Characterization of the intracellular survival of Mycobacterium avium ssp paratuberculosis: phagosomal pH and fusogenicity in J774 macrophages compared with other mycobacteria
Mp. Kuehnel et al., Characterization of the intracellular survival of Mycobacterium avium ssp paratuberculosis: phagosomal pH and fusogenicity in J774 macrophages compared with other mycobacteria, CELL MICROB, 3(8), 2001, pp. 551-566
The phagosomes containing viable pathogenic mycobacteria, such as Mycobacte
rium (M.) tuberculosis and Mycobacterium avium ssp. avium (M. avium), are k
nown to be limited in their ability to both acidify and fuse with late (but
not early) endocytic organelles. Here, we analysed the pH and fusogenicity
of phagosomes containing M. avium ssp. paratuberculosis (M. ptb), the caus
ative agent of paratuberculosis in ruminants. Using the murine J774 macroph
age cell line, we compared viable and heat-killed M. ptb and, in addition,
viable or dead M. avium, as well as two non-pathogenic mycobacteria, Mycoba
cterium smegmatis and Mycobacterium gordonae. Electron microscopic analysis
revealed that M. ptb persisted intracellularly in phagosomes for up to 15
days. The phagosomes containing live M. ptb and M. avium were significantly
reduced in their ability to acquire some markers for the endocytic pathway
, such as internalized calcein, BSA-gold or the membrane protein Lamp 2. Ho
wever, they were almost completely accessible to 70 kDa fluorescein isothio
cyanate, (FITC)-dextran and Lamp 1. Overall, the phagosomes containing dead
pathogenic mycobacteria behaved similarly to the ones containing live non-
pathogenic mycobacteria in all experiments. Using FITC-dextran in a novel f
luorescence-activated cell sorting (FACS)-based method, we could also show
that the bulk of endocytic compartments, including phagosomes, were only ve
ry mildly acidified to approximate to PH 6.3 over at least 72 h in J774 cel
ls infected with live M. ptb and M. avium. In contrast, J774 cells treated
with heat-killed M. ptb or BSA-coated latex beads showed substantial acidif
ication of the phagosome/endocytic compartments to a pH value of approximat
e to 5.2. After infection with M. smegmatis and M. gordonae, acidification
was initially (1-5 h after infection) inhibited, but increased after longer
infection to levels similar to those with dead mycobacteria.