔrfaL mutant, while infection of piglets with ΔrfaG and ΔrfaC did not induce expression of these cytokines above the levels observed in the non-infected controls. These results, together with the above-mentioned translocations and histological changes, indicate high virulence and the stimulatory effect of wild-type Salmonella Typhimurium and decreasing virulence with the decreasing completeness of the LPS chains. This is in agreement with in vitro observations in which the ΔrfaC mutant manifested lower protein secretion and invasion compared to wild-type Salmonella Typhimurium. So the total virulence of the Salmonella enterica mutants with affected LPS might be a sum of different structure, different length and other affected processes like protein secretion and motility [16].
Only a few data are available that characterize the presence of inflammatory cytokines in intestinal content during enteric infections. Jeong et al. found significantly elevated IL-8, TNF-α, and IL-10 levels in the jejunum and ileum of gnotobiotic piglets infected with Shigella dysenteriae at 24 h post-infection [47]. Our finding of increased levels of IL-8 in the distal small intestine corresponds to the presence of neutrophils in the ileum of both wild-type Salmonella Typhimurium and ΔrfaL mutant-infected piglets. We propose that high local levels of IL-8, together with high levels of TNF-α in the intestine, in the case of wild-type Salmonella Typhimurium, exceeded normal physiological levels and contributed to the damage of the intestine itself. Lower levels of IL-8 and TNF-α in the ΔrfaL group may correspond to the protective chemoattraction of neutrophils to the inflammatory site [14] as a mechanism of protection by rough Salmonella enterica strains against subsequent infection with virulent Salmonella Typhimurium [14,15,33]. Less understandable is the absence of secreted IL-10 in the ileum of all groups, since its transcription was highly induced in wild-type Salmonella Typhimurium and ΔrfaL mutant-infected piglets. A hypothesis on the possible immaturity of the intestine and absence of cells able to secrete IL-10, or the strong degrading effect of protease-rich surroundings can be excluded because IL-10 was found in the intestine of gnotobiotic piglets of the same age infected with E. coli O55 [48]. We propose that the secretion of IL-10 in the intestine might be delayed, and measurable later than 24 hrs post-infection. This delay is probably the reason why local IL-10 did not play a role in the regulation of the inflammatory response and did not ameliorate a cytokine storm and its deleterious consequences [10].
Increased mRNA levels for IL-8 and TNF-α in different parts of the intestine, in the conventional pig infected with Salmonella Typhimurium DT104, corresponded to the concurring serum values and showed significant increases with the highest levels at 1 dpi for IL-8 and 2 dpi for TNF-α [49]. Other conventional pigs infected with Salmonella Typhimurium X4232 showed increased serum levels of IL-8, TNF-α and IL-10 two days post-infection [50]. Systemic IL-8 was not found in blood plasma of the gnotobiotic piglets infected with Salmonella Typhimurium strain LT2 or colonized with probiotic E. coli Nissle O55 or avirulent E. coli O86. However, high systemic IL-8 levels were found in the piglets with E. coli O55 infection [48,51]. In our present study, we did not detect IL-8 in the plasma of the piglets infected with wild-type Salmonella Typhimurium or any of the Δrfa mutants. This likely supports our supposition that longer time would be needed for the development of detrimental consequences of the infection with the virulent Salmonella Typhimurium, as we concluded in the case of IL-10 in the intestinal content.
Both TNF-α and IL-10 were highly increased in the plasma of wild-type Salmonella Typhimurium-infected piglets. High levels of systemic IL-10 and TNF-α indicated a poor prognosis of survival in preterm infants [52] and adult patients [53]. Similarly, in the gnotobiotic piglets, both IL-10 and TNF-α were found in E. coli O55 infected piglets ante finem [48]. High levels of IL-10 were detected in the piglets infected with wild-type Salmonella, and in lower levels in the plasma of the piglets infected with the Δrfa mutants. They were absent, however, in the plasma of the control germ-free piglets. This further contrasted with the absence of IL-10 in the intestinal lavages, and the source of the plasma IL-10 is currently unknown.

4. Conclusions

In this study, we characterized the course of infection of germ-free piglets with wild-type and Δrfa mutants of Salmonella Typhimurium. Any defect in the LPS structure correlated with reduced virulence. However, the absence of O-antigen in the ΔrfaL mutant resulted in reduced, but still detectable, residual virulence. The absence of an outer core of LPS in both ΔrfaG and ΔrfaC mutants resulted in complete avirulence. This also means that additional defects in the structure of the inner core of LPS present in ΔrfaC resulted in no further reduction in virulence, even in an extremely sensitive model of colostrum-deprived germ-free piglets. These data will be used to plan future studies in gnotobiotic piglets colonized/infected for a longer period with wild-type Salmonella Typhimurium LT2 and its Δrfa mutants, to determine suitable candidates for the induction of innate and specific immune response and protection of the piglets against subsequent infection with wild-type Salmonella Typhimurium.

5. Materials and Methods

5.1. Ethical Statement

All experiments with animals were approved by the Animal Care and Use Committee of the Czech Academy of Sciences of the Czech Republic (protocol #63/2015; date of approval: 6 September, 2015).

5.2. Salmonella Typhimurium LT2 Strain and Its Isogenic Δrfa Mutants

The wild-type LT2 strain of Salmonella enterica serovar Typhimurium (WT) and its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants with various completeness of LPS chain (Figure 5) were obtained from a collection of microorganisms of the Institute of Microbiology (Novy Hradek, Czech Republic). The mutants with different LPS chemotype were prepared by the same methods as described elsewhere [17] (Appendix A).
The bacterial inocula were prepared by the cultivation of bacteria on meat peptone agar slopes (blood agar base; Oxoid, Basingstoke, UK) at 37 °C overnight. The bacteria were taken from the agar slopes and resuspended in PBS to an approximate density of 5 × 108 colony forming units CFU/mL. The number of CFU estimated by spectrophotometry at 600 nm was verified by a cultivation method on Luria-Bertani agar (Difco Laboratories, Detroit, MI, USA) at 37 °C for 24 h. The growth of the wild-type Salmonella Typhimurium and its Δrfa mutants on the agar was comparable.

5.3. Gnotobiotic Piglets

Miniature Minnesota-derived germ-free piglets were obtained by hysterectomy as described elsewhere [28]. Briefly, hysterectomies were performed on the 112th day of gestation under isoflurane (Isoflurane; Piramal Healthcare UK, Morpeth, UK) anesthesia. The total number of 40 gnotobiotic piglets were divided into five groups with eight piglets per group. Each piglet group was created from three independent hysterectomies. The piglet groups were reared separately in positive-pressure sterile fiberglass isolators with heated floors. They were fed to satiety 6–7 times a day with an autoclave-sterilized, condensed cow’s milk-based formula (Mlekarna Hlinsko, Hlinsko, Czech Republic), using a bottle with a nipple. The following were sampled and cultivated for the presence of aerobic and anaerobic bacteria, and mold: amniotic membranes, umbilical cords, meconium, mouth and isolator surface smears after hysterectomy and later mouth, isolator surface smears, and stool twice a week. Additionally, Gram-stained rectal swabs were inspected under a light microscope.

5.4. Colonization/Infection of the Germ-Free Piglets

One-week-old germ-free piglets were orally administered 1 × 108 CFU of Salmonella Typhimurium (WT) or its isogenic LPS deletion mutants (ΔrfaL, ΔrfaG, and ΔrfaC) in 5 mL of milk diet. The control germ-free piglets received 5 mL of milk without Salmonella. Each group of piglets was created from three hysterectomies. Twenty-four h after the challenge, the piglets were euthanized, bled out via cardiac puncture under isoflurane anesthesia, and samples were collected.

5.5. Clinical Signs

The piglets were observed for the appearance of fever, anorexia, somnolence, and diarrhea.

5.6. Bacterial Colonization and Translocation

Samples of peripheral blood were cultivated both undiluted and as serial log-dilutions with PBS. Ileum lavage was obtained by cutting off a 40-cm segment of a terminal part of the small intestine containing the whole ileum and part of the jejunum, filling it with 2 mL of Dulbecco’s PBS (Life Technologies, Carlsbad, CA, USA), followed by gentle kneading, and rinsing. The vortexed intestinal lavages were diluted logarithmically in PBS. One g of each type of tissue (mesenteric lymph nodes, the liver, spleen, and lungs, respectively) was homogenized in 4 mL of deionized water in a glass piston homogenizer and serially diluted in PBS, to allow for separate analyses. The serial dilutions were aerobically cultivated on plates with LB agar (Difco Laboratories) at 37 °C for 24 h. The CFU were counted from dishes containing less than 200 colonies.

5.7. Blood Plasma and Intestinal Lavages

Citrated blood was spun at 1200× g for 10 min at 8 °C, and protease inhibitor cocktail (Roche Diagnostics, Manheim, Germany) was added to the collected plasma. The ileum lavages with added protease inhibitor cocktail (Roche Diagnostic) were spun at 2500× g for 30 min at 8 °C and supernatants were filtered through 0.2 μm nitrocellulose filters (Sartorius, Goettingen, Germany). Both the plasma and the lavage supernatants were immediately frozen and stored at −45 °C until the cytokines were measured.

5.8. Histologic Assessment

Terminal ileum samples were fixed in Carnoy’s fluid for 30 min, dehydrated and embedded in paraffin. Five μm tissue sections were cut on a Leica microtome RM2245 (Leica Microsystems, Wetzlar, Germany), stained with hematoxylin-eosin and examined under an Olympus BX 40 microscope with an Olympus Camedia C-2000 digital camera (Olympus, Tokyo, Japan). Sections were evaluated in a blinded fashion. The histological scoring was adapted from experiments with preterm piglets [41]: (i) submucosal edema (0–2 score points), (ii) polymorphonuclear neutrophils infiltration into the lamina propria (0–2 score points), (iii) villus atrophy (0–3 score points), (iv) exudate in lumen (0–2 score points), (v) vessel dilation (0–2 score points), vi) inflammatory cellularity in lymphatic vessel lumen (0–2 score points), (vii) hyperemia (0–2 score points), (viii) hemorrhage (0–2 score points), (ix) peritonitis (0–1 score points), and (x) erosion of the epithelial layer (0–3 score points). Total scores of 0–21 points were obtained.

5.9. Isolation of Total RNA and Reverse Transcription

1–2 mm-thin cross sections of the terminal ileum were placed in RNAlater (Qiagen, Hilden, Germany), and stored at −20 °C until RNA purification was performed. A Teflon piston homogenizer (Institute of Microbiology of the CAS, Novy Hradek, Czech Republic) and a Spin Tissue RNA Mini Kit (Stratec Molecular, Berlin, Germany) were used for total RNA purification according to the manufacturer’s instructions. Five hundred ng of the total RNA, with ratio absorbance at 260 and 280 nm ≥2.0 as measured in 10 mM Tris-HCl buffer (pH 7.5), were used for reverse transcription with the QuantiTect Reverse Transcription kit (Qiagen). The RNA was incubated at 42 °C for 2 min with a genomic DNA wipeout buffer. The synthesis of cDNA with a mixture of random hexamers and oligo d(T) primers was performed at 42 °C for 20 min, and then heated at 95 °C for 3 min. 180 µl of PCR quality water (Life Technologies, Carlsbad, CA, USA) was added to 20 μl of the synthetized cDNA mixture to prepare the PCR template, which was stored at −25 °C until Real-Time PCR was performed.

5.10. Real-Time PCR

To quantify specific sequences in the cDNA templates, 2 µL of cDNA template was added to 18 µL of the FastStart Universal Probe Master, which contained 100 nM LNA probe (both Roche Diagnostic, Manheim, Germany) and 500 nM each of the forward and reverse primers (Generi-Biotech, Hradec Kralove, Czech Republic) (Table 1). A heating protocol (95 °C for 10 min (1×), 95 °C for 15 s and 60 °C for 60 s (45×)) was used in the iQ5 Real-Time PCR cycler with iQ5 Optical System Software 1.0 (Bio-Rad, Hercules, CA, USA). The Cq of claudin-1, claudin-2, occludin, IL-8, TNF-α, and IL-10 was measured in duplicate, and the obtained values were normalized to the β-actin and cyclophilin A. Relative expressions were calculated by 2−ΔCT method [54] using GenEx Pro 6 software (Multid Analyses AB, Gothenburg, Sweden).

5.11. ELISA

IL‑8 was detected as described elsewhere [55], while TNF-α and IL-10 were measured by commercial kits (Life Technologies, Carlsbad, CA, USA). IL-8, TNF-α, and IL-10 were measured with the sensitivities 20 pg/mL, 15 pg/mL, and 15 pg/mL, respectively. The assays were measured in two dilutions in duplicate at 450 nm and 620 nm with the Infinite M200 microplate reader (Tecan, Grodig, Austria), and results were evaluated with Magellan 6.3 software (Tecan, Grodig, Austria).

5.12. Statistical Analysis

The counts of wild-type Salmonella Typhimurium and its isogenic Δrfa mutants in the small intestine, their translocations into different organs, and the cytokine transcription and protein levels were compared among the groups with a Kruskal-Wallis multiple comparisons test with a post-hoc Dunn’s test. One-way analysis of variance (ANOVA) with Tukey’s post-hoc test was used in the evaluation of differences in the tight junction protein transcription levels. The statistical comparisons at p < 0.05 and graphs were processed by GraphPad 6 software (GraphPad Software, La Jolla, CA, USA).

Author Contributions

Conceptualization: A.S., I.R., and I.S.; Methodology: A.S., Z.S., I.R., and I.S.; Validation: A.S. and I.S.; Formal Analysis: I.S.; Investigation: A.S., Z.S., D.K., I.R., P.T., M.S., and I.S.; Resources: A.S. and I.S.; Data Curation: A.S. and I.S.; Writing—original draft preparation: A.S., Z.S., D.K., I.R., P.T., M.S., and I.S.; Writing—Review and Editing: A.S., I.R., and I.S.; Visualization: A.S. and I.S.; Supervision: I.S.; Project Administration: A.S. and I.S.; Funding Acquisition: I.R. and I.S.

Funding

This research was funded by the grants COST LD15090 of the Ministry of Education, Youth and Sports of the Czech Republic and COST Action FA1401 of the European Cooperation in Science and Technology and by the Institutional Research concept RVO 61388971 of the Institute of Microbiology of the CAS. I.R. and D.K. were supported by the project CZ.02.1.01/0.0/0.0/16_025/0007404 of the Ministry of Education, Youth and Sports of the Czech Republic.

Acknowledgments

We give special thanks to Jana Machova, Hana Sychrovska, Jarmila Jarkovska and Vera Jenistova for animal care, microbiological work, and the processing of samples. We are grateful to Rashada Alexander for editing of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

All the mutations were generated by the one-step PCR inactivation method [56] using the primers and protocol as described previously [17]. After the selection of antibiotic-resistant clones, in which the gene of interest was replaced either with a chloramphenicol or kanamycin gene cassette, the mutation was confirmed by PCR using primers from the sequence flanking the deleted gene sequence in combination with c1 and c2, or k1 and k2 primers [56]. In all the mutants, the chloramphenicol or kanamycin gene cassettes used for the gene replacement were removed from the mutant’s genome.
The Δrfa mutants have been repeatedly characterized and tested for sensitivity to serum, resistance to P22 phage infection, and by PCR using primers both inside and also flanking the deleted sequences. All gradually accumulated data confirmed expected characteristics and therefore the identity of the Δrfa mutants.

References

  1. Hurley, D.; McCusker, M.P.; Fanning, S.; Martins, M. Salmonella-host interactions—Modulation of the host innate immune system. Front. Immunol. 2014, 5, 481. [Google Scholar] [CrossRef] [PubMed]
  2. Haraga, A.; Ohlson, M.B.; Miller, S.I. Salmonellae interplay with host cells. Nat. Rev. Microbiol. 2008, 6, 53–66. [Google Scholar] [CrossRef] [PubMed]
  3. Robarge, M.E.; Ramos-Vara, J.A. Pathology in practice. Enteric salmonellosis. J. Am. Vet. Med. Assoc. 2014, 245, 643–645. [Google Scholar] [CrossRef] [PubMed]
  4. Keestra-Gounder, A.M.; Tsolis, R.M.; Bäumler, A.J. Now you see me, now you don’t: The interaction of Salmonella with innate immune receptors. Nat. Rev. Microbiol. 2015, 13, 206–216. [Google Scholar] [CrossRef] [PubMed]
  5. Santos, R.L.; Tsolis, R.M.; Bäumler, A.J.; Adams, L.G. Pathogenesis of Salmonella-induced enteritis. Braz. J. Med. Biol. Res. 2003, 36, 3–12. [Google Scholar] [CrossRef] [PubMed]
  6. Nikaido, H. Prevention of drug access to bacterial targets: Permeability barriers and active efflux. Science 1994, 264, 382–388. [Google Scholar] [CrossRef] [PubMed]
  7. Raetz, C.R.; Whitfield, C. Lipopolysaccharide endotoxins. Annu. Rev. Biochem. 2002, 71, 635–700. [Google Scholar] [CrossRef]
  8. Beveridge, T.J. Structures of gram-negative cell walls and their derived membrane vesicles. J. Bacteriol. 1999, 181, 4725–4733. [Google Scholar]
  9. Mikolajczyk, A.; Zlotkowska, D. Subclinical lipopolysaccharide from Salmonella Enteritidis induces dysregulation of bioactive substances from selected brain sections and glands of neuroendocrine axes. Toxins 2019, 11, 91. [Google Scholar] [CrossRef]
  10. Wang, H.; Ma, S. The cytokine storm and factors determining the sequence and severity of organ dysfunction in multiple organ dysfunction syndrome. Am. J. Emerg. Med. 2008, 26, 711–715. [Google Scholar] [CrossRef]
  11. Caroff, M.; Karibian, D. Structure of bacterial lipopolysaccharides. Carbohydr. Res. 2003, 338, 2431–2447. [Google Scholar] [CrossRef] [PubMed]
  12. Kong, Q.; Yang, J.; Liu, Q.; Alamuri, P.; Roland, K.L.; Curtiss, R., III. Effect of deletion of genes involved in lipopolysaccharide core and O-antigen synthesis on virulence and immunogenicity of Salmonella enterica serovar Typhimurium. Infect. Immun. 2011, 79, 4227–4239. [Google Scholar] [CrossRef] [PubMed]
  13. Leyman, B.; Boyen, F.; Van, P.A.; Verbrugghe, E.; Haesebrouck, F.; Pasmans, F. Salmonella Typhimurium LPS mutations for use in vaccines allowing differentiation of infected and vaccinated pigs. Vaccine 2011, 29, 3679–3685. [Google Scholar] [CrossRef] [PubMed]
  14. Foster, N.; Lovell, M.A.; Marston, K.L.; Hulme, S.D.; Frost, A.J.; Bland, P.; Barrow, P.A. Rapid protection of gnotobiotic pigs against experimental salmonellosis following induction of polymorphonuclear leukocytes by avirulent Salmonella enterica. Infect. Immun. 2003, 71, 2182–2191. [Google Scholar] [CrossRef] [PubMed]
  15. Splichal, I.; Trebichavsky, I.; Splichalova, A.; Barrow, P.A. Protection of gnotobiotic pigs against Salmonella enterica serotype Typhimurium by rough mutant of the same serotype is accompanied by the change of local and systemic cytokine response. Vet. Immunol. Immunopathol. 2005, 103, 155–161. [Google Scholar] [CrossRef] [PubMed]
  16. Crhanova, M.; Malcova, M.; Mazgajova, M.; Karasova, D.; Sebkova, A.; Fucikova, A.; Bortlicek, Z.; Pilousova, L.; Kyrova, K.; Dekanova, M.; et al. LPS structure influences protein secretion in Salmonella enterica. Vet. Microbiol. 2011, 152, 131–137. [Google Scholar] [CrossRef] [PubMed]
  17. Karasova, D.; Sebkova, A.; Vrbas, V.; Havlickova, H.; Sisak, F.; Rychlik, I. Comparative analysis of Salmonella enterica serovar Enteritidis mutants with a vaccine potential. Vaccine 2009, 27, 5265–5270. [Google Scholar] [CrossRef]
  18. Matiasovic, J.; Stepanova, H.; Volf, J.; Kubala, L.; Ovesna, P.; Rychlik, I.; Faldyna, M. Influence of the lipopolysaccharide structure of Salmonella enterica serovar Enteritidis on interactions with pig neutrophils. Vet. Microbiol. 2011, 150, 167–172. [Google Scholar] [CrossRef]
  19. Stepanova, H.; Volf, J.; Malcova, M.; Matiasovic, J.; Faldyna, M.; Rychlik, I. Association of attenuated mutants of Salmonella enterica serovar Enteritidis with porcine peripheral blood leukocytes. FEMS Microbiol. Lett. 2011, 321, 37–42. [Google Scholar] [CrossRef]
  20. Lunney, J.K. Advances in swine biomedical model genomics. Int. J. Biol. Sci. 2007, 3, 179–184. [Google Scholar] [CrossRef]
  21. Meurens, F.; Summerfield, A.; Nauwynck, H.; Saif, L.; Gerdts, V. The pig: A model for human infectious diseases. Trends Microbiol. 2012, 20, 50–57. [Google Scholar] [CrossRef] [PubMed]
  22. Goldfarb, R.D.; Dellinger, R.P.; Parrillo, J.E. Porcine models of severe sepsis: Emphasis on porcine peritonitis. Shock 2005, 24 (Suppl. S1), 75–81. [Google Scholar] [CrossRef] [PubMed]
  23. Michie, H.R. The value of animal models in the development of new drugs for the treatment of the sepsis syndrome. J. Antimicrob. Chemother. 1998, 41 (Suppl. S1), 47–49. [Google Scholar] [CrossRef] [PubMed]
  24. Stecher, B.; Hardt, W.D. Mechanisms controlling pathogen colonization of the gut. Curr. Opin. Microbiol. 2011, 14, 82–91. [Google Scholar] [CrossRef] [PubMed]
  25. Tremaroli, V.; Backhed, F. Functional interactions between the gut microbiota and host metabolism. Nature 2012, 489, 242–249. [Google Scholar] [CrossRef] [PubMed]
  26. Mooser, C.; de Agüero, M.G.; Ganal-Vonarburg, S.C. Standardization in host-microbiota interaction studies: Challenges, gnotobiology as a tool, and perspective. Curr. Opin. Microbiol. 2018, 44, 50–60. [Google Scholar] [CrossRef]
  27. Salmon, H.; Berri, M.; Gerdts, V.; Meurens, F. Humoral and cellular factors of maternal immunity in swine. Dev. Comp. Immunol. 2009, 33, 384–393. [Google Scholar] [CrossRef]
  28. Splichalova, A.; Slavikova, V.; Splichalova, Z.; Splichal, I. Preterm life in sterile conditions: A study on preterm, germ-free piglets. Front. Immunol. 2018, 9, 220. [Google Scholar] [CrossRef]
  29. McClelland, M.; Sanderson, K.E.; Spieth, J.; Clifton, S.W.; Latreille, P.; Courtney, L.; Porwollik, S.; Ali, J.; Dante, M.; Du, F.; et al. Complete genome sequence of Salmonella enterica serovar Typhimurium LT2. Nature 2001, 413, 852–856. [Google Scholar] [CrossRef]
  30. Clarke, R.C.; Gyles, C.L. Virulence of wild and mutant strains of Salmonella typhimurium in ligated intestinal segments of calves, pigs, and rabbits. Am. J. Vet. Res. 1987, 48, 504–510. [Google Scholar]
  31. Trebichavsky, I.; Splichalova, A.; Rychlik, I.; Hojna, H.; Muneta, Y.; Mori, Y.; Splichal, I. Attenuated aroA Salmonella enterica serovar Typhimurium does not induce inflammatory response and early protection of gnotobiotic pigs against parental virulent LT2 strain. Vaccine 2006, 24, 4285–4289. [Google Scholar] [CrossRef] [PubMed]
  32. Barthel, M.; Hapfelmeier, S.; Quintanilla-Martinez, L.; Kremer, M.; Rohde, M.; Hogardt, M.; Pfeffer, K.; Russmann, H.; Hardt, W.D. Pretreatment of mice with streptomycin provides a Salmonella enterica serovar Typhimurium colitis model that allows analysis of both pathogen and host. Infect. Immun. 2003, 71, 2839–2858. [Google Scholar] [CrossRef] [PubMed]
  33. Dlabac, V.; Trebichavsky, I.; Rehakova, Z.; Hofmanova, B.; Splichal, I.; Cukrowska, B. Pathogenicity and protective effect of rough mutants of Salmonella species in germ-free piglets. Infect. Immun. 1997, 65, 5238–5243. [Google Scholar] [PubMed]
  34. Galen, J.E.; Buskirk, A.D.; Tennant, S.M.; Pasetti, M.F. Live Attenuated Human Salmonella Vaccine Candidates: Tracking the Pathogen in Natural Infection and Stimulation of Host Immunity. EcoSal Plus 2016, 7. [Google Scholar] [CrossRef] [PubMed]
  35. Zhang, K.; Griffiths, G.; Repnik, U.; Hornef, M. Seeing is understanding: Salmonella’s way to penetrate the intestinal epithelium. Int. J. Med. Microbiol. 2018, 308, 97–106. [Google Scholar] [CrossRef] [PubMed]
  36. Gunzel, D.; Fromm, M. Claudins and other tight junction proteins. Compr. Physiol. 2012, 2, 1819–1852. [Google Scholar] [CrossRef]
  37. Liu, X.; Xia, B.; He, T.; Li, D.; Su, J.H.; Guo, L.; Wang, J.F.; Zhu, Y.H. Oral administration of a select mixture of Lactobacillus and Bacillus alleviates inflammation and maintains mucosal barrier integrity in the ileum of pigs challenged with Salmonella Infantis. Microorganisms 2019, 7, 135. [Google Scholar] [CrossRef]
  38. Edelblum, K.L.; Shen, L.; Weber, C.R.; Marchiando, A.M.; Clay, B.S.; Wang, Y.; Prinz, I.; Malissen, B.; Sperling, A.I.; Turner, J.R. Dynamic migration of gammadelta intraepithelial lymphocytes requires occludin. Proc. Natl. Acad. Sci. USA 2012, 109, 7097–7102. [Google Scholar] [CrossRef]
  39. Kohler, H.; Sakaguchi, T.; Hurley, B.P.; Kase, B.A.; Reinecker, H.C.; McCormick, B.A. Salmonella enterica serovar Typhimurium regulates intercellular junction proteins and facilitates transepithelial neutrophil and bacterial passage. Am. J. Physiol. Gastrointest. Liver Physiol. 2007, 293, G178–G187. [Google Scholar] [CrossRef]
  40. Loetscher, Y.; Wieser, A.; Lengefeld, J.; Kaiser, P.; Schubert, S.; Heikenwalder, M.; Hardt, W.D.; Stecher, B. Salmonella transiently reside in luminal neutrophils in the inflamed gut. PLoS ONE 2012, 7, e34812. [Google Scholar] [CrossRef]
  41. Splichalova, A.; Jenistova, V.; Splichalova, Z.; Splichal, I. Colonization of preterm gnotobiotic piglets with probiotic Lactobacillus rhamnosus GG and its interference with Salmonella Typhimurium. Clin. Exp. Immunol. 2019, 195, 381–394. [Google Scholar] [CrossRef] [PubMed]
  42. Eichner, M.; Protze, J.; Piontek, A.; Krause, G.; Piontek, J. Targeting and alteration of tight junctions by bacteria and their virulence factors such as Clostridium perfringens enterotoxin. Pflugers Arch. 2017, 469, 77–90. [Google Scholar] [CrossRef] [PubMed]
  43. Splichal, I.; Splichalova, A. Experimental enteric bacterial infections in pigs. J. Infect. Dis. 2018, 218, 504–505. [Google Scholar] [CrossRef] [PubMed]
  44. Baggiolini, M.; Walz, A.; Kunkel, S.L. Neutrophil-activating peptide-1/interleukin 8, a novel cytokine that activates neutrophils. J. Clin. Investig. 1989, 84, 1045–1049. [Google Scholar] [CrossRef] [PubMed]
  45. Sedger, L.M.; McDermott, M.F. TNF and TNF-receptors: From mediators of cell death and inflammation to therapeutic giants—past, present and future. Cytokine Growth Factor Rev. 2014, 25, 453–472. [Google Scholar] [CrossRef] [PubMed]
  46. Penaloza, H.F.; Schultz, B.M.; Nieto, P.A.; Salazar, G.A.; Suazo, I.; Gonzalez, P.A.; Riedel, C.A.; Alvarez-Lobos, M.M.; Kalergis, A.M.; Bueno, S.M. Opposing roles of IL-10 in acute bacterial infection. Cytokine Growth Factor Rev. 2016, 32, 17–30. [Google Scholar] [CrossRef]
  47. Jeong, K.I.; Zhang, Q.; Nunnari, J.; Tzipori, S. A piglet model of acute gastroenteritis induced by Shigella dysenteriae Type 1. J. Infect. Dis. 2010, 201, 903–911. [Google Scholar] [CrossRef] [PubMed]
  48. Splichalova, A.; Splichal, I. Local and systemic occurrences of HMGB1 in gnotobiotic piglets infected with E. coli O55 are related to bacterial translocation and inflammatory cytokines. Cytokine 2012, 60, 597–600. [Google Scholar] [CrossRef]
  49. Collado-Romero, M.; Arce, C.; Ramirez-Boo, M.; Carvajal, A.; Garrido, J.J. Quantitative analysis of the immune response upon Salmonella typhimurium infection along the porcine intestinal gut. Vet. Res. 2010, 41, 23. [Google Scholar] [CrossRef]
  50. Knetter, S.M.; Bearson, S.M.; Huang, T.H.; Kurkiewicz, D.; Schroyen, M.; Nettleton, D.; Berman, D.; Cohen, V.; Lunney, J.K.; Ramer-Tait, A.E.; et al. Salmonella enterica serovar Typhimurium-infected pigs with different shedding levels exhibit distinct clinical, peripheral cytokine and transcriptomic immune response phenotypes. Innate Immun. 2015, 21, 227–241. [Google Scholar] [CrossRef]
  51. Splichalova, A.; Splichal, I.; Chmelarova, P.; Trebichavsky, I. Alarmin HMGB1 is released in the small intestine of gnotobiotic piglets infected with enteric pathogens and its level in plasma reflects severity of sepsis. J. Clin. Immunol. 2011, 31, 488–497. [Google Scholar] [CrossRef] [PubMed]
  52. Ng, P.C.; Li, K.; Wong, R.P.; Chui, K.; Wong, E.; Li, G.; Fok, T.F. Proinflammatory and anti-inflammatory cytokine responses in preterm infants with systemic infections. Arch. Dis. Child. Fetal Neonatal Ed. 2003, 88, F209–F213. [Google Scholar] [CrossRef] [PubMed]
  53. Gogos, C.A.; Drosou, E.; Bassaris, H.P.; Skoutelis, A. Pro- versus anti-inflammatory cytokine profile in patients with severe sepsis: A marker for prognosis and future therapeutic options. J. Infect. Dis. 2000, 181, 176–180. [Google Scholar] [CrossRef] [PubMed]
  54. Schmittgen, T.D.; Livak, K.J. Analyzing real-time PCR data by the comparative C(T) method. Nat. Protoc. 2008, 3, 1101–1108. [Google Scholar] [CrossRef] [PubMed]
  55. Splichal, I.; Muneta, Y.; Mori, Y.; Takahashi, E. Development and application of a pig IL-8 ELISA detection system. J. Immunoass. Immunochem. 2003, 24, 219–232. [Google Scholar] [CrossRef] [PubMed]
  56. Datsenko, K.A.; Wanner, B.L. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc. Natl. Acad. Sci. USA 2000, 97, 6640–6645. [Google Scholar] [CrossRef] [PubMed]
Toxins 11 00534 g001 550
Figure 1. Bacterial counts in the small intestine, mesenteric lymph nodes, liver, spleen, lungs, and blood of the gnotobiotic piglets. Salmonella Typhimurium (WT) and its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutant colony forming units (CFU) were counted in the ileum (A), mesenteric lymph nodes (MLN) (B), the liver (C), the spleen (D), the lungs (E), and the blood (F) 24 h post infection. Individual log CFU counts are depicted by circles (n = 8 in each group) and the median by a horizontal line. The Kruskal-Wallis test with Dunn’s post-hoc multiple comparisons test was used, and statistical differences p < 0.05 are denoted with different letters above the groups. The same letter above the groups indicates no statistically significant differences.
Figure 1. Bacterial counts in the small intestine, mesenteric lymph nodes, liver, spleen, lungs, and blood of the gnotobiotic piglets. Salmonella Typhimurium (WT) and its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutant colony forming units (CFU) were counted in the ileum (A), mesenteric lymph nodes (MLN) (B), the liver (C), the spleen (D), the lungs (E), and the blood (F) 24 h post infection. Individual log CFU counts are depicted by circles (n = 8 in each group) and the median by a horizontal line. The Kruskal-Wallis test with Dunn’s post-hoc multiple comparisons test was used, and statistical differences p < 0.05 are denoted with different letters above the groups. The same letter above the groups indicates no statistically significant differences.
Toxins 11 00534 g001
Toxins 11 00534 g002 550
Figure 2. Representative hematoxylin and eosin-stained cross sections of the ileum in the gnotobiotic piglets and a histological score. The ileum of one-week-old gnotobiotic piglets: germ-free piglets (GF; A,B), piglets colonized/infected with Salmonella Typhimurium strain LT2 for 24 hrs (WT; C,D) or its isogenic mutants ΔrfaL (E,F), ΔrfaG (G,H) or ΔrfaC (I,J). Bars represent 1 mm (A,C,E,G,I) and 500 μm (B,D,F,H,J) cross sections, respectively. Histological scores from the ileum of six piglets per group are depicted (K).
Figure 2. Representative hematoxylin and eosin-stained cross sections of the ileum in the gnotobiotic piglets and a histological score. The ileum of one-week-old gnotobiotic piglets: germ-free piglets (GF; A,B), piglets colonized/infected with Salmonella Typhimurium strain LT2 for 24 hrs (WT; C,D) or its isogenic mutants ΔrfaL (E,F), ΔrfaG (G,H) or ΔrfaC (I,J). Bars represent 1 mm (A,C,E,G,I) and 500 μm (B,D,F,H,J) cross sections, respectively. Histological scores from the ileum of six piglets per group are depicted (K).
Toxins 11 00534 g002
Toxins 11 00534 g003 550
Figure 3. Transcription levels of claudin-1, claudin-2, and occludin in the ileum of the gnotobiotic piglets. Claudin-1 (A), claudin-2 (B), and occludin (C) mRNA were normalized to β-actin and cyclophilin A. The relative expressions (fold change) were evaluated in the germ-free piglets (GF) and the piglets colonized/infected with wild-type Salmonella Typhimurium (WT), or its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants. One-way analysis of variance (ANOVA) with Tukey’s multiple comparisons post-hoc test was used to compare differences among the groups. The values are presented as mean + SEM. Statistical differences p < 0.05 are denoted with different letters above the columns, and the same letter shown above the column indicates no statistically significant differences. Six samples in each group were analyzed.
Figure 3. Transcription levels of claudin-1, claudin-2, and occludin in the ileum of the gnotobiotic piglets. Claudin-1 (A), claudin-2 (B), and occludin (C) mRNA were normalized to β-actin and cyclophilin A. The relative expressions (fold change) were evaluated in the germ-free piglets (GF) and the piglets colonized/infected with wild-type Salmonella Typhimurium (WT), or its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants. One-way analysis of variance (ANOVA) with Tukey’s multiple comparisons post-hoc test was used to compare differences among the groups. The values are presented as mean + SEM. Statistical differences p < 0.05 are denoted with different letters above the columns, and the same letter shown above the column indicates no statistically significant differences. Six samples in each group were analyzed.
Toxins 11 00534 g003
Toxins 11 00534 g004 550
Figure 4. Transcription levels of IL-8, TNF-α, and IL-10 in the ileum tissue and their protein levels in the ileum lavage and plasma. Transcriptions of IL-8 (A), TNF-α (B), and IL-10 (C) in the terminal ileum tissue of the germ-free piglets (GF) and the piglets colonized/infected with wild-type Salmonella Typhimurium (WT), or its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants, were normalized to β-actin and cyclophilin A. The protein levels of the same cytokines—IL-8 (D), TNF-α (E), and IL-10 (F)—in the ileum lavage and the plasma (G,H,I, respectively) were estimated. Kruskal-Wallis test with Dunn’s multiple comparison post-hoc test was used to compare the groups. The transcriptions (A–C) were measured in six piglets per group, and the protein levels (D–I) in eight piglets per group. The values are presented as mean + SEM. Statistical differences p < 0.05 are denoted with different letters above the columns and the same letter shown above the column indicates no statistically significant differences.
Figure 4. Transcription levels of IL-8, TNF-α, and IL-10 in the ileum tissue and their protein levels in the ileum lavage and plasma. Transcriptions of IL-8 (A), TNF-α (B), and IL-10 (C) in the terminal ileum tissue of the germ-free piglets (GF) and the piglets colonized/infected with wild-type Salmonella Typhimurium (WT), or its isogenic ΔrfaL, ΔrfaG, and ΔrfaC mutants, were normalized to β-actin and cyclophilin A. The protein levels of the same cytokines—IL-8 (D), TNF-α (E), and IL-10 (F)—in the ileum lavage and the plasma (G,H,I, respectively) were estimated. Kruskal-Wallis test with Dunn’s multiple comparison post-hoc test was used to compare the groups. The transcriptions (A–C) were measured in six piglets per group, and the protein levels (D–I) in eight piglets per group. The values are presented as mean + SEM. Statistical differences p < 0.05 are denoted with different letters above the columns and the same letter shown above the column indicates no statistically significant differences.
Toxins 11 00534 g004
Toxins 11 00534 g005 550
Figure 5. General structure of lipopolysaccharide [7,11]. The complete lipopolysaccharide (LPS) chain corresponds to the wild-type Salmonella Typhimurium (WT). The incompleteness of the LPS chain and corresponding chemotypes of the ΔrfaC, ΔrfaG, and ΔrfaL mutants are depicted.
Figure 5. General structure of lipopolysaccharide [7,11]. The complete lipopolysaccharide (LPS) chain corresponds to the wild-type Salmonella Typhimurium (WT). The incompleteness of the LPS chain and corresponding chemotypes of the ΔrfaC, ΔrfaG, and ΔrfaL mutants are depicted.
Toxins 11 00534 g005
Table
Table 1. LNA probe-based Real-Time PCR systems.
Table 1. LNA probe-based Real-Time PCR systems.
Gene5′-Reverse Primer-3′5′-Forward Primer-3′#LNA Probe
BACT 1TCCCTGGAGAAGAGCTACGAAAGAGCGCCTCTGGACAC9
CYPA 2 CCTGAAGCATACGGGTCCTAAAGACCACATGTTTGCCATC48
CLD-1 3CACCACTTTGCAAGCAACCTGGCCACAAAGATGGCTATT3
CLD-2 4CTCGCGCCAAAGACAGAGATGAAGATTCCACGCAACG77
OCLN 5AAAGAGCTCTCTCGACTGGATAAAAGCAGCAGCCATGTACTCTTC42
IL-8TTCTTCTTTATCCCCAAACTGGCCACATGTCCTCAAGGTAGGA41
TNF-αTCAGGGATTCAGGGATGTGTGAAGCCCCAGTTCCAATTC77
IL-10TGCCTCCCACTTTCTCTTGTTTCCTATGAGTGTAAGCGACTTTG23
1 β-actin, 2 cyclophilin A, 3 claudin-1, 4 claudin-2, 5 occludin.

Share and Cite

MDPI and ACS Style

Splichalova, A.; Splichalova, Z.; Karasova, D.; Rychlik, I.; Trevisi, P.; Sinkora, M.; Splichal, I. Impact of the Lipopolysaccharide Chemotype of Salmonella Enterica Serovar Typhimurium on Virulence in Gnotobiotic Piglets. Toxins 2019, 11, 534. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11090534

AMA Style

Splichalova A, Splichalova Z, Karasova D, Rychlik I, Trevisi P, Sinkora M, Splichal I. Impact of the Lipopolysaccharide Chemotype of Salmonella Enterica Serovar Typhimurium on Virulence in Gnotobiotic Piglets. Toxins. 2019; 11(9):534. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11090534

Chicago/Turabian Style

Splichalova, Alla, Zdislava Splichalova, Daniela Karasova, Ivan Rychlik, Paolo Trevisi, Marek Sinkora, and Igor Splichal. 2019. "Impact of the Lipopolysaccharide Chemotype of Salmonella Enterica Serovar Typhimurium on Virulence in Gnotobiotic Piglets" Toxins 11, no. 9: 534. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11090534

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop