Adhesion patterns of commensal and pathogenic Escherichia coli from humans and wild animals on human and porcine epithelial cell lines
https://doi.org/10.1186/1757-4749-5-31
© Frömmel et al.; licensee BioMed Central Ltd. 2013
Received: 25 July 2013
Accepted: 19 October 2013
Published: 4 November 2013
Abstract
Background
Different strategies of colonization or infection by E. coli result in formation of certain adhesion patterns which help also in classifying intestinal E. coli into pathotypes. Little is known about adhesion patterns and host- and tissue adaption of commensal E. coli and about E. coli originating in clinically healthy hosts carrying pathotype-specific virulence-associated genes.
Findings
Adhesion pattern of E. coli (n = 282) from humans and from 18 animal species were verified on intestinal human Caco-2 and porcine IPEC-J2 cells and, furthermore, for comparison on human urinary bladder 5637, porcine kidney PK-15 epithelial and HEp-2 cells. The analysis was carried out on 150,000 images of adhesion assays.
Adhesion patterns were very diverse; 88 isolates were completely non-adherent, whereas 194 adhered to at least one cell line with the dominant adhesion patterns “diffusely distributed” and “microcolony formation”. Adhesion patterns “chains” and “clumps” were also visible. Chain formation was mediated by the presence of epithelial cells. Clump formation was very specific on only the 5637 cell line. All enteropathogenic (eae+) E. coli (EPEC; n = 14) were able to form microcolonies which was cell line specific for each isolate. Most EPEC formed microcolonies on intestinal IPEC-J2 and Caco-2 but several also on urinary tract cells. Shigatoxin-producing (stx+) E. coli (n = 10) showed no specific adhesion patterns.
Conclusions
E. coli isolates were highly diverse. Commensal and pathogenic isolates can adhere in various forms, including diffuse distribution, microcolonies, chains and clumps. Microcolony formation seems to be a global adhesion strategy also for commensal E. coli.
Keywords
Findings
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.
Results
Adhesion patterns of E. coli
Species of isolated E. coli and detected intestinal E. coli pathotypes
Species | Number of E. coli isolates | aEPEC | tEPEC | STEC | ETEC | DAEC | |
---|---|---|---|---|---|---|---|
Mammals | |||||||
Homo sapiens | Human | 19(a) | - | - | 1 | - | 1 |
Sus scrofa domestica | Domestic pig | 22(b) | - | - | - | 1 | - |
Capreolus capreolus | Roe deer | 23(c,d) | - | - | 9 | 1 | - |
Erinaceus europaeus | European hedgehog | 22(c) | - | 1 | - | - | - |
Lepus europaeus | European hare | 8(c) | 3 | - | - | - | - |
Lutra lutra | European otter | 7(c) | - | - | - | - | - |
Martes sp. | Marten | 19(c) | 3 | - | - | - | - |
Meles meles | European badger | 7(c) | 1 | - | - | - | - |
Mus musculus | House mouse | 9(c) | - | - | - | - | - |
Oryctolagus cuniculus | European rabbit | 6(c) | - | 1 | - | - | - |
Procyon lotor | Raccoon | 22(c) | 2 | - | - | - | - |
Rattus norvegicus | Brown rat | 4(c) | - | - | - | - | - |
Sciurus vulgaris | Red squirrel | 17(c) | 2 | - | - | - | - |
Sus scrofa | Wild boar | 22(c,d) | - | - | - | - | - |
Vulpes vulpes | Red fox | 21(c) | 1 | - | - | 1 | - |
Birds | |||||||
Accipiter nisus | Eurasian sparrowhawk | 13(c) | - | - | - | - | - |
Asio otus | Long-eared owl | 5(c) | - | - | - | - | - |
Buteo buteo | Common buzzard | 14(c) | - | - | - | - | - |
Turdus merula | Common blackbird | 22(c) | - | - | - | - | - |
E. coli adhesion patterns: cell line, tissue, host cell specificity
Adhesion pattern specificity | Cell lines | Diffusely distributed | Micro-colonies | Chains | Various pattern |
---|---|---|---|---|---|
Cell line | Caco-2 | 28 | 6 | 1 | - |
IPEC-J2 | 12 | 3 | - | - | |
5637 | 10 | - | - | - | |
PK-15 | 1 | - | - | - | |
Tissue | Intestinal epithelium (Caco-2, IPEC-J2) | 16 | 9 | - | 1 |
Urinary epithelium (5637, PK-15) | 1 | - | - | - | |
Host cell | Human (Caco-2, 5637) | 9 | 8 | - | 1 |
Porcine (IPEC-J2, PK-15) | 3 | 3 | - | - | |
Unspecific | All cell lines | 8 | 20 | 3 | 12 |
Other groups of cell lines | 21 | 8 | 2 | 8 |
Number of E. coli isolates from human and 18 animal species and its adhesion patterns on Caco-2, IPEC-J2, 5637 and PK-15
Human | Domestic pig | Roe deer | Europ. hedgehog | Europ. hare | Europ. otter | Mar ten | Europ. badger | House mouse | Europ. rabbit | Rac coon | Brown rat | Red squirrel | Wild boar | Red fox | Eurasian sparrow hawk | Long-eared owl | Common buzzard | Common blackbird | sum | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Isolates | 19 | 22 | 23 | 22 | 8 | 7 | 19 | 7 | 9 | 6 | 22 | 4 | 17 | 22 | 21 | 13 | 5 | 14 | 22 | 282 |
Caco-2 | ||||||||||||||||||||
Microcolonies | 5 | 4 | 3 | 6 | 4 | - | 6 | 2 | - | 1 | 6 | 2 | 8 | 1 | 4 | - | - | 2 | 8 | 62 |
Chains | - | - | 2 | - | - | - | 3 | - | - | - | - | - | - | 2 | - | - | - | 1 | 1 | 9 |
Distributed | 5 | 5 | 5 | 1 | 3 | 5 | 2 | 4 | 3 | 4 | 8 | 1 | 8 | 1 | 3 | 8 | 3 | 7 | 8 | 84 |
Non-adherent | 9 | 13 | 13 | 15 | 1 | 2 | 8 | 1 | 6 | 1 | 8 | 1 | 1 | 18 | 14 | 5 | 2 | 4 | 5 | 127 |
IPEC-J2 | ||||||||||||||||||||
Microcolonies | 3 | 3 | 2 | 6 | 3 | - | 7 | 2 | - | 2 | 2 | 2 | 5 | - | 6 | 1 | - | 1 | 7 | 52 |
Chains | - | - | - | 1 | - | - | - | - | - | - | - | - | - | 2 | - | - | - | 1 | 1 | 5 |
Distributed | 7 | 4 | 3 | 5 | - | 2 | 7 | 2 | 3 | 1 | 1 | - | 3 | 1 | - | 3 | 1 | 3 | 9 | 55 |
Non-adherent | 9 | 15 | 18 | 10 | 5 | 5 | 5 | 3 | 6 | 3 | 19 | 2 | 9 | 19 | 15 | 9 | 4 | 9 | 5 | 170 |
5637 | ||||||||||||||||||||
Microcolonies | 1 | 2 | 4 | 5 | 1 | - | 5 | 1 | - | 1 | 4 | 2 | 4 | 1 | 3 | - | - | 1 | 4 | 39 |
Chains | - | - | 1 | - | - | - | 1 | - | - | - | - | - | - | 2 | - | - | - | - | 2 | 6 |
Clumps | 1 | - | - | - | - | - | - | - | - | - | - | - | 1 | - | - | - | - | - | - | 2 |
Distributed | 6 | 5 | 2 | 2 | 2 | 2 | 3 | - | - | - | 3 | - | 3 | 5 | 3 | 2 | 1 | 2 | 2 | 43 |
Non-adherent | 11 | 15 | 16 | 15 | 5 | 5 | 10 | 6 | 9 | 5 | 15 | 2 | 9 | 14 | 15 | 11 | 4 | 11 | 14 | 192 |
PK-15 | ||||||||||||||||||||
Microcolonies | 6 | 2 | 3 | 2 | 2 | - | 4 | 1 | - | 2 | 2 | 2 | 2 | - | 4 | - | - | 1 | 6 | 39 |
Chains | - | - | 1 | - | - | - | 1 | - | - | - | - | - | - | 2 | - | - | - | 1 | 1 | 6 |
Distributed | 2 | 3 | 1 | 1 | 1 | - | 3 | 1 | 1 | 2 | - | 1 | 3 | 1 | 4 | 3 | 1 | 5 | 1 | 34 |
Non-adherent | 11 | 17 | 18 | 19 | 5 | 7 | 11 | 5 | 8 | 2 | 20 | 1 | 12 | 19 | 13 | 10 | 4 | 7 | 14 | 203 |
E. coli adhesion patterns of commensal E. coli and tEPEC. Fluorescent images of epithelial cells and adherent bacteria which were stained with propidium iodide are depicted. A) E. coli isolate from a domestic pig adhering diffusely distributed to IPEC-J2 cells. B) E. coli isolate from a European hare forming microcolonies on Caco-2 cells. C) E. coli isolate from a human forming clumps on 5637 cells. D) E. coli isolate from a common blackbird forming microcolonies on 5637 cells. E) E. coli isolate from a wild boar forming chains on PK-15 cells. F) tEPEC isolate from a European hedgehog forming microcolonies on 5637 cells. Scale: 10 μm.
Chain formation of one E. coli isolate from a common blackbird. Fluorescence images were taken after incubation in LB medium (overnight), cell culture media (four hours) and after incubation on epithelial cells (four hours). Chain formation is induced by cell culture media, and stimulated by epithelial cells. Isolate in A) LB medium: no chains, B) Caco-2 cell culture medium, C) 5637 cell culture medium, D) IPEC-J2 and PK-15 cell culture medium. Isolate after four-hour adhesion assay with cell culture media on E) Caco-2, F) 5637, G) PK-15 cells. H) Isolate after four-hour adhesion assay with LB media on IPEC-J2 cells. A- D) Phase contrast microscopy. E- H) Fluorescence microscopy. Scale: 10 μm.
Associations between pathotypes and adhesion patterns
Adhesion pattern formation of 14 eae A + E. coli isolates on four epithelial cells and on HEp- 2 cells after six- hour incubation. Microcolonies were formed on IPEC-J2 (10 aEPEC, 2 tEPEC), Caco-2 (10 aEPEC, no tEPEC), HEp-2 (7 aEPEC, 1 tEPEC), PK-15 (2 aEPEC, 1 tEPEC) and 5637 cells (2 aEPEC, no tEPEC).
Discussion and conclusion
In contrast to conventional adhesion studies which include relatively low numbers of isolates and cell lines, the present study included 282 E. coli isolates and their adhesion patterns on four cell lines. To handle such large sample numbers, assays were adapted to the 96-well cell culture format and to the fluorescence microscopy-based technology[5].
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.
Methods
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
Primers for VAGs of E. coli
Genes | Primer and probe sequences | Fragment length | Accession | Source of primer | |
---|---|---|---|---|---|
(5′ 3 f: forward; r: reverse) | |||||
Multiplex PCR | |||||
ipa H | f | GTTCCTTGACCGCCTTTCCGATACCGTC | 619 | M32063 | [17] |
r | GCCGGTCAGCCACCCTCTGAGAGTAC | ||||
daa D | f | TGAACGGGAGTATAAGGAAGATG | 371 | AY525531.1 | [17] |
r | GTCCGCCATCACATCAAAA | ||||
elt B | f | TCTCTATGTGCATACGGAGC | 322 | EU113252.1 | [17] |
r | CCATACTGATTGCCGCAAT | ||||
eae A | f | CCTGGTTACAACATTATGGAACG | 287 | AJ308550.1 | [4] |
r | TGAAATAGTCTCGCCAGTATTCG | ||||
stx 2 | f | GGCACTGTCTGAAACTGCTCC | 255 | FN252459 | [17] |
r | TCGCCAGTTATCTGACATTCTG | ||||
agg R | f | CGTAAGCCGGGTATGAAAGA | 188 | Z32523.1 | [4] |
r | GCCAGTTCAGAAGCAGGAAC | ||||
est 1a | f | TTTCCCCTCTTTTAGTCAGTCAA | 159 | M25607.1 AY342057.1 | [17] |
r | GCAGGATTACAACACAATTCACAGCAG | ||||
stx 1 | f | CTGGATTTAATGTCGCATAGTG | 150 | HM367099.1 | [17] |
r | AGAACGCCCACTGAGATCATC | ||||
est 2 | f | CTATTGCTACAAATGCCTATGC | 126 | M35586.1 | [4] |
r | CTCCAGCAGTACCATCTCTA | [18] | |||
Single PCR | |||||
pEAF | f | CAGGGTAAAAGAAAGATGATAA | 397 | X76137.1 | [16] |
r | TATGGGGACCATGTATTATCA |
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.
Declarations
Acknowledgements
This work was supported by InnoProfile IP 03 IP 611 funded by the Bundesministerium für Bildung und Forschung (BMBF, Germany).
Authors’ Affiliations
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