##plugins.themes.bootstrap3.article.main##

ID Adelia Gita Prasasti https://orcid.org/0000-0002-6603-1630
ID Teguh Hari Sucipto https://orcid.org/0000-0003-0512-2990
ID Muhammad Ridho Hafid Kurniawan https://orcid.org/0009-0009-2793-2637
ID Shifa Fauziyah https://orcid.org/0000-0002-2928-2967
ID Anak Agung Istri Dalem Cinthya Riris https://orcid.org/0000-0003-4085-2059
ID Yohana Djurumana https://orcid.org/0000-0001-6456-5914
ID Nafisah Nurul Hapsari https://orcid.org/0009-0006-3331-8607
ID Neni Isna Farihah https://orcid.org/0009-0006-9227-8676
ID Alvia Rachma Wijayanti https://orcid.org/0009-0008-9486-0453
ID Nita Kusumawati https://orcid.org/0000-0001-7119-682X
ID Hariyono Hariyono https://orcid.org/0000-0002-5243-5925
ID Puspa Wardhani https://orcid.org/0000-0003-2202-8090

Abstract

Indonesia recorded the highest dengue mortality rate in Asia in 2022, with 45,387 cases and 432 deaths.  This study aimed to investigate the coexistence of arboviruses and insecticide resistance mechanisms in Aedes vectors mosquitos’ populations in Mulyorejo District, Surabaya, during the early monsoon season of 2021. A cross-sectional survey was conducted in January 2021, and Aedes larvae were collected and reared to adulthood under laboratory conditions. A total of 309 Aedes larvae (comprising 65% Aedes aegypti and 35% Aedes albopictus) were collected from 36 breeding sites, identified, and georeferenced using QGIS software. RNA extraction and RT-PCR assays were performed to detect Dengue virus (DENV), Japanese encephalitis virus (JEV), West Nile virus (WNV), and knockdown resistance (KDR) mutations. Results showed seven samples positive for DENV-2 and seven for JEV, with two samples (codes 9 and 12) exhibiting co-infection with both viruses, while no WNV was detected. The detection of JEV in Aedes larvae is a notable finding, suggesting a potential secondary vector role for these species in the study area, as Culex mosquitoes are the primary vectors of JEV. Mutations at codons 1016 (V1016G) and 1534 (F1534C), associated with pyrethroid and DDT resistance, were detected in eight and seven samples, respectively. These findings confirm the circulation of DENV-2 and JEV in local Aedes populations, highlighting the presence of KDR mutations that confer insecticide resistance. The results underscore the urgent need for integrated vector management in Surabaya, combining arbovirus surveillance, insecticide resistance monitoring, and community-based source reduction to mitigate arboviral disease transmission.

Downloads

Download data is not yet available.

##plugins.themes.bootstrap3.article.details##

How to Cite
Prasasti, A. G. (2026) “Characterization of Aedes sp. larvae: Detection of dengue, Japanese encephalitis and West Nile virus with knockdown resistance mutations in Mulyorejo, Surabaya, Indonesia”, Indonesian Journal of Medical Laboratory Science and Technology, 8(1), pp. 1–13. doi: 10.33086/ijmlst.v8i1.6654.
Section
Articles
Aedes sp., Dengue virus, Japanese encephalitis virus, Knockdown resistance, West Nile virus

References

Phadungsombat J, Nakayama EE, Shioda T. Unraveling Dengue virus diversity in Asia: An epidemiological study through genetic sequences and phylogenetic analysis. Viruses. 2024;16(7):1046. https://doi.org/10.3390/v16071046

Widyawati. Dengue fever cases continue to rise, Anung urges the public to maximize mosquito nest eradication. [Kasus DBD terus bertambah, Anung imbau masyarakat maksimalkan pemberantasan sarang nyamuk]. Jakarta: Kementerian Kesehatan RI; 2019. From: https://kemkes.go.id/id/kasus-dbd-terus-bertambah-anung-imbau-masyarakat-maksimalkan-psn

Dinas Kesehatan Kota Surabaya. Surabaya City Health Profile 2021. [Profil kesehatan Kota Surabaya 2021]. 2021. Available from: https://dinkes.surabaya.go.id/portal_dinkes/d/dkk/dokumen?kategori=3&page=1

Dinas Kesehatan Kota Surabaya. Surabaya City Health Profile 2019. [Profil kesehatan Kota Surabaya 2019]. Vol. 1, Dinkes Kota Surabaya. 2019. Available from: https://dinkes.surabaya.go.id/portal_dinkes/d/dkk/dokumen

Dinas Kesehatan Kota Surabaya. Surabaya City Health Profile 2020. [Profil Kesehatan Surabaya 2020]. Dinkes Kota Surabaya. Available from: https://dinkes.surabaya.go.id/portal_dinkes/d/dkk/dokumen

Mackenzie JS, Gubler DJ, Petersen LR. Emerging flaviviruses: The spread and resurgence of Japanese encephalitis, West Nile and Dengue viruses. Nat Med. 2004;10(12 Suppl):S98-109. https://doi.org/10.1038/nm1144

Van den Eynde C, Sohier C, Matthijs S, De Regge N. Japanese encephalitis virus interaction with mosquitoes: A review of vector competence, vector capacity and mosquito immunity. Pathogens. 2022;11(3):317. https://doi.org/10.3390/pathogens11030317

Yamanaka A, Mulyatno KC, Susilowati H, Hendrianto E, Utsumi T, Amin M, Lusida MI, Soegijanto S, Konishi E. Prevalence of antibodies to Japanese encephalitis virus among pigs in Bali and East Java, Indonesia, 2008. Jpn J Infect Dis. 2010;63(1):58–60. https://doi.org/10.7883/yoken.63.58

Kramer LD, Li J, Shi PY. West Nile virus. Lancet Neurol. 2007;6(2):171–81. https://doi.org/10.1016/S1474-4422(07)70030-3

Myint KS, Kosasih H, Artika IM, Perkasa A, Puspita M, Ma'roef CN, Antonjaya U, Ledermann JP, Powers AM, Alisjahbana B. Short report: West Nile virus documented in Indonesia from acute febrile illness specimens. Am J Trop Med Hyg. 2014;90(2):260–262. https://doi.org/10.4269/ajtmh.13-0445

Othman M, Indawati R, Suleiman AA, Qomaruddin MB, Sokkalingam R. Model forecasting development for Dengue fever incidence in Surabaya City using time series analysis. Processes. 2022;10(11):1-17. https://doi.org/10.3390/pr10112454

Abernathy HA, Hollingsworth BD, Giandomenico DA, Moser KA, Juliano JJ, Bowman NM, George PJ, Reiskind MH, Boyce RM. Prevalence of knock-down resistance F1534S mutations in Aedes albopictus (Skuse) (Diptera: Culicidae) in North Carolina. J Med Entomol. 2022;59(4):1363–7. https://doi.org/10.1093/jme/tjac054

Andriyoko B, Parwati I, Tjandrawati A, Lismayanti L. Determination of Dengue virus serotype and description of clinical manifestations and routine hematology in Dengue virus infection. [Penentuan serotipe virus Dengue dan gambaran manifestasi klinis serta hematologi rutin pada infeksi virus Dengue]. Maj Kedokt Bandung. 2012;44(4):253–60. http://dx.doi.org/10.15395/mkb.v44n4.138

Fauziyah S, Subekti S, Utomo B, Sucipto TH, Adrianto H, Aryati A, Wardhani P, Soegijanto S. Detection of knockdown-resistance mutations (V1016G and F1534C) in Dengue vector from urban park, Surabaya, Indonesia. J Trop Viodivers Biotechnol. 2021;6(3):1–12. https://doi.org/10.22146/jtbb.65357

Auteri M, La Russa F, Blanda V, Torina A. Insecticide resistance associated with kdr mutations in Aedes albopictus: An update on worldwide evidences. Biomed Res Int. 2018;2018:3098575. https://doi.org/10.1155/2018/3098575

Faizah AN, Kobayashi D, Maekawa Y, Amoa-Bosompem M, Fauziyah S, Mulyatno KC, Subekti S, Rohmah EA, Lusida MI, Mori Y, Miura K, Hirayama K, Isawa H, Sawabe K. Identification and isolation of Japanese encephalitis virus genotype IV from Culex vishnui collected in Bali, Indonesia in 2019. Am J Trop Med Hyg. 2021;105(3):813-817. https://doi.org/10.4269/ajtmh.20-1554

Lanciotti RS, Calisher CH, Gubler DJ, Chang GJ, Vorndam AV. Rapid detection and typing of Dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction. J Clin Microbiol. 1992;30(3):545–51. https://doi.org/10.1128/jcm.30.3.545-551.1992

Patel P, Landt O, Kaiser M, Faye O, Koppe T, Lass U, Sall AA, Niedrig M. Development of one-step quantitative reverse transcription PCR for the rapid detection of flaviviruses. Virol J. 2013;10:58. https://doi.org/10.1186/1743-422X-10-58

Md Naim D, Kamal NZM, Mahboob S. Population structure and genetic diversity of Aedes aegypti and Aedes albopictus in Penang as revealed by mitochondrial DNA cytochrome oxidase I. Saudi J Biol Sci. 2021;27(3):953–967. https://doi.org/10.1016/j.sjbs.2020.01.021

Kitching RL. An ecological study of water-filled tree-holes and their position in the woodland ecosystem. J Anim Ecol. 1971;40(2):281. https://doi.org/10.2307/3247

Gao S, Xu H, Li H, Feng X, Zhou J, Guo R, Liang Z, Ding J, Li X, Huang Y, Liu W, Liang S. Identification and functional analysis of C-type lectin from mosquito Aedes albopictus in response to Dengue virus infection. Parasites and Vectors. 2024;17(1):375. https://doi.org/10.1186/s13071-024-06453-9

Cuellar-Quimbaya AF, Muñoz AL, Yepez-Perez Y, C ID, Rodríguez AK, Segura NA, Bello F, Losada-Barragán M. Quantitative detection of chikungunya, Zika, and Dengue viruses by one-step real-time PCR in different cell substrates. Braz J Microbiol. 2024;55(2):1083–1090. https://doi.org/10.1007/s42770-023-01226-5

Fang Y, Tambo E, Xue JB, Zhang Y, Zhou XN, Khater EIM. Molecular analysis of targeted insecticide resistance gene mutations in field-caught mosquitos of medical importance from Saudi Arabia. J Med Entomol. 2021;58(4):1839–48. https://doi.org/10.1093/jme/tjab048

Mundim-Pombo APM, Carvalho HJC, Rodrigues Ribeiro R, León M, Maria DA, Miglino MA. Aedes aegypti: Egg morphology and embryonic development. Parasit Vectors. 2021;14(1):531. https://doi.org/10.1186/s13071-021-05024-6

Rebora M, Salerno G, Piersanti S, Kovalev A, Gorb SN. The origin of black and white coloration of the Asian tiger mosquito Aedes albopictus (Diptera: Culicidae). Beilstein J Nanotechnol. 2023;14:496–508. https://doi.org/10.3762/bjnano.14.41

Wulandhani S. Analisis keberadaan nyamuk Aedes aegypti Linnaeus dan Aedes albopictus Skuse di berbagai tempat umum kecamatan Somba Opu Kabupaten Gowa. Celebes Biodiversitas. 2020;3(1):27. https://doi.org/10.51336/cb.v3i1.204

Kraemer MUG, Reiner RC Jr, Brady OJ, Messina JP, Gilbert M, Pigott DM, Yi D, Johnson K, Earl L, Marczak LB, Shirude S, Davis Weaver N, Bisanzio D, Perkins TA, Lai S, Lu X, Jones P, Coelho GE, Carvalho RG, Van Bortel W, Marsboom C, Hendrickx G, Schaffner F, Moore CG, Nax HH, Bengtsson L, Wetter E, Tatem AJ, Brownstein JS, Smith DL, Lambrechts L, Cauchemez S, Linard C, Faria NR, Pybus OG, Scott TW, Liu Q, Yu H, Wint GRW, Hay SI, Golding N. Past and future spread of the arbovirus vectors Aedes aegypti and Aedes albopictus. Nat Microbiol. 2019;4(5):854–63. https://doi.org/s41564-019-0376-y

Rezza G. Aedes albopictus and the reemergence of Dengue. BMC Public Health. 2012;12(1):72. https://doi.org/10.1186/1471-2458-12-72

Rabaan AA, Alshengeti A, Alrasheed HA, Al-Subaie MF, Aljohani MH, Almutawif YA, Yousuf AA, Alsuliman SA, Al-Jishi JM, Almalki F, Alshiekheid MA, Alahmed HE, Alramadan AM, Turkistani SA, Hajissa K. Dengue virus infection in Saudi Arabia from 2003 to 2023: A systematic review and meta-analysis. Pathog Glob Health. 2024;118(7-8):549-558. https://doi.org/10.1080/20477724.2024.2425493

Bhatnagar P, Sreekanth GP, Murali-Krishna K, Chandele A, Sitaraman R. Dengue virus non-structural protein 5 as a versatile, multi-functional effector in host–pathogen interactions. Front Cell Infect Microbiol. 2021:11:574067. https://doi.org/10.3389/fcimb.2021.574067

Zuharah WF, Sufian M. The discovery of a novel knockdown resistance (kdr) mutation A1007G on Aedes aegypti (Diptera: Culicidae) from Malaysia. Sci Rep. 2021;11(1):5180 https://doi.org/10.1038/s41598-021-84669-w

Mashlawi AM, Al-Nazawi AM, Noureldin EM, Alqahtani H, Mahyoub JA, Saingamsook J, Debboun M, Kaddumukasa M, Al-Mekhlafi HM, Walton C. Molecular analysis of knockdown resistance (kdr) mutations in the voltage-gated sodium channel gene of Aedes aegypti populations from Saudi Arabia. Parasit Vectors. 2022;15(1):375. https://doi.org/10.1186/s13071-022-05525-y

Barrera-Illanes AN, Micieli MV, Ibáñez-Shimabukuro M, Santini MS, Martins AJ, Ons S. First report on knockdown resistance mutations in wild populations of Aedes aegypti from Argentina determined by a novel multiplex high-resolution melting polymerase chain reaction method. Parasit Vectors. 2023;16(1):222. https://doi.org/10.1186/s13071-023-05840-y

Campbell GL, Martin AA, Lanciotti RS, Gubler. Reviews West Nile virus. Lancet Infectious Disease. 2002;2(9):519–29. https://doi.org/10.1016/s1473-3099(02)00368-7

García-Alegría AM, Anduro-Corona I, Pérez-Martínez CJ, Guadalupe Corella-Madueño MA, Rascón-Durán ML, Astiazaran-Garcia H. Quantification of DNA through the nanodrop spectrophotometer: Methodological validation using standard reference material and sprague dawley rat and human DNA. Int J Anal Chem. 2020;2020:8896738. https://doi.org/10.1155/2020/8896738

Reinhart D, Damjanovic L, Castan A, Ernst W, Kunert R. Differential gene expression of a feed-spiked super-producing CHO cell line. J Biotehcnol. 2018;285:23–37. https://doi.org/10.1016/j.jbiotec.2018.08.013

Yeh JY, Lee JH, Seo HJ, Park JY, Moon JS, Cho IS, Lee JB, Park SY, Song CS, Choi IS. Fast duplex one-step reverse transcriptase PCR for rapid differential detection of West Nile and Japanese encephalitis viruses. J Clin Microbiol. 2010;48(11):4010–4. https://doi.org/10.1128/jcm.00582-10

Kotaki T, Yamanaka A, Mulyatno KC, Churrotin S, Sucipto TH, Labiqah A, Ahwanah NL, Soegijanto S, Kameoka M, Konishi E. Divergence of the Dengue virus type 2 Cosmopolitan genotype associated with two predominant serotype shifts between 1 and 2 in Surabaya, Indonesia, 2008-2014. Infect Genet Evol. 2016;37:88–93. https://doi.org/10.1016/j.meegid.2015.11.002

Setiawan AR, Fadila SZ, Sucipto TH, Fauziah S, Madaniyah S, Dewi EC, Naw SW, Tukiran, Cahyaningrum SE. Detection of homozygous wildtype V1016V using allele-specific polymerase chain reaction in Aedes albopictus. Biodiversitas. 2023;24(1):62–7. https://doi.org/10.13057/biodiv/d240109

Adelia Gita Prasasti, Universitas Airlangga

Master of Basic Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia

Teguh Hari Sucipto, Universitas Airlangga

Dengue Study Group, Institute of Tropical Disease, Universitas Airlangga, Surabaya, Indonesia

Muhammad Ridho Hafid Kurniawan, Universitas Negeri Surabaya

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Surabaya, Surabaya, Indonesia

Shifa Fauziyah, Delima Husada Gresik Health Analyst Academy

Delima Husada Gresik Health Analyst Academy, Gresik, Indonesia

Anak Agung Istri Dalem Cinthya Riris, Public Health Office of Surabaya

Public Health Office of Surabaya, Surabaya, Indonesia

Yohana Djurumana, Universitas Kristen Indonesia Maluku

Department of Public Health, Faculty of Health, Universitas Kristen Indonesia Maluku, Maluku, Indonesia

Nafisah Nurul Hapsari, Universitas Negeri Surabaya

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Surabaya, Surabaya, Indonesia

Neni Isna Farihah, Universitas Negeri Surabaya

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Surabaya, Surabaya, Indonesia

Alvia Rachma Wijayanti, Universitas Negeri Surabaya

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Surabaya, Surabaya, Indonesia

Nita Kusumawati, Universitas Negeri Surabaya

Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Surabaya, Surabaya, Indonesia

Hariyono Hariyono, Universitas Airlangga

Postgraduate School, Universitas Airlangga, Surabaya, Indonesia

Puspa Wardhani, Universitas Airlangga

Department of Clinical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia

Similar Articles

<< < 1 2 3 > >> 

You may also start an advanced similarity search for this article.