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Attachment of Burkholderia Pseudomallei to Pharyngeal Epithelial Cells: a Title Highly Pathogenic Bacteria with Low Attachment Ability

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Attachment of Burkholderia Pseudomallei to Pharyngeal Epithelial Cells: a Title Highly Pathogenic Bacteria with Low Attachment Ability NAOSITE: Nagasaki University's Academic Output SITE Attachment of Burkholderia pseudomallei to pharyngeal epithelial cells: a Title highly pathogenic bacteria with low attachment ability Ahmed, Kamruddin; Enciso, Hernan D. R.; Masaki, Hironori; Tao, Misao; Author(s) Omori, Akemi; Tharavichikul, Prasit; Nagatake, Tsuyoshi American Journal of Tropical Medicine and Hygiene, 60(1), pp.90-93; Citation 1999 Issue Date 1999-01 URL http://hdl.handle.net/10069/20119 Copyright (c) 1999 by The American Society of Tropical Medicine and Right Hygiene This document is downloaded at: 2020-09-17T21:56:37Z http://naosite.lb.nagasaki-u.ac.jp Am. J. Trop. Med. Hyg., 60(1), 1999, pp. 90±93 Copyright q 1999 by The American Society of Tropical Medicine and Hygiene ATTACHMENT OF BURKHOLDERIA PSEUDOMALLEI TO PHARYNGEAL EPITHELIAL CELLS: A HIGHLY PATHOGENIC BACTERIA WITH LOW ATTACHMENT ABILITY KAMRUDDIN AHMED, HERNAN D. R. ENCISO, HIRONORI MASAKI, MISAO TAO, AKEMI OMORI, PRASIT THARAVICHIKUL, AND TSUYOSHI NAGATAKE Department of Internal Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan; Department of Microbiology, Chiang Mai University, Chiang Mai, Thailand Abstract. Respiratory infections are initiated by the attachment of bacteria to pharyngeal epithelial cells. We studied the attachment of Burkholderia pseudomallei to pharyngeal epithelial cells. After one, two, three, and four washes, there were 22.6 6 8.9, 15.7 6 7.0, 6.8 6 3.1, and 4.6 6 1.1 (mean 6 SD) attached bacteria/cell, respectively. If the bacterial concentration was maintained at 1 3 108 colony-forming units (cfu)/ml and three washes were done, at concentrations of 2.5 3 104,53 104, and 1 3 105 cells/ml there were 9.9 6 3.6, 3.3 6 0.8, and 2.5 6 1.1 attached bacteria/cell, respectively. If the cell concentration was kept at 2.5 3 104 cells/ml and three washes were done, at bacterial concentrations of 1 3 105,13106,13 107,13 108, and 1 3 109 cfu/ml, there were 0.3 6 0.3, 0.6 6 0.6, 1.0 6 0.2, 5.1 6 2.3, and 9.6 6 1.9 attached bacteria/cell, respectively. There were 4.8 6 1.9, 5.5 6 2.5, 5.6 6 1.9, and 6.4 6 2.6 attached bacteria/cell at 0, 30, 120, and 240 min of incubation, respectively. Pharyngeal cells from 10 persons (seven men and three women, mean 6 SD age 5 30.7 6 8.1 years, 12 experiments with a single isolate) showed that there were 7.8 6 4.3 attached bacteria/cell. It was found that the ef®ciency of attachment of this bacteria was very low (7.0 6 3.3 bacteria/cell). Electron microscopy revealed that there were no ®mbriae but a thin capsular polysaccharide layer on the surface of B. pseudomallei. Attachment to pharyngeal epithelial cells appeared to be mediated by this structure. Burkholderia pseudomallei, a gram-negative bacilli, is a the bacteria in laboratory conditions, virulence was validated natural saprophyte that can be isolated from soil, stagnant by challenging mice with B. pseudomallei. Five-week-old, streams, ponds, and rice paddies in areas endemic for me- pathogen±free, female ICR mice (Shizuoka Agricultural Co- lioidosis. This bacteria is usually transmitted by cutaneous operation Association for Laboratory Animals, Shizuoka, Ja- and respiratory routes; however cutaneous transmission is pan) were used. Animals were housed in clean conditions signi®cantly more prevalent than the respiratory route.1±3 The and were given sterile food and water. Mice were anesthe- most common form of this disease is a pulmonary infections tized by injecting them with 0.15 ml (7.5 mg) of pentobar- that ranges from acute bronchitis to overwhelming necrotiz- bital sodium (Dainabot Company Ltd., Osaka, Japan) intra- ing pneumonia. Burkholderia pseudomallei is one of the life- peritoneally. Groups of ®ve mice were challenged intraper- threatening causes of pneumonia in Southeast Asia and itoneally and intrabronchially with bacterial suspensions in northern Australia. The initial step in the pathogenesis of sterile phosphate-buffered saline (PBS) containing 1 3 105, respiratory infection is the attachment of the bacteria to the 1 3 107, and 1 3 109 colony-forming units (cfu)/ml in an pharyngeal epithelial cells. Until now no studies have been inoculum volume of 0.2 ml. Control mice were challenged done on the adherence of this bacteria to respiratory cells. intrabronchially and intraperitoneally with 0.2 ml of sterile A recent study has shown that B. pseudomallei was present PBS. After 24 hr, mortality and morbidity were determined in the pharynx of approximately half of the patients with and mice were killed by cervical dislocation. After dissec- pulmonary melioidosis, but absent in the controls.4 This in- tion, the heart and lungs were removed, suspended in an dicates that colonization of the pharynx by B. pseudomallei appropriate volume of sterile saline, homogenized, diluted in might be associated with the pathogenesis of this infection. a 10-fold series in sterile saline, inoculated onto brain-heart Therefore, this study was conducted to describe the basic infusion agar plates, and incubated overnight at 378C. aspects of attachment of B. pseudomallei to pharyngeal ep- Attachment assay. Pharyngeal cells were obtained by ithelial cells. This will lay the groundwork for exploring the scrapping the human pharynx with a swab. Cells were sus- pathogenic mechanisms of melioidosis. pended in phosphate buffer, pH 7.2, and washed three times by centrifugation at 80 3 g for 10 min (per wash) at room MATERIALS AND METHODS temperature. The attachment assay was done as described elsewhere with modi®cations.6 Unless otherwise stated, cell Bacteria. All eight strains of B. pseudomallei used were and bacterial concentrations of 2.5 3 104 cells/ml and 1 3 obtained from Chiang Mai University (Chiang Mai, Thai- 108 cfu/ml, respectively, were mixed in equal volumes, in- land) and their identi®cation was con®rmed with the API cubated in a shaking water bath at 378C for 30 min, and test system (Biomerieux S. A., Marcy l9Etoile, France).5 washed three times by centrifugation at 80 3 g for 10 min Strain SP 186 was the predominant strain used in this study. (per wash) at room temperature to remove the nonattached Bacteria were stocked in Mueller Hinton broth (Difco Lab- bacteria. Smears were made on glass slides using a cytospin oratories, Detroit, MI) containing 5% horse blood and kept procedure (Shandon Southern Products Ltd., Astmoor, Unit- at 2408C until used. Bacteria were cultured on brain-heart ed Kingdom) and Gram staining was done. Fifty cells per infusion agar (BBL, Becton Dickinson Microbiology Sys- slide were observed with the oil-immersion lens of a micro- tem, Cockeysville, MD) overnight at 378C. scope to count the attached bacteria. Virulency test in mice. To determine adverse effects on Electron microscopy. To reveal the surface structures on 90 ATTACHMENT OF B. PSEUDOMALLEI TO PHARYNGEAL EPITHELIUM 91 TABLE 1 TABLE 2 Mean number of colonies (cfu/g) isolated from lung and heart of Attachment of seven strains of Burkholderia pseudomallei to pha- mouse after different challenge doses of Burkholderia pseudom- ryngeal epithelial cells* allei No. of attached Challenge Intraperitoneal route Intrabronchial route bacteria per cell dose* Strain no.* (mean 6 SD) (cfu/ml) Lung Heart Lung Heart SP 335 3.7 6 1.1 1 3 105 No growth No growth 2 3 107 No growth SP 140 2.7 6 0.2 1 3 107 No growth No growth 3 3 109 1.1 3 104 SP 235 4.2 6 1.7 1 3 109 3.1 3 107 3 3 106 1.5 3 109 0.6 3 106 SP 237 2.3 6 0.3 * The inoculum volume was 0.2 ml. cfu 5 colony-forming units. SP R3 2.8 6 1.5 H99 1.8 6 1.0 U 232 1.9 6 0.3 * SP, H, and U indicate strains isolated from sputum, blood and urine, respectively, from B. pseudomallei and the involvement of these structures on patients with melioidosis. attachment, bacteria were analyzed by electron microscopy after the attachment assay. Specimens were prepared for transmission electron microscopy and scanning electron mi- gether for different times and washed three times. There croscopy according to a method described elsewhere.6 were 4.8 6 1.9, 5.5 6 2.5, 5.6 6 1.9, and 6.4 6 2.6 attached Statistical analysis. The Student's t-test was used for sta- bacteria/cell at 0, 30, 120, and 240 min of incubation, re- tistical analysis. Data were considered statistically signi®cant spectively. There was a signi®cant difference (P , 0.05) when P values were less than 0.05. only between the attachment at 0 and 240 min of incubation. To elucidate the attachment ability of other isolates of B. RESULTS pseudomallei, the attachment assay was done with seven strains isolated from different sources. All isolates showed After 24 hr, all mice challenged with 1 3 109 cfu/ml and similar, low-level attachment to pharyngeal epithelial cells two mice challenged with 1 3 105 cfu/ml (intrabronchially) (Table 2). Pharyngeal cells from 10 persons (seven males died. Three of the mice challenged with 1 3 105 cfu/ml and three females, mean 6 SD age 5 30.7 6 8.1 years, 12 (intrabronchially) and all mice challenged with 1 3 107 cfu/ experiments with a single isolate) showed that there were ml were sick. All mice challenged intrabronchially and all 7.8 6 4.3 attached bacteria/cell. In each attachment experi- challenged intraperitoneally with 1 3109 cfu/ml had pneu- ment, identi®cation of the gram-negative bacilli that actually monia.
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