Hs. Costa et al., MYCETOCYTE INCLUSION IN THE OOCYTES OF BEMISIA-ARGENTIFOLII (HOMOPTERA, ALEYRODIDAE), Annals of the Entomological Society of America, 89(5), 1996, pp. 694-699
This study investigates the process of transfer of endosymbiotic organ
isms from adult silverleaf whitefly, Bemisia argentifolii Bellows & Pe
rring (Bellows et al. 1994) (also known as Bemisia tabaci B biotype),
into the developing ova. In dissected females, individual mycetocyte c
ells containing microorganisms were scattered singly among developing
oocytes. Oocytes with mycetocytes included were first observed in fema
les 16 h after emergence. The mean number of oocytes >0.1 mm in length
per female increased through the 4th d after adult eclosion then leve
led off. The number of oocytes containing mycetocytes followed a simil
ar pattern. Stages of mycetocyte inclusion followed a pattern based on
the size of the oocyte. Oocytes became associated with a single mycet
ocyte cell when they were a mean of length of 0.135 +/- 0.003 mm (mini
mum of 0.11 mm). All mature oocytes examined contained a mycetocyte. M
ycetocytes were observed inside a common membrane with oocytes, at wha
t becomes the pedicel end of the ova, when oocytes were an average of
0.147 +/- 0.004 mm long. In the final stages of ovum development, the
plasma of the oocyte completely surrounded the mycetocyte and the chor
ion was thickened. Mycetocytes included in oocytes had a mean length o
f 33 +/- 0.4 mu m and width of 27 +/- 0.5 mu m. Although the females t
hat were dissected had the opportunity to oviposit, some retained seve
ral fully developed ova. Because inclusion of mycetocytes into oocytes
is a continuous process, manipulations of endosymbionts before inclus
ion into the oocytes should be possible at any time during adult life;
however, earlier treatment of an individual would probably affect a g
reater proportion of their offspring.