Porras O, Caugant D A, Gray B, Lagergård T, Levin B R, Svanborg-Edén C
Infect Immun. 1986 Jul;53(1):79-89. doi: 10.1128/iai.53.1.79-89.1986.
The extent of chromosomal genetic variability and the genetic structure of Haemophilus influenzae populations was analyzed. A total of 119 isolates from humans in Göteborg, Sweden, and Birmingham, Ala., and 16 strains from a type culture collection were characterized for capsular type, biotype, outer membrane protein profile, and enzyme electrophoretic type (ET). The results of this study indicate that the bacteria identified as H. influenzae are a genetically extremely variable array of organisms. For the six enzymes studied, the estimated mean genetic diversity was 0.57 (approximately 20% higher than the corresponding estimate for Escherichia coli). Two lines of evidence indicate that despite its ability to recombine by transformation, H. influenzae maintains a largely clonal population structure. Although there is considerable potential for generating different genotypes, there were only 88 distinct ETs among the 135 strains, and isolates of the same ET and biotype were recovered at frequencies greater than would be anticipated at random. This evidence for a clonal population structure holds for uncapsulated as well as capsulated strains. However, these data also suggest that the stability of H. influenzae clones (clone persistence time) may be less than that of the nontransforming species E. coli. The ET data indicate that there is somewhat less variability among H. influenzae strains that express the same capsular antigens, biotype, and outer membrane proteins than among randomly chosen isolates. Nevertheless, there is substantial genetic variation among isolates within each of these classes and combinations thereof. There is also variation in these typing characteristics among strains of the same ET. These observations and those on genetic variability and population structures have implications for the characterization of H. influenzae isolates in clinical and epidemiological studies.
分析了流感嗜血杆菌群体的染色体遗传变异性程度和遗传结构。对来自瑞典哥德堡、美国阿拉巴马州伯明翰的119株人类分离株以及16株来自标准菌种保藏中心的菌株进行了荚膜类型、生物型、外膜蛋白谱和酶电泳类型(ET)的鉴定。本研究结果表明,鉴定为流感嗜血杆菌的细菌是一组遗传上极具变异性的生物体。对于所研究的六种酶,估计的平均遗传多样性为0.57(比大肠杆菌的相应估计值高约20%)。两条证据表明,尽管流感嗜血杆菌能够通过转化进行重组,但其群体结构在很大程度上保持克隆性。尽管产生不同基因型的潜力很大,但在135株菌株中只有88种不同的ET,并且相同ET和生物型的分离株的回收频率高于随机预期。这种克隆群体结构的证据适用于无荚膜菌株和有荚膜菌株。然而,这些数据也表明,流感嗜血杆菌克隆的稳定性(克隆持续时间)可能低于非转化物种大肠杆菌。ET数据表明,表达相同荚膜抗原、生物型和外膜蛋白的流感嗜血杆菌菌株之间的变异性略低于随机选择的分离株之间的变异性。然而,在这些类别及其组合中的每一个类别内的分离株之间存在大量遗传变异。同一ET的菌株在这些分型特征上也存在变异。这些观察结果以及关于遗传变异性和群体结构的观察结果对临床和流行病学研究中流感嗜血杆菌分离株的鉴定具有重要意义。