1 Insect Pest Control Laboratory, Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture, International Atomic Energy Agency, Vienna, Austria.
J Insect Sci. 2011;11:79. doi: 10.1673/031.011.7901.
The sterile insect technique has been successfully used to eliminate tsetse populations in a number of programs. Program monitoring in the field relies on the ability to accurately differentiate released sterile insects from wild insects so that estimates can be made of the ratio of sterile males to wild males. Typically, released flies are marked with a dye, which is not always reliable. The difference in isotopic signatures between wild and factory-reared populations could be a reliable and intrinsic secondary marker to complement existing marking methods. Isotopic signatures are natural differences in stable isotope composition of organisms due to discrimination against the heavier isotopes during some biological processes. As the isotopic signature of an organism is mainly dependent on what it eats; by feeding factory-reared flies isotopically different diets to those of the wild population it is possible to intrinsically mark the flies. To test this approach unlabeled samples of Glossina pallidipes (Austen) (Diptera: Glossinidae) from a mass rearing facility and wild populations were analyzed to determine whether there were any natural differences in signatures that could be used as markers. In addition experiments were conducted in which the blood diet was supplemented with isotopically enriched compounds and the persistence of the marker in the offspring determined. There were distinct natural isotopic differences between factory reared and wild tsetse populations that could be reliably used as population markers. It was also possible to rear artificially isotopically labeled flies using simple technology and these flies were clearly distinguishable from wild populations with greater than 95% certainty after 85 days of "release". These techniques could be readily adopted for use in SIT programs as complimentary marking techniques.
不育昆虫技术已成功用于消除一些项目中的采采蝇种群。实地计划监测依赖于准确区分释放的不育昆虫和野生昆虫的能力,以便能够估算不育雄虫与野生雄虫的比例。通常,释放的苍蝇会被标记上染料,但这并不总是可靠的。野生和工厂饲养种群之间同位素特征的差异可能是一种可靠的、内在的辅助标记方法,以补充现有的标记方法。同位素特征是由于在某些生物过程中对较重同位素的歧视,导致生物体稳定同位素组成的自然差异。由于生物体的同位素特征主要取决于它所吃的东西;通过给工厂饲养的苍蝇喂食与野生种群不同的同位素饮食,可以内在地标记这些苍蝇。为了验证这种方法,对来自大规模饲养设施的未标记的 Glossina pallidipes (Austen) (双翅目:Glossinidae)样本和野生种群进行了分析,以确定是否存在可以用作标记的自然签名差异。此外,还进行了实验,在实验中血液饮食中补充了同位素富集的化合物,并确定了标记在后代中的持久性。工厂饲养和野生采采蝇种群之间存在明显的自然同位素差异,可以可靠地用作种群标记。使用简单的技术也可以人工饲养同位素标记的苍蝇,这些苍蝇在“释放” 85 天后与野生种群的可区分度超过 95%。这些技术可以很容易地被采用作为 SIT 计划的补充标记技术。