Adhesion patterns of commensal and pathogenic Escherichia coli from humans and wild animals on human and porcine epithelial cell lines

Background

The occurrence of bacterial virulence factors coded by virulence-associated genes (VAGs) indicates different host infection mechanisms and adhesion patterns, and can be used to define intestinal E. coli pathotypes[1]. Pathotype-specific VAGs frequently detected in E. coli from diarrheic hosts can also be found in E. coli from clinically healthy hosts[2, 3]. It is neither known if such isolates display adhesion patterns similar to their pathogenic counterparts nor whether their adhesion or infection patterns are host-specific and tissue-specific. Moreover, no information is available regarding host- or tissue-specific adhesion patterns of E. coli without VAGs (commensals). We analyzed adhesion patterns of 282 intestinal E. coli isolates on four epithelial cell lines. Due to such a large amount of isolates, we created an automatic imaging method based on fluorescence microscopy.

Adhesion patterns of E. coli

We identified four adhesion pattern of all E. coli: (i) diffusely distributed single bacteria; (ii) microcolonies; (iii) chains; and (iv) clumps (Figure 1). Isolates formed one adhesion pattern on one cell line only (cell line-specific), on all cell lines (both, host cell-unspecific and tissue-unspecific), on urinary tract or intestinal cells (tissue-specific) or on human or porcine cells (host cell-specific) (Table 2). There was no species-specific adhesion pattern which means that E. coli isolates from one animal host displayed diverse adhesion patterns on one cell line (Table 3). Two isolates formed clumps on cell line 5637 (Figure 1C) but were distributed diffusely or formed microcolonies on other cell lines. Chain formation could be identified in eleven isolates and was unspecific. Chain formation was inducible by cell culture medium as well as by the epithelial cells themselves (Figure 2).

Associations between pathotypes and adhesion patterns

EPEC: We tested the microcolony formation of EPEC on intestinal and urinary tract cells and on the model cell line HEp-2. All eae A⁺ isolates formed microcolonies on at least two cell lines but no isolate formed microcolonies on all cell lines. aEPEC formed microcolonies on IPEC-J2 (10 aEPEC), Caco-2 (10), HEp-2 (7), PK-15 (2) and 5637 cells (2) (Figure 3) STEC: All STEC were non-adherent to any tested cell line with the exception of 6 STEC; 5 were low adherent on Caco-2 cells; one was low adherent on human cells ETEC: A consistent adhesion pattern was not observed for the three ETEC daa D⁺ DAEC. The one human daa D⁺ DAEC adhered diffusely to human intestinal and urinary tract and also to HEp-2 cells but did not adhere to porcine cells.

Adhesion patterns of commensals

The expression of different bacterial adhesins binding on host cell receptors drives bacterial tissue and host specificity[6, 7]. We demonstrated that most isolates had different adhesion patterns on different cell lines. However, there were also isolates which had one adhesion pattern on all cell lines. This indicates the broad spectrum of adhesin-receptor interactions of E. coli in the intestinal and urinary tract. Microcolony formation was more unspecific than diffuse distribution, thus indicating that microcolony formation is less dependent on cell type specific receptors or response.

It is well known that EPEC forms microcolonies. This has also been demonstrated in the case of our 14 eae A⁺ isolates. However, there were other 61 isolates which also formed microcolonies but were intimin-negative according to our PCR which was able to detect all known intimin types. This shows that microcolony formation is more of a global adhesion and colonization strategy which ensues resistance to environmental or host immunological stresses[8, 9].

E. coli chain formation was just recently published by Gioppo et al. (2000) and Vejborg and Klemm (2009)[10, 11]. Our isolates did not form chains in pure LB medium but in cell culture media or on epithelial cells which is in contrast to these previous studies[11]. This, and the fact that chains were longer on cells than chains in cell culture media alone, showed that epithelial cells mediated E. coli chain formation.

Two isolates of our study exhibited a very unique adhesion pattern on 5637 cells only. They formed large clumps of several thousand bacteria which was not been described so far. We assume these two isolates have a high potential for biofilm formation.

Adhesion patterns of intestinal pathogens

EPEC: All 14 intimin-positive isolates formed microcolonies on at least two cell lines verifying that these isolates are indeed EPEC. Host cell-unspecific and tissue-unspecific microcolony formation of some isolates showed that microcolony formation can be a universal infection mechanism. Other isolates showed tissue or host tropism which often depends on different intimin subtypes. Interestingly, several EPEC formed microcolonies on urinary tract epithelial cells, a fact which has not previously been recorded and which might contribute to E. coli urinary tract infections. Finally, IPEC-J2 turned out to be a better model cell line for the verification of the EPEC phenotype than HEp-2 cells and may represent an additional valuable diagnostic tool. STEC: In general, the adhesion of STEC isolates to any tested cell line was very low, supporting the non-adhesive infection mechanism of STEC[12]. ETEC and DAEC: As we detected only 3 ETEC and only 1 DAEC, we have not gone into any discussion about adhesion pattern specificity here.

In conclusion, adhesion patterns as well as host and tissue specificity varied broadly between isolates. Since diffuse adherence was also detected for many commensal E. coli, any characterization of pathogenic DAEC based solely on the determination of pattern formation would appear to be unsuitable. Since many commensal isolates also formed microcolonies, this adhesion pattern must be recognized as a global colonization strategy.

Bacterial isolates

Isolates are listed in Table 1. Identification and confirmation of E. coli is extensively described elsewhere[4, 13–15]. Hemolytic isolates were excluded from analysis as they destroy cell monolayers. For human samples, sample collection was performed by individuals themselves using sterile collection tubes. The samples represented the negative controls of a clinical study. Participants were prospectively informed about the potential usage of redundant stool samples for research purpose; no written informed consent was obtained from patients. All associated information relating to these samples was anonymous. This study was approved by the Ministry of Environment, Health and Consumer Protection of the Federal State of Brandenburg, Germany (V3-2347-8-39-1-2011).

Multiplex PCR assay

E. coli adhesion assays

All cells were grown and adhesion assays were carried out as previously described[4, 19]. E. coli were grown overnight to an OD₆₀₀ of 0.8-1.2. Cells were inoculated with an infection dose of 62,500 bacteria per mm² of a monolayer using a conversion of 3x10⁸ bacteria/mL/OD₆₀₀. After four hour incubation and washing with 1xPBS, cells and adherent bacteria were fixed with 4% paraformaldehyde. Cells and bacteria were stained with propidium iodide (10 μg/mL in ddH₂O) and analyzed. All tests were repeated at least three times in triplicates. To verify the EPEC phenotype, eae A⁺ isolates were carried out with six hours incubation time on epithelial cells including one additional washing step after three hours. The term “diffuse adherent” was used exclusively to refer to daa D⁺ DAEC. A similar pattern of isolates not containing daa D was defined as “diffuse distributed”.

VideoScan/Aklides­: fluorescence imaging technology

The VideoScan technology implemented in the commercially available Aklides System (Medipan GmbH, Dahlewitz/Berlin, Germany) is a versatile fluorescence microscope imaging technology which can be used to analyze fluorescent objects[4, 5, 20–22]. The VideoScan/Aklides instrument automatically aligned itself to each well on a 96-well plate, focused on the cell monolayer surface and captured images[4]. A minimum cell monolayer area of 0.3 mm² per well was investigated. All 150,000 images were visually analyzed for E. coli pattern formation. Isolates whose images resembled those of the negative control (cells without bacterial incubation) were defined as non-adherent.