Professional Documents
Culture Documents
Wolbachia
Wolbachia
The uncertainty concerning the naming of Wolbachia has for quite some time been a
problem for organizing and understanding strain diversity. In fact, one problem for traditional
phylogeny methods is the rising findings of extensive recombination among strains because it
accelerates the modification of genomic characteristics specifically surface protein, housekeeping
genes, and prophage genes together with intergenic regions (Baldo, Bordenstein, Wernegreen,
& Werren, 2005).
Invertebrates have no excuse to Wolbachia as it has the ability to grow and to operate
their reproductive process and cellular mechanism on them. Moreover, on the study of Baldo,
Clark, & Werren (2008), it has been found that a particular group of bacteria, with the genus
Candidatus Cardinium on the class of Bacteroidetes, to have a unique particular set of
reproductive manipulation.
Studies had shown that Wolbachia infection causes phenotypical effects including
Cytoplasmic incompatibility, Parthenogenesis induction, feminization, male killing, and multi-
potent Wolbachia.
Fourth, same cause of Wolbachia infection is male killing. During the stage of
embryogenesis of an arthropod, male killing occurs. Because it happens on the beginning stage
of life cycle, higher rate of survival on female progeny because more food materials for them.
According to Kageyama, Nishimura, Hoshizaki, & Isikawa the reason for male killing in
lepidopteran host namely Ostrinia scapulalis was brought from feminization induced by
Wolbachia. Genetic females die during larval development when there is an absence of
Wolbachia, while in the presence of Wolbachia, feminization happen to genetic males and
eventually die during the stage of larval development. Hence, Wolbachia-induced male killing
happens through lethal feminization (Kageyama & Traut, 2004).
Fifth, there are selected strains that can induce multiple phenotype. One evidence is a
Wolbachia strain that infects the lepidopteran host Cadra cautella normally causes CI, but when
cases that the strain transferred into different host, the same strain cause male killing but not CI
(Sasaki & Ishikawa, 2000).
Given all these phenotypical effects that make the dark side of Wolbachia, there are things
that could be bright side of the bacteria. In the world full of darkness disease and terror of pests,
Wolbachia is our light for combatting such things (Bourtzis, 2008; Pfarr & Houerauf, 2006). Not
only that, but it also fights the filarial pathogenicity (Saint André, 2002). Its mechanism is to target
bacteria that causes the pathogen by taking action using anti-Wolbachia treatment together with
the use of vermicides which causes reduction of nematode load (Debrah, et. al., 2007; Debrah,
et. al., 2006; Turner, et. al., 2006; Bazzocchi, et. al., 2008). Currently, the Wolbachia genomes
are being utilized to identify possible targets for therapeutic agents. Wolbachea can also be used
in proliferation of arthropod population by means of phenotypic alteration by cytoplasmic
incapability. Wolbachia-infected males is manipulated and use as a tool in controlling pest
population by inducing elevated cytoplasmic incapability (Xi, Koo, & Dobson, 2005; Zabalou, et.
al., 2004; Dogson, Fox, & Jiggins, 2002). Moreover, the use of Wolbachia in resolving problem is
not limited with filarial pathogenicity and proliferation of the arthropod population. It is useful in
resolving world problems such as dengue fever by shortening the lives of its vectors such us
Aedes mosquitoes by also phenotypic alteration with the aid of Wolbachia (Brownstein, Hett &
O’Neill, 2003).
Though given these information, Wolbachia has a lot more to discover. Its capacity to
infect is not just for negative but also can be useful in other aspects in life. If this organism has its
effect on shortening the lives of Aedes mosquitoes, then it has the potential on killing other pest
and pathogenic vectors. To end this discussion, Wolbachia is a good counter evidence for
misconception about all bacteria are harmful. We only need to open our scientific minds and look
for the bright side of everything.
REFERENCES
Baldo, L., Bordenstein, S., Wernegreen, J. J., & Werren, J. H. (2005). Widespread
recombination throughout Wolbachia genomes. Molecular biology and evolution, 23(2),
437-449.
Bazzocchi, C., Mortarino, M., Grandi, G., Kramer, L. H., Genchi, C., Bandi, C., ... & McCall, J.
W. (2008). Combined ivermectin and doxycycline treatment has microfilaricidal and
adulticidal activity against Dirofilaria immitis in experimentally infected dogs. International
journal for parasitology, 38(12), 1401-1410.
Bourtzis, K. (2008). Wolbachia-based technologies for insect pest population control. In
Transgenesis and the management of vector-borne disease (pp. 104-113). Springer,
New York, NY.
Brownstein, J. S., Hett, E., & O’Neill, S. L. (2003). The potential of virulent Wolbachia to
modulate disease transmission by insects. Journal of invertebrate pathology, 84(1), 24-
29.
Debrah, A. Y., Mand, S., Marfo‐Debrekyei, Y., Batsa, L., Pfarr, K., Buttner, M., ... & Hoerauf, A.
(2007). Macrofilaricidal effect of 4 weeks of treatment with doxycycline on Wuchereria
bancrofti. Tropical medicine & international health, 12(12), 1433-1441.
Debrah, A. Y., Mand, S., Specht, S., Marfo-Debrekyei, Y., Batsa, L., Pfarr, K., ... & Hoerauf, A.
(2006). Doxycycline reduces plasma VEGF-C/sVEGFR-3 and improves pathology in
lymphatic filariasis. PLoS pathogens, 2(9), e92.
Dobson, S. L., Fox, C. W., & Jiggins, F. M. (2002). The effect of Wolbachia-induced cytoplasmic
incompatibility on host population size in natural and manipulated systems. Proceedings
of the Royal Society of London. Series B: Biological Sciences, 269(1490), 437-445.
Kageyama, D., & Traut, W. (2004). Opposite sex–specific effects of Wolbachia and interference
with the sex determination of its host Ostrinia scapulalis. Proceedings of the Royal
Society of London. Series B: Biological Sciences, 271(1536), 251-258.
Lassy, C. W., & Karr, T. L. (1996). Cytological analysis of fertilization and early embryonic
development in incompatible crosses of Drosophila simulans. Mechanisms of
development, 57(1), 47-58.
Narita, S., Kageyama, D., Nomura, M., & Fukatsu, T. (2007). Unexpected mechanism of
symbiont-induced reversal of insect sex: feminizing Wolbachia continuously acts on the
butterfly Eurema hecabe during larval development. Appl. Environ. Microbiol., 73(13),
4332-4341.
O'Neill, S. L., Giordano, R., Colbert, A. M., Karr, T. L., & Robertson, H. M. (1992). 16S rRNA
phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic
incompatibility in insects. Proceedings of the National Academy of Sciences, 89(7),
2699-2702.
Pannebakker, B. A., Pijnacker, L. P., Zwaan, B. J. & Beukeboom, L. W. (2004). Cytology of
Wolbachia-induced parthenogenesis in Leptopilina clavipes (Hymenoptera Figitidae).
Genome 47, 299–303.
Pfarr, K. M., & Hoerauf, A. M. (2006). Antibiotics which target the Wolbachia endosymbionts of
filarial parasites: a new strategy for control of filariasis and amelioration of pathology.
Mini reviews in medicinal chemistry, 6(2), 203-210.
Poinsot, D., Charlat, S., & Mercot, H. (2003). On the mechanism of Wolbachia‐induced
cytoplasmic incompatibility: Confronting the models with the facts. Bioessays, 25(3),
259-265.
Reed, K. M., & Werren, J. H. (1995). Induction of paternal genome loss by the paternal‐sex‐ratio
chromosome and cytoplasmic incompatibility bacteria (Wolbachia): a comparative study
of early embryonic events. Molecular reproduction and development, 40(4), 408-418.
Ros, V. I. D., Fleming, V. M., Feil, E. J., & Breeuwer, J. A. J. (2009). How Diverse Is the Genus
Wolbachia? Multiple-Gene Sequencing Reveals a Putatively New Wolbachia
Supergroup Recovered from Spider Mites (Acari: Tetranychidae). Retrieved from
https://aem.asm.org/content/75/4/1036
Saint André, A. V., Blackwell, N. M., Hall, L. R., Hoerauf, A., Brattig, N. W., Volkmann, L., ... &
Diaconu, E. (2002). The role of endosymbiotic Wolbachia bacteria in the pathogenesis of
river blindness. Science, 295(5561), 1892-1895.
Sasaki, T., & Ishikawa, H. (2000). Transinfection of Wolbachia in the Mediterranean flour moth,
Ephestia kuehniella, by embryonic microinjection. Heredity, 85(2), 130.
Stouthamer, R., & Kazmer, D. J. (1994). Cytogenetics of microbe-associated parthenogenesis
and its consequences for gene flow in Trichogramma wasps. Heredity, 73(3), 317.
Turner, J. D., Mand, S., Debrah, A. Y., Muehlfeld, J., Pfarr, K., McGarry, H. F., ... & Hoerauf, A.
(2006). A randomized, double-blind clinical trial of a 3-week course of doxycycline plus
albendazole and ivermectin for the treatment of Wuchereria bancrofti infection. Clinical
Infectious Diseases, 42(8), 1081-1089.
Vandekerckhove, T., Watteyne, S., Bonne, W., Vanacker, D., Devaere, S., Rumes, B., ... &
Mertens, J. (2003). Evolutionary trends in feminization and intersexuality in woodlice
(Crustacea, Isopoda) infected with Wolbachia pipientis (alpha-Proteobacteria). Belgian
journal of zoology, 133(1), 61-69.
Weeks, A. R., & Breeuwer, J. A. J. (2001). Wolbachia–induced parthenogenesis in a genus of
phytophagous mites. Proceedings of the Royal Society of London. Series B: Biological
Sciences, 268(1482), 2245-2251.
Werren, J. H., Baldo, L., & Clark, M. E. (2008). Wolbachia: master manipulators of invertebrate
biology. Nature Reviews Microbiology, 6(10), 741–751. doi:10.1038/nrmicro1969
World Mosquito Program (n.d.). Wolbachia. Retrieved from
http://www.eliminatedengue.com/our-research/wolbachia
Xi, Z., Khoo, C. C., & Dobson, S. L. (2005). Wolbachia establishment and invasion in an Aedes
aegypti laboratory population. Science, 310(5746), 326-328.
Zabalou, S., Riegler, M., Theodorakopoulou, M., Stauffer, C., Savakis, C., & Bourtzis, K. (2004).
Wolbachia-induced cytoplasmic incompatibility as a means for insect pest population
control. Proceedings of the National Academy of Sciences, 101(42), 15042-15045.