Adderson E E, Byington C L, Spencer L, Kimball A, Hindiyeh M, Carroll K, Mottice S, Korgenski E K, Christenson J C, Pavia A T
Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, USA.
Pediatrics. 2001 Jul;108(1):E18. doi: 10.1542/peds.108.1.e18.
Haemophilus influenzae type b causes severe disease in nonimmune infants and young children; other serotypes are uncommon pathogens and thought to have low virulence. Some have hypothesized that with the virtual elimination of H influenzae type b, other serotypes might acquire virulence traits and emerge as important pathogens of children. We describe the clinical, epidemiologic, and molecular biologic features of 5 cases of severe disease attributable to Haemophilus influenzae type a.
After observing 4 cases of invasive disease caused by H influenzae type a, we reviewed microbiology records at 3 reference laboratories that perform all serotyping in Utah and surveillance databases. Strains of H influenzae type a and control strains were examined by Southern blotting with the use of the cap probe pUO38 and by pulsed-field gel electrophoresis. The putative virulence mutation, the IS1016-bexA deletion, was detected by polymerase chain reaction amplification and sequencing.
During a 10-month period, we observed 5 children with severe invasive disease caused by H influenzae type a. No isolates of H influenzae type a had been submitted to the reference laboratories between 1992 and 1998. The median age of patients was 12 months (range: 6-48 months). Four of 5 had meningitis and bacteremia; 1 had purpura fulminans. Three isolates, representing 1 of 2 pulsed-field gel electrophoresis patterns, contained the IS1016-bexA deletion and were associated with particularly severe disease.
We describe an unusual cluster of severe disease caused by H influenzae type a that resembles the clinical and epidemiologic features of H influenzae type b disease. Our data support the hypothesis that the IS1016-bexA deletion may identify more virulent strains of H influenzae. Haemophilus influenzae, epidemiology, virulence, serotyping, pathogenicity.
b型流感嗜血杆菌可在未免疫的婴幼儿中引发严重疾病;其他血清型是罕见的病原体,且被认为毒力较低。一些人推测,随着b型流感嗜血杆菌的实际消除,其他血清型可能会获得毒力特征并成为儿童的重要病原体。我们描述了5例由a型流感嗜血杆菌引起的严重疾病的临床、流行病学和分子生物学特征。
在观察到4例由a型流感嗜血杆菌引起的侵袭性疾病后,我们查阅了犹他州进行所有血清分型的3个参考实验室的微生物学记录以及监测数据库。使用帽探针pUO38通过Southern印迹法和脉冲场凝胶电泳对a型流感嗜血杆菌菌株和对照菌株进行检测。通过聚合酶链反应扩增和测序检测推定的毒力突变,即IS1016-bexA缺失。
在10个月的时间里,我们观察到5名儿童患有由a型流感嗜血杆菌引起的严重侵袭性疾病。1992年至1998年期间,没有a型流感嗜血杆菌分离株被提交到参考实验室。患者的中位年龄为12个月(范围:6至48个月)。5例中有4例患有脑膜炎和菌血症;1例患有暴发性紫癜。代表2种脉冲场凝胶电泳模式之一的3株分离株含有IS1016-bexA缺失,并且与特别严重的疾病相关。
我们描述了一组不寻常的由a型流感嗜血杆菌引起的严重疾病,其临床和流行病学特征类似于b型流感嗜血杆菌疾病。我们的数据支持这样的假设,即IS1016-bexA缺失可能识别出毒力更强的流感嗜血杆菌菌株。流感嗜血杆菌、流行病学、毒力、血清分型、致病性。