Cytotoxicity of Pseudomonas aeruginosa internal lectin PA-I to respiratory epithelial cells in primary culture
- PMID: 7927712
- PMCID: PMC303133
- DOI: 10.1128/iai.62.10.4481-4487.1994
Cytotoxicity of Pseudomonas aeruginosa internal lectin PA-I to respiratory epithelial cells in primary culture
Abstract
Pseudomonas aeruginosa is the most important bacterial pathogen associated with chronic airway infection, especially in cystic fibrosis. We addressed the question of whether the galactophilic internal lectin of P. aeruginosa (PA-I) could represent a virulence factor for the respiratory epithelium. PA-I lectin was localized in all the bacteria of P. aeruginosa ATCC 33347 as determined by immunofluorescence staining. We investigated the dose-dependent effect of P. aeruginosa PA-I lectin on the growth, the ciliary beating frequency, and the morphology of human respiratory cells in primary culture of nasal polyps collected from non-cystic fibrosis patients. PA-I lectin significantly (P < 0.01) inhibited the growth of respiratory cells at a concentration of > or = 10 micrograms/ml. The percentage of active ciliated cell surface of the cultures decreased significantly (P < 0.05) at a PA-I lectin concentration of 50 micrograms/ml. Exposed to a low concentration of PA-I lectin (10 micrograms/ml), respiratory epithelial cells showed intracytoplasmic vacuoles when examined by light and transmission electron microscopy. At a higher concentration of PA-I lectin (100 micrograms/ml), major cell damage and severe epithelial shedding occurred. These results demonstrate that the P. aeruginosa internal PA-I lectin has a dose-dependent cytotoxic effect on respiratory epithelial cells in vitro. The P. aeruginosa PA-I lectin may represent a virulence factor by contributing to the respiratory epithelial damage during P. aeruginosa respiratory infections.
Similar articles
-
Blocking of Pseudomonas aeruginosa and Chromobacterium violaceum lectins by diverse mammalian milks.J Dairy Sci. 2010 Feb;93(2):473-82. doi: 10.3168/jds.2009-2381. J Dairy Sci. 2010. PMID: 20105519
-
Purified Pseudomonas aeruginosa PA-I lectin induces gut growth when orally ingested by rats.FEMS Immunol Med Microbiol. 1995 Jun;11(3):191-5. doi: 10.1111/j.1574-695X.1995.tb00116.x. FEMS Immunol Med Microbiol. 1995. PMID: 7581270
-
Protection of human respiratory epithelium from Pseudomonas aeruginosa adherence by phosphatidylglycerol liposomes.Infect Immun. 1994 Feb;62(2):704-8. doi: 10.1128/iai.62.2.704-708.1994. Infect Immun. 1994. PMID: 8300228 Free PMC article.
-
Adhesins and receptors of Pseudomonas aeruginosa associated with infection of the respiratory tract.Microb Pathog. 1992 Oct;13(4):251-60. doi: 10.1016/0882-4010(92)90035-m. Microb Pathog. 1992. PMID: 1363702 Review.
-
Receptors in the Pseudomonas aeruginosa adherence to injured and repairing airway epithelium.Am J Respir Crit Care Med. 1996 Oct;154(4 Pt 2):S155-62. doi: 10.1164/ajrccm/154.4_Pt_2.S155. Am J Respir Crit Care Med. 1996. PMID: 8876535 Review.
Cited by
-
Cinnamide Derivatives of d-Mannose as Inhibitors of the Bacterial Virulence Factor LecB from Pseudomonas aeruginosa.ChemistryOpen. 2015 Oct 13;4(6):756-67. doi: 10.1002/open.201500162. eCollection 2015 Dec. ChemistryOpen. 2015. PMID: 27308201 Free PMC article.
-
Synthesis of β-d-galactopyranoside-Presenting Glycoclusters, Investigation of Their Interactions with Pseudomonas aeruginosa Lectin A (PA-IL) and Evaluation of Their Anti-Adhesion Potential.Biomolecules. 2019 Nov 1;9(11):686. doi: 10.3390/biom9110686. Biomolecules. 2019. PMID: 31683947 Free PMC article.
-
Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis.Int J Mol Sci. 2021 Apr 24;22(9):4448. doi: 10.3390/ijms22094448. Int J Mol Sci. 2021. PMID: 33923202 Free PMC article. Review.
-
The key role of Pseudomonas aeruginosa PA-I lectin on experimental gut-derived sepsis.Ann Surg. 2000 Jul;232(1):133-42. doi: 10.1097/00000658-200007000-00019. Ann Surg. 2000. PMID: 10862206 Free PMC article.
-
Repair Process Impairment by Pseudomonas aeruginosa in Epithelial Tissues: Major Features and Potential Therapeutic Avenues.Front Cell Infect Microbiol. 2019 May 31;9:182. doi: 10.3389/fcimb.2019.00182. eCollection 2019. Front Cell Infect Microbiol. 2019. PMID: 31214514 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources