Kato Hirotomo, Jochim Ryan C, Lawyer Phillip G, Valenzuela Jesus G
Vector Molecular Biology Unit, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852, USA.
J Exp Biol. 2007 Mar;210(Pt 5):733-40. doi: 10.1242/jeb.001289.
Two transcripts coding for an adenosine deaminase (ADA) were identified by sequencing a Phlebotomus duboscqi salivary gland cDNA library. Adenosine deaminase was previously reported in the saliva of the sand fly Lutzomyia longipalpis but it was not present in the saliva of the sand flies Phlebotomus papatasi, P. argentipes, P. perniciosus and P. ariasi, suggesting that this enzyme is only present in the saliva of sand flies from the genus Lutzomyia. In the present work, we tested the hypothesis that the salivary gland transcript coding for ADA in Phlebotomus duboscqi, a sister species of Phlebotomus papatasi, produces an active salivary ADA. Salivary gland homogenates of P. duboscqi converted adenosine to inosine, suggesting the presence of ADA activity in the saliva of this species of sand fly; furthermore, this enzymatic activity was significantly reduced when using either salivary glands of recently blood-fed sand flies or punctured salivary glands, suggesting that this enzyme is secreted in the saliva of this insect. This enzymatic activity was absent from the saliva of P. papatasi. In contrast to other Phlebotomus sand flies, we did not find AMP or adenosine in P. duboscqi salivary glands as measured by HPLC-photodiode array. To confirm that the transcript coding for ADA was responsible for the activity observed in the saliva of this sand fly, we cloned this transcript into a prokaryotic expression vector and produced a soluble and active recombinant protein of approximately 60 kDa that was able to convert adenosine to inosine. Extracts of bacteria transformed with control plasmids did not show this activity. These results suggest that P. duboscqi transcripts coding for ADA are responsible for the activity detected in the salivary glands of this sand fly and that P. duboscqi acquired this activity independently from other Phlebotomus sand flies. This is another example of a gene recruitment event in salivary genes of blood-feeding arthropods that may be relevant for blood feeding and, because of the role of ADA in immunity, it may also play a role in parasite transmission.
通过对杜氏白蛉唾液腺cDNA文库进行测序,鉴定出了两种编码腺苷脱氨酶(ADA)的转录本。腺苷脱氨酶此前曾在长须罗蛉的唾液中被报道,但在巴氏白蛉、银足白蛉、有害白蛉和阿氏白蛉的唾液中未发现,这表明这种酶仅存在于罗蛉属白蛉的唾液中。在本研究中,我们检验了一个假设,即与巴氏白蛉为姐妹种的杜氏白蛉唾液腺中编码ADA的转录本会产生一种有活性的唾液ADA。杜氏白蛉的唾液腺匀浆将腺苷转化为次黄苷,这表明该种白蛉的唾液中存在ADA活性;此外,当使用刚吸食过血液的白蛉的唾液腺或被刺破的唾液腺时,这种酶活性显著降低,这表明这种酶是在这种昆虫的唾液中分泌的。巴氏白蛉的唾液中没有这种酶活性。与其他白蛉属白蛉不同,通过高效液相色谱 - 光电二极管阵列检测,我们在杜氏白蛉的唾液腺中未发现AMP或腺苷。为了证实编码ADA的转录本是造成这种白蛉唾液中所观察到的活性的原因,我们将该转录本克隆到原核表达载体中,并产生了一种约60 kDa的可溶性活性重组蛋白,该蛋白能够将腺苷转化为次黄苷。用对照质粒转化的细菌提取物未显示出这种活性。这些结果表明,杜氏白蛉中编码ADA的转录本是造成该种白蛉唾液腺中检测到的活性的原因,并且杜氏白蛉独立于其他白蛉属白蛉获得了这种活性。这是吸血节肢动物唾液基因中基因招募事件的另一个例子,这可能与吸血有关,并且由于ADA在免疫中的作用,它也可能在寄生虫传播中发挥作用。