Literature DB >> 16842419

Bacteriophage WO-B and Wolbachia in natural mosquito hosts: infection incidence, transmission mode and relative density.

N Chauvatcharin1, A Ahantarig, V Baimai, P Kittayapong.   

Abstract

Bacteriophages of Wolbachia bacteria have been proposed as a potential transformation tool for genetically modifying mosquito vectors. In this study, we report the presence of the WO-B class of Wolbachia-associated phages among natural populations of several mosquito hosts. Eighty-eight percent (22/25) of Wolbachia-infected mosquito species surveyed were found to contain WO-B phages. WO-B phage orf7 sequence analysis suggested that a single strain of WO-B phage was found in most singly (23/24) or doubly (1/1) Wolbachia-infected mosquitoes. However, the single Wolbachia strain infecting Aedes perplexus was found to harbour at least two different WO-B phages. Phylogenetic analysis suggested that horizontal transmission of WO-B phages has occurred on an evolutionary scale between the Wolbachia residing in mosquitoes. On an ecological scale, a low trend of co-transmission occurred among specific WO-B phages within Wolbachia of each mosquito species. Assessment of the density of WO-B phage by real-time quantitative polymerase chain reaction (RTQ-PCR) revealed an average relative density of 7.76 x 10(5)+/- 1.61 x 10(5) orf7 copies per individual mosquito for a single Wolbachia strain infecting mosquitoes, but a threefold higher density in the doubly Wolbachia-infected Aedes albopictus. However, the average combined density of WO-B phage(s) did not correlate with that of their Wolbachia hosts, which varied in different mosquito species. We also confirmed the presence of WO-B-like virus particles in the laboratory colony of Ae. albopictus (KLPP) morphologically, by transmission electron microscopy (TEM). The viral-like particles were detected after purification and filtration of Ae. albopictus ovary extract, suggesting that at least one WO-B-like phage is active (temperate) within the Wolbachia of this mosquito vector. Nevertheless, the idea of utilizing these bacteriophages as transformation vectors still needs more investigation and is likely to be unfeasible.

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Year:  2006        PMID: 16842419     DOI: 10.1111/j.1365-294X.2006.02947.x

Source DB:  PubMed          Journal:  Mol Ecol        ISSN: 0962-1083            Impact factor:   6.185


  19 in total

1.  Tripartite associations among bacteriophage WO, Wolbachia, and host affected by temperature and age in Tetranychus urticae.

Authors:  Ming-Hong Lu; Kai-Jun Zhang; Xiao-Yue Hong
Journal:  Exp Appl Acarol       Date:  2012-06-06       Impact factor: 2.132

2.  Detection and phylogenetic analysis of bacteriophage WO in spiders (Araneae).

Authors:  Qian Yan; Huping Qiao; Jin Gao; Yueli Yun; Fengxiang Liu; Yu Peng
Journal:  Folia Microbiol (Praha)       Date:  2015-04-23       Impact factor: 2.099

3.  Diverse phage-encoded toxins in a protective insect endosymbiont.

Authors:  Patrick H Degnan; Nancy A Moran
Journal:  Appl Environ Microbiol       Date:  2008-09-12       Impact factor: 4.792

4.  Infection incidence and relative density of the bacteriophage WO-B in Aedes albopictus mosquitoes from fields in Thailand.

Authors:  Arunee Ahantarig; Nopmanee Chauvatcharin; Toon Ruang-areerate; Visut Baimai; Pattamaporn Kittayapong
Journal:  Curr Microbiol       Date:  2010-10-28       Impact factor: 2.188

Review 5.  Horizontal gene transfers with or without cell fusions in all categories of the living matter.

Authors:  Joseph G Sinkovics
Journal:  Adv Exp Med Biol       Date:  2011       Impact factor: 2.622

6.  Diversity of Wolbachia pipientis strain wPip in a genetically admixtured, above-ground Culex pipiens (Diptera: Culicidae) population: association with form molestus ancestry and host selection patterns.

Authors:  Rebecca J Morningstar; Gabriel L Hamer; Tony L Goldberg; Shaoming Huang; Theodore G Andreadis; Edward D Walker
Journal:  J Med Entomol       Date:  2012-05       Impact factor: 2.278

7.  Complete WO phage sequences reveal their dynamic evolutionary trajectories and putative functional elements required for integration into the Wolbachia genome.

Authors:  Kohjiro Tanaka; Seiichi Furukawa; Naruo Nikoh; Tetsuhiko Sasaki; Takema Fukatsu
Journal:  Appl Environ Microbiol       Date:  2009-07-10       Impact factor: 4.792

Review 8.  Phage WO of Wolbachia: lambda of the endosymbiont world.

Authors:  Bethany N Kent; Seth R Bordenstein
Journal:  Trends Microbiol       Date:  2010-01-18       Impact factor: 17.079

9.  Impacts of Low Temperatures on Wolbachia (Rickettsiales: Rickettsiaceae)-Infected Aedes aegypti (Diptera: Culicidae).

Authors:  Meng-Jia Lau; Perran A Ross; Nancy M Endersby-Harshman; Ary A Hoffmann
Journal:  J Med Entomol       Date:  2020-09-07       Impact factor: 2.278

10.  Large proportion of genes in one cryptic WO prophage genome are actively and sex-specifically transcribed in a fig wasp species.

Authors:  Guan-Hong Wang; Li-Ming Niu; Guang-Chang Ma; Jin-Hua Xiao; Da-Wei Huang
Journal:  BMC Genomics       Date:  2014-10-13       Impact factor: 3.969

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