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Biomedical subjects

R L Blackman

Publications and source records attributed to R L Blackman.

15 recordsLinked to original sources
PubMed2006

Morphological discrimination of Aphis gossypii (Hemiptera: Aphididae) populations feeding on Compositae.

Aphis gossypii Glover is a polyphagous aphid pest with a worldwide distribution. However, there is evidence that on a global scale the name A. gossypii is being applied to a number of forms with different life cycles and/or host-plant associations. Morphometric variation of A. gossypii samples from crops and non-cultivated plants in many parts of the world was examined, to determine whether this variation is correlated with the hosts from which the aphids originated. Samples of A. gossypii were collected from Cucurbitaceae and Malvaceae in Europe, and from Compositae in various parts of the world. Morphometric data for 13 parameters measured from 97 clonal lineages (728 specimens) and 27 field-collected samples (313 specimens) were analysed by a series of canonical variates analyses, using the field sample/clonal lineage as grouping factor. Clonal lineages were reared on a common host in controlled conditions to standardize the effect of host and environment on morphology. The analyses provided a clear morphometric separation of the aphids originating from Compositae and those collected on Cucurbitaceae and Malvaceae, regardless of the geographical origin of the aphids and the host plant on which they were reared. This indicates that within A. gossypii there are two widely distributed host races or subspecies with different plant family associations. The taxonomic implications are discussed.

Animals↗
PubMed2003

Co-existence of different host-adapted forms of the Myzus persicae group (Hemiptera: Aphididae) in southern Italy.

Multivariate morphometric analysis (method of canonical variates) was used to compare 38 parthenogenetic lineages and three field collections of aphids of the Myzus persicae (Sulzer) group sampled on peach and tobacco in the Caserta region of southern Italy. Comparisons were also made with the morphology of lineages collected on peach in Lehonia, in central eastern Greece away from tobacco-growing regions, and on tobacco in Naphplion, in southern Greece. The lineages were measured after parthenogenetic rearing for one to three generations on the same host (potato) under constant conditions. As in previous work, the multivariate morphometric approach separated the aphids from peach from those feeding on tobacco. The life cycle category of the lineages was also examined. Almost all the lineages from peach in Caserta were holocyclic, yet the lineages from tobacco in the same region were unable to produce sexual morphs. The results suggest that tobacco-adapted and non-tobacco-adapted forms co-exist in the same region in southern Italy, not only because they colonize different host plants, but also because they have different life cycles. This is in complete contrast to the situation in peach-growing areas of northern Greece, and shows that the ecology and population structure of M. persicae is different in neighbouring counties of the Mediterranean area, even where climatic conditions and cultivated crops are similar.

Adaptation, Physiological↗
PubMed2002

Microsatellite variation in cyclically parthenogenetic populations of Myzus persicae in south-eastern Australia.

We examined the population structure of the introduced aphid, Myzus persicae collected mainly from its primary host, Prunus persica, in south-east Australia. Myzus persicae has been present in Australia since at least 1893. Samples were collected in the spring of 1998 from two mainland and three Tasmanian localities and isofemale lines were established in the laboratory. The reproductive mode (life cycle), karyotype and 17-locus microsatellite genotype of each clone were determined. All populations showed significant population differentiation (F(ST) 0.058-0.202) even over small geographic distances (<50 km). All clones were karyotypically normal except for a subset of clones from one site that was exposed to the carbamate insecticide, Pirimor, the week prior to sampling. Those clones were heterozygous for an autosomal 1,3 translocation frequently associated in M. persicae with insecticide resistance. In contrast to other loci and despite being on different chromosomes, loci myz2(A) and M55(A) showed general and significant linkage disequilibrium. These loci may be affected by epistatic selection. We discuss the observed high clonal diversity, moderate but significant population differentiation, general conformance to Hardy-Weinberg equilibria and low linkage disequilibria with particular focus on the global population biology of M. persicae.

Animals↗
PubMed2002

Life cycle variation of Myzus persicae (Hemiptera: Aphididae) in Greece.

During the years 1995-1999 the life cycle category of 2797 clones of Myzus persicae (Sulzer) was examined. The clones originated from primary and secondary hosts from different localities of North and Central Greece and the island of Crete in the south. Four different overwintering life cycle strategies were found that have also been described for M. persicae and other heteroecious species previously. A geographical variation was found in the proportion of holocyclic clones from tobacco and other secondary hosts associated with the abundance of the primary host in the sampling regions. In Central Macedonia, around the main peach-growing regions, the proportion of holocyclic clones was mostly above 50% and in some cases reached 100%. In localities of East Macedonia, holocyclic clones were also frequent. On the other hand, further south or in north-eastern Greece, where peach is not common, the proportion of holocyclic clones varied between 0 and 33%. Fifty seven percent of examined anholocyclic clones produced males under short day conditions, suggesting that androcyclic clones in Greece represent an important factor of genetic variability. Intermediate clones were sampled from all host-plants but at low frequencies (3.6% of total examined clones and 6.9% of non-holocyclic ones). Moreover, a regional variation was found in different colour forms feeding on tobacco plants. Red clones were predominant in regions where aphids overwinter parthenogenetically on weeds or winter crops. However, almost all clones from the primary host were green. The ecological aspects of life cycle variation are discussed.

Animals↗
PubMed2000

Inheritance and meiotic behaviour of a de novo chromosome fusion in the aphid Myzus persicae (Sulzer).

A de novo tandem fusion between autosomes 2 and 3 (A2+3), arising in the course of laboratory crosses of sexual morphs of two clones of the aphid Myzus persicae, was stable through more than 180 generations of parthenogenetic (clonal) reproduction. Studies of its inheritance through the sexual phase, and segregation from an amplified esterase marker gene, showed that crossing over occurred during oogenesis, but not in spermatogenesis, confirming previous cytological observations. Only a small number of progeny resulted from attempts at selfing fusion heterozygotes, and none of these was homozygous for the fusion. A2+3 paired in parallel alignment with the separate A2 and A3 to form a trivalent at prophase I of spermatogenesis. Fusion heterozygotes had a segregation problem at anaphase I of meiosis, A2+3 forming a chromatin bridge between the daughter spermatocytes in about 42% of dividing cells, which could be attributed to alternate orientation in the trivalent (A2 and A3 paired with opposite sides of A2+3) in the preceding metaphase I. Males heterozygous for an A2 dissociation were also studied and found to have much less of a segregation problem, despite showing similar orientation patterns at metaphase I. Possible reasons for this difference and the significance of the findings in relation to karyotype evolution in aphids are discussed.

Animals↗
PubMed2000

Host-correlated morphological variation of Myzus persicae (Hemiptera: Aphididae) populations in Greece.

Morphological variation in nine characters of 157 clones of Myzus persicae (Sulzer) was examined by multivariate analysis. The clones were collected from peach, Prunus persica, the primary host and the secondary hosts tobacco, Nicotiana tabacum, cabbage, Brassica oleracea, sugarbeet, Beta vulgaris and pepper Capsicum annuum. The 156 clones originated from various regions of Greece, both in the north, where a large part of the population has an annual bisexual generation on peach, and in more southerly regions, where populations are predominantly unisexual. One clone was collected from tobacco in Caserta, Italy. All clones were laboratory-reared on potato. Canonical variate analysis, hierarchical cluster analysis and a non-parametric classification tree method both revealed morphological differences associated with the host-plant on which they were collected. The scores of the first two canonical variates separated the tobacco-feeding clones from those originating from other secondary host-plants. However, in tobacco-growing areas the tobacco-feeding form predominated in spring populations on peach, and was sometimes found on other secondary hosts. In addition, using cluster analysis, the clones from tobacco which were sampled in the most southeasterly region showed a relatively large phenotypic distance from those collected further north and west. Moreover, clonal phenotypes were affected both by host plant and by long-term parthenogenetic rearing. However, in spite of these effects, the tobacco form was generally distinguishable from aphids originating from other hosts, indicating that the difference must have a genetic basis. In separate analyses of the clones originating from secondary hosts no association was found between morphology and either life cycle category or colour. Discriminant analysis showed that 89% of 1723 specimens could be correctly classified into the two groups.

Animals↗
PubMed2000

High diversity of structurally heterozygous karyotypes and rDNA arrays in parthenogenetic aphids of the genus Trama (Aphididae: Lachninae).

Karyotypes of permanently parthenogenetic aphids of three species of the genus Trama show great diversity, particularly in the number and distribution of chromosomal elements containing highly repetitive sequences. Sampling at only a few sites in southern England, chromosome number varied from 14 to 23 in T. troglodytes, 9-12 in T. caudata and 10-14 in T. maritima, with some colonies having individuals of more than one karyotype. This variation was paralleled by differences in the number and distribution of rDNA arrays revealed by in situ hybridization. This high intraspecific karyotype diversity contrasts with very low genetic diversity in the same populations, suggesting rapid karyotype evolution. Although T. troglodytes feeds on many species of composite plants there was no evidence of any karyotype-associated host race formation.

Animals↗
PubMed1999

Relationship between amount of esterase and gene copy number in insecticide-resistant Myzus persicae (Sulzer).

Overproduction of the insecticide-degrading esterases, E4 and FE4, in peach-potato aphids, Myzus persicae (Sulzer), depends on both gene amplification and transcriptional control, the latter being associated with changes in DNA methylation. The structure and function of the aphid esterase genes have been studied but the determination of their copy number has proved difficult, a common problem with gene amplification. We have now used a combination of pulsed-field gel electrophoresis and quantitative competitive PCR to determine relative esterase gene copy numbers in aphid clones with different levels of insecticide resistance (R1, R2 and R3). There are approx. 4-fold increases between susceptible, R1, R2 and R3 aphids, reaching a maximum of approx. 80 times more genes in R3; this gives proportionate increases in esterase protein relative to susceptible aphids. Thus there is no overexpression of the amplified genes, in contrast with what was thought previously. For E4 genes, the loss of 5-methylcytosine is correlated with a loss of expression, greatly decreasing the amount of enzyme relative to the copy number.

5-Methylcytosine↗
PubMed1998

Orientation of the 'stretched' univalent X chromosome during the unequal first meiotic division in male aphids.

In situ hybridization was used to label the ends of the X chromosomes of two aphid species, Myzus persicae and Amphorophora tuberculata, in order to study the peculiar behaviour and orientation of the univalent X in aphid spermatogenesis. Anaphase I begins with the long axis of the X chromosome at right angles to the spindle and its two chromatids closely associated, but as the division proceeds the chromatids separate along most of their lengths, retaining only a midway connection as the X chromosome becomes stretched on the spindle. Both ends of one chromatid move towards one pole, while both ends of the other chromatid move towards the other pole. However, the midway connection is retained and the whole X chromosome eventually passes into one daughter cell. This form of X chromosome behaviour is common to all aphids and therefore presumably dates back to the Permian. It is independent of the type of meiosis, which in aphids can be 'normal' (reductional first division) or 'inverted' (reductional second division).

Animals↗
PubMed1998

A 169-base pair tandem repeat DNA marker for subtelomeric heterochromatin and chromosomal rearrangements in aphids of the Myzus persicae group.

Numerous copies of a 169-base pair DNA sequence (Myzus persicae group repeat; MpR) occur at subtelomeric locations on all chromosomes of three members of the Myzus persicae species group (Myzus persicae, M. antirrhinii, M. certus). MpR occurs in large tandem arrays at both ends of all autosomes of the standard 2n = 12 karyotype, and near one end of the X chromosome (the end opposite to the nucleolar organizer) and is estimated to make up about 5% of the genome (a total of about 200000 copies). Locations of MpR were compared in various karyotypes to determine the likely nature of the rearrangements (fusions, dissociations, translocations) that are found in this species group which, like other Hemiptera, has holocentric chromosomes that are devoid of morphological markers. Aphid clones heterozygous for autosome dissociations do not have any detectable MpR at 'new' chromosome ends, indicating that this sequence is not involved in 'capping' of chromosomes. However, a clone with a de novo autosome fusion had an interstitial block of MpR marking the point of fusion, and clones heterozygous for an autosomal 1,3 translocation had MpR from autosome 1 translocated to a new site on autosome 3. The isolation from M. antirrhinii of the telomeric repeat TTAGG, which is found in several insect groups, is also reported.

Animals↗
PubMed1996

Ribosomal DNA is frequently concentrated on only one X chromosome in permanently apomictic aphids, but this does not inhibit male determination.

The ribosomal DNA arrays in the nucleolar organizer regions (NORs) of aphids are generally-located in a telomeric or subtelomeric position on the X chromosomes. In aphid populations or species that have lost the sexual part of their life cycle and become permanent apomicts, multiple rDNA copies are often concentrated on only one of the original X chromosomes. This situation has been found in apomictic members of three aphid subfamilies, although not as yet in the tribe Aphidini, which includes several permanent apomicts that are important pests. Some clonal cultures of Acyrthosiphon pisum and Myzus persicae reared for many years in conditions that prolong apomixis and inhibit sexual reproduction also have their rDNA arrays concentrated on one X chromosome. A 50-year-old clone of Aphis fabae, however, still retains a pair of similar-sized rDNA arrays on its X chromosomes. Although pairing of the X chromosomes by their NORs during prophase of the maturation division seems to be required for determination of XO males in aphids, a clone of A. pisum with one rDNA array was nevertheless able to produce males when subjected to appropriate environmental conditions.

Animals↗
PubMed1976

Cytogenetics of two species of Euceraphis (Homoptera, Aphididae).

Somatic cell divisions, spermatogenesis, and the prophase stages of primary oocytes, are described for two species of birch aphid, Euceraphis betulae (Koch) and E. punctipennis (Zettersted). Females of E. betulae have two autosome pairs, two pairs of X-chromosomes of different lengths, and two B-chromosomes. Females of E. punctipennis have the same number of X-chromosomes. The sex determination system is X1X2O. E. punctipennis males sometimes have only one B-chromosome. In the spermatogenesis of E. Betulae, pairing of homologous autosomes occurs in early prophase I, but no evidence was found of chiasmata or end-to-end alignment of homologues. Instead, homologues remain closely aligned in parallel as they condense into metaphase, and anaphase I separates the products of pairing in a strictly reductional manner. The two unpaired X-chromosomes and both B-chromosomes are stretched on the anaphase I spindle and all four pass into the larger secondary spermatocyte. The second division is equational. The B-chromosomes thus show accumulation in spermatogenesis, which must be compensated in some way by an elimination mechanism in oogenesis. Meiosis of E. punctipennis is highly anomalous. The two autosomes pair but separate again in early prophase I, then one homologue becomes heterchromatic and is apparently rejected from the late prophase nucleus. A single, equational maturation division follows. In female neiosis I, both species show highly characteristic diplotene figures with multiple chiasmata, the B-chromosomes remaining unpaired. These results are discussed in relation to previous work on aphid cytogenetics.

Animals↗