Department of Natural Resource Sciences, Macdonald Campus, McGill University, 21111 Lakeshore Road, Ste. Anne de Bellevue, Que., Canada H9X 3V9.
Vet Microbiol. 2010 Mar 24;141(3-4):332-41. doi: 10.1016/j.vetmic.2009.09.030. Epub 2009 Sep 25.
Actinobacillus minor and "Actinobacillus porcitonsillarum" are distinguished by their haemolytic activities, the latter organism being haemolytic and the former, non-haemolytic. Analysis of a whole genome shotgun sequence, however, revealed that A. minor strain 202, like "A. porcitonsillarum", possesses a haemolysin-encoding apxII operon. The purpose of this study was therefore to investigate haemolysin production by this organism and also by three additional members of the A. minor/"porcitonsillarum" complex, strains 33PN and 7ATS and A. minor strain NM305(T). Primers based on sequences within the apxII genes of strain 202 allowed the amplification of appropriately sized fragments from DNA from strain 33PN suggesting that this organism also possesses an apxII operon. Analysis of a whole genome shotgun sequence failed to reveal any trace of an apxII operon in strain NM305(T) and attempts to amplify apxII genes from DNA from strain 7ATS also failed. Strains 202 and 33PN, and surprisingly, the type strain of A. minor and strain 7ATS, were all found to be haemolysin-positive as growth media from cultures of these organisms could promote the lysis of erythrocytes in suspension. The erythrocyte specificities of the haemolysins produced by strains 202 and 33PN indicated that the haemolytic activities exhibited by these organisms were due to ApxII. In keeping with the apparent lack of apxII genes in strains NM305(T) and 7ATS, the haemolysins produced by these organisms were not erythrocyte-specific and with both organisms, haemolytic activity appeared to be due to a combination of heat-stable and heat-labile components. The identities of these components, however, remain unknown.
小巴斯德氏菌和“猪扁桃体巴斯德氏菌”通过其溶血活性来区分,后者是溶血的,而前者是非溶血的。然而,全基因组鸟枪法序列分析表明,像“猪扁桃体巴斯德氏菌”一样,A. minor 菌株 202 也拥有编码溶血素的 apxII 操纵子。因此,本研究旨在研究该菌以及 A. minor/“猪扁桃体巴斯德氏菌”复合体的另外三个成员(菌株 33PN、7ATS 和 A. minor 菌株 NM305(T))产生溶血素的情况。基于 202 株 apxII 基因序列设计的引物能够从 33PN 株的 DNA 中扩增出适当大小的片段,表明该菌也拥有 apxII 操纵子。对全基因组鸟枪法序列的分析未能在 NM305(T)株中发现任何 apxII 操纵子的痕迹,而且从 7ATS 株的 DNA 中扩增 apxII 基因的尝试也失败了。令人惊讶的是,202 株和 33PN 株以及 A. minor 标准株和 7ATS 株均被发现为溶血素阳性,因为这些菌的培养液能够促进悬浮红细胞的溶解。202 株和 33PN 株产生的溶血素的红细胞特异性表明,这些菌表现出的溶血活性归因于 ApxII。与 NM305(T)株和 7ATS 株明显缺乏 apxII 基因相一致,这些菌产生的溶血素不是红细胞特异性的,而且对于这两种菌,溶血活性似乎是由热稳定和热不稳定成分的组合引起的。然而,这些成分的身份仍然未知。