Maintenance of Acanthamoeba culbertsoni by Cryopreservation

1998 ◽  
Vol 84 (6) ◽  
pp. 1261 ◽  
Author(s):  
Ricardo Alejandre-Aguilar ◽  
Ma. Lourdes Calvo-Mendez ◽  
Benjamin Nogueda-Torres ◽  
Fernando de la Jara-Alcocer
Author(s):  
Ahmad Z Al-Herrawy ◽  
Mohamed A Marouf ◽  
Mahmoud A. Gad

Genus Acanthamoeba causes 3 clinical syndromes amebic keratitis, granulomatous amebic encephalitis and disseminated granulomatous amebic disease (eg, sinus, skin and pulmonary infections). A total of 144 tap water samples were collected from Giza governorate, Egypt. Samples were processed for detection of Acanthamoeba species using non-nutrient agar (NNA) and were incubated at 30oC. The isolates of Acanthamoeba were identified to species level based on the morphologic criteria. Molecular characterization of the Acanthamoeba isolates to genus level was performed by using PCR. The obtained results showed that the highest occurrence percentage of Acanthamoeba species in water samples was observed in summer season (38.9%), then it decreased to be 30.6% in spring and 25% in each of autumn and winter. PCR analysis showed that 100% of 43 Acanthamoeba morphologically positive samples were positive by genus specific primer. In the present study eight species of Acanthamoeba can be morphologically recognized namely Acanthamoeba triangularis, Acanthamoeba echinulata, Acanthamoeba astronyxis, Acanthamoeba comandoni, Acanthamoeba griffini, Acanthamoeba culbertsoni, Acanthamoeba quina and Acanthamoeba lenticulata. In conclusion, the most common Acanthamoeba species in tap water was Acanthamoeba comandoni


1989 ◽  
Vol 66 (10) ◽  
pp. 690-693 ◽  
Author(s):  
CHARLES G. CONNOR ◽  
YVONNE BLOCKER ◽  
DONALD G. PITTS

Steroids ◽  
1988 ◽  
Vol 51 (5-6) ◽  
pp. 551-558 ◽  
Author(s):  
Haider Mehdi ◽  
H.S. Garg ◽  
N.K. Garg ◽  
D.S. Bhakuni

2001 ◽  
Vol 8 (4) ◽  
pp. 724-730 ◽  
Author(s):  
Cynthia L. Chappell ◽  
John A. Wright ◽  
Michael Coletta ◽  
Anthony L. Newsome

ABSTRACT Acanthamoeba species can cause serious, debilitating, and sometimes life-threatening infections. Three groups have been identified using morphological and immunological comparisons. Previous serological studies have utilized a variety of antigen preparations and assay methods and reported disparate (3 to 100%) results. This study was designed to (i) optimize an enzyme-linked immunosorbent assay for detecting serum antibodies to each of the Acanthamoebaserogroups and (ii) test 55 healthy individuals for specific immunoglobulin G reactivity. The highest signal-to-background ratio was found when 3,000 fixed, intact trophozoites per well were used with a 1:10 serum dilution. Sera yielding optical densities of <0.25 against all three Acanthamoeba serogroups were used to define the cutoff for positive results. The highest background reactivity with these sera was seen with Acanthamoeba polyphaga (serogroup 2), followed by Acanthamoeba culbertsoni (serogroup 3) andAcanthamoeba astronyxis (serogroup 1). Of 55 subjects tested, the highest number of positive results was seen with A. polyphaga (81.8%), followed by A. astronyxis(52.8%) and A. culbertsoni (40%). Seven serum samples (12.7%) were negative for all three Acanthamoebaserogroups, 16 (29.1%) were positive for one serogroup only, 16 were positive for two serogroups, and 16 reacted to all three serogroups. Further analysis showed no significant associations between serogroup reactivity and age or gender. However, some ethnic differences were noted, especially with A. polyphaga antigens. In that case, serum samples from Hispanic subjects were 14.5 times less likely to be positive (P = 0.0025) and had lower mean absorbance values (P = 0.047) than those from Caucasian subjects. Overall, these data suggest that Acanthamoeba colonization or infection is more common than previously thought. Mild or asymptomatic infections may contribute to the observed serum reactivities.


Sign in / Sign up

Export Citation Format

Share Document