Tissue migration capability of larval and adult Brugia pahangi
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作者:
Chirgwin, SR
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Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USALouisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
Chirgwin, SR
[1
]
Coleman, SU
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Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USALouisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
Coleman, SU
[1
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Porthouse, KH
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Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USALouisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
Porthouse, KH
[1
]
Klei, TR
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Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USALouisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
Klei, TR
[1
]
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[1] Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
Infection with mosquito-born filarial nematodes occurs when hosts are bitten by a vector carrying the infective third Stage larvae (L3) of the parasites. These larvae, deposited oil the skin by the feeding mosquito, are presumed to enter the,;kill via the vector-induced puncture wound. Larvae of Brugia spp. must then migrate from the entry site, penetrate various skin layers. and locate I lymphatic vessel that leads to their lymphatic predilection site. We have recently established an intradermal (11)) infection Model using B. pahangi and (lie Mongolian gerbil. allowing LIS to investigate the migratory capability of B. pahangi. Larval and adult parasites recovered from the peritoneal cavities of gerbils were capable of establishing an infection following ID (larvae) or subcutaneous (adult) injection. Third and fourth stage larvae both migrated away from the injection site within hours, although data suggest they localize to different lymphatic tissues at 3 days postinfection (DPI). Immature adult (28 day) B. pahangi also migrated away front their SC inoculation site within 7 DPI. Mature (45 day) adult B. pahangi displayed little migration away front the SC infection site, suggesting tissue migration may be limited to developing stages of the parasite.