Forecasting seasonal population growth of Aphis glycines (Hemiptera: Aphididae) in soybean in Illinois.

From 2001 to 2004, 252 fifty-plant samples were collected from commercial soybean, Glycine max L., fields in three townships (93-km2 area) in Illinois. Townships were sampled every 3 wk from late June or early July when aphids (Aphis glycines Matsumura) first invaded the townships to early August. We used linear regression of 18 mean township field densities to calibrate several simple models to predict the change in aphid population density in a township from one sampling date to the next. The best exponential model for the complete data set has an r2 = 0.54, Y2 = Ylexp (0.09659 x DAY), where Y1 and Y2 are the first and second samples of aphids separated by a 3-wk period (the number of days, DAY). Our intrinsic rate of increase for the population is much lower than rates calculated in other studies. The best single-variable linear model has an r2 = 0.88, Y2 = Y1 + 0.1084 x Y1 x DAY. The latter model indicates the value of including monitoring data in the prediction. The best two-variable model has an R2 = 0.98, Y2 = Y1 + 0.08136 x Y1 x DAY + 0.000080 x N1(2) x DAY, where N1(2) x DAY is the interaction term for initial, squared, sample density of the season multiplied by the number of days between samples. The latter two models indicate that the change in the population density is greater for more dense populations. Degree-days were generally inferior to days as the time component in the simple models.

Solanaceous Weeds as Possible Sources of Cucumber mosaic virus in Southern Illinois for Aphid Transmission to Pepper.

Over 5,000 individual plants representing approximately 55 species from an area in southern Illinois where Cucumber mosaic virus (CMV) has been a major problem in pepper (Capsicum annuum) were tested for the presence of CMV by enzyme-linked immunosorbent assay (ELISA). Representative ELISA-positive samples were checked by western blot tests to confirm virus-specific reactions. Nearly all of the infected plants detected were either Solanum ptycanthum (eastern black nightshade) or Physalis spp. (principally P. heterophylla, groundcherry). Over 1,000 pepper transplants and approximately 500 tomato transplants, collected prior to planting, were negative for CMV by ELISA. In aphid transmission (arena) experiments, all five aphid species tested were capable of transmitting CMV from nightshade to pepper: Aphis fabae subsp. solanella, Aphis gossypii, Myzus persicae, Rhopalosiphum padi, and Sitobion avenae. Aphis fabae subsp. solanella, A. gossypii, and A. nerii were able to transmit CMV from P. heterophylla to pepper. Aphis fabae subsp. solanella was commonly found colonizing nightshade from May through October in southern Illinois.

The tryptophan biosynthetic pathway of aphid endosymbionts (Buchnera): genetics and evolution of plasmid-associated anthranilate synthase (trpEG) within the aphididae.

The bacterial endosymbionts (Buchnera) from the aphids Rhopalosiphum padi, R. maidis, Schizaphis graminum, and Acyrthosiphon pisum contain the genes for anthranilate synthase (trpEG) on plasmids made up of one or more 3.6-kb units. Anthranilate synthase is the first as well as the rate-limiting enzyme in the tryptophan biosynthetic pathway. The amplification of trpEG on plasmids may result in an increase of enzyme protein and overproduction of this essential amino acid, which is required by the aphid host. The nucleotide sequence of trpEG from endosymbionts of different species of aphids is highly conserved, as is an approximately 500-bp upstream DNA segment which has the characteristics of an origin of replication. Phylogenetic analyses were performed using trpE and trpG from the endosymbionts of these four aphids as well as from the endosymbiont of Schlechtendalia chinensis, in which trpEG occurs on the chromosome. The resulting phylogeny was congruent with trees derived from sequences of two chromosome-located bacterial genes (part of trpB and 16S ribosomal DNA). In turn, trees obtained from plasmid-borne and bacterial chromosome-borne sequences were congruent with the tree resulting from phylogenetic analysis of three aphid mitochondrial regions (portions of the small and large ribosomal DNA subunits, as well as cytochrome oxidase II). Congruence of trees based on genes from host mitochondria and from bacteria adds to previous support for exclusively vertical transmission of the endosymbionts within aphid lineages. Congruence with trees based on plasmid-borne genes supports the origin of the plasmid-borne trpEG from the chromosomal genes of the same lineage and the absence of subsequent plasmid exchange among endosymbionts of different species of aphids.

Detection of Buchnera, the primary prokaryotic endosymbiont of aphids, using the polymerase chain reaction.

Members of the genus Buchnera constitute a distinct prokaryotic lineage containing the primary endosymbionts of aphids (Homoptera: Aphidoidea). Using synthetic oligonucleotides in conjunction with the polymerase chain reaction, we propose three approaches for the identification of members of this genus. The first is based on unique sequences within rrs (gene coding for 16S ribosomal RNA). The second is based on a different and unique organization of the ribosomal RNA operons of Buchnera and the close proximity of aroE upstream of rrl (gene coding for 23S rRNA). The third is based on the linkage relationship of argS which is upstream of rrs. Validation of these three approaches requires their more extensive application.

Evidence for the establishment of aphid-eubacterium endosymbiosis in an ancestor of four aphid families.

Aphids (superfamily Aphidoidea) contain eubacterial endosymbionts localized within specialized cells (mycetocytes). The endosymbionts are essential for the survival of the aphid hosts. Sequence analyses of the 16S rRNAs from endosymbionts of 11 aphid species from seven tribes and four families have indicated that the endosymbionts are monophyletic. Furthermore, phylogenetic relationships within the symbiont clade parallel the relationships of the corresponding aphid hosts. Our findings suggest that this endocytobiotic association was established in a common ancestor of the four aphid families with subsequent diversification into the present species of aphids and their endosymbionts.