Expression of a peroxiredoxin–glutaredoxin by Haemophilus influenzae in biofilms and during human respiratory tract infection

Timothy F. Murphy , Charmaine Kirkham , Sanjay Sethi , Alan J. Lesse
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引用次数: 53

Abstract

Evidence is mounting that nontypeable Haemophilus influenzae grows as a biofilm in the middle ear of children with otitis media and the airways of adults with chronic obstructive pulmonary disease. To begin to assess antigens expressed by H. influenzae in biofilms, cell envelopes of bacteria grown as a biofilm were compared to those grown planktonically. A ∼30 kDa peroxiredoxin–glutaredoxin was present in greater abundance during growth in biofilms. Mutants deficient in expression of peroxiredoxin–glutaredoxin were constructed by homologous recombination in four clinical isolates. The mutants showed a 25–50% reduction in biofilm formation compared to the corresponding parent strains. To study in vivo expression of peroxiredoxin–glutaredoxin during human respiratory tract infection, paired pre- and post-exacerbation serum from adults with chronic obstructive pulmonary disease and H. influenzae in sputum were assayed using an enzyme-linked immunosorbent assay and purified recombinant peroxiredoxin–glutaredoxin. Eight from 18 (44.4%) paired serum samples showed a significant increase in antibody to peroxiredoxin–glutaredoxin from pre- to post-infection. These results indicate that (1) peroxiredoxin–glutaredoxin is present in greater abundance in H. influenzae biofilms compared to planktonically grown bacteria; (2) peroxiredoxin–glutaredoxin is involved in biofilm formation by H. influenzae and the degree of involvement varies among strains; and (3) peroxiredoxin–glutaredoxin is expressed by H. influenzae during infection of the human respiratory tract and is recognized by the human immune system.

流感嗜血杆菌在生物膜和人呼吸道感染过程中表达过氧化物氧还蛋白-戊二氧还蛋白
越来越多的证据表明,不可分型的流感嗜血杆菌在患有中耳炎的儿童中耳和患有慢性阻塞性肺病的成人气道中以生物膜的形式生长。为了开始评估流感嗜血杆菌在生物膜中表达的抗原,将作为生物膜生长的细菌的细胞包膜与浮游生长的细菌进行比较。在生物膜的生长过程中,A ~ 30 kDa的过氧化物还毒素-谷胱甘肽的丰度更高。通过同源重组,在4个临床分离株中构建了过氧化物还蛋白-谷胱甘肽缺乏表达的突变体。与相应的亲本菌株相比,突变体的生物膜形成减少了25-50%。为了研究人呼吸道感染期间过氧化物还蛋白-谷氨酰胺的体内表达,使用酶联免疫吸附法和纯化的重组过氧化物还蛋白-谷氨酰胺,对慢性阻塞性肺疾病成人和流感嗜血杆菌加重前和加重后的血清进行了检测。18个配对血清样本中有8个(44.4%)显示感染前后过氧化物还毒素-谷氨还毒素抗体显著增加。这些结果表明:(1)与浮游生长的细菌相比,流感嗜血杆菌生物膜中过氧化物还毒素-谷胱甘肽的含量更高;(2)过氧化物还毒素-谷胱甘肽参与流感嗜血杆菌生物膜的形成,不同菌株参与程度不同;(3)流感嗜血杆菌在感染人呼吸道时表达过氧化物还蛋白-谷胱甘肽,并被人体免疫系统识别。
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