scholarly journals Experimental lagochilascariosis in X-chromosome-linked immunodeficient mice

2009 ◽  
Vol 42 (4) ◽  
pp. 381-385 ◽  
Author(s):  
Jaqueline Aparecida Gleice de Freitas ◽  
Mariana Félix de Souza Prudente ◽  
Mara Silvia Carvalhaes

Lagochilascaris minor is the etiological agent of lagochilascariosis, a disease that affects the neck region and causes exudative abscesses, with eggs, adult parasites and L3/L4 larvae in the purulent exudates. Mice are now considered to be intermediate hosts for the parasite. To determine the pattern of infection in B1 cell-deficient mice, experimental lagochilascariosis was studied in BALB/c and X-chromosome-linked immunodeficient (xid) mice. BALB.xid-infected mice showed lower numbers of larvae. Third-stage larvae, fourth-stage larvae and adult parasites were found in both strains. BALB/c mice produced IgM, IgG, IgA and IgE against the crude extract and secreted/excreted antigens of the parasite. On the other hand, BALB.xid mice did not produce IgM and produced lower levels of IgG and IgA, and similar quantities of IgE.

2009 ◽  
Vol 42 (3) ◽  
pp. 325-328 ◽  
Author(s):  
Mariana Félix de Souza Prudente ◽  
Adriana de Moraes Costa Crespo ◽  
Mara Silvia Carvalhaes

Lagochilascaris minor is the causative agent of lagochilascariosis, a disease that affects the neck region and causes festering abscesses, with eggs, adult parasites and L3/L4 larvae within the purulent exudates. Today, mice are considered to be intermediate hosts for the parasite. C57BL/6 mice produce immunoglobulin IgM, IgA and IgG against the crude extract of the parasite; on the other hand, antibodies produced against the secreted/excreted antigens of Lagochilascaris minor present lower levels of IgM, IgA and IgG. This is the first description of antibody detection against different antigens of Lagochilascaris minor.


Parasitology ◽  
1970 ◽  
Vol 60 (1) ◽  
pp. 97-122 ◽  
Author(s):  
J. F. A. Sprent

Several species of Australian python, Morelia spilotes variegatus, Liasis amethy-stinus, L. fuscus and L. childreni, were experimentally infected with eggs of Ophidascaris moreliae and the development of the larvae described. The first moult occurred in the egg, which survived and remained infective for over 7 years in moist conditions. The first moult occurred in 12 days and the second-stage larva in the egg was infective to mice in 14–21 days. After ingestion the larvae migrated to liver and lungs and in 21 days were mainly distributed throughout the subcutaneous tissues, particularly in the neck region and behind the ears. Growth occurred to about 8 mm; the larvae attained their infectivity for pythons after 5 weeks and retained it for more than a year. The second moult was not observed but it was assumed that the third stage was infective for pythons. Development to about the same length occurred in guinea-pigs and indigenous and laboratory rats and in the bandicoot (Isoodon obesulus). In the possum (Tricho-surus sp.) a more rapid growth occurred to about the same length. No growth occurred in tadpoles.After ingestion by pythons larvae migrated to the lungs, where they remained for 3 months or more, grew to a length of 45 mm and underwent the third moult. Larvae removed from the lungs and reingested by pythons returned to the lungs if they had been in the first python for less than 60 days. After this time, they remained in the stomach of the second python. During the third moult larvae underwent a marked constriction of the anterior end, moved up the trachea and became attached in the upper oesophagus as fourth-stage larvae. In mouse-infected M. spilotes the third moult occurred at 117 days at a length of 23–45 mm; fourth-stage larvae measured 34–50 mm. The fourth moult occurred in the stomach at 318 days at a length of 37–55 mm. The smallest adult specimens found were a 55 mm male and a 63 mm female. Development to the adult stage was only observed in M. spilotes variegatus. In other python species only pre-adult forms were recovered. It appeared that development may be retarded at the fourth moult during the winter. The morphology of the larvae during the five stages of development is described. It is concluded that the main growth phases are the third stage in the lungs of the python and the adult stage in the stomach of the python. Encapsulated forms were found only in the tissues of intermediate hosts. The larvae from mouse tissues emerged from the capsules during putrefaction and survived for several weeks in water.Acknowledgement is made to the able technical assistance of Miss Marian Hollis. Financial assistance for this study was provided under grants from the Australian Research Grants Committee and the United States Department of Health, Education and Welfare no. A 107023–02.


2009 ◽  
Vol 46 (4) ◽  
pp. 205-208 ◽  
Author(s):  
M. Prudente ◽  
R. Lino-Junior ◽  
M. Carvalhaes

AbstractLagochilascaris minor is the causative agent of lagochilascariosis, a disease that affects the neck region causing exudative abscesses with eggs, adult parasites and L3/L4 larvae within purulent exudates. Nowadays, mice are considered intermediate hosts for the parasite. To determine the pattern of infection in B1 cell-defective mice, experimental lagochilascariosis was studied in BALB/c and X-chromosome-linked immunodeficient (Xid) mice. BALB.xid infected mice showed higher survival ratios and less intense lung lesions than BALB/c mice. Serum levels of IL-10 was higher in BALB/c infected mice when compared to BALB.xid animals; however, serum levels of IFNγ, in control and infected BALB.xid mice, were statistically different from that seen in BALB/c mice. We discuss the participation of B1 cells and their cytokines in the resistance to infection.


1988 ◽  
Vol 66 (10) ◽  
pp. 2212-2222 ◽  
Author(s):  
Lena N. Measures

In Guelph Lake, a man-made reservoir in Ontario, Canada, prevalence of larval Eustrongylides tubifex in pumpkinseed (Lepomis gibbosus), rock bass (Ambloplites rupestris), and yellow perch (Perca flavescens) was 12.9% and mean intensity ranged from 1 to 1.8. Larvae were encapsulated on the mesentery of fish. Pumpkinseed and yellow perch were the important fish hosts in Guelph Lake as most larvae in these fish were alive. In contrast, 40% of larvae in rock bass were dead and calcified. Third- and fourth-stage larvae from naturally infected fish are described. Larvae in the three species of fish elicited a granulomatous inflammatory reaction. Attempts to transfer third-stage larvae from experimentally infected oligochaetes and third-stage larvae from naturally infected fish to laboratory-reared pumpkinseed were unsuccessful. Fourth-stage larvae from naturally infected fish were transferred successfully to pumpkinseed. Eutropic lakes such as Guelph Lake are particularly suitable enzootic areas because of the abundant populations of tubificid intermediate hosts and the presence of fish hosts such as pumpkinseed and perch. The advanced stage and development of larvae (to the fourth stage) in fish likely represents an adaptation for a parasite that occurs in a migratory host such as Common Mergansers (Mergus merganser), which frequent Guelph Lake for only about 1 month in spring and fall.


2006 ◽  
Vol 66 (1b) ◽  
pp. 199-204 ◽  
Author(s):  
N. M. S. Banevicius ◽  
E. M. Zanotti-Magalhães ◽  
L. A. Magalhães ◽  
A. X. Linhares

Some terrestrial mollusks are natural hosts of Angiostrongylus costaricensis. In the laboratory, this nematode can be maintained in certain planorbids, which are aquatic mollusks and intermediate hosts of Schistosoma mansoni. Mollusks can be infected with Angiostrongylus costaricensis by ingestion of or active penetration by the first-stage larvae. In this work we assessed the ability of Biomphalaria glabrata to attract first-stage larvae of A. costaricensis. Movement of the nematode larvae towards the mollusks was observed after 15 min, 30 min and 1 h. B. glabrata did not attract the first-stage larvae of A. costaricensis in any of the three intervals. The susceptibility of two populations of Biomphalaria tenagophila to infection by A. costaricensis was also determined. One population was genetically selected for the susceptibility to S. mansoni while the other was not. Third-stage larvae were recovered from the snails 30 days after exposure of the two populations to 120 first-stage larvae. All the mollusks were infected. However, a significantly higher number of third-stage larvae were recovered in mollusks not genetically selected.


1976 ◽  
Vol 54 (4) ◽  
pp. 522-525 ◽  
Author(s):  
Richard J. Cawthorn ◽  
Roy C. Anderson

The stomachs of 162 (89%) of 183 striped skunk (Mephitis mephitis) collected in the area of Guelph, Ontario, between September 1973 and August 1974 were infected with Physaloptera maxillaris. Adult worms were most abundant in midsummer (June–July) and rare in winter (December–March). Third-stage larvae were most abundant in late fall and midwinter (October–January) and least abundant in midsummer (June–July). Fourth-stage larvae were most abundant in spring (April–May) and least abundant in early fall (August–September). It is suggested that adults appear mainly when skunk are feeding regularly in spring and midsummer. Third-stage larvae acquired in late summer and fall fail to develop (probably because of inadequate food consumption by skunk) and persist over the winter. In spring when skunk start to feed again, overwintering larvae grow into adults and initiate the annual cycle in skunk and intermediate hosts.


1998 ◽  
Vol 76 (1) ◽  
pp. 33-38 ◽  
Author(s):  
Murray W Lankester ◽  
Ing-Marie C Olsson ◽  
Margareta Stéen ◽  
Alvin A Gajadhar

Dimensions and illustrations of the first-, second-, and third-stage larvae of Elaphostrongylus alces are presented for the first time. First-stage larvae were 417 ± 16 µm long (mean ± SD) (range 377-445 µm) and similar in size to those of E. cervi (420 ± 13 µm long; range 392-445 µm) and E. rangiferi, the other recognized members of the genus. The mean length of third-stage E. alces larvae (714 ± 23 µm long; range 675-756 µm) recovered from gastropod intermediate hosts was significantly less than that of E. cervi (831 ± 78 µm long; range 669-954 µm) and E. rangiferi, providing further evidence of the distinct status of E. alces, a recently described species from moose in Fennoscandia.


2011 ◽  
Vol 48 (3) ◽  
pp. 162-166
Author(s):  
M. Prudente ◽  
J. Freitas ◽  
E. Ribeiro ◽  
M. Carvalhaes

Abstract Lagochilascaris minor is the causative agent of human lagochilascariosis, a disease that affects the neck region causing abscesses with eggs, adult parasites and L3/L4 larvae within purulent exudates. Nowadays, mice are considered intermediary hosts for the parasite. In previous study we observed that A/J mice experimentally infected with Lagochilascaris minor showed higher survival ratios than B10.A mice. Now, we denoted that A/J mice (resistant to experimental infection) produced higher levels of IgM, IgG and IgA against the crude extract (excepted for IgM) and secreted/excreted antigens of the parasite; on the other hand, B10.A mice (susceptible to experimental infection) produced higher levels of IgE in the later period of the experimental infection than A/J infected mice.


2000 ◽  
Vol 74 (4) ◽  
pp. 323-328 ◽  
Author(s):  
M. Køie

AbstractMature specimens of Cucullanus heterochrous Rudolphi, 1802 (Nematoda: Cucullanidae) were obtained from the intestine of the flounder, Platichthys flesus, from Danish waters. Eggs embryonate in seawater but do not hatch. Fully developed larvae pressed out of eggs are 430 μm long with amphids and dereids and enclosed within the cuticle of a previous larval stage. Infective larvae are believed to be in their third stage. Experimental studies showed that the polychaetes, Nereis spp., Scoloplos armiger, Brada villosa and Capitella sp., may act as intermediate hosts. In N. diversicolor the larvae increase their length to 1 mm within four weeks (15°C) without moulting. Experimental infections showed that larvated eggs are not infective to fish, whereas >550 μm long larvae from polychaetes survived in 4–24 cm long flounders and plaice, Pleuronectes platessa. Third-stage larvae 550 μm to 1.1 mm long were found in the submucosa of the intestine one week post infection. At a length of about 800 μm to 1.4 mm they moult to fourth-stage larvae. Fourth-stage larvae, immature and mature worms occur in the intestine and rectum. Fourth-stage larvae and adults survived experimental transfer from one flounder to another. Similar developmental stages survived for two weeks in the intestine of experimentally infected cod, Gadus morhua.


1962 ◽  
Vol 40 (7) ◽  
pp. 1175-1186 ◽  
Author(s):  
Roy C. Anderson

Eggs of Diplotriaena bargusinica from worms found in a Hylocichla fuscescens from Algonquin Park, Ontario, hatched and developed in the fat body of grasshoppers (Melanoplus bilituratus, M. fasciatus, Camnula pellucida). At approximately 30–33 °C the first molt took place on the 9–11th day, the second on the 14–16th day. Most second- and third-stage larvae were enveloped in capsules, more than one larva often being present in a single capsule. The larval stages from grasshoppers are described. Grasshoppers with infective larvae were fed to two H. fuscescens, one H. ustulata. one Turdus migratorius, and one Quiscalus quiscula. Subadult worms were found in the two H. fuscescens and the H. ustulata 55–301 days later but none was found in the other birds examined 78–97 days later. Late fourth-stage larvae from the heart and aorta of a nestling H. ustulata captured in the field are described. It is believed tridents first make their appearance during development in the definitive host from the infective stage to the fourth stage. Observations on the morphology of adult D. bargusinica are also reported.


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