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. 2021 May 13;11:671913. doi: 10.3389/fcimb.2021.671913

Table 2.

Methods employed for analysis and characterization of Leishmania Sias.

Methods Leishmania species/strain Main objectives/findings References
Fluorimetric quantification by acetyl acetone method L.tropica K27,
L. major JISH118,
L. mexicana LV4,
L. braziliensis L280,
L. amazonensis LV81,
L. infantum MON29
Quantity of total Sias is proportional to virulence (Ghoshal et al., 2010)
HPLC K27, LV4, LV81 Different proportions of Neu5Gc, Neu5Ac, Neu5,7Ac2 and other derivatives (Chatterjee et al., 2003; Chava et al., 2004; Ghoshal et al., 2010; Karmakar et al., 2012)
ELISA  K27, JISH118, L280, MON29, LV4, LV81, and L. donovani AG83 Sias correlation with host responses (Chatterjee et al., 2003; Ghoshal et al., 2010)
Lectin blot (Western blot)-employing labeled achatinin MHOM/IN/83/AG83 Identification of Sias on amastigotes and adsorbed serum sialoglycans on promastigotes (Chatterjee et al., 2003; Chava et al., 2004)
Lectin blot (Western blot)- MAA e SNA labeled lectins K27, JISH118, L280, MON29, LV4, LV81, AG83 The role of Sias in Leishmania infection (Chatterjee et al., 2003; Chava et al., 2004; Ghoshal et al., 2010; Karmakar et al., 2012)
Flow cytometry employing lectins conjugated with fluorophores K27, JISH118, L280, MON29, LV4, LV81, AG83 Sias and the host susceptibility response (Chava et al., 2004; Ghoshal et al., 2010; Karmakar et al., 2012)