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. 2016 Dec 19;15:595. doi: 10.1186/s12936-016-1646-2

Spatial and space–time distribution of Plasmodium vivax and Plasmodium falciparum malaria in China, 2005–2014

Samuel H Hundessa 1, Gail Williams 1, Shanshan Li 1, Jinpeng Guo 2, Linping Chen 1, Wenyi Zhang 2,✉, Yuming Guo 1,✉
PMCID: PMC5168843  PMID: 27993171

Abstract

Background

Despite the declining burden of malaria in China, the disease remains a significant public health problem with periodic outbreaks and spatial variation across the country. A better understanding of the spatial and temporal characteristics of malaria is essential for consolidating the disease control and elimination programme. This study aims to understand the spatial and spatiotemporal distribution of Plasmodium vivax and Plasmodium falciparum malaria in China during 2005–2009.

Methods

Global Moran’s I statistics was used to detect a spatial distribution of local P. falciparum and P. vivax malaria at the county level. Spatial and space–time scan statistics were applied to detect spatial and spatiotemporal clusters, respectively.

Results

Both P. vivax and P. falciparum malaria showed spatial autocorrelation. The most likely spatial cluster of P. vivax was detected in northern Anhui province between 2005 and 2009, and western Yunnan province between 2010 and 2014. For P. falciparum, the clusters included several counties of western Yunnan province from 2005 to 2011, Guangxi from 2012 to 2013, and Anhui in 2014. The most likely space–time clusters of P. vivax malaria and P. falciparum malaria were detected in northern Anhui province and western Yunnan province, respectively, during 2005–2009.

Conclusion

The spatial and space–time cluster analysis identified high-risk areas and periods for both P. vivax and P. falciparum malaria. Both malaria types showed significant spatial and spatiotemporal variations. Contrary to P. vivax, the high-risk areas for P. falciparum malaria shifted from the west to the east of China. Further studies are required to examine the spatial changes in risk of malaria transmission and identify the underlying causes of elevated risk in the high-risk areas.

Electronic supplementary material

The online version of this article (doi:10.1186/s12936-016-1646-2) contains supplementary material, which is available to authorized users.

Keywords: Plasmodium falciparum, Plasmodium vivax, Malaria, Spatial clustering, Space–time clustering

Background

Malaria is a life-threatening infectious disease severely affecting vulnerable communities in tropical and subtropical regions where the environment is suitable for transmission [1, 2] Although malaria transmission appears to be declining worldwide as a result of control interventions [2, 3], the 2015 estimation indicates that there are 214 million cases and 438,000 malaria deaths [4]. Malaria is caused by five species of Plasmodium: Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae and Plasmodium knowlesi [1]. In China, P. vivax and P. falciparum are the main malaria parasites, with the former being the most dominant species [5]. Anopheles sinensis, Anopheles minimus, Anopheles dirus, and Anopheles lesteri are common malaria vectors in China [6].

Prior to 1949, the annual number of malaria cases in China was estimated to be 30 million. Owing to its substantial public health importance, a Malaria Control Programme was initiated in 1955 [7]. Since then, the malaria burden has greatly declined [8, 9], but it has remained a serious public health problem in China with periodic outbreaks [10]. Following an epidemic peak in 2006 [11], control efforts were consolidated with the formulation of the National Malaria Control Programme (NMCP) in 2006 [12]. Overall, malaria cases have sharply declined with only 14,491 malaria cases reported in 2009 [13]. The National Malaria Elimination Programme (NMEP) was launched in 2010 [12]. Since then, substantial progress has been made. P. vivax malaria cases were reduced by 57.7% in one year [14], followed by a decline in geographical coverage [5]. However, P. falciparum greatly increased dominating the overall confirmed malaria cases since 2007. The proportion of P. falciparum malaria increased from 7.1% in 2009 [13] to 71.2% in 2013 [15]. Areas affected by P. falciparum have consistently increased from 17 provinces in 2006 to 20 in 2010, 22 in 2011 [14], and to 30 provinces in 2013 [14–16], involving formerly non-endemic provinces [17].

The distribution of malaria in China shows considerable variation at fine spatial resolution such as county [18, 19]. A better understanding of the spatiotemporal change in disease distribution is crucial for improving control interventions and health resource allocation. Several studies have used the spatial and space–time scan statistics to detect clustering of malaria [18–22] and other public health problems [23] in space and time. These techniques detect disease clusters while adjusting for varying population size among spatial and temporal scales under study. In China, these have been used to identify high-risk areas and periods of malaria in some endemic provinces [18–22, 24, 25]. However, few studies have analysed the spatial and space–time distribution of both P. vivax and P. falciparum malaria at the national level. The purpose of the present study is to fill this gap in the understanding of the spatial and spatiotemporal distribution malaria in China during 2005–2014.

Methods

The study was conducted in mainland China, which encompass 31 provinces/autonomous region/municipalities, and more than two thousand county-level divisions. According to the sixth national census in 2010, mainland China has a population of 1.3 billion [26].

Data sources and its management

Malaria case data between 2005 and 2014 were obtained from the China Information System for Disease Control and Prevention (CISDCP). Malaria is a notifiable disease in China. The laboratory-confirmed and suspected cases are reported to the county-level CDC within one day through an online infectious disease reporting system in use since 2004 [27]. Case investigation and identification are conducted within three days of receiving the case report. Cases are identified according to national standard criteria issued by the Chinese Ministry of Health [28]. Malaria case data includes the county name and associated county code (i.e., identification number), demographic information, date of diagnosis and travel history. These counties are the living addresses for malaria cases. The surveillance-response system covers the whole country which enabled us to conduct a national level study.

Malaria case data, population, and geo-coordinates of each county were linked via county code in R Software version 3.2.2 [29]. As input for the clustering analysis in SaTSan software (version 8.0), a coordinate file, case file and population files were separately generated in text format. To indicate locations of the clusters, the output of the clustering analysis was mapped in ArcGIS software version 10.3.1 [30].

Spatial autocorrelation analysis

A descriptive analysis was performed to explore county-level annual trends of P. falciparum and P. vivax malaria cases in China during 2005–2014, and the results were plotted to reveal the annual trend. County level counts of P. vivax and P. falciparum malaria case for each year were used to test for the spatial distribution of the malaria in China. To explore the overall spatial autocorrelation within-country level local malaria cases, Global Moran’s I statistics was applied in ArcGIS software version 10.3.1 [30]. Row standardization of spatial weight was allowed as criteria for identifying neighbouring counties [31]. If counties share a boundary the spatial weight element was assumed to be 1; otherwise it was assumed to be 0. Based on this assumption, Global Moran’s I values were calculated for P. falciparum and P. vivax malaria separately. The value varies between −1.0 and +1.0, where a value close to +1 indicates a tendency for spatial clustering (positive spatial autocorrelation) of areas with similar numbers of malaria cases, whereas −1.0 and 0.0 respectively indicate spatial dispersion (negative spatial autocorrelation) and a random spatial pattern. Global Moran’s I tests the null hypothesis that the distribution of malaria in China is random in space [32]. Significance (p < 0.05) of the test statistic suggests that malaria cases are spatially clustered or dispersed. Following this, spatial scan statistics was used to identify locations of the significant cluster (i.e., high-risk areas) [33].

Spatial and space–time cluster analysis

In this study, two spatial scan statistics were performed: purely spatial cluster analysis and mixed space–time cluster analysis. The purely spatial cluster analysis (with the Poisson model) was performed for P. vivax and P. falciparum malaria separately in SaTScan Software. These techniques impose circular windows of different sizes to scan for spatial clustering. Kuldorff’s spatial cluster detection statistics [34], was used to scan for counties with high rates of malaria. The maximum spatial cluster size was set to the default of 50% of the population at risk in the circular spatial window [18]. In addition to avoiding pre-selection bias, this enables scanning for clusters of different sizes [34]. The most likely and secondary clusters were not permitted to overlap. The space–time scan statistic was also performed with the Poisson model. The length of time aggregation was set to one year. The maximum temporal cluster sizes to be scanned were also set at the default of 50% of the populationat risk and 50% of the study period, respectively.

Results

Overall trend of malaria

A total of 247,540 malaria cases were reported in China during 2005–2014. An annual variation in number of malaria cases was observed with most cases in 2006 (N = 73, 283), comprising 56,258 P. vivax and 3113 P. falciparum malaria. Overall, P. vivax accounted for 75.2% of malaria cases, while 8.7% were P. falciparum. 16.2% of all malaria cases reported during this period were unidentified.

A substantial decrease in the yearly number of vivax malaria case was observed during the study period (Fig. 1a). The most rapid reduction in the number of P. vivax cases occurred after 2006. The number of areas with P. vivax cases declined from 791 counties in 2006 to 303 counties in 2014 with an overall reduction of 60.7%. Numbers of P. falciparum malaria cases reached a peak in 2005, fell until 2008, then slightly increased, and have dominated since 2012 (Fig. 1a). Consequently, areas with P. falciparum greatly increased from 228 counties to 783. Compared to 2005, areas with P. falciparum increased by more than 100%.

Fig. 1.

Fig. 1

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Annual trend of overall, local and imported P. vivax and P. falciparum malaria in China from 2005 to 2014. a Overall trend of P. vivax and P. falciparum malaria. b Annual trends of local P. vivax and P. falciparum malaria. c Annual trends of imported P. vivax and P. falciparum malaria

Sources of infection

The data from 2005 to 2014 indicated 153, 051 local P. vivax and 19, 666 local P. falciparum malaria cases. Declining trends of local transmission were observed for both malaria types (Fig. 1b). Local P. vivax and P. falciparum malaria transmission declined by 99.79 and 98.42%, respectively. The geographical distribution of the counties with local P. vivax and P. falciparum during this period was shown in Additional file 1.

In contrast to the decline in local malaria cases, an increasing trend was observed for imported malaria during this study period (Fig. 1c). Imported P. falciparum consistently increased from 2005 to 2014, reaching a peak in 2013. However, the imported P. vivax didn’t show a significant change over the study period. Regarding the origin of infection, P. falciparum was mainly imported from Africa (72.70%, N = 7, 700) and Myanmar (17.7%, N = 1, 878) while the remaining cases were imported from Indonesia (0.69%, N = 73), Cambodia (0.23%, N = 24), Laos (0.19%, N = 20), Pakistan (0.13%, N = 14), India (0.09%, N = 10), Papua New Guinea (PNG) (0.06%, N = 6), and Vietnam (0.06%, N = 6), and. P. vivax was mainly imported from Myanmar (N = 5, 613), Oceania and unspecified countries (N = 1, 171) (Additional file 2).

Spatial autocorrelation analysis of annual local malaria cases in China showed the existence of significant overall spatial autocorrelation each year during the study period. The tendency of spatial clustering was observed for both P. vivax and P. falciparum malaria (Table 1).

Table 1.

Spatial autocorrelation (Global Moran’s I) of P. vivax and P. falciparum in China during 2005–2014

Year P. vivax P. falciparum
I Z p value I Z p value
2005 0.42 20.1 < 0.001 0.11 43.01 <0.001
2006 0.53 21.5 <0.001 0.10 52.19 <0.001
2007 0.49 21.25 <0.001 0.07 42.35 <0.001
2008 0.53 29.24 <0.001 0.08 51.45 <0.001
2009 0.52 24.03 <0.001 0.08 45.56 <0.001
2010 0.34 20.85 <0.001 0.07 38.32 <0.001
2011 0.28 17.97 <0.001 0.05 24.18 <0.001
2012 0.19 14.86 <0.001 0.02 9.42 <0.001
2013 0.09 5.90 <0.001 0.01 1.86 <0.01
2014 0.07 38.22 <0.001 0.03 16.61 <0.001
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I Moran’s Index, Z z-score

Spatial clustering

A purely spatial cluster analysis of annual P. vivax malaria indicated a non-random distribution of malaria cases in China during 2005–2014. The analysis detected significant spatial clusters (most likely and secondary) each year during the study period. The number of counties per most likely cluster ranged from 7 to 35. The most likely cluster with the highest number of counties was detected in 2007 and that with the lowest number in 2013. The most likely spatial cluster of P. vivax included several counties in the Northern Anhui province from 2005 to 2009. Throughout the rest of the study period, the most likely cluster covered bordering counties along the western Yunnan province. The secondary clusters were also identified in many provinces, each year during the study period. Most of these clusters, especially those with a high relative risk were detected in Western Yunnan from 2005 to 2009 and in Northern Anhui until 2011 (Fig. 2). Overall, more than half of the local P. vivax cases were reported from the most likely and secondary cluster areas except in 2013, when the clusters contributed to 42.62% of the local P. vivax malaria cases reported in the country (Table 2).

Fig. 2.

Fig. 2

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The locations of the detected spatial clusters of P. vivax malaria in China from 2005 to 2014

Table 2.

Pure spatial clustering of P. vivax cases in China during 2005–2014

Year Clusters Latitude Longitude N Observed cases Expected cases RR p value
2005 Most likely 33.68399 116.72312 15 15,241 570.93 48.44 0.001
Secondary 24.03683 97.80955 22 5590 105.74 63.35 0.001
2006 Most likely 33.68399 116.72312 15 35,053 958.00 97.94 0.001
Secondary 24.03683 97.80955 23 5595 177.28 34.99 0.001
2007 Most likely 33.21876 116.58207 35 31,436 1543.33 66.53 0.001
Secondary 24.03683 97.80955 29 3122 143.51 23.32 0.001
2008 Most likely 33.03381 117.03400 32 15,766 717.31 57.44 0.001
Secondary 24.03683 97.80955 28 2091 109.56 20.73 0.001
2009 Most likely 33.03381 117.03400 32 6533 345.07 39.07 0.001
Secondary 24.03683 97.80955 21 1561 53.42 33.31 0.001
2010 Most likely 24.03683 97.80955 13 1320 30.02 57.20 0.001
Secondary 33.03381 117.03400 39 1872 151.63 18.03 0.001
2011 Most likely 24.03683 97.80955 12 799 11.67 95.57 0.001
Secondary 33.03381 117.03400 39 678 72.60 12.01 0.001
2012 Most likely 24.03683 97.80955 23 516 9.26 101.22 0.001
Secondary 28.20380 120.13838 22 20 1.06 19.19 0.001
2013 Most likely 24.85646 97.91907 7 289 2.31 183.35 0.001
Secondary 32.00298 117.56783 9 22 0.76 29.67 0.001
2014 Most likely 25.27506 98.49739 14 324 4.49 113.70 0.001
Secondary 32.94082 104.77725 7 47 0.19 261.31 0.001
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N number of counties per cluster, RR indicates relative risk for malaria case in the location

The distribution of P. falciparum malaria also showed spatial clustering during 2005–2014. From 2005 to 2011, the most likely cluster was consistently detected in western Yunnan province along the China–Myanmar border (Fig. 3). The number of counties per most likely clusters during this period ranged from 7 to 13. The cluster with the highest number of counties (n = 13) was detected in 2006. This cluster contributed to more than half of the local P. falciparum malaria cases reported each year from 2005 to 2011 (i.e., 78.52, 77.54, 65.97, 58.22, 55.00, 54.61 and 46.71%, respectively). During 2012–2014, the most likely spatial cluster was detected in the counties of central Guangxi (in 2012 & 2013) and Anhui (in 2014). The most likely spatial cluster detected during this period included a small number of counties. However, 48.90% of the total counties per secondary spatial clusters were detected during 2012–2014. Overall, the spatial cluster areas contributed to more than half (53.2%) of the local P. falciparum malaria cases reported during 2012–2014 (Table 3).

Fig. 3.

Fig. 3

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Location of the detected spatial clusters of P. falciparum malaria cases in China from 2005 to 2014

Table 3.

Pure spatial clustering of P. falciparum cases in China during 2005–2014

Year Clusters Latitude Longitude N Observed cases Expected cases RR p value
2005 Most likely 24.73918 98.31948 10 2545 27.18 335.72 0.001
Secondary 21.08838 110.32950 25 198 103.24 1.97 0.001
2006 Most likely 24.03683 97.80955 13 2265 28.68 348.14 0.001
2007 Secondary 24.73918 98.31948 9 1118 12.66 249.20 0.001
Most likely 29.52352 119.90339 1 20 1.55 13.08 0.001
2008 Secondary 24.85646 97.91907 7 590 5.02 255.22 0.001
Most likely 34.55674 118.78395 4 26 2.85 9.33 0.001
2009 Secondary 24.85646 97.91907 7 508 4.97 192.20 0.001
Most likely 37.52641 103.33228 8 22 0.92 24.47 0.001
2010 Secondary 24.85646 97.91907 7 529 6.35 133.89 0.001
Most likely 30.53620 106.41193 11 61 4.63 13.74 0.001
2011 Secondary 24.85646 97.91907 7 213 5.67 45.08 0.001
Most likely 32.10585 118.76075 38 297 54.25 6.88 0.001
2012 Secondary 23.52086 108.63520 1 112 0.75 167.01 0.001
Most likely 24.85646 97.91907 31 144 4.39 37.48 0.001
2013 Secondary 23.52086 108.63520 1 955 1.46 1081.9 0.001
Most likely 32.00298 117.56783 21 134 3.58 39.53 0.001
2014 Secondary 32.00298 117.56783 1 90 1.82 52.79 0.001
Most likely 23.52086 108.63520 32 56 0.75 77.63 0.001
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N number of counties per cluster, RR indicates relative risk for malaria case in the location

Space–time clustering

The space–time scan statistics identified both the most likely and secondary clusters of locations with an elevated risk of P. vivax and P. falciparum malaria (Table 4). The most likely space–time cluster of P. vivax encompassing 32 counties was in a northern part of Anhui province in 2005–2009 (Fig. 4a). A secondary space–time cluster of P. vivax encompassing 20 counties was identified in the western part of Yunnan (2005–2009) and Hainan (2005–2008) provinces. For P. falciparum, the most likely space–time cluster included 10 counties in the western part of Yunnan province during the same period. A secondary space–time cluster of P. falciparum was detected in Anhui, Guangxi, and Zhejiang province from 2012 to 2013 (Fig. 4b).

Table 4.

Space–time clustering of P. vivax and P. falciparum malaria in China, 2005–2014

Malaria parasites Clusters Latitude Longitude Start/end date N Observed cases Exp. case RR p value
P. vivax Most likely 24.73918 98.31948 2005/2009 10 7011 67.29 170.70 0.001
Secondary 23.52086 108.63520 2013/2013 24 955 1.13 895.75 0.001
P. falciparum Most likely 33.03381 117.03400 2005/2009 32 10,829 2538.07 103.88 0.001
Secondary 24.03683 97.80955 2005/2009 26 18,919 385.80 54.61 0.001
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N number of counties per cluster, RR indicates relative risk for malaria case in the location. Obs. case observed number of case in the cluster, Exp. case expected number of cases in the cluster

Fig. 4.

Fig. 4

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Location of space–time clustering of malaria in China from 2005 to 2014. a locations of spatiotemporal clusters of P. vivax; b locations of spatiotemporal clusters of P. falciparum

Discussion

Using a surveillance dataset of 10 years, the present study demonstrated substantial changes occurring with respect to annual trends and the geographical distribution of malaria in China. The annual number of P. vivax malaria cases showed a considerable decrease, especially after 2006 when the NMCP was launched [12]. However, the number of P. falciparum cases remained relatively stable at a higher level. P. falciparum cases malaria peaked in 2005, fell until 2008, then slightly increased, and has dominated cases since 2012. The steady decline in P. vivax cases and increase in P. falciparum cases was similar to that noted previously [5].

The present study also indicated a shrinking in the geographical distribution of P. vivax malaria and a substantial expansion in areas with P. falciparum. These findings coincide with previous research [15, 35]. Different interventions have been formulated with the aim of controlling malaria in China. These have been effectively implemented with support from the Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM) [36]. This may have increased the ability of counties to effectively control local malaria transmission dominated by P. vivax [15, 16]. A possible reason for the geographical expansion of P. falciparum malaria could be the rising number of overseas imported malaria cases in recent years [14, 37]. As of 2013, 97.9% of the national malaria cases reported came from overseas [15]. Most overseas-imported malaria in recent years was P. falciparum. One study conducted in Jiangsu province showed that P. falciparum accounted for 79.8% of the total malaria cases imported to the province during 2001–2011 [38]. In recent years, a dramatic increase in overseas investments increased the number of Chinese persons working abroad and paved the way for international travel to and from countries where P. falciparum is highly endemic. In 2012, about 0.5 million people left the country for work and 83.2 million for other reasons. Compared to 2010, an increase of 24.6 and 44.9% were observed, respectively [39]. Available evidence indicated that P. falciparum was mostly imported via Chinese people returning from Africa [17, 38, 40–44].

Identifying a high-risk area is crucial for spatial targeting of interventions against malaria transmission. Spatial cluster analysis identified most likely clusters of P. vivax malaria located in North Anhui province from 2005 to 2009. The area where most likely clusters of P. vivax were identified in this study was similar to the previous transmission foci detected in the northern part of Anhui province [18], where An. sinensis is a principal vector. A study suggested that increased vector capacity of An. sinensis related with the mosquito host reduction (livestock), and human behavioural change contributed to P. vivax malaria outbreak in Huaiyuan county of Anhui province [45]. This area, especially north of the Huai River, is one of the high-risk areas with unstable malaria transmission [46], possibly due to environmental conditions associated with geographical location [11, 14, 18]. Malaria transmission in this province has been an important issue in China, responsible for the outbreak in 2006 which was dominated by P. vivax [11]. From 2006 to 2009, Anhui had been the number one province in China in terms of number of malaria cases [11, 13, 47].

The present study also identified most likely spatial clusters of P. vivax malaria in western Yunnan province, along the China–Myanmar border after 2009. The cluster persisted for five years (2010–2014), contributing more than half the total number of P. vivax cases reported each year. Although the high-risk area identified in this area agrees with previous studies [20, 48, 49], a shift of the geographical location from Anhui to Yunnan province after 2009 is new. The reduction in Anhui may be explained by intensive malaria control in the central China provinces [50]. Since the initiation of the NMEP in 2010 [12, 51], national malaria, especially local cases greatly declined [8, 15]. One study showed that overall malaria cases in Anhui province decreased by 65.5% (in 2011) compared to those in 2010 [9]. The total number of P. vivax cases in the country, therefore, decreased by 57.7% in one year, with most of the local cases in Yunnan province [16]. The province remained endemic, ranking first in the country in terms of an overall number of malaria cases [8, 9, 15, 52], particularly P. vivax [16]. For example, 73.1% (171/234) of the national P. vivax malaria cases in 2012 were contributed by Yunnan [16], and P. vivax malaria appeared to be dominant along the China–Myanmar border [53]. Malaria transmission in this area is a major concern in the disease elimination stage. This could be attributed to environmental conditions conducive for transmission and efficiency of the dominant An. minimus vectors in this area [17]. Unlike An. sinensis [54, 55], An. minimus shows a strong attraction to human than other hosts [56] and has a high human blood index [57] which has an implication for vector control interventions even though An. minimus is endophilic, endophagic, and susceptible to insecticides [55, 58]. Human behavioural factors [59] could be another reason for malaria transmission and control in this area. For example, some counties of Yunnan province along the international border have been recognized as high-risk areas in China because of sharing a boundary with malaria endemic countries which put them at risk of reintroduction [20, 60]. One study revealed that imported P. vivax to China had increased between 2004 and 2012, most of which were from malaria endemic countries of South East Asia (Myanmar, Cambodia and Laos) [16]. 59.3% of the total P. vivax malaria cases imported from South East Asia (n = 697) were introduced from Myanmar, and 56.7% (n = 6832) of the total introduced P. vivax cases (n = 12, 060) were in Yunnan [17]. However, other evidence shows lack of significant association between travel to Myanmar and transmission of P. vivax along the China–Myanmar border [53]. Residents in this area have a relatively low educational level, limited knowledge of malaria transmission and utilization of personal protection, especially during outdoor activities [61, 62], and exhibit poor treatment-seeking behaviour [62]. These factors could contribute to sustained malaria transmission in this area [17].

Similarly, the current study identified the most likely spatial clusters of P. falciparum malaria in the western Yunnan province along the China–Myanmar border every year from 2005 to 2011. This is consistent with previous studies [20, 48, 49]. This is the only area where the local P. falciparum cases were reported by several studies [9, 15]. It implies that these counties are at high-risk of achieving stable falciparum malaria transmission. Most of the national P. falciparum cases during 2005–2011 were reported from Yunnan province, although counties were not frequently specified [9, 11, 47, 52]. In addition to behavioural and lifestyle factors for malaria transmission [61], travel to Myanmar was significantly associated with acquiring P. falciparum infection, indicating cross-border movement is a key factor for the stable transmission of P. falciparum in the China–Myanmar border [17, 53, 61, 62]. However, 84.5% of the imported P. falciparum cases were imported from Africa. Climatic factors have also been found to be an important factor for malaria transmission in this area [48]. According to one study [20], temperature was significantly associated with vivax malaria in clustered areas of Yunnan province. Further research is required to better understand the importance of climatic factors in the spatial distribution of malaria in China.

The present study also identified high-risk areas for P. falciparum in central Anhui province from 2013 to 2014. This foci (Feidong county) is different from the previously identified high-risk area in the Northern Anhui province [18], indicating spatial variation in foci of P. falciparum cases, was and its less importance in this area than P. vivax [11]. In the present study, the most likely spatial cluster of P. falciparum was not detected in Anhui province until 2012. However, a spatial cluster of P. vivax was observed consistently in the northern Anhui province from 2005 to 2009. This result verified that P. falciparum played a relatively insignificant role in the previously identified high-risk area in Anhui province [18].

The high-risk area for P. falciparum malaria shifted from Yunnan to Anhui province, and very large secondary clusters were detected in some counties of the northern and eastern provinces, especially after 2011. This could be attributed to the increased proportion of overseas imported malaria from the parasite endemic countries in recent years [14, 46]. P. falciparum dominates overseas imported malaria cases, which are distributed in different parts of China, including non-endemic provinces. Nevertheless, the study of disease clustering focused only on local malaria cases. Spatial variations among P. vivax and P. falciparum malaria followed different patterns indicating differences in the biological features of parasites, which might have facilitated their transmission. Climatic factors are associated with an increased risk of malaria because of their impact on vector activities and the parasite incubation period [63]. Compared to P. vivax, P. falciparum requires a slightly higher temperature for parasite development. The minimum threshold temperature for P. falciparum and P. vivax are approximately 18 and 15 °C, respectively [64], indicating increased opportunity for P. falciparum to spread to previously cooler areas, following global climate change. Further studies are required to fully understand the risk factors driving spatial shifting and geographic expansion of P. falciparum across mainland China.

The most likely space–time cluster of P. vivax malaria was detected in the northern Anhui province. These areas coincided with results of the purely spatial analysis in this study as well those of previous studies [18]. The time frame for all significant space–time clusters of P. vivax malaria was 2005–2009. This implies a declining burden of P. vivax malaria in China since 2010. Control interventions, especially those following the establishment of the Chinese NMEP [12, 51] are a likely factor in this substantial reduction of this malaria.

For P. falciparum, the most likely space–time cluster was detected in western Yunnan province during 2005–2009. Although this is consistent with the previous study [65], the secondary space–time cluster was scattered mostly in the eastern and north-eastern provinces after 2012 (Fig. 4b). This could imply the spreading of P. falciparum malaria to previously non-endemic areas, probably due to an increased number of overseas-imported P. falciparum [8, 15, 35]. Although an imported case can be distributed randomly to any provinces, the present study showed a greater expansion of P. falciparum to the east and northeast of China than to any other parts of the country. A better understanding of the direction of malaria expansion or spatial change and underlying risk factors for the malaria transmission in these formerly non-endemic areas is important for the malaria elimination goal of China.

This study is the first to identify the spatial and spatiotemporal distribution of P. vivax and P. falciparum at the national level in China. A separate analysis was conducted for both important malaria parasites in the country. The study identified high-risk areas and the spatial extent of both P. vivax and P. falciparum. Spatial and space–time scan statistics were performed using SaTScan software [66]. These techniques were designed particularly to perform spatial clustering of disease or health related events, and to test the statistical significance of clustering under the null hypothesis of a random distribution of the diseases in space, time and space–time [66, 67]. These techniques are most effective at identifying disease clusters [68], and have been widely used in fields of epidemiology for similar purpose [18, 19, 21, 24, 25].

Although purely spatial scan statistics are most effective at identifying a cluster of malaria with a circular shape [68], the spatial distribution of the disease may not always assume this shape and some irregularly shaped clusters might have been undetected.

Conclusion

Overall, the spatial and space–time cluster detection statistics identified a high-risk areas for both P. vivax and P. falciparum malaria. The counties in the clusters should be given priority in the control programs, and for further operational research. Both malaria types showed significant spatial and spatiotemporal variations. Contrary to P. vivax, the high-risk areas for P. falciparum malaria shifted from southwest to east of China. Thus, further studies are required to examine spatial changes in the risk of malaria transmission and identify the underlying causes of elevated risk in emerging high-risk areas.

Authors’ contributions

SH and YG designed the study protocol, WZ and JG provided original dataset, SL and LC compiled and prepared the dataset for analysis. SH and YG did the analysis and interpretation of the results, and drafted the manuscript. YG, GW, SL, and WZ critically revised the manuscript for intellectual content. All authors read and approved the final manuscript.

Acknowledgements

SH is a Ph.D student supported by an International Postgraduate Research (IPRS) and The University of Queensland Scholarship; YG is supported by the Career Development Fellowship of Australian National Health and Medical Research Council (#APP1107107).

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The dataset of this article is available upon request.

Ethical approval

Prior to the start of this research, the study protocol was approved by the Ethics Committee of the University of Queensland, Australia. The data was de-identified and aggregated to county-level prior to commencement of the data analysis.

Abbreviations

CISDCP

China information system for disease control and prevention

NMCP

National Malaria Control Programme

NMEP

National Malaria Elimination Programme

CDC

Center for Disease Control and Prevention

I

Moran’s index

Z

z-score

RR

indicates relative risk

AIDS

acquired human immuno deficiency syndrome

Additional files

12936_2016_1646_MOESM1_ESM.pdf (618.5KB, pdf)

Additional file 1. Distribution maps of imported malaria cases.

12936_2016_1646_MOESM2_ESM.docx (13.5KB, docx)

Additional file 2. Number of malaria cases imported from other countries, 2005–2014.

Contributor Information

Samuel H. Hundessa, Email: s.hundessa@uq.edu.au

Gail Williams, Email: g.williams@sph.uq.edu.au.

Shanshan Li, Email: uqshany0601@gmail.com.

Jinpeng Guo, Email: pengpla@126.com.

Linping Chen, Email: l2.chen@uq.edu.au.

Wenyi Zhang, Phone: +86 10 66948384, Email: zwy0419@126.com.

Yuming Guo, Phone: +61 7 3346 5265, Email: y.guo1@uq.edu.au.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The dataset of this article is available upon request.

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