key: cord-0001099-68eblcke
authors: Gallego, Carolina; Middleton, Andrew M.; Martínez, Nhora; Romero, Stefany; Iregui, Carlos
title: Interaction of Bordetella bronchiseptica and Its Lipopolysaccharide with In Vitro Culture of Respiratory Nasal Epithelium
date: 2013-03-11
journal: Vet Med Int
DOI: 10.1155/2013/347086
sha: 5ff8a6df6aa6e3ec16db9ff91702f691c18541df
doc_id: 1099
cord_uid: 68eblcke

The nasal septa of fetal rabbits at 26 days of gestation were harvested by cesarean section of the does while under anesthesia and then exposed to Bordetella bronchiseptica or its lipopolysaccharide (LPS) for periods of 2 and 4 hours. A total of 240 explants were used. The tissues were examined using the Hematoxylin & Eosin technique. Then, semithin sections (0.5 μm) were stained with toluidine blue and examined with indirect immunoperoxidase (IPI) and lectin histochemistry. The most frequent and statistically significant findings were as follows: (1) cell death and increased goblet cell activity when exposed to bacteria and (2) cell death, cytoplasmic vacuolation and infiltration of polymorphonuclear leukocytes when exposed to LPS. The lesions induced by the bacterium were more severe than with LPS alone, except for the cytoplasmic vacuolation in epithelial cells. IPI stained the ciliated border of the epithelium with the bacterium more intensely, while LPS lectin histochemistry preferentially labeled the cytoplasm of goblet cell. These data indicate that B. bronchiseptica and its LPS may have an affinity for specific glycoproteins that would act as adhesion receptors in both locations.

Bordetella bronchiseptica is a Gram-negative bacterium capable of colonizing the respiratory tract of a large range of mammalian hosts, including mice, rats, guinea pigs, rabbits, cats, dogs, pigs, sheep, horses, and bears [1] . B. bronchiseptica is responsible for a wide spectrum of overt respiratory diseases such as kennel cough in dogs, atrophic rhinitis in pigs, and snuffles and pneumonia in rabbits [2] [3] [4] . B. bronchiseptica can also lead to permanent asymptomatic colonization of the respiratory tract [1, 5] .

In dogs, B. bronchiseptica causes tracheobronchitis with two patterns of histological lesions. One pattern consists of focal areas of epithelial degeneration, necrosis, and cellular disorganization with vacuolation and pyknosis represented by congestion in the lamina propria, infiltrated with macrophages and lymphocytes. The second pattern consists of mucopurulent exudates that accumulate in the lumen of the airway with edema in the lamina propria, marked infiltration of polymorphonuclear leukocytes and clumps of bacteria located between the cilia of the tracheobronchial epithelium [10] .

In piglets, B. bronchiseptica can cause upper respiratory illness, leading to nonprogressive atrophic rhinitis; histologically, other common lesions include hyperplasia of the epithelium with metaplasia and deciliated cells. In rabbits, B. bronchiseptica causes a suppurative bronchopneumonia with interstitial pneumonia; histologically, peribronchial lymphocytic cuffing has been described in [1, 11] . In species other than piglets [12] [13] [14] , detailed descriptions of the initial changes in the respiratory epithelium of the nasal cavity have not been reported. Numerous B. bronchiseptica virulence factors have been implicated as being responsible for damaging the host cells. These factors include toxins such as adenylate cyclase toxin, dermonecrotic toxin, the type III secretion system, and adhesins such as filamentous hemagglutinin, pertactin, and fimbriae [15, 16] . Most of the effects of these factors have been described from in vitro studies working with isolated cell cultures exposed to the respective virulence factor.

Despite the importance of B. bronchiseptica infection in rabbits [1, 17] , as well as of the lipopolysaccharide (LPS) of B. bronchiseptica as a virulence factor, no reports on the effects of the whole microorganism or its LPS using a nasal septum culture have been documented in this species. Recent work from our group with another respiratory pathogen of rabbits, Pasteurella multocida, showed damage caused by the LPS of this pathogen to the respiratory epithelium of rabbit fetuses using the same model presented in this study [18] . In addition, the author found that the LPS of P. multocida significantly increased the number of bacteria adhering to the epithelium when this molecule was applied 30 minutes before or simultaneously with exposure to the microorganism. A similar effect has been described for the LPS of other Gram negative bacteria, such as Salmonella enterica [19] and Helicobacter pylori [20] .

The goal of this work was to detail the changes caused by B. bronchiseptica in the respiratory epithelium of the nasal septum of rabbits during the first hours of infection. Additionally, we sought to examine whether the LPS of this pathogen by itself could cause lesions that would complicate the damages caused by the bacterium. To test this, a novel experimental approach more similar to natural conditions was used, namely, a tissue culture from the nasal septum of fetal rabbits.

2.1. Bacteria. B. bronchiseptica 0301 was isolated from rabbits having clinical symptoms of rhinitis or pneumonia; the animals originated from commercial farms located on the flat plain near Bogotá, Colombia (2,600 m.a.s.l.). Samples were collected from nares or trachea, cultured on brain heart infusion agar (BHI), and were stored in 10% glycerol at −70 ∘ C until use.

Large-scale virulent B. bronchiseptica cultures were collected in BHI agar and its biomass was harvested. The bacterium was suspended in distilled water (DW) with 0.1% thimerosal at 4 ∘ C for inactivation and conservation. The cells were centrifuged at 2,500 g for 50 min in sterile DW.

Westphal and Jann's [24] phenol-hot water method was used. Inactivated bacteria were suspended in DW, treated with 90% phenol v/v for 30 min at 68 ∘ C, and stored at 4 ∘ C for 24 h. When phase separation (aqueous, phenolic interphase, and precipitate) was evident, the samples were centrifuged at 3,000 g for 30 min at 4 ∘ C [25] . The aqueous phase was separated and treated with 1 : 10 volume of 95% ethanol that was then stored for 18 h at −20 ∘ C and then centrifuged at 2,500 g for 15 min to obtain crude LPS. LPS precipitate was suspended in physiological saline solution (PSS), centrifuged at 2,000 g for 30 min, and then dialyzed against sterile DW. The LPS was quantified by the Lee and Tsai's colorimetric method [26] . LPS (25 g in 100 L PSS) was intraperitoneally inoculated into five mice to evaluate its biological activity. An additional five mice were injected with sterile PSS. The first five mice were euthanized when clinical signs appeared, and their tissues were processed by routine histopathological technique.

Hyperimmune Antisera Production. One mature sheep was used for hyperimmune antiserum production against B. bronchiseptica 0301. Next, 35 days after the first inoculation of killed B. bronchiseptica 0301 with complete Freund adjuvant was administered, one repetition with incomplete Freund adjuvant and one repetition with only the bacterium, the animal was bled. The antiserum was immunoadsorbed with fetal rabbit turbinate macerates to eliminate cross-reaction with rabbit tissues, and they were washed with PSS and diluted 1 : 25 in sterile buffer (Tris saline, pH 7.6). One mL of antiserum was admixed with 1 mL macerate, washed with PSS, and centrifuged at 133 g for 1 h at room temperature. The supernatant contained the immunoadsorbed antiserum and was kept at -20 ∘ C until use. The antiserum titer was calculated by indirect immunodot at 1 : 25-1 : 400 dilutions.

Culture. Twenty-six day pregnant does ( = 10, 240 explants) were subjected to cesarean section under aseptic conditions; they had been previously anesthetized with 5 mg/Kg xylazine, 35 mg/Kg ketamine. Fetuses were immediately euthanized by medullar sectioning. Three sequential 2-mm-thick transversal sections were obtained from the nasal cavity. The sections were then freed of skin, bone and turbinate, retaining only the nasal septum. The septa were washed tree times with Dulbecco's modified Eagle medium (MEM) high in glucose and were treated as shown in Tables 1 and 2. The septa were placed in Veterinary Medicine International 3 Changes to the respiratory epithelium exposed to whole B. bronchiseptica and to B. bronchiseptica LPS were quantitatively and semiquantitatively evaluated. Changes such as the number of vacuolated cells, number of dead cells, desquamated cells (for descriptive morphological purposes the following were accepted as cell death criteria: pyknosis and karyorrhexis, desquamated cells in the lumen with such nuclear changes and cell detritus in the lumen), and polymorphonuclear neutrophils (PMN) infiltrating the epithelium were quantified over 120 epithelial cells with a 100x objective. A semiquantitative analysis of the activity of the goblet cells, detritus and mucus in the lumen was also performed. Four fields were examined for each tissue section.

The presence and localization of bacteria on the respiratory epithelium were evaluated using Walker and Mayer's [28] IIP technique, with some modifications. The immunoadsorbed anti-B. bronchiseptica polyclonal antiserum described in Section 2.3 was used as a primary antibody; as a secondary conjugate, protein G (Sigma Biochemicals, St. Louis, MO, USA) labeled with peroxidase was used. Septa not exposed to bacteria and septa in which the primary antiserum was replaced with preimmune ovine sera were included as negative controls. Septa of rabbits suffering from a natural disease and from which B. bronchiseptica had been isolated and diagnosed by IIP and histopathology were included as positive controls. A final 1 : 50 dilution of the immunoadsorbed antiserum was used.

To detect the LPS of B. bronchiseptica in the respiratory epithelium of the nasal septum a lectin histochemical technique was implemented [29] . Briefly, nasal septa were incubated with a lectin-enzyme conjugate which consisted of lectin from Limulus polyphemus (LPA) conjugated to the alkaline phosphatase enzyme (Alkaline Phosphatase Conjugated Limulus polyphemus Lectin Horseshoe Crab, EY Laboratories Inc., USA), which binds specifically to the sugar 2-keto-3-deoxyoctonate (KDO) in the core of LPS [30] .

Experimental error was controlled for as follows: random application of treatments, blind evaluation of tissue, independence with the Durbin-Watson test and normality with Shapiro-Wilk's test. A test for comparing means was used for the proposed hypotheses, which proved to be significant.

Mice intraperitoneally inoculated with LPS showed signs compatible with endotoxemia after 36 h, including depression, nasal and ocular secretion, bristled hair, and watery feces. Macroscopically, the lungs were congested and had petechial hemorrhages in their serous membranes. Histopathologically, microcirculatory changes in the lung consisting of edema, congestion, alveolar hemorrhages and infiltration of PMN in the alveolar septa and the alveolar space were observed. In the liver, mild perivascular mononuclear inflammatory infiltrate and moderate congestion were the main findings.

Respiratory epithelial cells of the nasal septa experimentally incubated with B. bronchiseptica for 2 h or 4 h showed no statistically significant changes; in consequence, for statistical purposes the results of both experimental time points were grouped. However, the changes in the epithelium of exposed septa were significantly different than those at 0, 2, and 4 h that had not been exposed to the microorganism. Respiratory epithelial cell death (Figure 1(a) ) and PMN infiltration into the respiratory epithelium of the septa exposed to B. bronchiseptica were significantly different ( < 0.005) than negative controls. Cellular degeneration, such as cytoplasmic vacuolation and reactive changes, such as increased goblet cell activity (defined by a larger cytoplasm of the GC, protrusion above the ciliated cells and the GC liberating their content into the lumen (Figure 1(b) )), were also significantly different ( < 0.05) than the control groups (Figure 1(c) ). Cytoplasmic vacuolation of respiratory epithelial cells was present in some of the control tissues at 0 hours but was minimal (Figure 1(d) ). (e) Fetal rabbit nasal septum respiratory epithelium exposed to B. bronchiseptica. Positive staining of ciliated border is indicated (arrow). A 100x magnified IIP is shown. (f) Negative control fetal rabbit nasal septum respiratory epithelium not exposed to B. bronchiseptica. A 100x magnified IIP is shown.

of PMN into the epithelium, and increased goblet cell activity (Figure 2(a) ). All of these lesions, including death of the epithelial cells, were statistically significant when compared to control tissues ( < 0.05) (Figure 2(b) ).

3.4. Nasal Septa Exposed to B. bronchiseptica: IIP. B. bronchiseptica was observed attaching to the ciliated border over the course of 2 hours (Figure 1(e) ). Conversely, no specific staining was found in control tissues (Figure 1(f) ).

Histochemistry. The specific reaction of B. bronchiseptica LPS with lectin histochemistry was found mostly within goblet cell cytoplasm (Figure 2(c) ); controls did not show a similar reaction. 

While descriptions of the respiratory nasal epithelial lesions caused by B. bronchiseptica in piglets are well documented [12] [13] [14] , they are less so for dogs, cats, and rabbits. Additionally, a detailed study of the cellular changes caused by some of the virulence factors of this pathogen in cell cultures has been reported [31] [32] [33] . However, to the best of our knowledge, a thorough study of the cellular changes during the initial stages of the infection and the distribution of B. bronchiseptica or its LPS in an isolated manner by using a model that more closely reflects the in vivo conditions (i.e., reconstructing the architecture and cell relationships of the respiratory epithelium in a natural host of this microorganism) has not been documented. In this work, we successfully developed a nasal septa tissue culture from fetal rabbits to study the first steps of infection with B. bronchiseptica and its LPS. Tissue culture models from human trachea, lung, nasopharynx, and nasal turbinates for studying the colonization, invasion, and pathogenic effects of other microorganisms, such as Streptococcus pneumoniae, Neisseria meningitides, and Mycobacterium tuberculosis, have been previously developed [34] [35] [36] [37] [38] [39] [40] [41] . Here, we cultured the nasal septum from fetal rabbits at 26-day of gestation for 4 h without major morphological changes in the epithelial cells. Importantly, we also examined the earliest changes during the interaction between B. bronchiseptica or its LPS with that epithelium, as that is the time during which the first steps of adhesion and colonization take place.

As early as 2 hours postexposure to B. bronchiseptica or its LPS, several degenerative, reactive, and deadly changes were present in the respiratory epithelial cells. These consisted of cytoplasmic vacuolation, activation of GC, infiltration of PMN and dead cells within the epithelial layer or desquamated into the lumen.

Vacuolation is considered a sign of cellular degeneration and cell death [42, 43] . A similar finding has been described in vivo in rabbits experimentally infected with Pasteurella multocida and in rabbits with natural respiratory disease [44, 45] . Nevertheless, no previous publications have documented this lesion within the respiratory epithelium of rabbits or other species during the first hours of infection induced by B. bronchiseptica or its LPS, using similar experimental conditions as those employed in this study.

Goblet cell activity was observed after challenge with either B. bronchiseptica or its LPS; the cells were enlarged due to an apparent accumulation and enlargement of their cytoplasmic content, and a higher number of GC were observed protruding above the normal apical limit of the respiratory epithelium or were found extruding their content, which led to mucus accumulation in the luminal septa. Tesfaigzi et al. [46] stated that LPS induces an increase in the number of epithelial cells in the respiratory mucosa by increasing the quantity of GC (i.e., hyperplasia). This contention has been contradicted by other authors who have proposed that the synthesis and secretion of mucus are synchronic and do not alter the number or size of GC [47, 48] . Our study was not intended to determine whether there was GC hyperplasia, metaplasia, or hypertrophy; however, the enlargement of these cells observed in the epithelia exposed to B. bronchiseptica or its LPS could not be explained without any increase in the size of their cytoplasm. This increase need not be due to a higher synthesis of mucin, but it is more likely due to a looser arrangement (due to hygroscopy) of the granula contents or the fusion of their membranes prior to expulsion.

The mechanism by which the LPS induces mucus production is not completely understood. However, it is known that LPS increases mRNA expression of MUC5AC, MUC5B, and IL-8 and that it stimulates the secretion of both mucins (MUC5AC up to 39%, MUC5B up to 31%) and the inflammatory cytokine IL8 [49] . In vivo, increased expression of genes coding for mucin and inducing mucous metaplasia due to LPS have been demonstrated [46] ; the LPS stimulates inflammatory mediator synthesis by the PMN, which in turn drives the expression of the aforementioned genes. Given the short experimental time in our study, it would be quite difficult for a cell to perform some of these elaborated processes, during which the activation of several genes must take place. Typical morphological changes of cell death in human tracheal cell line cultures induced by B. bronchiseptica have been described [32] . Studies using B. bronchisepticainfected macrophages and various epithelial cell lineages have also documented cytotoxicity in a nonapoptotic mechanism that is type III secretory system-dependent. Nogawa et al. [31] and Kuwae et al. [33] reported that the mechanism by which B. bronchiseptica induces necrosis is mediated by the complex BopC and BopB-BopD proteins, with tyrosine phosphatase activity translocated through the secretory type III system. The activity apparently lies in the ability of BopD and BopB to induce the formation of pores in the cytoplasmic membrane of eukaryotic cells through which other effector proteins are introduced into the cytoplasm. Morphologically, the dying cells seem necrotic rather than apoptotic, showing cytoplasmic swelling and extensive membrane blebbing without nuclear changes [50] . Qualitatively, the changes induced by the B. bronchiseptica LPS were similar to those caused by the bacterium. Quantitatively, however, the two differed in that, with the exception of PMN infiltration into the epithelium, the lesions were less severe with the LPS than with the bacterium. It has been previously indicated that other pathogen-associated molecular patterns (PAMPs) expressed by the bacterium, in addition to the LPS, can induce genomic expression in host cells mediated by TLRs other than TLR4. This is further supported by the observation that live B. bronchiseptica induces a small subset of genes that are not activated by the LPS [51, 52] .

In this work, LPS induced a higher infiltration of PMN in the respiratory epithelium and the propria of nasal septa than did the bacterium. Multiple studies have demonstrated that the main inflammatory cells in tracheobronchial lavages of rats that were intranasally and intratracheally exposed to different doses (20 to 1000 g) of Pseudomonas aeruginosa LPS were neutrophils, with macrophages, lymphocytes, and eosinophils being absent. Such LPS doses are enough to initiate neutrophilic inflammation in the lungs [48, 53] . The dose used in our work was 10 g/mL (150 g final concentration); this dose closely resembles those reported by others [21] [22] [23] be explained by selective activation induced by the LPS of the PMN through its PAMP recognition receptors, more specifically through TLR4. Mann et al. [51, 54, 55] and Kirimanjeswara [56] documented TLR4 activation by B. bronchiseptica LPS and they noted its importance for PMN recruitment and cytokine production. Several proteins are required for the migration of a PMN from the venular lumen to its final destination in the epithelium, be it in the interstitial tissues or the respiratory track; all of these proteins were present and most likely expressed at high levels in the experimental tissue cultures employed in this study. However, the question of where the increased numbers of PMN observed infiltrating the epithelium of the septum came from still remains. This PMN infiltration cannot be easily explained in this study as the nasal septa were completely separated from the vascular bed of the fetuses. One hypothesis could be that these cells are in an inactive state within the remaining blood vessels or in the interstitial matrix of the nasal septum and that they are not recognizable until activated by the bacteria or their products. Additional studies are required to address this issue. However, the importance of PMN in LPS-mediated processes cannot be ignored.

Considering the similarity of the lesions caused by B. bronchiseptica and its LPS and the fact that the differences were only in quantitative terms, it is tempting to hypothesize that the lesions caused by the bacterium could simply be the result of the LPS still attached to its outer membrane. This hypothesis should be addressed in future studies. B. bronchiseptica and its LPS distribution on the nasal septum respiratory epithelium were evaluated by the indirect immunoperoxidase and lectin histochemistry techniques. B. bronchiseptica immunostaining indicated that bacteria were distributed mainly on the ciliated border of the epithelium and less frequently in detritus and mucus accumulated in the lumen. In both cases, the staining was granular in nature. On the other hand, B. bronchiseptica LPS was visualized mainly within GC cytoplasm. These results suggest that B. bronchiseptica, as well as its LPS, adhered to receptors containing glycoconjugates, be it in the glycocalyx of the interciliary space or in those produced by the GC. Filamentous hemagglutinin (FHA) of B. bronchiseptica is necessary and sufficient to mediate in vitro rat lung epithelial cell adherence [15] . The FHA of B. pertussis possesses a carbohydrate recognition domain (CRD) that mediates its attachment to the ciliated respiratory epithelial cells and macrophages in vitro. A lectinlike activity for heparin and other sulfated carbohydrates has also been identified in B. bronchiseptica and B. pertussis, which can mediate adherence to nonciliated epithelial cell lines [57] [58] [59] [60] . Regarding the LPS, it is possible that a short duration of time is needed for it to bind to its receptors, as our experiments found LPS within GC cytoplasm in the early stages of exposure. These findings could be explained by Alexander and Rietschel's [52] results, which indicated that LBP and CD14 mediated rapid cellular internalization of high molecular weight LPS aggregates. Furthermore, Huber et al. [61] proposed that the LPS could bind soluble CD14 receptors, which would permit CD14-negative cells to respond to the LPS.

In this research, we successfully established a nasal septum culture from rabbit fetuses for studying the first steps of the relationship between B. bronchiseptica or its LPS with the respiratory epithelium. Models such as these, which use a complete tissue culture instead of isolated cells, more closely reflect the natural processes of an infection and allow for an improved understanding of the initial phases of the pathogen-host interaction and further examine new preventive avenues. We also demonstrated that B. bronchiseptica and its LPS induce very similar lesions on the septal respiratory epithelium after 2 h of exposure. The lesions in the epithelial cells were mainly degenerative, early reactive, and deadly in nature and the changes induced by the whole bacterium were even more severe. The labeling of the bacterium and its GC cytoplasm mucosubstance-associated LPS suggests that B. bronchiseptica and its LPS have an affinity for interciliar and GC glycoproteins, representing their respective initial adhesion locations.

Bacterial and parasitic diseases of rabbits

The pathogenesis of turbinate atrophy in pigs caused by Bordetella bronchiseptica

Pasteurella multocida and Bordetella bronchiseptica infections in rabbits

Role of Bordetella bronchiseptica in infectious tracheobronchitis in dogs

Rabbit respiratory system: clinical anatomy, physiology and disease

Adherence of Bordetella bronchiseptica 276 to porcine trachea maintained in organ culture

Adherence of Pasteurella multocida or Bordetella bronchiseptica to the swine nasal epithelial cell in vitro

Bordetella bronchiseptica persists in the nasal cavities of mice and triggers early delivery of dendritic cells in the lymph nodes draining the lower and upper respiratory tract

Prior infection with Bordetella bronchiseptica increases nasal colonization by Haemophilus parasuis in swine

An improved system for studying the effect of Bordetella bronchiseptica on the ciliary activity of canine tracheal epithelial cells

Bordetellain

Effects of intranasal inoculation of porcine reproductive and respiratory syndrome virus, Bordetella bronchiseptica, or a combination of both organisms in pigs

Detection of respiratory pathogens in porcine lung tissue and lavage fluid

Coinfection of pigs with porcine respiratory coronavirus and Bordetella bronchiseptica

Filamentous hemagglutinin of Bordetella bronchiseptica is required for efficient establishment of tracheal colonization

Mechanisms of Bordetella pathogenesis

Epidemiology and susceptibility of pathogenic bacteria responsible for upper respiratory tract infections in pet rabbits

Exposición simultánea y secuencial al lipopolisacárido de Pasteurella multocida y a Pasteurella multocida en cultivos de fosa nasal de conejo

Different sugar residues of the lipopolysaccharide outer core are required for early interactions of Salmonella enterica serovars Typhi and Typhimurium with epithelial cells

Effects of a HP0859 (rfaD) knockout mutation on lipopolysaccharide structure of Helicobacter pylori 26695 and the bacterial adhesion on AGS cells

Endotoxin potentiates ozone-induced mucous cell metaplasia in rat nasal epithelium

Production of the acute-phase protein lipopolysaccharide-binding protein by respiratory type II epithelial cells: implications for local defense to bacterial endotoxins

Synergistic action of E. coli endotoxin and Pasteurella multocida type A for the induction of bronchopneumonia in pigs

Bacterial lipopolysaccharides: extraction with phenol-water and further applications of this procedure

Isolement et caractérisation chimique des lipopolysaccharides de type R dans une souche hypovirulente de Yersinia pestis

Quantification of bacterial lipopolysaccharides by the purpald assay: measuring formaldehyde generated from 2-keto-3-deoxyoctonate and heptose at the inner core by periodate oxidation

Histologic fixatives suitable for diagnostic light and electron microscopy

Lectin binding to formalin-fixed paraffin sections

Interaction of bacteria and fungi with lectins and lectin-like substances

The type III secreted protein BopD in Bordetella bronchiseptica is complexed with BopB for pore formation on the host plasma membrane

Ultrastructural analysis of the interactions between Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica and human tracheal epithelial cells

BopC is a novel type III effector secreted by Bordetella bronchiseptica and has a critical role in type III-dependent necrotic cell death

Smoke exposure exacerbates an ethanol-induced defect in mucociliary clearance of Streptococcus pneumoniae

Neisseria meningitidis lactate permease is required for nasopharyngeal colonization

The role of Mycobacterium avium complex fibronectin attachment protein in adherence to the human respiratory mucosa

Interaction of Mycobacterium tuberculosis with human respiratory mucosa

Investigation of mycobacterial colonisation and invasion of the respiratory mucosa

Inhibition of adherence of Mycobacterium avium complex and Mycobacterium tuberculosis to fibronectin on the respiratory mucosa

Interaction between mycobacteria and mucus on a human respiratory tissue organ culture model with an air interface

Interpreting the results of the amplified Mycobacterium tuberculosis direct test for detection of M. tuberculosis rRNA

Lesión, adaptación y muerte celular

Cellular and tissue responses to injury

Ultrastructural pathology of the upper respiratory tract of rabbits experimentally infected with Pasteurella multocida A:3

Comparación ultraestructural de fosa nasal y nasofaringe de Conejos sanos y enfermos con el síndrome de neumonía enzoótica

DNA synthesis and Bcl-2 expression during development of mucous cell metaplasia in airway epithelium of rats exposed to LPS

Noninvasive detection of endotoxin-induced mucus hypersecretion in rat lung by MRI

Ozone exposure enhances endotoxin-induced mucous cell metaplasia in rat pulmonary airways

LPS up-regulates mucin and cytokine mRNA expression and stimulates mucin and cytokine secretion in goblet cells

Bordetella type III secretion induces caspase 1-independent necrosis

Toll-like receptor 4-dependent early elicited tumor necrosis factor alpha expression is critical for innate host defense against Bordetella bronchiseptica

Bacterial lipopolysaccharides and innate immunity

LPS-induced neutrophilic inflammation and Bcl-2 expression in metaplastic mucous cells

Toll-like receptor 4 is critical to innate host defense in a murine model of bordetellosis

Comparative toll-like receptor 4-mediated innate host defense to Bordetella infection

The complex mechanism of antibody-mediated clearance of Bordetella from the lungs requires TLR4

Identification and purification of transferrin-and lactoferrin-binding proteins of Bordetella pertussis and Bordetella bronchiseptica

The adenylate cyclase toxin contributes to the survival of Bordetella pertussis within human macrophages

Adhesion of bacteria to mucosal surfaces

Combining sites of bacterial fimbriae

R-form LPS, the master key to the activation of TLR4/MD-2-positive cells