[Phenotypic evaluation of hydrophobicity and the ability to produce biofilm in coagulase-negative staphylococci isolated from infected very-low-birthweight newborns].

Monika Grzebyk, Wloch Monika Brzychczy-, Anna Piotrowska, Pawel Krzyściak, Piotr B Heczko, Malgorzata Bulanda
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Abstract

Introduction: Coagulase-negative staphylococci (CNS), particularly Staphylococcus epidermidis and Staphylococcus haemolyticus, are the leading cause of infection among infants with very low birth weight (<1500 g). The most important virulence factor of these pathogens is their ability to form biofilm. The aim of this study was to evaluate the surface properties, the ability to produce slime and biofilm formation of S. epidermidis and S. haemolyticus strains isolated from infections in very low birth weight neonates.

Methods: Isolates ofS. epidermidis (n=60) and S. haemolyticus (n=38) were obtained from neonates, hospitalized in two neonatal intensive care units in Poland. Cell surface hydrophobicity was determined by autoagglutination test (AA) in 0.9% NaCl and salt aggregation test (SAT) in ammonium sulphate solution. In order to determine the ability to produce slime, Christiensen's tube test with safranin staining and Congo Red Agar (CRA) test were carried out. The quantitative assessment of biofilm production was determined by crystal violet (CV) assay.

Results: Based on the AA test, it was demonstrated that almost all S. epidermidis and S. haemolyticus isolates showed no agglutination in sodium chloride saline. The SAT test indicated that the greatest number ofS. epidermidis isolates aggregated in concentration of 2 M, whereas, for S. haemolyticus, it was 0.5 M. In the Christiensen's method, the largest amount of the S. epidermidis isolates produced a small amount of slime (40%), whereas 68% of the S. haemolyticus isolates produced a large amount of slime. In CRA test, in both species, the most common result was the bacterial culture colour being almost black, which corresponds to low production of biofilm. Quantitative assessment of biofilm production in CV assay revealed that while 97% of the S. heamolyticus isolates produced high levels of biofilm, similar results were observed in only 43% of the S. epidermidis isolates.

Conclusions: Based on the results obtained by phenotypic methods, it was demonstrated that the S. haemolyticus isolates showed a statistically significant stronger ability to produce mucus and form biofilm than the isolates ofS. epidermidis.

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[从感染的极低出生体重新生儿中分离的凝固酶阴性葡萄球菌的疏水性和产生生物膜的能力的表型评估]。
导语:凝固酶阴性葡萄球菌(CNS),特别是表皮葡萄球菌和溶血葡萄球菌,是极低出生体重婴儿感染的主要原因。表皮病(n=60)和溶血链球菌(n=38)来自波兰两个新生儿重症监护病房住院的新生儿。采用0.9% NaCl自凝集试验(AA)和硫酸铵溶液盐聚集试验(SAT)测定细胞表面疏水性。为了确定产黏液的能力,进行了红花红染色Christiensen试管试验和刚果红琼脂(CRA)试验。采用结晶紫(CV)法对生物膜产量进行定量评价。结果:AA试验表明,几乎所有表皮葡萄球菌和溶血葡萄球菌分离株在氯化钠盐中均无凝集反应。SAT测试表明s。表皮分离株的聚集浓度为2 M,而溶血链球菌的聚集浓度为0.5 M。在christensen的方法中,最多的表皮分离株产生少量黏液(40%),而68%的溶血链球菌分离株产生大量黏液。在CRA试验中,在这两个物种中,最常见的结果是细菌培养颜色几乎是黑色的,这对应于生物膜的低产量。CV法对生物膜产量的定量评估显示,97%的溶血性葡萄球菌分离株产生高水平的生物膜,而只有43%的表皮葡萄球菌分离株产生类似的结果。结论:表型分析结果表明,溶血链球菌分离株产生黏液和形成生物膜的能力明显强于溶血链球菌分离株。epidermidis。
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