Females: twice in size (length) of the adult males
Larvae, also known as microfilariae
Slender and size ranges under 150 um to 350 um in length
Two key characteristics helpful in speciating the microfilariae forms:
Distribution of nuclei
Presence or absence of a delicate transparent covering known as a sheath
Only one to four infective larvae, injected by an infected arthropod at the feeding site, are required to initiate human infection
Larvae migrate to the tissues for their development
Resulting adult worms reside in the lymphatics, subcutaneous tissue, or intestinal body cavities
Fertilized adult female worms lay live microfilariae, which take up residence in the blood or dermis
Microfilariae exit the body via a blood meal by the appropriate arthropod vector
Intermediate host & vector of filaria: arthropod
Larvae development into the infective stage takes place in the insect host
Parasite is transferred into uninfected humans
Larvae development into the infective stage takes place in the insect host
Periodicity
A phenomenon whereby the parasites are present in the bloodstream during a specific time
This periodicity is connected to the corresponding vector’s feeding schedule
Nocturnal - occurring at night
Diurnal - occurring during the day
Subperiodic - the timing of occurrences is not clear-cut
Primary Method of Diagnosis: Microscopic examination of the microfilariae Giemsa-stained blood or a tissue scraping of an infected nodule
Whole blood samples may also be collected (the two are used for low microfilaremia - low amount of microfilariae in the blood)
Knott's technique
Membrane filtration
Knott’s Technique
1 mL of blood can be mixed with 140 mL of 2% formalin and then centrifuged
The supernatant is discarded and the sediment is studied (sediment: bottom; used for the thin blood film)
Spread like a thin blood film, fixed, and stained
Membrane Filtration - makes use of a syringe attached to a Swinney filter holder
1 mL of fresh or anticoagulated blood is drawn into the syringe and lyzed by adding 10 mL of distilled water
Lyzed blood is then passed through a Swinney membrane filter where microfilariae will be recovered
A membrane filter can be examined like a wet smear preparation or may be dried, fixed, and then stained
Although a number of serologic tests have been developed and are available, there is some concern as to their specificity, and thus, they are not universally considered as viable diagnostic techniques.
WUCHERERIA BANCROFTI Common name: Bancroft's Filaria
WUCHERERIA BANCROFTI Common associated disease/Condition Names:
Bancroft’s filariasis or Elephantiasis
WUCHERERIA BANCROFTI Microfilariae
240 to 300 um long
Sheath is present (thin and delicate)
Numerous nuclei in the body
Anterior end is blunt and round
Posterior end or tail end is free of nuclei
WUCHERERIA BANCROFTI Adult worm
White and threadlike appearance
Females: 40-100 mm
Males: 20-40 mm
WUCHERERIA BANCROFTI Specimen of Choice: Blood
WUCHERERIA BANCROFTI Lab Diagnostic Method of Choice: Examination of Giemsa-stained blood
WUCHERERIA BANCROFTI Heparinized blood
More sensitive for microfilariae recovery
Blood is filtered through nuclepore filter, and then the filtered contents are stained and examined
WUCHERERIA BANCROFTI
Knott Technique
Light infections
1 mL blood mixed with 10 mL of 2% solution of formalin and then centrifuged. Sediment is spread like a thin blood film, stained, and examined
WUCHERERIA BANCROFTI Periodicity: Nocturnal
Peak hours: 9:00 PM - 4:00 AM
Wuchereria bancrofti Serologic tests, including antigen and antibody detection and PCR assays, have been developed