The microbial flora of Aphis gossypii: Patterns across host plants and geographical space

Journal of Invertebrate Pathology

Volumn 100, Issue 2, 2009, Pages 123-126

  Najar Rodríguez, Adriana J ^a,c   McGraw, Elizabeth A ^a   Mensah, Robert K ^b,c   Pittman, Geoffrey W ^a   Walter, Gimme H ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b NSW DEPARTMENT OF PRIMARY INDUSTRIES   (Australia)

^c Australian Cotton Research Institute   (Australia)

Author keywords

Aphid; Aphis gossypii; Microbial flora; Symbiont

Indexed keywords

ANIMAL; APHID; ARTICLE; AUSTRALIA; BACTERIUM; BUCHNERA; CLASSIFICATION; GENETICS; GEOGRAPHY; ISOLATION AND PURIFICATION; JAPAN; MICROBIOLOGY; PHYLOGENY; PLANT; SPECIES DIFFERENCE; SYMBIOSIS;

ANIMALS; APHIDS; AUSTRALIA; BACTERIA; BUCHNERA; GEOGRAPHY; JAPAN; PHYLOGENY; PLANTS; SPECIES SPECIFICITY; SYMBIOSIS;

APHIDIDAE; APHIS GOSSYPII; BACTERIA (MICROORGANISMS); GOSSYPIUM HIRSUTUM;

EID: 58649091976     PISSN: 00222011     EISSN: 10960805     Source Type: Journal    
DOI: 10.1016/j.jip.2008.10.005     Document Type: Article

References (34)

1. Altschul S.F., et al. Basic local alignment search tool. J. Mol. Biol. 215 (1990) 403-410
2. Chen D.-Q., et al. A new rickettsia from a herbivorous insect, the pea aphid Acyrthosiphon pisum (Harris). Curr. Microbiol. 33 (1996) 123-128
3. Chen D.Q. Fitness effects of two facultative endosymbiotic bacteria on the pea aphid Acyrthosiphon pisumand the blue alfalfa aphid A. kondoi. Entomol. Exp. Appl. 95 (2000) 315-323
4. Duron O., et al. The diversity of reproductive parasites among arthropods: Wolbachia do not walk alone. BMC Biol. 6 (2008) 27
5. Ekukole G. Effects of some selected plants on the fecundity of Aphis gossypii Glover under laboratory conditions. Cotton et Fibres Tropicales 45 (1990) 263-266
6. Fukatsu T., et al. The secondary endosymbiotic bacterium of the pea aphid Acyrthosiphon pisum (Insecta: Homoptera). Appl. Environ. Microbiol. 66 (2000) 2748-2758
7. Fukatsu T., et al. Spiroplasma symbiont of the pea aphid, Acyrthosiphon pisum (Insecta: Homoptera). Appl. Environ. Microbiol. 67 (2001) 1284-1291
8. Gherna R., et al. Arsenophonus nasoniae gen. nov., sp. nov., the causative agent of the son-killer trait in the parasitic wasp Nasonia vitripennis. Int. J. Syst. Bacteriol. 41 (1991) 563-565
9. Guldemond J.A., et al. Host races of Aphis gossypii (Homoptera: Aphididae) on cucumber and chrysanthemum. Environ. Entomol. 23 (1994) 1235-1240
10. Haynes S., et al. Diversity of bacteria associated with natural aphid populations. Appl. Environ. Microbiol. 69 (2003) 7216-7223
11. Houhamdi L., and Raoult D. Experimental infection of human body lice with Acinetobacter baumannii. Am. J. Trop. Med. Hyg. 74 (2006) 526-531
12. Kikuchi Y., et al. Insect-microbe mutualism without vertical transmission: a stinkbug acquires a beneficial gut symbiont from the environment every generation. Appl. Environ. Microbiol. 73 (2007) 4308-4316
13. Kondo N., et al. Infection density of Wolbachia endosymbiont affected by co-infection and host genotype. Biol. Lett. 1 (2005) 488-491
14. Leonardo T.E., and Muiru G.T. Facultative symbionts are associated with host plant specialization in pea aphid populations. Proc. R. Soc. Lond. B 270 (2003) S209-S212
15. McKenzie C.L., and Cartwright B. Susceptibility of Aphis gossypii (Glover) to insecticides as affected by host plant using a rapid bioassay. J. Entomol. Sci. 29 (1994) 289-301
16. Moran N.A. Symbiosis as an adaptive process and source of phenotypic complexity. PNAS 104 Suppl. 1 (2007) 8627-8633
17. Moran N.A., et al. Evolutionary relationships of three new species of Enterobacteriaceae living as symbionts of aphids and other insects. Appl. Environ. Microbiol. 71 (2005) 3302-3310
18. Murrell A., et al. A survey of bacterial diversity in ticks, lice and fleas from Australia. Parasitol. Res. 89 (2003) 326-334
19. Muyzer G., et al. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16s rRNA. Appl. Environ. Microbiol. 59 (1993) 695-700
20. Oliver K.M., et al. Facultative bacterial symbionts in aphids confer resistance to parasitic wasps. PNAS 100 (2003) 1803-1807
21. Ronquist F., and Huelsenbeck J.P. MRBAYES 3: bayesian phylogenetic inference under mixed models. Bioinformatics 19 (2003) 1572-1574
22. Russell J., et al. Side-stepping secondary symbionts: widespread horizontal transfer across and beyond the Aphidoidea. Mol. Ecol. 12 (2003) 1061-1075
23. Sabater B., et al. Molecular evolution of aphids and their primary (Buchnera sp) and secondary endosymbionts: implications for the role of symbiosis in insect evolution. Interciencia 26 (2001) 508-512
24. Sakurai M., et al. Rickettsia symbiont in the pea aphid Acyrthosiphon pisum: novel cellular tropism, effect on host fitness, and interaction with the essential symbiont Buchnera. Appl. Environ. Microbiol. 71 (2005) 4069-4075
25. Simon J.-C., et al. Host-based divergence in populations of the pea aphid: insights from nuclear markers and the prevalence of facultative symbionts. Proc. R. Soc. Lond. B 270 (2002) 1703-1712
26. Takada H. Interclonal variability in the photoperiodic response for sexual morph production of Japanese Aphis gossypii Glover (Hom, Aphididae). J. Appl. Entomol. 106 (1988) 188-197
27. Thao M.L., and Baumann P. Evidence for Multiple Acquisition of Arsenophonus by Whitefly Species (Sternorrhyncha: Aleyrodidae). Curr. Microbiol. 48 (2004) 140-144
28. Thao M.L., et al. Secondary endosymbionts of psyllids have been acquired multiple times. Curr. Microbiol. 41 (2000) 300-304
29. Thompson J.D., et al. The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 24 (1997) 4876-4882
30. Tsuchida T., et al. Diversity and geographic distribution of secondary endosymbiotic bacteria in natural populations of the pea aphid, Acyrthosiphon pisum. Mol. Ecol. 11 (2002) 2123-2135
31. Tsuchida T., et al. Host plant specialization governed by facultative symbiont. Science 303 (2004) 1989
32. Wool D., and Hales D. Components of variation of morphological characters in Australian Aphis gossypii: host-plant effects predominate. Entomol. Exp. Appl. 80 (1996) 166-168
33. Yu Z., and Morrison M. Comparisons of different hypervariable regions of rrs genes for use in fingerprinting of microbial communities by PCR-denaturing gradient gel electrophoresis. Appl. Environ. Microbiol. 70 (2004) 4800-4806
34. Zahner V., et al. Application of 16S rDNA-DGGE and plate culture to characterization of bacterial communities associated with the sawfly, Acantholyda erythrocephala (Hymenoptera, Pamphiliidae). Curr. Microbiol. (2008) 10.1007/s00284-008-9243-4