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View Article - Biodiversity Heritage Library
1999
Journal of the American Mosquito Control Association, l5(2):ll7-127,
Copyright O 1999 by the American Mosquito Control Association, Inc.
A HISTORICAL REVIEW OF THE F-l STRAIN OF ANOPHELES
FREEBORNI AS A HOST AND VECTOR FOR STUDIES OF MALARIA
WILLIAM
E. COLLINS
AND GEOFFR-EY M. JEFFERY
Divisktn of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention,
Public Health Service, U.S. Department of Health and Humnn Services, Atlanta, GA 30341
ABSTRACT. A reveiw was made of the use of a specific strain of Anopheles freeborni from California
(F-1) that has been used extensively in experimental investigations ofmalaria for more than 50 years. The
F-l strain of An. freeborni has been shown to be a suitable experimental host and vector for different
species of Plasmodium that cause malaria in humans and nonhuman primates for biologic, immunologic,
and chemotherapeutic studies. Eleven species of Plasmodium ftlly completed sporogonic development;
development of sporozoites within mature oocysts occurred in an additional 7 species. Transmission through
An. .freeborni from human to human, monkey to human, or monkey to monkey has been demonstrated for
9 species of Plasmodium.
KEY
WORDS
Anopheles freeborni, Plasmodium, malaria, mosquitoes
INTRODUCTION
Over the last half century, several species of
anopheline mosquitoes have served as laboratory
hosts for experimental studies on malaria. Among
these are Anopheles quadrimaculatus Say, An.
atroparvus Thiel, An stephensi Liston, An. albimanus Wiedemann, and An. freeborni Aitken.
Here we summarize some of the studies that have
established An. freeborni as one of the most useful and suitable hosts for a variety of investigations of malaria.
The F-l strain of An. (An.) freeborni Aiken
was established from eggs laid by wild-caught females collected near Marysville, CA, on March
3, 1943. The colony was supplemented by an additional 800 wild-caught females on March 15
and 25O to 400 females collected from the same
location on April 30, 1943. On August 21, 1944,
eggs were shipped from the U.S. Public Health
Service laboratory at Letterman General Hospital, San Francisco, CA, to the U.S. Public Health
Service laboratory in Columbia, SC. This was
part of the wartime "Imported Malaria Studies"
effort to determine the potential of native anophelines to transmit malaria parasites from infected
returning servicemen. Since its establishment,
this strain of An. freeborni l;.as been maintained
continuously in various laboratories where it has
served as the standard host and vector for comparative studies with many species of Plasmodium causing human and nonhuman malaria.
A suitable experimental host and vector should
be able to be reared in relatively large numbers
using standard insectary techniques, should readily feed on animal or human hosts, should support sporogonic development to the production of
infectious sporozoites, and should be capable of
transmitting the infection by feeding on a susceptible host. Preferably, a laboratory vector will be
susceptible to infection with and be capable of
transmitting
a number of different species of
Plasmodium. A review of the use of this mosquito for studies with human and nonhuman primate malaria parasites indicates that this is a remarkably usefi.rl vector for biologic, immunologic,
and chemotherapeutic studies.
HUMAN
MALARIA
PARASITES
The earliest studies with the F-l strain involved the feeding of colony-reared mosquitoes
on Plasmodium vivax-infected soldiers returning
from the South Pacific and the Mediterranean
during World War II. Young et al. (1945) reported
that 1,358 of 2,581 mosquitoes that fed on these
patients became infected; several infections with
P. vivax originating from the Pacific were experimentally transmitted by An. freeborni. Moore et
al. (1945) reported on the feeding of 64 lots of
An. freeborni on relapsing P. vivax infections in
soldiers. Mosquitoes became infected and 8 infections were transmitted to other patients by this
vector. Oocyst counts as high as 8OOper gut were
found, although the usual oocyst counts ranged
from 1 to 24. Hardman (L947) summarized the
procedures being used at that time for the laboratory rearing of these mosquitoes. These early
studies indicated that An. freeborni had high potential for more extensive investigations. Of early
interest was the relative efficiency of different
laboratory-reared anopheline vectors in transmitting different species and strains of human malaria parasites. Using simultaneous feedings,
Young and Burgess (1948) reported on the comparative susceptibility of An. quadrimaculatus
from the southeastern United States and An. freeborni from California to foreign vivax malaria;
their studies indicated that the latter was more
susceptible (more oocysts per gut and higher percentage of infection). Young et al. (1948) reported the infection of An. freeborni witln P. vivax
from different geographic origins, including the
Il]]]
u8
Table 1.
JounNnLon rne AvnnrcaN Mosqurro CoNrnol AssocrATroN
Studies on the infection and transmission of Plasmodium vivax, P. falciparum,
by Anophe les freeborni.
Species of
Plasmodium
Strains (geographic origin)
Primate hosts
P. vivax
South Pacific and Mediteranean, Sal I and Sal II (El
Salvador), Chesson (New
Guinea), West Pakistan
(Pakistan), ONG and
NAM (Indonesia), St,
Elizabeth (U.S.A.), NICA
(Nicaragua), Panama
(Panama), Vietnam I-IV
(Vietnam), Vietnam Palo
Alto (Vietnam), Brazll U
CDC (Brazil), Mauritania
VCDC (Mauritania), New
Guinea (New Guinea),
North Korean (Korea),
India VII (India), and
others
Humans, night monkeys,
squirrel monkeys, chimpanzees
P. falciparum
Mclendon (U.S.A.), Panama II (Panama), Santa
Lucia (El Salvador), Malayan IV (Malaysia),
Cambodian I (Cambodia).
West Africa I (Nigeria),
NF-54 and 3D7 (Netherlands). and Indochina I
(Thailand-Cambodia),
Burma Thau. (Burma),
Montagnard (Vietnam),
Colombia (Colombia),
Thailand (Thailand), El
Limon (Panama), and
others
Humans, night monkeys,
squirrel monkeys, chimpanzees
Solomon Islands, New Guinea, New Britain, the
Mediterranean, Burma, and the Carribean. Burgess and Young (1950) reported on a comparative
study on the susceptibility of An. quadrimaculatus and An. freeborni to the St. Elizabeth strain
of P. vivax. Here again, An. freeborni was more
Vor-. 15, No. 2
p. malariae,
and.p. ovale
References
Moore et al. 1945; Young
et al. 1945, 1948; Young
and Burgess 1948; Burgess and Young 195O;
Collins and Roberts
1991: Collins et al.
1969c, 1972b, 1973c,
1973d, 1974c, 1976a,
1976b, 1977a, 1979a,
1979d, 1980a, 1980b.
1980c. 1983a. 1985b.
1985c, 1985e,1986a,
1986c, 1987b, 1987d,
1988, 1992b, 1994a,
1998a, 1998b; Coatney et
al. 1971t Singal et al.
1977; Warren and Collins
1981; Krotoski et al.
1982; Campbell et al.
1983: Wirtz et al. 1985:
Hollingdale et al. 1985,
1986; Millet et al. 1989;
Porter and Collins 1990;
Barr et al. l99l; Charenov i t e t a l l 9 9 l ; S u l l i v a ne t
al. 1996; Nayar et al. 1997
Beier et al. 19921,Burgess
and Young 1946; Burkot
et al. 1984; Campbell et
al. 1980a, 1980b, 1982,
1986; Chege et al. 1996;
Collins et al.1963,
1964a, 1968b, 1972,
1973e, 1973f, 19'77a,
1977b, 1978, r979a,
1979c, 1979d, 1981a,
1982a,1982b, 1983b,
1986d, 1991, 1996a,
1996b. 1997b: Contacos
and Collins 1968; Sodeman et al. 1969; Coatney
et al. 1971; Chin and
Collins 1980;Collins and
Contacos 1980; Ponnudurai et al. 1982; Mazier et
al. 1984; Techlehaimanot
et al. 1987; Graves et al.
1988: Renia et al. 1988:
Do Rosario et al. 1989:
Millet et al. 1991a; Shahabuddin et al. 1993;
Vaughn et al. 1994a,
1994b; Noden et aI.
1995; Vaidya et al. 1995;
Gozar et al. 1998
susceptible than was An. quadrimaculatus. This
strain, of probable U.S. origin, was frequently
used for the induction of malariotherapy of patients with neurosyphilis, a standard treatment at
that time. With the cessation of the use of malaria
studies on
for the treatment of neurosyphilis,
JUNE 1999
HISToRICAL
REvIEw
Table 1.
Species of
Plasmodium
ll9
oF ANoPHELES FREEBORNI
Strains (geographicorigin)
Continued.
Primate hosts
References
P. malariae
USPHS (U.S.A.), Philippines, Nigeria, Uganda,
China I/CDC
Humans, night monkeys,
squirrel monkeys, chimDanzees
P. ovale
Donaldson (South Pacific),
West Africa, Nigerian
Humans, chimpanzees
transmission to humans ceased. With the subsequent establishment of P. vivax in New World
monkeys, a large number of different isolates and
strains of P. vivax were now available for studv
it An. freebornl (Table 1).
Burgess and Young (1946) were the lst to report the experimental transmission by An. freeborni of Plasmodium falciparum
(Mclendon
strain) to 2 patients; prepatent periods were 15
and 29 days. Anopheles freeborni then became
one of the standard hosts and vectors for transmission studies with this parasite. Jeffery et al.
(1963) reported on studies with a multidrug-resistant strain of P. falciparum from Thailand in
which 6 patients were infected via the bites of
An. freeborni.
In a comparative susceptibility
study based on oocyst densities, Collins et al.
(L964a) demonstrated that, with a strain of P.
falciparum from Panama, An. freeborni was more
heavily infected than was An. quadrimaculatus or
even a coindigenous strain of An. albimanus.
However, the adaptation of various strains of P.
falciparum to New World monkeys opened up a
new field of study where An. freeborni was exposed to isolates and strains of the parasite from
distant geographic areas (Table 1).
Plasmodium malariae was first shown to be
transmissible by An- freeborni
by Young and
Burgess (1947). Little further success in the
transmission of this parasite was obtained until
Contacos and Collins (1969) reported the transmission of P. malariae from an infected night
monkey (Aotus sp.) to humans. Although subsequent studies indicated monkeys and chimpanzees would support the development of p. malariae gametocytes infective to An. freeborni,
transmission via sporozoites to other monkeys
and chimpanzees was not successful.
Chin et al. (1966) reported the transmission of
a West African strain of Plasmodium ovale from
human to human using An. freeborni. Successful
Young and Burgess 1961;
Collins and Contacos
1969: Contacos and Collins 1969; Coatney et al.
1971; Collins et al.
1973a, 1975a, 1984a,
1989a, r989b, l99Od,
1994b. 1997a:.Millet et
al. 1988a: Nagasawa et
al. 1988
Chin et al- 1966: Collins et
a1. I969c. 1987c: Coatney et al. l97l; Mazier
et al. 1987; Nagasawa et
al. 1987; Millet et al.
1994; Morris et al. 1996
experimental studies with P. ovale and An. freeborni have also been conducted in chimpanzees.
Different strains of this parasite readily infect An.
(liver stages) of
freeborni, and exoerythrocytic
the parasite have been demonstrated in squirrel
monkeys (Saimiri spp.). However, no erythrocytic-stage infections have been established in New
World monkeys.
The ready infectivity of many different strains
of human malaria parasites from diverse geographic areas to An. freeborni suggested that this
mosquito could serve as a universal host for a
variety of chemotherapeutic
and immunologic
studies. In fact, this has become the case in several laboratories in the United States.
NONHUMAN
PRIMATE
PARASITES
MALARIA
Monkeys have long been used a models for
chemotherapeutic and immunologic studies with
malaria parasites, and both Old World and New
World monkeys have been infected with various
species of Plasmodium. For almost 40 years, we
have usedAn. freeborni as a laboratory vector for
a variety of studies on malaria in nonhuman primates (Table 2). It early became apparent that,
although in most instances An. freeborni
was
highly susceptible to the development of the oocyst stage, some species of Plasmodium failed to
develop to the point of sporozoites being present
in the salivary glands. With all but a few species,
oocyst densities in An. freeborni were high; oocyst counts could be used as an indicator of gametocyte infectivity.
However, transmission via
sporozoites could only be obtained if oocysts
containing mature sporozoites were crushed and
then injected into the primate. Plasmodium cynomolgi, P. gonderi, P. simium, P. fragite, and
P. brasilianum, parasites of monkeys, developed
fully, including the presence of sporozoites in the
120
Table 2.
Species of
Plasmodium
JounNnl on tHe AlvrnnrclNMosqurro Corqrnol AssocterroN
Studies on the infection and transmission of nonhuman primate-infecting
Anopheles freeborni.
Strains (geographic origin)
Primate hosts
P. brasilianum
S (Colombia), AT (Panama) Peruvian I-III
Night monkeys, squirrel
monkeys, spider monkeys, humans
P. coatneyi
Hackeri (Malaysia)
Macaques
P. crynomolgi
B, Berok, M, Gombak
(Malaysia), ceylonensis
(Sri Lanka), RO (Assam-Burma), Celebes
(Philippines), Cambodian
Macaques, night monkeys,
squirrel monkeys
P. fieldi
Macaques
P. fragile
Hackeri, N-3, ABI, Malaysian
Sri Lanka, Nilgiri (India)
P. gonderi
Mandrill
P. hylobati
WAK
P. inui
Taiwanland2(Taiwan),
N-34, Perlis, Perak, I-eaf
Monkey I and II, kucosphyrus, Mulligan,
and others (Malaysia),
OS (India)
Malaysian
Macaques, night monkeys,
squirrel monkeys
P. knowlesi
H, Malaysian, Hackeri
(Malaysia)
P, reichenowi
Chimpanzee (West Africa)
Macaques, humans, night
monkeys, squirrel monkeys
Chimpanzees
P. schwetzi
Chimpanzee (West Africa)
Chimpanzees, humans
P. simiovale
Sri Lanka
Macaques
P. simium
Howler (Brazil)
Night monkeys, squirrel
monkeys
P. jefferyi
(West Africa)
(Indonesia)
salivary glands of An. freeborni. Plasmodium
schwetzi and P. reichenowi, parasites of chimpanzees and gorillas, and P. hylobati, a parasite
of gibbons, also developed to maturity in this
vector.
Some parasites failed to develop beyond the
presence of mature sporozoites in oocysts and
Macaques, Night monkeys,
squirrel monkeys
Macaques
Gibbons
Gibbons
Vor-. 15, No. 2
species of Plasmodium by
References
Collins et al. 1969b,
1985d, 1990b, 1993; Sodeman et al. 1969; Coatney et al. l97l
Held and Contacos 1967;
Coatney et al. l97l;'
Coffins et al.1992a
Coatney et al. 1971; Collins et al. 1972c, l9'15b,
1985a, 1998; Krotoski et
al. 1973: Omar and Collins 1973; Omar et al.
1973, 1974:' Atkinson et
al. 1989; Millet et al.
1989,1990
Coatney et al. 1971; Collins et al. 1984b,1992a
Collins et al. 1967, 1974b,
1975c, l990a, 1992a;
Coatney et al. 19'71
Collins et al. 1964b,
1992a; Coatney et aI.
1971; Collins and Contacos 1980
Coatney et al. l97l; Collins et al. 1972d
Collins et al. 1968a,
198lb; Held et al. 1968;
Coatney et al. l97l:'
Nguyen-Dinh et al.
1980; Collins and Warren 1998
Collins and Orihel 1969;
Coatney et al. 1971; Rodenberg 1985; Millet et
al.1988b
Coatney et al. 19'71
Coatney et al. 1971; Collins et al. 1986b
Collins et al. 1969c; Contacos et al. 1970; Coatney et al. t97l
Coatney et al. l97l; Collins et al. 1972a,1992a;
Collins and Contacos
1979
Collins et al.1969a,
1973b, 1974a, 1979b,
1987a; Coatney et al.
197 |
transmission could be obtained only through the
injection of mechanically harvested sporozoites.
Those parasites requiring mechanical harvesting
included Plasmodium knowlesi, P. simiovale, P.
coatneyi, P. fieldi, and P. inui.
Anopheles freeborni has been shown to support
the complete sporogonic development of many
Juxe 1999
HISToRICAL
70
Rgvrsw
oF ANoPHELES FREEBoRNI
SPOROZOIIESIN SALIVARYGLANDS
sPoRozotTEs
tNoocYsTs
'15 17 17
11 ?? 12 11 12 13 12 14
12r 12' 14' 14' 13* 161 16r
a
260
o
E
Qso
e
cr40
UJ
-
lil
=3 0
o20
z
uJ .^
0
inui
cynomolgi gondei lalcipmm simium reichenowimaliliae knowl$i simiovale ietleN
lngile
schweai viw
Nah brcilimm
coatneyi tieldi
Wobati
SPECIESOF PIASMODIUM
Q a o e v s ! r o o r v s f f i r z o r v sf f i r + o n v s
Fig. l.
Mean oocyst diameter at 8, 10, 12, and 14 days and days when sporozoites are present in salivary glands
or mature oocysts inAnophelesfreeborni
mosqtoitoes infected with 18 species of Plasmodium when incubated at 25
+ 1"C.
different species of Plasmodium, but fails to do
so for other parasites (Fig. 1). This mosquito
readily supports full development, to the presence of sporozoites in the salivary glands, of P.
vivax and P. ovale and the related nonhunman
tertian parasites P. cynomolgi, P. gonderi, P.
schwetfi, and P. simium; P. falciparum and the
related parasite P. reichenowi; P. malariae and
the related quartan parasite P. brasilianum:
and
the tertian parasite P. hylobati. Anopheles freeborni supports to a lesser extent the sporogonic
development of the tertian parasites P. fragile, P.
Table 3.
Transmission
j"ff"ryi,
P. fieldi, P. simiovale, and P. coatneyi;
the quartan parasite P. inui; and the quotidian
parasite P. knowlesi. In these latter species, infective sporozoites are present in mature oocysts,
but are rarely found in the salivary glands. Infectivity of these sporozoites has been demonstrated
by the injection of susceptible hosts with sporozoites mechanically released from mature oocysts. In our studies with monkeys (Table 3),
transmission via bite or the injection of sporozoites dissected from An. freeborni has been
demonstrated with 9 species of Plasmodium. Be-
of 9 species of Plasmodium from monkey to monkey by Anopheles freeborni
mosquitoes.
Transmissions
Species of
Plasmodium
Donor
P. brasilianum
Recipient
P. coatneyi
P. cynomolgi
Saimiri
Ateles
Macaca mulatta
M. mulatta
Saimiri
Ateles
M. mulatta
M. mulatta
P. falciparum
Aotus
Aotus
Aotus
Aotus
P.
P.
P.
P.
P.
M. mulatta
M. mulatta
M. mulatta
M. mulntta
Aotus
M. mulatta
M. mulatta
M. mulatta
M. mulatta
Aotus
Aotus
Samiri
Saimiri
Saimiri
Bite
Injectionr
9
3
0
32
0
0
6
a1
fieldi
gonderi
inui
knowlesi
vivax
3
0
44
0
1
0
8
3
0
o
0
37
2
3
l
0
0
l
a
'Intravenous
or intrahepatic injection of sporozoites dissected from omysts or infected salivry
glands.
Prepatentperiod(days)
Range
t8-42
t8-43
14-15
8-36
8-24
l5-19
10-69
t6-69
l8-30
t2-17
t2-15
5-6
14-55
1417
39
28
Median
34.O
36.0
15.0
I1.0
9.0
18.0
23.O
22.O
18.0
13.0
13.5
6.0
2t.o
20.s
39.0
28.0
122
JounNll
oF THE AMERlc,rN Mosquno
cause of the invariable success in all species tested, there is no reason to believe that sporozoites
from salivary glands or mature oocysts of the
other species of human and nonhuman primate
malaria parasites produced in An. freeborni could
not also be infective to susceptible primate hosts.
Ano p he I es fre eb o rni, after long-term establishment in the laboratory, has been shown to be
highly susceptible to many species of Plasmodium from widely separated geographic areas. In
addition, the susceptibility
to many different
strains of the parasites from widely separated
geographic areas allows us to use this mosquito
as a standard for all studies with human malaria
parasites and most of the nonhuman-infecting
species.
Many questions remain concerning the relationship between this mosquito host and the different species of human and nonhuman primate
malaria parasites. The reasons why one species
of Plasmodiun develops completely, whereas another does not, deserves investigation. Why are
oocyst densities higher in An. freeborni than rn
other mosquitoes when simultaneously fed on
certain strains of Plasmodium? Why is the reverse true with other species and strains of parasites when different species of anophelines simultaneously
feed on the same animal? The
extensive data available from studies on the F-l
strain of An. freebornl generate more questions
than answers on the vector-parasite relationships
for this extremely important group of human
pathogens.
REFERENCES CITED
CoNrnol
AssocrATloN
V o l . 1 5 ,N o . 2
of cultured Plasmodium falciparum. Trans. R. Soc.
Trop. Med. Hy g. 74:668-669.
Campbell, C. C., W. E. Collins, J. M. Roberts and A.
Armstead. 1986. Adaptation of the Indochina VCDC
stratn of Plasmodium falciparum to the squirrel monkey
(Saimiri sciureus). Am. J. Trop. Med. Hyg. 35:472-475.
Campbell, C. C., H. C. Spencer, W. Chin and W. E. Cotlins. 1980b. Adaption of cultured Plasmodiumfalciparum to the intact squirrel monkey (Saimiri sciureus).
Trans. R. Soc. Trop. Med. Hyg. 74:548-549.
Campbell, C. C., W. Chin, W. E. Collins, S. M. Teitsch
and D. M. Moss. 1979. Chloroquine-resistant Plasmodium falciparum from East Africa. Lancet 1:11511t54.
Campbell, C. C., W. E. Collins, W. Chin, J. M. Roberts
and J. R. Broderson. 1983. Studies on the Sal I strain
of Plasmodium vivrtx in the squirrel monkey (Saimiri
sciureus). J. Parasitol. 69:598-601.
Campbell, C. C., W. E. Collins, P Nguyen-Dinh, A. Barber and J. R. Broderson. 1982. Plasmodiumfalciparum
gametocytes from in vitro culture develop to sporozoites which are infectious to primates. Science 217:
1048-1050.
Charoenvit, Y., W. E. Collins, T, R. Jones, P. Millet, L.
Yuan, G. H. Campbell, R. L. Beaudoin, J. R. Broderson
and S. L. Hoffman. 1991. Inability of malaria vaccine
to induce antibodies to a protective epitope within its
sequence. Science 251:668-67 l.
Chege, G. M., C. B. Pumpuni and J. C. Beier. 1996. Proteolytic enzyme activity and Plasmodium falciparum
sporogonic development in three species of Anopheles
mosquitoes. J. Parasitol. 82: I 1-16Chin, W. and W. E. Collins. 1980. Comparative studies on
two strains of Plasmodium falciparum isolated by the
culture method of Trager and Jenson. Am. J. Tiop. Med.
Hyg. 29:1143-1146.
Chin. W.. P. G. Contacos and J. N. Buxbaum. 1966. The
transmission of a West African strain of Plasmodium
ovale by Anopheles freeborni and Anopheles maculatus.
Am. J. Trop. Med. Hyg. 15:690-693.
Coatney, G. R., W. E. Collins, McW Warren and P G.
Contacos. 1971. The primate malarias. U.S. Government Printing Office, Washington, DC.
Collins, W. E. and P G. Contacos. 1969. Infectivity of
Plasmodium malariae in the Aotus trivirgatus monkey
to Anopheles freeborni mosquitoes. J. Parasitol. 55:
1253-1257.
Collins, W. E. and P G. Contacos. 1972. Transmission of
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Plasmodiumfalciparum
bite of infected Anopheles freeborni mosquitoes. Tlans.
R. Soc. Trop. Med. Hyg.66:371-372.
Collins. W. E. and P G. Contacos. 1979. Infection and
transmission studies with Plasmodium simiovale in the
Macaca mulatta monkey. J. Parasitol. 65:6O9-612.
Collins, W. E. and P G. Contacos. 1980. Infection and
transmission of Plasmodium gondei inthe Macaca mulatta monkey. J. Parasitol. 66:998-1002.
Collins, W. E. and T. C. Orihel. 1969. The sporogonic cyle
of P Ia smodium j effe ry i. J. Parasitol. 55 : l24O -1246.
Atkinson, C. T,, P Millet, W. E. Collins and M. Aikawa.
1989.Localizationof the circumsporozoiteantigenin
exoerythrocytic schizonts of Plasmodium cynomolgi.
Am. J. Trop.Med. Hyg. 40:13l-140.
Barr, P J., K. M. Green, H. L. Gibson, I. C. Bathurst, I.
A. Quakyi and D. C. Kaslow. 1991.RecombinantPfs25
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Beier,J. C., M. S. Beier,J. A. Vaughn,C. B. Pumpuni,J.
R. Davis and B. H. Noden. 1992. Sporozoitetransmission by Anophelesfreeborni and Anopheles gambiae
experimentallyinfected with Plasmodiumfalc iparum. J.
Am. Mosq. Control Assoc. 8:404-408.
Burgess, R. W. and M. D. Young. 1946. Experimental
transmissionof P. falciparumby Anophelesmaculipennis freeborni. J. Natl. Malar. Soc. 57:150-151.
Burgess,R. W. and M. D. Young. 1950.The comparative
susceptibility of Anopheles quadrimaculatus and
Anophelesfreeborni to infection by Plasmodium vivax Collins, W. E. and J. M. Roberts. 1991. Anopheles Satnbiae as a host for geographic isolates of Plasmodium
(St. Elizabeth strain). J. Natl. Malar. Soc.9:218221.
vivttx. L Am. Mosq. Control Assoc. 7:569-573.
Burkot, T. R., J. L. Williams and I. Schneider.1984. InCollins, W. E. and McW. Warren. 1998. Studies on infecfectivity to mosquitoes of Plasmodium falciparum
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