Locusts are grasshoppers (Orthoptera: Acrididae) that are characterised by their capacity for extreme population density-dependent polyphenism, transforming between a cryptic solitarious phase that avoids other locusts, and a swarming gregarious phase that aggregates and undergoes collective migration. The two phases differ in many aspects of behaviour, physiology and ecology, making locusts a useful model through which to investigate the phenotypic interface of molecular processes and environmental cues. This review summarises recent progress in understanding the mechanisms and consequences of locust phase change, from differential gene expression and epigenetic regulation through to neuronal plasticity and altered behaviour. The impact of techniques such as RNA interference (RNAi), and the sequencing of the first locust genome is discussed, and we consider the evidence from comparative analyses between related locust species for the possible evolution of locust-like phenotypic plasticity. Collective movement, and new ways of measuring the behaviour of both migrating bands in the field and individuals in the laboratory, are analysed. We also examine the environmental factors that affect phase change, along with the wider impact of land use and management strategies that may unwittingly create environments conducive to outbreaks. Finally, we consider the human costs of locust swarming behaviour, and use combined social, economic and environmental approaches to suggest potential ways forward for locust monitoring and management.

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BackgroundThe Australian plague locust, Chortoicetes terminifera, is among the most promising species to unravel the suites of genes underling the density-dependent shift from shy and cryptic solitarious behaviour to the highly active and aggregating gregarious behaviour that is characteristic of locusts. This is because it lacks many of the major phenotypic changes in colour and morphology that accompany phase change in other locust species. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is the most sensitive method available for determining changes in gene expression. However, to accurately monitor the expression of target genes, it is essential to select an appropriate normalization strategy to control for non-specific variation between samples. Here we identify eight potential reference genes and examine their expression stability at different rearing density treatments in neural tissue of the Australian plague locust.ResultsTaking advantage of the new orthologous DNA sequences available in locusts, we developed primers for genes encoding 18SrRNA, ribosomal protein L32 (RpL32), armadillo (Arm), actin 5C (Actin), succinate dehydrogenase (SDHa), glyceraldehyde-3P-dehydrogenase (GAPDH), elongation factor 1 alpha (EF1a) and annexin IX (AnnIX). The relative transcription levels of these eight genes were then analyzed in three treatment groups differing in rearing density (isolated, short- and long-term crowded), each made up of five pools of four neural tissue samples from 5th instar nymphs. SDHa and GAPDH, which are both involved in metabolic pathways, were identified as the least stable in expression levels, challenging their usefulness in normalization. Based on calculations performed with the geNorm and NormFinder programs, the best combination of two genes for normalization of gene expression data following crowding in the Australian plague locust was EF1a and Arm. We applied their use to studying a target gene that encodes a Ca2+ binding glycoprotein, SPARC, which was previously found to be up-regulated in brains of gregarious desert locusts, Schistocerca gregaria. Interestingly, expression of this gene did not vary with rearing density in the same way in brains of the two locust species. Unlike S. gregaria, there was no effect of any crowding treatment in the Australian plague locust.ConclusionArm and EF1a is the most stably expressed combination of two reference genes of the eight examined for reliable normalization of RT-qPCR assays studying density-dependent behavioural change in the Australian plague locust. Such normalization allowed us to show that C. terminifera crowding did not change the neuronal expression of the SPARC gene, a gregarious phase-specific gene identified in brains of the desert locust, S. gregaria. Such comparative results on density-dependent gene regulation provide insights into the evolution of gregarious behaviour and mass migration of locusts. The eight identified genes we evaluated are also candidates as normalization genes for use in experiments involvi...