# Polymicrobial Infection in an Immigrant Female at the United States-Mexico Border

**Authors:** Eshani Kishore, Frederick Gyabaah, Abhizith Deoker

PMC · DOI: 10.7759/cureus.51400 · Cureus · 2023-12-31

## TL;DR

A female immigrant in the U.S. contracted malaria, dengue, and rhinovirus, highlighting the complexity of polymicrobial infections in travelers.

## Contribution

This case report highlights a rare polymicrobial infection involving malaria, dengue, and rhinovirus in an immigrant patient.

## Key findings

- The patient tested positive for dengue fever antibodies and was concurrently infected with rhinovirus.
- Malaria was confirmed via blood smear as Plasmodium vivax, with treatment initiated using chloroquine and later atovaquone-proguanil.
- The patient continued to experience fevers despite treatment until maintenance therapy was administered.

## Abstract

Malaria is a highly infectious disease transmitted through the bite of the Anopheles mosquito carrying the parasite of the Plasmodium genus; it presents with cyclical fevers, myalgias, and headaches. In the United States, the vast majority of malaria cases are reported in people who travel abroad, mainly to Africa. These cases are predominantly linked to Plasmodium falciparum or ovale and can be medically treated with artemisinin, chloroquine, or atovaquone-proguanil. We discuss a case of a 38-year-old female immigrant from Venezuela living at an immigration facility who presented to a hospital located on the United States-Mexico border with a two-day history of watery diarrhea, headache, and subjective fever. She had experienced mosquito bites and likely contracted the illness in Chiapas, Mexico during her trek from Peru to the United States. Her case was unique as she tested positive for dengue fever antibodies acquired from a previous infection and also contracted rhinovirus during her clinical course. Her diagnosis of malaria was confirmed with a peripheral blood smear that revealed ring forms with no gametocytes. This in tandem with her route of travel suggested infection with Plasmodium vivax. She was treated with chloroquine while the malaria culture was pending and continued to spike fevers every 24-36 hours while on medication. Once the culture was confirmed, she was treated with atovaquone-proguanil as maintenance therapy. She was subsequently discharged on primaquine for 14 days to prevent relapse.

## Linked entities

- **Diseases:** malaria (MONDO:0005136), dengue fever (MONDO:0005502)
- **Species:** Anopheles (taxon 7164), Plasmodium vivax (taxon 5855)

## Full-text entities

- **Genes:** ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}
- **Diseases:** hemolysis (MESH:D006461), death (MESH:D003643), hypertension (MESH:D006973), glucose-6-dehydrogenase deficiency (MESH:D005955), abdominal pain (MESH:D015746), headache (MESH:D006261), emesis (MESH:D014839), infectious disease (MESH:D003141), pain (MESH:D010146), parasitic infection (MESH:D010272), Polymicrobial Infection (MESH:D060085), acute pancreatitis (MESH:D010195), loss of kidney function (MESH:D007680), lymphadenopathy (MESH:D008206), infection (MESH:D007239), pancreatic necrosis (MESH:D019283), arthralgias (MESH:D018771), dehydration (MESH:D003681), Hepatitis C. (MESH:D019698), re-infection (MESH:D000084063), leukocytosis (MESH:D007964), fever (MESH:D005334), Malaria (MESH:D008288), hyponatremia (MESH:D007010), electrolyte abnormalities (MESH:D014883), tachycardia (MESH:D013610), lactic acidosis (MESH:D000140), liver damage (MESH:D056486), myalgias (MESH:D063806), weakness (MESH:D018908), dizziness (MESH:D004244), rhinorrhea (MESH:D012818), shortness of breath (MESH:D004417), malnourishment (MESH:D044342), migraine (MESH:D008881), nausea (MESH:D009325), sepsis (MESH:D018805), cough (MESH:D003371), hypokalemia (MESH:D007008), P. vivax malaria (MESH:D016780), diarrhea (MESH:D003967), hypoglycemia (MESH:D007003), chills (MESH:D023341), parasitemia (MESH:D018512), dengue (MESH:D003715), watery diarrhea (MESH:D003969)
- **Chemicals:** lactic acid (MESH:D019344), sodium (MESH:D012964), Primaquine (MESH:D011319), Atovaquone-proguanil (MESH:C109496), acetaminophen (MESH:D000082), ubiquinone (MESH:D014451), atovaquone (MESH:D053626), creatinine (MESH:D003404), biguanide (MESH:D001645), Zofran (MESH:D017294), hematin (MESH:D006427), artemisinin (MESH:C031327), glucose (MESH:D005947), Chloroquine (MESH:D002738), bilirubin (MESH:D001663), proguanil (MESH:D002727)
- **Species:** Clostridioides difficile (species) [taxon 1496], Human immunodeficiency virus 1 (no rank) [taxon 11676], Helicobacter pylori (species) [taxon 210], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Plasmodium vivax (malaria parasite P. vivax, species) [taxon 5855], Plasmodium malariae (species) [taxon 5858], Plasmodium knowlesi (species) [taxon 5850], Enterovirus (genus) [taxon 12059], Homo sapiens (human, species) [taxon 9606], Plasmodium (subgenus) [taxon 418103]

## Full text

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC10826631/full.md

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Source: https://tomesphere.com/paper/PMC10826631