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After large-scale control and treatment efforts, visceral leishmaniasis (VL) was well controlled in China by the 1960s and eliminated in the early 1980s as a major public health problem (1). However, the number of mountain-type zoonotic visceral leishmaniasis (MT-ZVL) cases has been increasing significantly in recent years. Conducting timely identification of this disease and implementing an early warning of MT-ZVL transmission risks are fundamental premises of generating targeted intervention measures. To identify the key risk areas, a risk-matrix was used to assess the transmission risk of MT-ZVL in six endemic provincial-level administrative divisions (PLADs) in China. Data such as the indigenous cases (2015–2020) and the occurrence probabilities of the main vector Phlebotomus chinensis (Ph. chinensis) were collected, and the comprehensive scores were calculated. The transmission risk areas showed a trend of patchy dissemination centered on major endemic areas and medium-high risk occurrence areas of the vector with discrete foci. Multi-point re-emergence and local outbreaks of MT-ZVL appeared in historically endemic areas. In the medium-high risk areas identified, the recommended strategies are more frequent monitoring of sandflies, canines, and mobile population, establishing a mechanism of joint prevention and control, and highlighting health education to the public.
The indigenous cases reported in 6 endemic PLADs were collected from the National Notifiable Disease Reporting System between 2015 and 2020 (Figure 1A). The data were verified by epidemiological investigations on individual cases and vector investigations conducted by county-level CDCs. According to the working guidelines of VL prevention and control, the endemic county-level administrative divisions (CLADs) were categorized into three classes with the number of reported cases based on experts’ experiences of onsite prevention and control. Class I CLADs were those with a cumulative case number of not less than 10. Class II and Class III CLADs had 3–9 and less than 3 cases, respectively. Non-endemic CLADs were those that have no indigenous case. The scores were 3, 2, 1, 0, from more cases to less.
Figure 1.Transmission risks of mountain-type zoonotic visceral leishmaniasis in six endemic PLADs, China. (A) The distribution of MT-ZVL indigenous cases in CLADs from 2015 to 2020; (B) The occurrence probabilities of Phlebotomus chinensis in CLADs; (C) The risk-matrix evaluation result of MT-ZVL in CLADs.
Note: The occurrence probabilities of Phlebotomus chinensis were calculated using the distribution data of the vector, and bioclimatic and geographical environment data in previous studies. The sandfly distribution data was derived from a national field survey and historical literature; the environment data was derived from the WorldClim database (https://www.worldclim.org/data/worldclim21.html) and Resource and Environment Science and Data Center database (http://www.resdc.cn/). Abbreviations: MT-ZVL=mountain-type zoonotic visceral leishmaniasis; PLADs=provincial-level administrative divisions; CLADs=county-level administrative divisions.The historical distribution of the vector, bioclimatic, and geographical environmental data were collected. MaxEnt software (version 3.4.1, American Museum of Natural History, New York, NY, USA) was used to calculate the occurrence probabilities of Ph. chinensis in a previous study (2). The continuous value of occurrence probabilities ranged from 0–1 (minimal–maximal probability). In this study, the occurrence probabilities were re-extracted by mean value based on CLADs and further categorized into three ranks. A 0.60–1.0 value was a high risk for the occurrence of Ph. chinensis, 0.30–0.59 was medium risk, and 0–0.29 was low risk, and these were assigned 3, 2, and 1 points, respectively.
The cumulative value of the comprehensive scores was calculated and presented in the transmission risk-matrix (Table 1). The assessment was under expert guidance and the results were already included in the investigation of vectors in potential MT-ZVL endemic areas. The data of indigenous cases and the vectors, and the risk warning assessment scores were analyzed by Microsoft Excel (version 2016, Microsoft, Redmond, WA, USA). The visual maps were made by ArcGIS (version 10.1, ESRI, Redlands, CA, USA).
Classification of Occurrence probabilities of
Phlebotomus chinensisClassification of MT-ZVL endemic CLADs ClassⅠ
(cases ≥10, 3)ClassⅡ
(cases 3–9, 2)Class Ⅲ
(cases <3, 1)Non-endemic
(no case, 0)High risk (0.60–1, 3) 6, RISK 1 5, RISK 2 4, RISK 2 3, RISK 3 Medium risk (0.30–0.59, 2) 5, RISK 2 4, RISK 2 3, RISK 3 2, RISK 3 Low risk (0–0.29, 1) 4, RISK 2 3, RISK 3 2, RISK 3 1, RISK 4 Note: MT-ZVL scores were calculated by the summation of the scores of endemic CLADs classification and the scores of occurrence probabilities of Phlebotomus chinensis. The corresponding risk levels were evaluated comprehensively by the scores and opinions of experts.
Abbreviations: MT-ZVL=mountain-type zoonotic visceral leishmaniasis; PLADs=provincial-level administrative divisions; CLADs=county-level administrative divisions.Table 1. Risk-matrix evaluation on the transmission risk of mountain-type zoonotic visceral leishmaniasis in 6 endemic PLADs in China, 2015–2020.
The number of MT-ZVL indigenous cases and its proportion of total VL cases increased significantly between 2015 and 2020, although the annual number of VL cases showed an overall downward trend. Re-emerged cases were defined as indigenous cases after epidemiological investigations that currently re-occurred in an area where local transmission was interrupted in the past 10 years, according to the literature (3). A total of 25 MT-ZVL re-emergent CLADs appeared between 2015 and 2020, with 88 re-emergent cases reported. The number of class I, Ⅱ, and Ш CLADs were 16, 20, and 23 in the study area, respectively. They were scattered in southern Gansu, northern Sichuan, and the mountainous cross-border areas of Shaanxi, Shanxi, Hebei, and Henan, showing significant local aggregation characteristic (Figure 1A). The occurrence probabilities map of Ph. chinensis showed 66 high risk areas, 154 medium risk areas, and 592 low risk areas on a county basis (Figure 1B).
According to the risk assessment results, RISK 1, RISK 2, RISK 3, and RISK 4 areas contained 16, 41, 143, and 592 CLADs, corresponding to super-high risk, high risk, moderate risk, and low risk, respectively. RISK 1 and RISK 2 areas included all major MT-ZVL endemic CLADs and the majority of high-risk areas for Ph. chinensis occurrence, while most of the RISK 3 areas were the vector’s medium risk occurrence areas. The risk areas showed a trend of patchy dispersion centered on major endemic CLADs and medium-high risk occurrence areas of the vectors. Multi-point re-emergence and local outbreaks appeared in historically endemic areas. Medium-high risks appeared in the suburbs of some large urban regions and their surrounding areas. The distribution of risk areas was concentrated in the Qinling Range in southern Gansu and Shaanxi, the northern Hengduan Range in northern Sichuan, the Lvliang Range and the extended region of Loess Plateau at the cross-border areas of Shaanxi and Shanxi, and hilly areas of the Yanshan-Taihang Range across Shanxi, Henan, and Hebei (Figure 1C).
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