Abstract
Background and Objectives: Mosquito-borne viral diseases (MBVDs) create a dramatic health situation worldwide. There is a need to improve the understanding of factors to be addressed in intervention programmes. This study explored community knowledge, attitudes, and practices (KAP) regarding MBVD in Kinshasa. Materials and Methods: A cross-sectional survey was carried out between January and April 2019. The socio-demographic and KAP data collected through a questionnaire were analysed using Epi Info 7. Results: The study included 1464 male and female respondents aged from 18 to 70 years old. Open garbage cans and outdoor water storage units were found in 61.2% and 33.4% of respondent residences, respectively. Polluted water bodies (80.3%) were the most mentioned as mosquito breeding places. Among 86.6% of the respondents that had heard about yellow fever, 12% knew that it is an MBVD. The majority of respondents (72.5%) were perceived to be at risk of contracting MBVD. Environment sanitation (58%) and insecticide use (25%) were among the measures implemented to control mosquitoes. The greater overall knowledge score and attitude were not associated with good practice. Conclusion: The residents of Kinshasa had limited knowledge of MBVD. Raising awareness and educational sessions are essential in empowering the community regarding the correct attitudes and practices to effectively manage the risk posed by MBVD.
Keywords: knowledge, attitude, practices, mosquitoes, mosquito-borne viruses, Democratic Republic of the Congo
1. Introduction
Mosquitoes transmit different pathogens that affect human and animal health and negatively impact food security and socio-economic wellbeing [1,2,3]. In addition to malaria and lymphatic filariasis, mosquitoes are also vectors of several viral diseases. The most important mosquito-borne viral diseases (MBVDs) include yellow fever, Zika, dengue, chikungunya, Rift Valley fever, and West Nile [4]. Transmission of MBVD to humans and animals includes multifaceted processes which are influenced by mosquito and viral genetic, environmental, socio-demographic, and anthropological factors [5,6].
For effective interventions, in addition to knowledge of biomedical aspects of the diseases, information on socio-anthropological aspects is equally important. It is critical to explore different local socio-cultural and demographic driving factors of MBVD in order to design appropriate interventions. In the current context of increasing insecticide resistance, limited vaccine options, and lack of curative resources, an integrated approach based on community and individual participation are critical in the effective prevention and control of MBVDs.
There is limited information on community knowledge, attitudes, and practices (KAP) on MBVD in Sub-Saharan Africa [7]. Studies outside Africa have shown that KAP on MBVD vary widely across populations and countries [8,9,10,11,12,13]. Inadequate knowledge is a significant barrier to appropriately empowering local communities and individual interventions against MBVD. Lack of or inadequate community knowledge is likely to be an obstacle in adopting specific prevention and control measures against some specific mosquito species and MBVD [11].
Indeed, mosquito species express different biting behaviour and breeding preferences. Generally, populations are often discussing mosquitoes in a global way and do not differentiate between mosquito species. Such conceptualisation could pose an obstacle to the adoption of specific prevention or control measures for some specific mosquito species and MBVDs [13]. Contrary to Anopheles, the main vector of malaria and o’nyong’nyong virus (ONNV), which present nocturnal activities, Aedes aegypti, the main vector of yellow fever virus (YFV), Zika virus (ZIKV), dengue virus (DENV), and chikungunya virus (CHIKV), present a diurnal activity and preferentially breed in domestic containers and bite in peridomestic locations. Culex pipiens complex, a major vector of WNV, tend to breed in polluted water bodies containing organic matter [14,15,16,17,18]. Considering such details in educating the population could raise their awareness of the vector, the viruses, and adapted control and prevention measures.
The Democratic Republic of the Congo (DRC) experiences both tropical and equatorial climates with long rains. The climatic and ecological conditions are optimal for almost all major MBVDs of public health importance. MBVDs are becoming common and a serious public health problem in the DRC [19]. The country is known to be at high risk of YFV transmission, morbidity, and mortality [20]. More than 400 people died during the yellow fever outbreaks of 2016–2017 [6,21]. Kinshasa, the capital city, has experienced four chikungunya outbreaks during the past two decades [22,23,24]. Recently, reports of dengue occurrence have increased [23,25,26,27], the presence of Zika virus (ZIKV) has been documented [27], and the overall seroprevalence of Rift Valley fever virus (RVFV) has increased [28]. To date, Aedes albopictus has been reported in Kinshasa [29]. These threats of MBVD are not only to the local population of the DRC but also to visitors. For instance, the majority of chikungunya virus infections in Belgium between 2007 and 2012 were imported from the DRC [30] and, recently, Japanese and Italian travelers returning from the DRC were diagnosed with DENV [31,32]. The evidence of circulating West Nile virus (WNV) in dogs, horses, and mosquitoes has been documented in Kinshasa [33,34,35]. In the context of inadequate resources for control, there is an immediate need to increase community awareness of MBVD in the DRC. This study was therefore carried out to determine community knowledge, attitudes, and practices as regards mosquitoes and MBVDs in Kinshasa, DRC.
2. Materials and Methods
2.1. Study Area and Design
In this cross-section study, a questionnaire survey was conducted in four districts of Kinshasa between January and April 2019. Kinshasa has 24 communes (municipalities) grouped into four districts and each commune is divided into neighbourhoods. It has an estimated human population of 11,855,000 [36]. A multistage sampling technique was carried out to select study participants. At the first level, three municipalities from each district of Kinshasa were chosen. At the second level, two neighbourhoods were selected to guarantee a good coverage of the geographical, demographic, and socio-economic profiles of the population. The head of the household or a representative was systematically selected from neighbourhoods. The participants included in this study have complied with the following criteria: (i) aged 18 years old or above, (ii) living in the selected neighbourhoods, and (iii) freely consent to participate in the study and being present during the interview.
A questionnaire was developed in English, translated into French, and administered by a face-to-face interview in either Lingala or French depending on the language proficiency of the respondent. The questionnaire contained both closed and open questions with the possibility for the respondent to provide more than one answer. The information sought was related to socio-demographic characteristics of respondents, knowledge about mosquitoes (breeding places, activities, behaviour, vector role, control measures, symptoms), attitudes and practices towards mosquitoes, and MBVD. The attitude questions were focused on the perception of mosquitoes’ impact on daily life and the consciousness about responsibility for individual and community protection against mosquitoes and MBVD. The practice questions captured the information about measures undertaken to reduce or avoid mosquito bites, and mosquito abundance on the property (environmental hygiene, use of chemical and physical means). To gain more insight and accuracy on the respondent’s practice, additional data were captured by inspection of their residential places and their surroundings (presence of vegetation, stagnant water collection, uncovered storage water unit set outdoors, any potential artificial or natural water container, opened garbage can).
2.2. Data Analysis
The data were entered into a Microsoft Excel spreadsheet and statistical analysis was performed using Epi Info Software Version 7 (CDC, Atlanta, GA, USA). A summary of the statistics is presented as frequencies and proportions in tables. Each correct response to the knowledge, attitude, and practice questions was scored on a scale of one to five while an incorrect response was assigned zero points. The sum of each knowledge component (breeding site, times of activity, vector role of mosquito in spreading viruses, arbovirus known or heard of before the survey, prevention, and control measures) was used to determine the overall knowledge score about MBVD by calculating the mean. The attitude questions sought information on how they perceived the impact of mosquitoes on daily life and their responsibility in prevention and protection. Awareness of health risks posed by mosquitoes and personal responsibilities at the household and community level for the prevention and protection of themselves, their households, and the community against mosquitoes and MBVD was considered to be a positive attitude. The preventive measures that have been undertaken and the information on the description of the immediate residential environment of the respondent were included in the determination of the overall practice score. Low scores were values less than the mean and high scores were values equal to or greater than the mean. The scoring procedures for each KAP component are provided in the Supplementary Materials. The total possible points were 30, 15, and 12 for overall knowledge, attitude, and practice, respectively.
The chi-square test was used to identify associated factors of the KAP scores by calculating the odds ratios (OR) and the 95% confidence interval (CI). p-values less than 0.05 were considered statistically significant. The socio-demographic characteristics (age, sex, education, occupation, marital status, religion) were considered independent variables.
3. Results
3.1. Socio-Demographic and Environmental Characteristics
Of 1464 respondents included in the study, 60.7% were females, 52.5% were above 33 years of age, and 43.2% had a higher level of education. About half of the respondents were married (Table 1), approximately half (47.8%) owned a house. The majority of the houses (61.2%) had open garbage cans and 38.7% had vegetation in their surroundings. One-third (33.4%) of the houses had water storage units set outdoors, 25.1% had stagnant water collections, and 22.5% had potential artificial or natural water containers outdoors (tyres, flower pots, small cans, boxes, coconut shells, plastic plates). Domestic animals were found in around one-third of the respondents’ homes. Only 36.4% of houses had insect screen windows. More details of the surveyed households are provided in Table 2.
Table 1.
Variable | No. of Respondents | Percent |
---|---|---|
Age Group | ||
18–33 years | 702 | 47.9 |
34–70 years | 762 | 52.5 |
Sex | ||
Male | 575 | 39.3 |
Female | 889 | 60.7 |
District | ||
Tshangu | 509 | 34.8 |
Mont-Amba | 388 | 26.5 |
Funa | 207 | 14.1 |
Lukunga | 360 | 24.6 |
Marital status | ||
Unmarried | 737 | 50.3 |
Married | 727 | 49.7 |
Education level | ||
Low education level | 831 | 56.7 |
High education level | 633 | 43.2 |
Occupation | ||
Medical personnel or student | 303 | 20.7 |
Other | 1161 | 79.3 |
Religion | ||
Christian | 1234 | 84.3 |
Other | 230 | 15.7 |
Table 2.
Variable | No. of Respondents | Percent |
---|---|---|
Household size | ||
≤5 | 632 | 43.1 |
6–10 | 706 | 48.2 |
>10 | 126 | 8.6 |
Presence of children under 5 years old in the household | 772 | 52.7 |
Homeownership | ||
Tenant | 764 | 52.2 |
Owner | 700 | 47.8 |
Source of water supply | ||
Tap water on the home premises | 1024 | 69.9 |
Tap water away from the home premises | 382 | 26.0 |
Well on the home premises | 17 | 1.2 |
Well away from the home premises | 49 | 3.3 |
Types of house walls | ||
Cement brick | 1385 | 94.6 |
Sheet metal | 53 | 3.6 |
Straw, clay, timber (wood) | 26 | 1.8 |
Types of house roof | ||
Sheet metal | 1370 | 93.6 |
Straw | 94 | 6.4 |
Presence of net (insect screens) on windows | 533 | 36.4 |
Description of house’s immediate surroundings | ||
Vegetation | 567 | 38.7 |
Stagnant water collection | 368 | 25.1 |
Storage water unit set outdoors | 490 | 33.4 |
Any potential artificial or natural water container outdoors | 330 | 22.5 |
An opened garbage can | 897 | 61.2 |
Domestic animal keeping (rearing) | 459 | 31.3 |
3.2. Knowledge
The majority of respondents stated that stagnant and draining polluted water (80.3%) and garbage (35%) were the major mosquito breeding sites. As regards mosquito biting time, 39% considered mosquitoes to bite during the night, 31% during sundown, and 30.5% any time of the day. The majority of respondents mentioned environmental measures such as cleaning and removal of garbage (64.2%), draining of standing water (24.8%), and proper disposal of empty containers (10.1%) as the most effective mosquito control measures. Other measures are detailed in Table 3. Yellow fever was the most frequent (86.6%) MBVD that respondents had heard of before our study. Others included chikungunya (13.9%), Zika (7.5%), and dengue (3.7%). Only a few respondents knew that YFV (12.2%), CHIKV (5.4%), ZIKV (1.8%), DENV (1.5%), and RVFV (0.6%) were transmitted by mosquitoes. Almost all respondents (97.2%) identified malaria as a disease that is spread by mosquitoes. Regarding knowledge of the role of the mosquito in spreading zoonoses, only 23.7% (348/1464) were aware that mosquitoes can transmit pathogens to animals or exchange pathogens between animals and humans. Of these, 348 respondents (39.0%) were unable to mention any zoonosis (Table 4).
Table 3.
Variable | No. of Respondents | Percent |
---|---|---|
Breeding places for mosquitoes | ||
Drain and stagnant polluted water | 1178 | 80.3 |
Garbage | 526 | 35.9 |
Unsafe waste disposal compost pit | 137 | 9.3 |
Pits, drainage open underground soakage pits | 141 | 9.6 |
Clean water collection | 66 | 4.5 |
Ditches, ponds | 148 | 10.1 |
Water storage tanks | 80 | 5.4 |
Small containers | 26 | 1.7 |
Storage and other water storage jars | 24 | 1.6 |
Vehicle tyres | 72 | 4.9 |
Coconut shells and broken utensils | 35 | 2.3 |
Cracks in walls, tree holes | 63 | 4.3 |
I don’t know | 62 | 4.2 |
Other | 28 | 1.9 |
Mosquito biting times | ||
Daytime (morning, afternoon) | 63 | 4.3 |
Sundown | 454 | 31.0 |
Night | 571 | 39.0 |
Anytime | 447 | 30.5 |
I don’t know | 36 | 2.4 |
Season of the year mosquitoes are the most frequent | ||
Rainy season | 704 | 48.0 |
Dry season | 354 | 24.1 |
Both seasons | 350 | 23.9 |
I don’t know | 56 | 3.8 |
Can mosquitoes transmit disease to animals? | ||
Yes | 288 | 19.7 |
No | 1134 | 77.4 |
I don’t know | 42 | 2.9 |
Can mosquitoes spread disease between animals and humans | ||
Yes | 348 | 23.7 |
No | 1090 | 74.5 |
I don’t know or don’t believe | 26 | 1.8 |
Preventive measures | ||
Keep the environment clean, remove garbage or any uncovered container | 1090 | 74.4 |
Use mosquito bed net | 601 | 41.0 |
Keep cover over water source/storage unit container | 151 | 10.3 |
Remove standing water/stagnant water | 363 | 24.8 |
Spray insecticide | 326 | 22.2 |
Fumigation | 102 | 6.2 |
Use repellent | 50 | 3.4 |
Use fan | 67 | 4.5 |
Put mosquito screen (net) on house windows | 130 | 8.8 |
Wear long clothes | 25 | 1.7 |
I don’t know | 33 | 2.2 |
Other (gasoline oil, detergent, etc.) | 22 | 1.8 |
Table 4.
The Disease Can Be Transmitted by a Mosquito (n = 1464) | Being Aware of MBVD before the Survey (n = 1464) | MBVD That Can Be Transmitted between Humans and Animals (n = 348) | |
---|---|---|---|
n (%) | n (%) | n (%) | |
Malaria | 1423 (97.2) | 119 (34.2) | |
Yellow fever | 179 (12.2) | 1269 (86.6) | 9 (2.5) |
Chikungunya | 79 (5.4) | 204 (13.9) | 3 (0.8) |
Zika | 27 (1.8) | 111 (7.5) | 0.4 |
Dengue | 22 (1.5) | 55 (3.7) | |
Rift Valley fever | 9 (0.6) | 26 (1.7) | 3 (0.8) |
West Nile fever | 11 (0.7) | ||
O’nyong’nyong | 2 (0.1) | 8 (0.5) | 3 (0.8) |
Arbovirus | 14 (0.9) | ||
Filariasis | 1 (0.07) | 3 (0.8) | |
Trypanosomiasis | 17 (1.2) | 29 (8.3) | |
Typhoid fever | 69 (4.7) | 11 (3.1) | |
Ebola | 28 (1.9) | 20 (5.7) | |
HIV | 17 (1.1) | 3 (0.8) | |
Rabies | 16 (4.6) | ||
Others | 49 (3.4) | 8 (2.2) | |
I don’t know | 22 (1.5) | 136 (39.0) |
The majority (70.1%) of respondents who knew about any MBVD stated fever as the most common symptom, followed by headache (52.4%), general body pain (21.2%), and joint pain (18.7%). Only a few respondents mentioned jaundice (9.9%), back pain (4.2%), haemorrhage (2.2%), skin rashes (1.8%), and others (5.7%).
A total of 1346 (91.9%) participants had a low overall score of knowledge related to mosquitoes and MBVD (Table 5). Knowledge scores related to mosquito breeding places were significantly associated with the respondent’s age, marital status, educational level, and sex. Respondents above 33 years of age (OR: 2.4; 95%CI: 1.4–4.2; p = 0.0002), married (OR: 2.2; 95%CI: 1.3–3.7; p = 0.0016), and having higher educational level (OR: 2.0; 95%CI: 1.2–3.2; p = 0.002) had higher knowledge on mosquito breeding places. Compared to males, female respondents had low knowledge scores regarding mosquito breeding places (OR: 0.3; 95%CI: 0.2–0.6; p = 0.0001) and times of mosquito biting activity (OR: 0.8; 95%CI: 0.6–1; p = 0.03). The non-Christians (OR: 1.3; 95%CI: 0.9–1.7; p = 0.03) had higher scores than Christians about times of mosquito activity. The age, sex, occupation, religion, marital status, and level of education of respondents were not significantly associated with the knowledge of the role of the mosquitoes in transmission of zoonosis and arboviruses, arboviral disease, prevention and control measures, as well as the overall knowledge (Table 6).
Table 5.
Variable | Effective | Percent | IC 95% |
---|---|---|---|
Score of knowledge about breeding site | |||
Low | 1392 | 95.1 | 93.8–96.1 |
High | 72 | 4.9 | 3.8–6.1 |
Score of knowledge about mosquitoes’ period of activity | |||
Low | 1018 | 69.5 | 67.0–71.8 |
High | 446 | 30.5 | 28.1–32.9 |
Score of knowledge about the role of mosquitoes in spreading zoonoses | |||
Low | 977 | 66.7 | 64.2–69.1 |
High | 487 | 33.3 | 30.6–35.7 |
Score of knowledge about vector role of mosquitoes in arbovirus transmission | |||
Low | 1208 | 82.5 | 80.4–84.4 |
High | 256 | 17.5 | 15.5–19.5 |
Score of knowledge about arbovirosis | |||
Low | 1407 | 96.1 | 94.9–97.0 |
High | 57 | 3.9 | 2.9–5.0 |
Score of knowledge about mosquito control and prevention | |||
Low | 1358 | 92.8 | 91.2–94.0 |
High | 106 | 7.2 | 5.9–8.7 |
Overall score of knowledge | |||
Low | 1346 | 92.0 | 90.4–93.2 |
High | 118 | 8.0 | 6.7–9.6 |
Overall score of attitude | |||
Low | 298 | 20.3 | 36.9–42.0 |
High | 1166 | 79.7 | 57.9–63.3 |
Overall score of practice | |||
Low | 1255 | 85.7 | 83.8–87.4 |
High | 209 | 14.3 | 12.5–16.2 |
Table 6.
Variable | OR | X2 | IC 95% | p |
---|---|---|---|---|
Factors associated with a high score of knowledge about breeding site | ||||
Age group of 34–70 years | 2.4 | 11.5 | 1.4–4.2 | 0.0002 |
Female sex | 0.3 | 14.1 | 0.2–0.6 | 0.0001 |
Married | 2.2 | 9.6 | 1.3–3.7 | 0.0016 |
Post-secondary educational level | 2.0 | 7.6 | 1.2–3.2 | 0.002 |
Medical personnel or student | 0.8 | 0.003 | 0.4–1.5 | 0.5 |
Non-Christian | 0.9 | 0.003 | 0.5–1.8 | 0.5 |
Factors associated with a high score of knowledge about mosquitoes’ period of activity | ||||
Age group of 34–70.years | 1.3 | 7.6 | 1.1–1.7 | 0.002 |
Female sex | 0.8 | 3.1 | 0.6–1.0 | 0.03 |
Married | 1.0 | 0.1 | 0.8–1.3 | 0.3 |
Post-secondary education level | 0.00 | 0.8 | 0.8–1.2 | 0.4 |
Medical personnel or student | 1.0 | 0.15 | 0.7–1.2 | 0.3 |
Non-Christian | 1.3 | 0.003 | 0.5–1.8 | 0.003 |
Factors associated with a high score of knowledge about role of mosquitoes in spreading zoonosis | ||||
Age group of 34–70.years | 0.9 | 0.0 | 0.7–1.2 | 0.5 |
Female sex | 0.8 | 2.6 | 0.6–1.0 | 0.05 |
Married | 0.9 | 1.1 | 0.7–1.0 | 0.1 |
Post-secondary education level | 1.0 | 0.6 | 0.8–1.3 | 0.4 |
Medical personnel or student | 0.9 | 0.3 | 0.6–1.1 | 0.2 |
Non-Christian | 1.1 | 0.5 | 0.8–1.5 | 0.2 |
Factors associated with a high score of knowledge about vectors and the role of mosquitoes in arbovirus transmission | ||||
Group age of 34–70.years | 1.0 | 0.3 | 0.8–1.4 | 0.2 |
Female sex | 0.8 | 1.9 | 0.6–1.1 | 0.08 |
Married | 1.0 | 0.2 | 0.8–1.4 | 0.4 |
Post-secondary education level | 0.9 | 0.3 | 0.6–1.2 | 0.2 |
Medical personnel or student | 1.2 | 1.2 | 0.8–1.6 | 0.1 |
Non-Christian | 1.3 | 2.4 | 0.9–1.9 | 0.06 |
Factors associated with a high score of knowledge about arboviruses | ||||
Group age of 34–70.years | 0.8 | 0.09 | 0.5–1.5 | 0.3 |
Female sex | 0.6 | 2.0 | 0.3–1.1 | 0.07 |
Married | 0.7 | 1.0 | 0.4–1.2 | 0.1 |
Post-secondary education level | 1.1 | 0.2 | 0.6–2.0 | 1.2 |
Medical personnel or student | 1.0 | 0.0 | 0.5–1.9 | 0.5 |
Non-Christian | 1.7 | 2.8 | 0.9–3.3 | 0.05 |
Factors associated with a high score of knowledge about mosquito control and prevention | ||||
Group age of 34–70.years | 0.9 | 0.00 | 0.6–1.4 | 0.5 |
Female sex | 1.1 | 2.0 | 0.7–1.6 | 0.3 |
Married | 0.7 | 1.0 | 0.5–1.2 | 0.1 |
Post-secondary education level | 1.2 | 0.9 | 0.8–1.8 | 0.1 |
Medical personnel or student | 0.8 | 0.4 | 0.5–1.3 | 0.2 |
Non-Christian | 1.1 | 0.05 | 0.6–1.8 | 0.3 |
Factors associated with a high global score of knowledge | ||||
Group age of 34–70.years | 1.1 | 0.16 | 0.7–1.6 | 0.3 |
Female sex | 1.1 | 0.3 | 0.7–2.0 | 0.2 |
Married | 1.2 | 1.3 | 0.8–1.8 | 0.1 |
Post-secondary education level | 1.0 | 0.08 | 0.7–1.5 | 0.3 |
Medical personnel or student | 0.8 | 0.4 | 0.5–1.3 | 0.2 |
Non-Christian | 1.2 | 0.6 | 0.7–1.6 | 0.2 |
3.3. Attitudes and Perceptions
Approximately three-quarters (72.5%) of the respondents perceived the impact of mosquitoes on their daily life. Most (60.7%) of them reported being bitten by mosquitoes outdoor in their home places, fewer at recreational places or workplaces, and half responded that they were bitten indoors. In all, 44.6% of respondents were regularly bitten and 31.2% reported sometimes. Overall, 90% of participants were bitten during dark hours (sundown 36%, night 53%); fewer reported being bitten during the day (7.0%). According to their experience, the respondents associated the mosquito abundance in residential places with the presence of drainage and blocked draining water channels (21%), garbage (17.7%), farming activities (14%), house/road construction (10%), and animal rearing (7.7%). The most familiar sources for searching for information about MBVDs were health professionals/hospitals (40.2%) and their relatives or family members (26.1%), radio or television (25.3%), and schools (17.7%), and the others reported in Table 7.
Table 7.
Variable | No. of Respondents | Percent |
---|---|---|
Main source of the information | ||
Health professional/hospital | 529 | 40.2 |
Family | 344 | 26.1 |
Radio/television | 333 | 25.3 |
School, college, university | 233 | 17.7 |
Neighbours | 117 | 8.9 |
Community leaders and volunteers | 100 | 7.6 |
Megaphone public or government announcements | 74 | 5.0 |
Internet, newspapers, SMS | 74 | 5.0 |
Church/mosque | 15 | 1.2 |
Other (traditional healer) | 25 | 1.9 |
Impact of mosquitoes on daily life | ||
Health risk | 1061 | 72.5 |
Nuisance | 380 | 25.9 |
No concern | 7 | 0.4 |
I don’t know | 30 | 2.0 |
Other (disease, malaria, death) | 103 | 7.0 |
In which locations are you often bitten? | ||
Indoors | 741 | 50.6 |
Outdoors while I am at home | 890 | 60.7 |
At workplace indoors | 14 | 0.9 |
Outdoors while at workplace, recreational place | 119 | 8.1 |
Everywhere | 62 | 4.2 |
Nowhere | 24 | 1.6 |
How often do you get bitten? | ||
Rarely | 343 | 23.4 |
Sometimes | 468 | 31.9 |
Regularly | 653 | 44.6 |
During which time of the day are you often bitten? | ||
Daytime (morning, afternoon) | 102 | 7.0 |
Sundown | 528 | 36.0 |
Night | 778 | 53.8 |
Anytime | 177 | 12.0 |
Activity in your community leading to mosquito abundance | ||
Agriculture | 206 | 14.0 |
Animal rearing | 113 | 7.7 |
House building, road construction | 157 | 11.6 |
Drainage and all blocked draining water channels | 310 | 21.1 |
Garbage | 260 | 17.7 |
Mechanic or automobile garage | 12 | 0.8 |
Church services/prayers | 14 | 0.9 |
Witchcraft/sorcery | 14 | 0.9 |
Absence of sewage water draining system | 29 | 1.9 |
Erosion, flooding, proximity to the river | 15 | 1.1 |
Market, high population density | 5 | 0.3 |
None | 279 | 19 |
I don’t know | 223 | 15.2 |
Most respondents (72.9%) perceived that they were responsible for the prevention and protection of themselves and their households against mosquitoes and MBVD. However, only 37.3% were aware of their responsibilities at the community level. They perceived that mosquitoes and MBVD control and prevention should be the responsibility of the health authorities and national government (Table 8).
Table 8.
Self-Protection and Household | Community | |
---|---|---|
n (%) | n (%) | |
Individual responsibility | 1068 (72.9) | 546 (37.3) |
Household head | 128 (8.7) | 114 (7.7) |
Family members | 40 (2.7) | 7 (0.5) |
Local community population | 17 (1.2) | 62 (4.2) |
Health authorities | 223 (15.2) | 326 (22.2) |
Local government administration | 24 (1.6) | 50 (3.4) |
National government | 173 (11.8) | 245 (11.8) |
Both government and population | 96 (6.6) | |
God | 8 (0.5) | 2 (0.1) |
None one | 18 (1.2) | 153 (10.4) |
I don’t know | 84 (5.7) |
About 80% appeared to observe the correct attitude towards MBVDs (Table 5). The overall attitude scores were significantly associated with the respondent’s age and occupation. Respondents aged over 33 years (OR: 0.8; 95%CI: 0.6–1.0; p = 0.02) had lower attitude scores compared to those aged 18 to 33 years. Considered together, students and medical personnel (OR: 0.002; 95%CI: 1.1–1.9; p = 0.002) had a correct attitude towards mosquitoes and MBVDs. The sex, religion, marital status, education, and overall knowledge were not significantly associated with the respondents’ attitudes (Table 9).
Table 9.
Variable | OR | X2 | IC 95% | p |
---|---|---|---|---|
Factors associated with appropriate attitude towards MBDs | ||||
Age group of 34–70 years | 0.8 | 3.5 | 0.6–1.0 | 0.02 |
Female sex | 0.9 | 0.3 | 0.7–1.1 | 0.2 |
Married | 1.0 | 0.006 | 0.8–1.2 | 0.4 |
Post-secondary education level | 1.0 | 0.1 | 0.8–1.2 | 0.3 |
Medical personnel or student | 1.4 | 7.7 | 1.1–1.9 | 0.002 |
Non-Christian | 0.8 | 0.9 | 0.6–1.1 | 0.1 |
High score of knowledge | 1.2 | 0.9 | 0.8–1.8 | 0.1 |
3.4. Practices Regarding Vector Control
Slightly more than a half (58.6%) of the respondents reported cleaning the environment, one-quarter used insecticides, and another one-quarter reported emptying garbage containers and emptying flower pots (11%) as the measures undertaken to reduce mosquito abundance around their homes. The draining of standing water was mentioned by 16.3% of respondents and garbage cleaning by 11.3%. Covering of water sources or drinking water and/or storage containers was stated by only 10.4% of respondents.
As regards measures undertaken to reduce or avoid mosquito bites, a large proportion of the respondents (79%) stated the use of mosquito nets, fumigation and spraying of insecticide (15.8%), mosquito screens on windows (13%), use of fans (10%), wearing long clothes (0.3%), and praying to God (1%). High proportions of residents (67.7%) confirmed that they did not have any challenge in taking action to prevent or control mosquitoes. Challenges in mosquito control and prevention included lack of money and other resources (42.9%), limited access to necessary items (19.3%), not having time (19%), and disbelief in the effectiveness of these preventive measures (12.8%). Although 87.4% of the respondents had at least one mosquito net, only 67% confirmed to have slept under a mosquito net during the previous night. The source of the mosquito nets included a national mass distribution campaign (68.8%), healthcare facilities (15%), and procurement from shops/markets (18.8%). Almost 45% of these mosquito nets had holes (Table 10). The overall practice score was lower among 85.7% of participants. The age, sex, occupation, marital status, and education of participants were not significantly associated with their practices. Believers other than Christians (OR: 0.5; 95%CI: 0.3–0.8; p = 0.003) had lower practices compared to the latter. A high overall knowledge (OR: 1.4; 95%CI: 0.8–2.3; p = 0.1) and attitude (OR: 1.22; 95%CI: 0.9–1.6; p =0.1) were not significantly associated with the respondents’ good practice (Table 11).
Table 10.
Variable | No. of Respondents | Percent |
---|---|---|
Measures were undertaken to reduce mosquito abundance on the property | ||
Put a cover over the water source/drinking water/storage unit/container | 153 | 10.4 |
Empty flower pots/vases regularly | 160 | 10.9 |
Cleaning environment | 858 | 58.6 |
Empty other water containers serving as garbage collection | 363 | 24.8 |
Fumigating | 95 | 6.5 |
Remove garbage | 166 | 11.3 |
Use of insecticides | 380 | 25.9 |
Remove standing/stagnant water | 239 | 16.3 |
Nothing | 42 | 2.9 |
Use bed net | 68 | 4.6 |
Close the house door | 6 | 0.4 |
Measures that were undertaken to reduce or avoid mosquito bites | ||
Put mosquito screen on house windows | 197 | 13.4 |
Sleep under bed net during the day | 138 | 9.4 |
Sleep under bed net during the night | 1158 | 79.1 |
Use of mosquito repellent during the day | 19 | 1.3 |
Use of mosquito repellent during the night | 44 | 3.0 |
Stay indoors | 34 | 2.3 |
Use of fans | 153 | 10.4 |
Fumigate and spray the home | 232 | 15.8 |
Pray to God | 15 | 1.0 |
Nothing | 48 | 3.2 |
Wear long clothes | 5 | 0.3 |
Other | 48 | 3.2 |
Households having at least a mosquito bed net | 1280 | 87.4 |
Slept under mosquito bed net last night | 982 | 67.0 |
Source of mosquito bed net supply | ||
Mass distribution campaign | 873 | 68.8 |
Shop/market | 239 | 18.8 |
Health facilities | 191 | 15.0 |
Other | 26 | 2.0 |
Mosquito bed net with a hole in it | 538 | 43.4 |
Any challenges in implementing preventive measures | ||
Yes | 474 | 32.3 |
No | 990 | 67.7 |
Types of challenges | ||
Have no time to apply these preventive measures | 72 | 15 |
Lack of money and resources | 204 | 42.9 |
Limited access to necessary items | 92 | 19.3 |
Not a priority for me | 34 | 7.1 |
I don’t believe these preventive measures are effective | 61 | 12.8 |
Risk is low | 15 | 2.9 |
Other | 13 | 2.7 |
Table 11.
Variable | OR | X2 | IC 95% | p |
---|---|---|---|---|
Factors associated with appropriate attitude towards MBD | ||||
Age group of 34–70.years | 1.0 | 0.01 | 0.7–1.3 | 0.4 |
Female sex | 1.2 | 2.1 | 0.9–1.7 | 0.07 |
Married | 1.0 | 0.00 | 0.7–1.3 | 0.4 |
Post-secondary education level | 1.0 | 0.02 | 0.7–1.3 | 0.4 |
Medical personnel and student | 0.8 | 0.2 | 0.6–1.2 | 0.3 |
Non-Christian | 0.5 | 6.4 | 0.3–0.8 | 0.003 |
High score in knowledge | 1.4 | 1.6 | 0.8–2.3 | 0.1 |
Appropriate attitude | 1.2 | 1.5 | 0.9–1.6 | 0.1 |
4. Discussion
The present study explored the level of community KAP concerning mosquitoes and MBVD in Kinshasa, DRC. The majority of respondents reported being frequently bitten by mosquitoes either outdoors or indoors and most stated that mosquito activities were more intense from sundown to night. Only a few participants knew about the daily activity of mosquitoes. A high proportion of study participants felt more concerned about health problems that are brought by mosquitoes. The observation of the residential environment of the respondents allowed taking inventory of the diverse types of human-made and natural containers that could serve as mosquito breeding places. This observation was in contrast with a good level of general knowledge about environmental preventive measures noted among the majority of respondents and what they confirmed as their usual practices towards control and prevention of mosquitoes. This confirms that often people do not properly understand the meaning of the concept of environmental management [13].
The majority of respondents emphasised environmental cleaning although a high percentage of uncovered garbage cans, vegetation, stagnant water collections, and abandoned domestic containers were present in residential places. In addition, probably due to inadequate water supply in some homes, people have set up different water storage units outdoors being unaware of a possible invasion of Aedes mosquitoes [37]. This confirms that the common Aedes breeding habitats are not well known by the majority of the respondents [38]. The most common mosquito breeding places known by the study population were polluted water bodies. Garbage places were perceived as the main drivers leading to mosquito abundance. This was in line with studies carried out in India [39,40].
The mechanical automobile activities that take place in the city might also contribute to mosquito abundance. Similar reports from Tanzania have indicated that tyres are among the most prolific breeding sites for Aedes mosquitoes [41]. Agriculture and construction of roads and houses were also reported among the activities leading to mosquito abundance in Kinshasa. These observations were consistent with findings reported from Kenya, Tanzania, Sudan, France, and the French Antilles [1,42,43,44]. Therefore, the messages for MBVD prevention should raise awareness among the stakeholders engaged in the design, materials, and all human resources such as architects, landscapers, construction professionals, distributors, and installers [44].
Nevertheless, the majority of respondents in the current study were unaware of the vector role of mosquitoes in spreading pathogens to animals and their involvement. Although the majority of study participants had heard of an Aedes-transmitted virus such as yellow fever, chikungunya, Zika, and dengue, the majority of them did not know that these viruses are transmitted to humans by mosquitoes. The Democratic Republic of the Congo has experienced four chikungunya and four yellow fever outbreaks during the past two decades [22,23,24,45,46,47,48]. This could be one of the reasons why the majority of the respondents were aware of these diseases.
The lack of knowledge on the role of mosquitoes in spreading viruses to both humans and animals could explain some contradictory attitudes, behaviours, and practices noted among study participants. Similar observations have been reported in Jamaica, where the population had poor knowledge of MBVD and poor prevention practices [49]. On the contrary, in Belize, more than 85% of the respondents confirmed that DENV, ZIKV, CHIKV, and YVFV are viruses transmitted by mosquitoes and that communities were regularly draining standing water or using insecticides to control mosquitoes [2]. Similar observations have been reported in Colombia, the USA, and China where the majority of the population was positively involved in source reduction preventive practices [12,50,51].
The appropriate knowledge of MBVD can empower individuals to make some effort to prevent or control MBVD in their properties instead of waiting for government intervention. Poor knowledge of MBVD has also been reported for RVF in Kenya, Tanzania, and Sudan [1,42,43]. The lack of knowledge is driving MBVD into new areas and leads to loss of life and economic losses [1,43]. The high level of dirt, multiple fortuitous markets, high demographic pressure, and inadequate urbanisation of the Kinshasa metropolitan area are suitable conditions to support the Culex mosquito, the main vector of WNV and RVFV [52,53,54]. In the DRC, currently, RVFV activities are increasing [28] and evidence of WNV in domestic dogs and horses has been documented from Kinshasa [34,35]. Regarding the number of households rearing either domestic or livestock animals in this study area, there is also an urgent need to raise awareness of the population about the role of the mosquito in spreading zoonosis.
Participants in the current study were less aware of how their involvement in the local population can boost the control of mosquitoes and MBVD in their community. The study participants thought that their duty was only for self-protection and their households but not for local community mosquito prevention and control. Similar observations have been reported in a study in Western Australia [55]. These positive attitudes of trusting in government action offer an opportunity for decision makers and health actors to maximise their educational activities in this community and to get closer to the population through its local structures. Even practically, the respondents did not perceive the responsibility of the local community and their role as a source of information. The population must perceive that control of mosquito-borne diseases does not only have to rely on individual or household protection but also protection at the community level. Strengthening cooperation between neighbouring households can also serve as an information channel to improve the knowledge levels of this study population. The financial limitation was mentioned as the main hindrance in taking action against mosquitoes for the majority of the study population. This could be the reason that the majority of study participants would resort less to control measures that incur expenditures. Once the health risk is perceived as a real threat and priority, the population can transfer their knowledge into action [13]. However, embracing protective behaviours is a multifactorial procedure influenced by socio-economic and cognitive factors [56]. In general, household expenditure on protective measures using chemicals is high [2,3]. So, in limited resource settings, it is better to emphasise environmental measures which are more accommodated, simple to implement, and very effective too. Simple actions such as removing garbage and domestic use containers can reduce over 90% of larval abundance and putting in window screens and closing doors can contribute to excluding over 80% of mosquito adults from homes [13]. Social mobilisation and communication programmes including modern channels should be developed with all national and local partners and community leaders. The integration of awareness-raising activities on the prevention and control of mosquito-borne diseases should be encouraged in church, school, and university programmes to educate church followers and students and use them as multipliers.
Moreover, our findings are very interesting, especially for local health authorities, epidemiologists, and other involved stakeholders; significant inferences can assist to accommodate the prevention strategies of MBVDs. The interpretation of the results concerning the perception is subject to certain limitations. The study design and the declarative nature of the data did not allow us to have absolute confidence in the different cognitive and behavioural statements. The high attitude score in this study could be explained by the fact that only the perceived risk and the perception of the responsibility of participants in the individual and collective prevention and control of mosquitoes were considered in the scoring of attitude. The importance of the perception of risk lies in its ability to determine our emotional, behavioural, and social reactions. Observational longitudinal studies would help to better understand the dynamics of the perceptions and practices of the population. Since KAP studies are more likely to be descriptive in nature, they often do not provide an in-depth insight into the reasons underlying the results. A complementary qualitative approach to our survey is therefore essential.
In the current study, the association between the qualitative binary variables of interest was assessed by using contingency analysis with a significance level of 0.05, as this p-value is commonly used to identify statistically significant associations. It could also increase the family-wise Type I error rate.
5. Conclusions
The findings of this study indicate that the population of Kinshasa lives in an environment conducive to the proliferation of mosquitoes and the spread of mosquito-borne diseases. However, the overall community knowledge regarding MBVD was poor in terms of mosquito biology, prevention, and control. Therefore, there is an urgent need to introduce multiple education programmes to raise their awareness and improve their knowledge. Particular emphasis should be placed on environmental sanitation, as it is essential to encourage this population to invest themselves in the hygiene of their living environment since it is also within their reach.
Acknowledgments
The authors would like to thank both authorities of the Department of Tropical Medicine and the Faculty of Medicine of the University of Kinshasa for granting permission to carry out this study. The authors are also grateful to the finalist students from the Faculties of Medicine of both Université Libre de Kinshasa and Université Réverend Kim of Kinshasa for being helpful during the fieldwork.
Abbreviations
MBVD | Mosquito-borne viral disease |
YFV | Yellow fever virus |
CHIKV | Chikungunya virus |
DENV | Dengue virus |
ZIKV | Zika virus |
RVFV | Rift Valley fever virus |
WNV | West Nile virus |
ONNV | O’nyong’nyong virus |
EVD | Ebola virus disease |
KAP | Knowledge, attitude, and practice |
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/epidemiologia4010001/s1, File S1: Survey questionnaire; File S2: The scoring detail procedures for each KAP component.
Author Contributions
K.M.M. designed the study, conducted the fieldwork, performed the statistical analysis, and prepared the manuscript for publication; L.E.G.M. assisted in developing the study questionnaire, and critically revised the manuscript; R.W. assisted in developing the study questionnaire, study design, and participated in writing the manuscript; J.K.Z. participated in study design, and conducted the fieldwork, F.K.L. participated in the field, and assisted in writing the manuscript; G.M. participated in study design and revised the manuscript; S.I.K. participated in designing the study, assisted in developing the study questionnaire. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
The study protocol obtained approval from the Ethical Review Committee of the Public Health School of the University of Kinshasa, DRC (approval number ESP/CE/058/2019). Informed consent was obtained from all the respondents prior to survey questionnaire administration.
Informed Consent Statement
Ethical clearance for the study was obtained from the Ethics Committee of the Kinshasa School of Public Health (approval number: ESP/CE 058/2019). Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
All data supporting the study findings are included in this published article.
Conflicts of Interest
The authors declare no conflict of interest.
Funding Statement
This study received financial assistance through a scholarship from the Government of the United Republic of Tanzania through World Bank WB-ACE II Grant PAD1436. The funder had a role in the study.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
- 1.Abdi I.H., Affognon H.D., Wanjoya A.K., Onyango-Ouma W., Sang R. Knowledge, Attitudes and Practices (KAP) on Rift Valley Fever among Pastoralist Communities of Ijara District, North Eastern Kenya. PLoS Negl. Trop. Dis. 2015;9:e0004239. doi: 10.1371/journal.pntd.0004239. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Duman-Scheel M., Eggleson K.K., Achee N.L., Grieco J.P., Hapairai L.K. Mosquito control practices and perceptions: An analysis of economic stakeholders during the Zika epidemic in Belize, Central America. PLoS ONE. 2018;13:e0201075. doi: 10.1371/journal.pone.0201075. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Thuilliez J., Bellia C., Dehecq J.-S., Reilhes O. Household-level expenditure on protective measures against mosquitoes on the island of La Réunion, France. PLoS Negl. Trop. Dis. 2014;8:e2609. doi: 10.1371/journal.pntd.0002609. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Statistics for Mosquito-Borne Diseases & Deaths. [(accessed on 10 August 2019)]. Available online: http://www.mosquitoreviews.com/mosquito-statistics.
- 5.Gulich G.A. Epidemiology, Driving Factors, Transmission and Control Options of Zika Virus. Rev. J. Infect. Dis. Ther. 2016;4:278. [Google Scholar]
- 6.Kraemer M.U.G., Faria N.R., Reiner R.C., Golding N., Nikolay B., Stasse S., Johansson M.A., Salje H., Faye O., Wint G.R.W., et al. Spread of yellow fever virus outbreak in Angola and the Democratic Republic of the Congo 2015–16: A modelling study. Lancet Infect. Dis. 2017;17:330. doi: 10.1016/S1473-3099(16)30513-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Braack L., de Almeida A.P.G., Cornel A.J., Swanepoel R., de Jager C. Mosquito-borne arboviruses of African origin: Review of key viruses and vectors. Parasit. Vectors. 2018;11:29. doi: 10.1186/s13071-017-2559-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Whiteman A., Mejia A., Hernandez I., Loaiza J.R. Socioeconomic and demographic predictors of resident knowledge, attitude, and practice regarding arthropod-borne viruses in Panama. BMC Public Health. 2018;18:1261. doi: 10.1186/s12889-018-6172-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Corrin T., Waddell L., Greig J., Young I., Hierlihy C., Mascarenhas M. Risk perceptions, attitudes, and knowledge of chikungunya among the public and health professionals: A systematic review. Trop. Med. Health. 2017;45:21. doi: 10.1186/s41182-017-0061-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Mouchtouri V.A., Papagiannis D., Katsioulis A., Rachiotis G., Dafopoulos K., Hadjichristodoulou C. Knowledge, Attitudes, and Practices about the Prevention of Mosquito Bites and Zika Virus Disease in Pregnant Women in Greece. Int. J. Environ. Res. Public Health. 2017;14:367. doi: 10.3390/ijerph14040367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Potter A., Jardine A., Neville P.J. A Survey of Knowledge, Attitudes, and Practices in Relation to Mosquitoes and Mosquito-Borne Disease in Western Australia. Front. Public Health. 2016;4:32. doi: 10.3389/fpubh.2016.00032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Liu X., Wan F., Cirendunzhu, Cirenwangla, Bai L., Pengcuociren, Zhou L., Baimaciwang, Guo Y., Dazhen, et al. Community knowledge and experience of mosquitoes and personal prevention and control practices in Lhasa, Tibet. Int. J. Environ. Res. Public Health. 2014;11:9919–9937. doi: 10.3390/ijerph110909919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Leslie T.E., Carson M., van Coeverden E., De Klein K., Braks M., Krumeich A. An analysis of community perceptions of mosquito-borne disease control and prevention in Sint Eustatius, Caribbean Netherlands. Glob. Health Action. 2017;10:1350394. doi: 10.1080/16549716.2017.1350394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Harrington L.C., Fleisher A., Ruiz-Moreno D., Vermeylen F., Wa C.V., Poulson R.L., Edman J.D., Clark J.D., Jones J.W., Kitthawee S., et al. Heterogeneous Feeding Patterns of the Dengue Vector, Ae aegypti, on Individual Human Hosts in Rural Thailand. PLoS Negl. Trop. Dis. 2014;8:e3048. doi: 10.1371/journal.pntd.0003048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Dambach P., Schleicher M., Korir P., Ouedraogo S., Dambach J., Sié A., Dambach M., Becker C. Nightly Biting Cycles of Anopheles Species in Rural Northwestern Burkina Faso. J. Med. Entomol. 2018;55:1027–1034. doi: 10.1093/jme/tjy043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Skiff J.J., Yee D.A. Behavioral Differences Among Four Co-occurring Species of Container Mosquito Larvae: Effects of Depth and Resource Environments. J. Med. Entomol. 2014;51:375–381. doi: 10.1603/ME13159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Ajamma Y.U., Villinger J., Omondi D., Salifu D., Onchuru T.O., Njoroge L., Muigai A.W.T., Masiga D.K. Composition and Genetic Diversity of Mosquitoes (Diptera: Culicidae) on Islands and Mainland Shores of Kenya’s Lakes Victoria and Baringo. J. Med. Entomol. 2016;53:1348–1363. doi: 10.1093/jme/tjw102. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Djoufounna J., Mayi M.P.A., Bamou R., Ningahi L.G., Falone Ornela Magatsing F.O., Djiappi-Tchamen B., Djamouko-Djonkam L., Antonio-Nkondjio C., Tchuinkam T. Larval habitats characterization and population dynamics of Culex mosquitoes in two localities of the Menoua Division, Dschang and Santchou, West Cameroon. JoBAZ. 2022;83:30. doi: 10.1186/s41936-022-00290-x. [DOI] [Google Scholar]
- 19.Mbanzulu K.M., Mboera L.E.G., Luzolo F.K., Wumba R., Misinzo G., Kimera S.I. Mosquito-borne viral diseases in the Democratic Republic of the Congo: A review. Parasit. Vectors. 2020;13:103. doi: 10.1186/s13071-020-3985-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.WHO Africa . Mapping the Risk and Distribution of Epidemics in the WHO African Region. WHO Regional Office for Africa; Brazzaville, Republic of Congo: [(accessed on 10 August 2019)]. A technical report. Available online: https://apps.who.int/iris/handle/10665/206560. [Google Scholar]
- 21.Otshudiema J.O., Ndakala N.G., Mawanda E.-T.K., Tshapenda G.P., Kimfuta J.M., Nsibu L.-R.N., Gueye A.S., Dee J., Philen R.M., Giese C., et al. Yellow Fever Outbreak—Kongo Central Province, Democratic Republic of the Congo, August 2016. MMWR Morb. Mortal. Wkly. Rep. 2017;66:335–338. doi: 10.15585/mmwr.mm6612a5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Muyembe-Tamfum J.J., Peyrefitte C.N., Yogolelo R., Mathina Basisya E., Koyange D., Pukuta E., Mashako M., Tolou H., Durand J.P. Epidemic of Chikungunya virus in 1999 and 200 in the Democratic Republic of the Congo. Med. Trop. Rev. Corps. Sante. Colon. 2003;63:637–638. [PubMed] [Google Scholar]
- 23.Ido E., Ahuka S., Karhemere S., Shibata K., Kameoka M., Muyembe J.J. Dengue Virus Infection during an Outbreak of Chikungunya Virus in Democratic Republic of Congo Annales Africaines de Médecine. [(accessed on 9 August 2019)]. Available online: https://anafrimed.net/dengue-virus-infection-during-an-outbreak-of-chikungunya-virus-in-democratic-republic-of-congo-infection-virus-de-dengue-survenue-lors-dune-epidemie-virus-chikungunya-republique-democr/
- 24.Mintela C. Epidémie de Chikungunya Confirmée à Kinshasa. [(accessed on 9 August 2019)]. Available online: https://www.academia.edu/38387381.
- 25.Malekani M.J., Mccollum A.M., Monroe B., Malekani V., Mulumba M., Nguete BKarhemere S.R. Cas de Dengue Chez Les Patients Suspects de Chikungunya à Kinshasa. Annales Africaines de Médecine. [(accessed on 10 August 2019)]. Available online: https://anafrimed.net/cas-de-dengue-chez-les-patients-suspects-de-chikungunya-a-kinshasa/
- 26.Makiala-Mandanda S., Ahuka-Mundeke S., Abbate J.L., Pukuta-Simbu E., Nsio-Mbeta J., Berthet N., Leroy E.M., Becquart P., Muyembe-Tamfum J.-J. Identification of Dengue and Chikungunya Cases Among Suspected Cases of Yellow Fever in the Democratic Republic of the Congo. Vector Borne Zoonotic Dis. 2018;18:364–370. doi: 10.1089/vbz.2017.2176. [DOI] [PubMed] [Google Scholar]
- 27.Willcox A.C., Collins M.H., Jadi R., Keeler C., Parr J.B., Mumba D., Kashamuka M., Tshefu A., de Silva A.M., Meshnick S.R. Seroepidemiology of Dengue, Zika, and Yellow Fever Viruses among Children in the Democratic Republic of the Congo. Am. J. Trop. Med. Hyg. 2018;99:756–763. doi: 10.4269/ajtmh.18-0156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Georges T.M., Justin M., Victor M., Marie K.J., Mark R., Léopold M.M.K. Seroprevalence and Virus Activity of Rift Valley Fever in Cattle in Eastern Region of Democratic Republic of the Congo. J. Vet. Med. 2018;2018:4956378. doi: 10.1155/2018/4956378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Bobanga T., Moyo M., Vulu F., Irish S.R. First Report of Aedes albopictus (Diptera: Culicidae) in the Democratic Republic of Congo. Afr. Entomol. 2018;26:234–236. doi: 10.4001/003.026.0234. [DOI] [Google Scholar]
- 30.VAN DEN Bossche D., Cnops L., Meersman K., Domingo C., VAN Gompel A., VAN Esbroeck M. Chikungunya virus and West Nile virus infections imported into Belgium, 2007–2012. Epidemiol. Infect. 2015;143:2227–2236. doi: 10.1017/S0950268814000685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Yamamoto S.P., Kasamatsu Y., Kanbayashi D., Kaida A., Shirano M., Kubo H., Goto T., Iritani N. Dengue Virus in Traveler Returning to Japan from the Democratic Republic of the Congo, 2015. Jpn. J. Infect. Dis. 2019;72:426–428. doi: 10.7883/yoken.JJID.2018.554. [DOI] [PubMed] [Google Scholar]
- 32.Colavita F., Vairo F., Carletti F., Boccardo C., Ferraro F., Iaiani G., Moghazi S.A., Galardo G., Lalle E., Selvaggi C., et al. Full-length genome sequence of a dengue serotype 1 virus isolate from a traveler returning from Democratic Republic of Congo to Italy, July, 2019. Int. J. Infect. Dis. 2020;92:46–48. doi: 10.1016/j.ijid.2019.12.023. [DOI] [PubMed] [Google Scholar]
- 33.Mbanzulu K.M., Wumba R., Mukendi J.K., Zanga J.K., Shija F., Bobanga T.L., Aloni M.N., Misinzo G. Mosquito-borne viruses circulating in Kinshasa, Democratic Republic of the Congo. Int. J. Infect. Dis. 2017;57:32–37. doi: 10.1016/j.ijid.2017.01.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Cabre O., Grandadam M., Marié J.-L., Gravier P., Prangé A., Santinelli Y., Rous V., Bourry O., Durand J.-P., Tolou H., et al. West Nile Virus in horses, sub-Saharan Africa. Emerg. Infect. Dis. 2006;12:1958–1960. doi: 10.3201/eid1212.060042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Davoust B., Leparc-Goffart I., Demoncheaux J.-P., Tine R., Diarra M., Trombini G., Mediannikov O., Marié J.-L. Serologic surveillance for West Nile virus in dogs, Africa. Emerg. Infect. Dis. 2014;20:1415–1417. doi: 10.3201/eid2008.130691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Wikipedia Kinshasa Population. [(accessed on 10 August 2019)]. Available online: https://en.wikipedia.org/w/index.php.
- 37.Baak-Baak C.M., Arana-Guardia R., Cigarroa-Toledo N., Puc-Tinal M., Coba-Tún C., Rivero-Osorno V., Lavalle-Kantun D., Loroño-Pino M.A., Machain-Williams C., Reyes-Solis G.C., et al. Urban Mosquito Fauna in Mérida City, México: Immatures Collected from Containers and Storm-water Drains/Catch Basins. Southwest. Entomol. 2014;39:291–306. doi: 10.3958/059.039.0207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Medone P., Hernï Ndez-Suï Rez C.M. ‘Swimming mosquitoes’: A key stepping stone to prevent Dengue, Zika and Chikungunya: An educative experience in Colima, Mexico. Health Educ. Res. 2019;34:389–399. doi: 10.1093/her/cyz012. [DOI] [PubMed] [Google Scholar]
- 39.Boratne A.V., Jayanthi V., Datta S.S., Singh Z., Senthilvel V., Joice Y.S. Predictors of knowledge of selected mosquito-borne diseases among adults of selected peri-urban areas of Puducherry. J. Vector Borne Dis. 2010;47:249–256. [PubMed] [Google Scholar]
- 40.Tenglikar P.V., Hussain M., Nigudgi S., Ghooli S. Knowledge and Practices Regarding Mosquito borne disease among people of an urban area in Kalaburgi, Karnataka. Natl J. Community Med. 2016;7:223–225. [Google Scholar]
- 41.Mboera L.E.G., Mweya C.N., Rumisha S.F., Tungu P.K., Stanley G., Makange M.R., Misinzo G., Nardo P.D., Vairo F., Oriyo N.M. The risk of Dengue virus transmission in Dar es Salaam, Tanzania during an epidemic period of 2014. PLoS Negl. Trop. Dis. 2016;10:e0004313. doi: 10.1371/journal.pntd.0004313. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Shabani S.S., Ezekiel M.J., Mohamed M., Moshiro C.S. Knowledge, attitudes and practices on Rift Valley fever among agro pastoral communities in Kongwa and Kilombero districts, Tanzania. BMC Infect. Dis. 2015;15:363. doi: 10.1186/s12879-015-1099-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Hassan O.A., Affognon H., Rocklöv J., Mburu P., Sang R., Ahlm C., Evander M. The One Health approach to identify knowledge, attitudes and practices that affect community involvement in the control of Rift Valley fever outbreaks. PLoS Negl. Trop. Dis. 2017;11:e0005383. doi: 10.1371/journal.pntd.0005383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Claeys C., Robles C., Bertaudiere-Montes V., Deschamps-Cottin M., Megnifo H.T., Pelagie-Moutenda R., Evander M. Facteurs socio-écologiques contribuant à l’exposition des populations humaines aux piqûres des moustiques vecteurs de la dengue, du chikungunya et du zika: Une comparaison entre France métropolitaine et Antilles françaises. Environ. Risques Santé. 2016;15:318–325. [Google Scholar]
- 45.WHO . Yellow Fever in the Democratic Republic of the Congo. World Health Organisation; Geneva, Switzerland: [(accessed on 9 August 2019)]. Available online: https://www.who.int/emergencies/disease-outbreak-news/item/2010_07_19a-en. [Google Scholar]
- 46.WHO . Yellow Fever in the Democratic Republic of Congo. World Health Organisation; Geneva, Switzerland: [(accessed on 9 August 2019)]. Available online: https://www.who.int/emergencies/disease-outbreak-news/item/2013_06_14_yellowfever-en. [Google Scholar]
- 47.WHO . Yellow Fever Democratic Republic of the Congo. World Health Organisation; Geneva, Switzerland: [(accessed on 9 August 2019)]. Available online: https://www.who.int/emergencies/disease-outbreak-news/item/2014_04_24_yellowfever-en. [Google Scholar]
- 48.WHO . Situation Report Yellow Fever. World Health Organisation; Geneva, Switzerland: [(accessed on 9 August 2019)]. Available online: http://apps.who.int/iris/bitstream/10665/250661/1/yellowfeversitrep28Oct16-eng.pdf?ua/ [Google Scholar]
- 49.Alobuia W.M., Missikpode C., Aung M., Jolly P.E. Knowledge, Attitude, and Practices Regarding Vector-borne Diseases in Western Jamaica. Ann. Glob. Health. 2015;81:654–663. doi: 10.1016/j.aogh.2015.08.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Ramírez G.I.J., Álvarez L.S.B. Knowledge, Attitudes and Practices Regarding Dengue, Chikungunya, and Zika and their Vector Aedes Aegypti in Villavicencio, Colombia. Open Public Health J. 2017;10:80–89. doi: 10.2174/1874944501710010080. [DOI] [Google Scholar]
- 51.Morse W., Izenour K., McKenzie B., Lessard S., Zohdy S. Perceptions and practices of mosquito-borne diseases in Alabama: Is concern where it should be? BMC Public Health. 2019;19:987. doi: 10.1186/s12889-019-7308-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Karch S., Asidi N., Manzambi Z., Sa-Laun J. Culicidianfauna and its nuisance in Kinshasa (Zaire) Bull. Société Pathol. Exot. 1993;86:68–75. [PubMed] [Google Scholar]
- 53.Herrington J.E. Pre-West Nile virus outbreak: Perceptions and practices to prevent mosquito bites and viral encephalitis in the United States. Vector Borne Zoonotic Dis. 2003;3:157–173. doi: 10.1089/153036603322662156. [DOI] [PubMed] [Google Scholar]
- 54.Mweya C.N., Kimera S.I., John Bukombe J.K., Mboera L.E.G. Predicting distribution of Aedes aegypti and Culex pipiens complex, potential vectors of Rift Valley fever virus in relation to disease epidemics in East Africa. Infect. Ecol. Epidemiol. 2013;3:21748. doi: 10.3402/iee.v3i0.21748. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Mainali S., Lamichhane R.S., Clark K., Beatty S., Fatouros M., Neville P., Oosthuizen J. Looking over the Backyard Fence: Householders and Mosquito Control. Int. J. Environ. Res. Public Health. 2017;14:246. doi: 10.3390/ijerph14030246. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Fritzell C., Raude J., Adde A., Dusfour I., Quenel P., Flamand C. Knowledge, Attitude and Practices of Vector-Borne Disease Prevention during the Emergence of a New Arbovirus: Implications for the Control of Chikungunya Virus in French Guiana. PLoS Negl. Trop. Dis. 2016;10:e0005081. doi: 10.1371/journal.pntd.0005081. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All data supporting the study findings are included in this published article.