Assessment of the resilience of canine leishmaniasis to control or, more ambitiously, the effort needed to eradicate infection, requires an estimate of the basic case reproduction number (R0). This paper applies the theoretical results of Hasibeder, Dye & Carpenter (1992) to data from a cross-sectional survey on the Maltese island of Gozo in which dogs of known age, sex and occupation (pet, guard etc) were subjected to three different serological tests for the presence of specific antibody (IFAT, DAT and ELISA). Difficulties in interpreting these test results, and hence of determining the proportion of dogs infected, present the main obstacle to estimating R0: estimates are critically dependent on the choice of threshold separating seropositives from seronegatives. The data do, however, allow a robust comparative analysis of risk which shows that the force of infection experienced by working dogs is about three times higher than that of pet dogs, a degree of non-homogeneous contact which actually has little effect on estimates of R0. We suggest a cautious point estimate of R0 ≃ 11, and comment briefly on its significance for leishmaniasis control.

The surface lipophosphoglycans (LPG) of Leishmania promastigotes express stage- and species-specific polymorphisms that are defined by variations in the type and number of phosphorylated oligosaccharide repeats. We have studied how these polymorphic structures control the development of transmissible infections in the sandfly vector as well as the species-specificity of vectorial competence. Procyclic promastigotes displayed an inherent capacity to bind to midgut epithelial cells of a competent vector. This capacity was lost during their transformation to metacyclic promastigotes, permitting the selective release and anterior migration of infective-stage parasites for subsequent transmission by bite. Midgut attachment and release were found to be controlled by developmental modifications in terminally exposed saccharides on LPG, which, depending on the species of Leishmania, involved either substitution or capping of terminal side-chain sugars, loss of terminal side-chain sugars, substitution or loss of neutral capping sugars. The stage-specific terminal sugars involved in midgut adhesion are, in some cases, also species-specific, and the extent to which these differences affect midgut attachment, forcefully predicted vectorial competence.

Investigations were made on possible reservoir hosts of Leishmania donovani in 2 zoonotic foci of visceral leishmaniasis (VL) in Dinder National Park (DNP) and the peri-domestic habitats of adjacent villages of eastern Sudan. Animals were captured, in November 1997–1998 and April–May 1999 and examined for L. donovani infection using light microscopy and 2 sensitive Polymerase Chain Reaction (PCR) systems. Microscopy and PCR investigations were also used to determine the infection rates of L. donovani in Phlebotomus orientalis captured from the uninhabited site of DNP. Infections of L. donovani were detected in 2 out of 14 Egyptian mongooses (Herpestes ichneumon), 1 out of 168 Arviconthus niloticus and 1 out of 8 Mastomys natalensis. Samples from 68 other animals captured from the study area were all negative for the infection. Active zoonotic transmission of L. donovani at the time of animal sampling in the uninhabited site of DNP was demonstrated by finding the parasite in 3.4% (7 out of 184) and 3.2% (5 out of 157) of flies collected in March 1998 and May 1999, respectively. We suggest that the Egyptian mongoose is a possible reservoir host of L. donovani. The importance of other animals in maintaining the infection is also discussed.

A number of natural and man-made habitats in Marigat area of Kenya were surveyed for sandflies in 1985/86. Of the 98,573 adult sandflies collected, 2.7 % belonged to the genus Phlebotomus and 97.3% to Sergentomyia. Relative abundance of sandflies of the genus Phlebotomus was four times higher in burrows than in termite hills, while sandflies of the genus Sergentomyia collected from termite hills were twice as numerous as those from burrows. Termite hills had the highest sandfly population compared to other sites, followed by tree holes and animal burrows. Fifteen species were identified, of which five belonged to Phlebotomus and 10 to Sergentomyia. The most abundant and widespread species were Sergentomyia antennatus, S. bedfordi, S. ingrami, Phlebotomus martini, S. schwetzi, S. africanus and P. duboscqi. Sandflies of both genera were present for the greater part of the year. Most species of sandflies decreased in numbers during the dry season. High population densities of sandflies were recorded during the wet period. Correlations between relative abundance of sandfly vectors of leishmaniases and rainfall were positive. However, none of the correlation coefficients was statistically significant.

—In order to evaluate the effect of permethrin-treated wall cloth against phlebotomine sandflies, a study lasting 26 months (February 1989 to March 1991) was conducted in Marigat Location of Baringo District, Kenya, an endemic focus of both visceral and cutaneous leishmaniases. In six experimental villages, a total of 2000 houses were fitted with cloth made of cotton and impregnated with permethrin EC 20% at a dosage of 0.5 g/m2 diluted in water. Houses in the two control villages were not fitted with cloths and were located 1.5 km away from the experimental area. Traps made of clear polythene sheeting were coated with castor oil and placed inside houses to collect endophilic sandflies. In the experimental villages, the permethrin-treated wall cloth (called Mbu cloth) reduced the population of sandflies found inside houses by 52–73%. Phlebotomus martini and P. duboscqi, vectors of visceral and cutaneous leishmaniases, were reduced by 76 and 85% respectively. In the experimental villages, highly significant differences were observed between the average numbers of sandflies collected before deployment of the treated wall cloth and those observed after thethird treatment of the cloth. No major sandfly reduction was observed however, in the control villages. There was also evidence of feeding reduction due to the permethrin.

Animal burrows are major habitats for both P. martini and P. duboscqi, vectors of visceral and cutaneous leishmaniases in Kenya. In burrows, both species were collected throughout the year. The highest relative abundance of P. martini and P. duboscqi was recorded in August and in April, respectively. The lowest relative abundance was observed in july for P. martini and in October for P. duboscqi. In termite mounds, P. martini was present all the year round, but P. duboscqi was absent for the greater part of the year. The highest relative abundance of P. martini was observed in November and April, while that of P. duboscqi was seen in March and April. The lowest relative abundance of P. martini was recorded in July. In termite mounds, P. duboscqi showed a significant positive correlation with rainfall, contrary to P. martini which did not afford any significant correlation with any environmental factor. Rainfall, relative humidity and ambient temperature did not correlate with relative sandfly abundance in animal burrows.

Field investigations were carried out in northern Nigeria to determine the prominent natural habitats of phlebotomine sandflies. Two biotopes, termite hills and rock crevices, were identified as the major habitats with the termite hills being the most significant. All the 12 species (Phlebotomus duboscqi, P. rodhaini, Sergentomyia antennula, S. bedfordi, S. africana, S. schwetzi, S. ingrami, S. adleri, S. clydei, S. buxtoni, S. affinis and S. christophersi) identified in this study came from this source. Only a small number of samples representing a few species were collected from the three other habitats (tree holes, animal burrows and a cave) investigated. The distribution of the sandflies was found to be influenced by the availability of suitable biotopes and physico-chemical composition of the soil.

Five (Sergentomyia antennatus, S. garnhami, S. schwetzi, S. ingrami and S. adleri) of the six species of sandflies fed on mammalian blood containing cultured Leishmania donovani promastigotes on day 0, were able to feed through cockerel skin membranes at 5.5, 10, 34.3, 45.7 and 95% feeding rates, respectively. Sergentomyia bedfordi was able to feed on mammalian blood only through a lizard skin membrane at 100% feeding rate. Promastigotes were found in 9.3, 25 and 37.5% of S. schwetzi, S. adleri and S. ingrami respectively, dissected on days 3–9.

The results open way for artificial feeding of Kenyan sandflies on mammalian blood through membranes, and indicate that it is necessary to select the type of membrane depending on sandfly species. The ability of L. donovani to develop in Kenyan sandflies is being investigated to experimentally establish and confirm the importance of various genera and species in the epidemiology of leishmaniasis.

Studies of outer chorionic sculpturing of eggs of four species of sandflies were carried out by the use of scanning electron microscope. Two species, P. martini and S. garnhami, which utilize similar resting sites, termite hill ventilation shafts, had similar chorionic sculpturing, while two other species (S. bedfordi and S. kirki) which use several resting sites, i.e. rock crevices, tree holes and termite ventilation shafts, had chorionic sculpturings which were dissimilar.

A survey of phlebotomine sandflies was carried out in northern Nigeria to determine the distribution of Phlebotomus (Phlebotomus) duboscqi which is suspected to be the vector of cutaneous leishmaniasis in West Africa. P.(P.) duboscqi was found to be confined to the very dry areas of the Sudan savanna vegetation zone, where it utilizes termite hills as the main breeding habitats in association with rodents and lizards. Rock hyrax were located in some adjacent rocky areas. The restricted distribution range includes locations where cutaneous leishmaniasis has been recorded in Nigeria.

Investigation of sandfly vectors of visceral leishmaniasis (kala-azar) was intensified after the epidemic outbreak of the latter in Machakos District, Kenya, in the early 1970s. Studies were carried out to assess the infection rate of potential vectors using human baits during the height of the 1978 epidemic outbreak. The results presented here indicated that, in Machakos District, sandflies captured when coming to human baits had higher infection rates than those collected in the natural resting sites using suction tubes.

Ultrastructural studies were carried out on wild Kenyan sandflies (Phlebotomus pedifer) naturally infected with Leishmania aethiopica. The promastigotes were attached to structures resembling pieces of a peritrophic membrane. They were located amongst long microvilli and also deep in the cytoplasm of the gut cells. The factors which influence the invasion of the parasites into cells are not known and need to be investigated.

Wild-caught phlebotomine sandflies were captured from rock crevices and termite hills and released into feeding cages containing various species of laboratory animals, to find suitable hosts for feeding flies for experimental or breeding purposes. Flies captured from rock crevices did not feed as well as those human-baited at termite hills. The ubiquitous species from the termite hills was Phlebotomus martini, the major vector of kala-azar in the study area (Machakos District of Kenya). This anthropophilic species feeds readily on the mammalian laboratory animals. Cooling flies before feeding stimulated them to feed.