The order of prime-boost vaccination of neonatal calves with Mycobacterium bovis BCG and a DNA vaccine encoding mycobacterial proteins Hsp65, Hsp70, and Apa is not critical for enhancing protection against bovine tuberculosis.

Priming neonatal calves at birth with a Mycobacterium bovis bacillus Calmette-Guérin (BCG) vaccine and boosting with a DNA vaccine consisting of plasmids encoding mycobacterial antigens Hsp65, Hsp70, and Apa or the reverse prime-boost sequence induced similar levels of protection against experimental challenge with Mycobacterium bovis. When M. bovis was isolated from a thoracic lymph node following challenge, the two groups of calves given the prime-boost regimen had significantly lower numbers of M. bovis isolates than those vaccinated with BCG alone. These observations suggest that the exact sequence of administration of a prime-boost vaccination regimen in a neonatal animal model is not critical to the development of immunity.

Development of the lung of the brushtail possum, Trichosurus vulpecula.

The developing lung of the brushtail possum, Trichosurus vulpecula, was studied by light microscopy, and transmission electron microscopy was used to study the morphology of the conducting airways in the adult. Bronchi did not extend beyond the hilus of each of the six lobes of the lung, and lobules were supplied by major bronchioles. By 105 days post partum, bronchi and bronchioles were fully formed, coinciding with the emergence of mucosal associated lymphoid tissue (MALT), which preceded alveolar maturation by approximately 20 days. In the adult lung, goblet cells were rarely observed in the mucosal epithelium of bronchi, whereas Clara cells were present in the mucosa of all airways, increasing proportionately as the conducting and respiratory portions narrowed distally. Although the airways of the possum lung have a poorly developed mucociliary blanket, this may be compensated for by the large numbers of Clara cells and adequate supply of MALT.