Research Roundup: Forest loss and Ebola, antibody-caused dengue complications, and a mosquito-monitoring platform

In this regular feature on Breakthroughs, we highlight some of the most interesting reads in global health research from the past we. A quick and inexpensive test may make it easier to diagnose and distinguish betweenZika and dengue. Both viruses produce the same NS1 protein, making it is impossible for current NS1 protein-based diagnostic tests to discern between the two. To overcome this problem, scientists developed a set of antibodies produced from immune cells that can distinguish between an NS1 protein produced by the Zika virus and an NS1 protein produced by the dengue virus. In a study, the diagnostic test was able to discern between the two viruses, even when there was a lowNS1 protein count in the body. While further studies are required, this tool could become an essential diagnostic tool in areas of the world where both Zika and dengue are endemic. A series of papers exploring the impact of group B streptococcus (GBS) was published in Clinical Infectious Diseases. GBS is an infection a mother can pass to her fetus that can cause septicemia, meningitis, and even death. The papers argue that there are 410,000 cases of GBS every year with 147,000 associated stillbirths and infant deaths. There is also a major disparity of GBS cases between developed and developing countries: Many at-risk women in developed countries receive prophylactic antibiotics during labor, but those resources are often not available to women in developing countries. Scientists believe the solution to this problem is a GBS-specific vaccine, which could save over 100,000 infant lives.This vaccine may be critically important as scientists believe “immunizing expecting mothers is a potentially groundbreaking approach that could dramatically reduce the number of maternal and child deaths.”There is currently no GBS vaccine available, but there are candidates in development. The US Environmental Protection Agency approved the release of lab-reared “killer mosquitoes” to help reduce the population of disease-carrying mosquitoes in certain American states. A biotechnology start-up based in Kentucky—MosquitoMate—will rear these mosquitoes with a lethal bacterium that impedes reproduction and release the infected males into the wild. When the infected males mate with wild females, the offspring will not be viable due to malformed chromosomes. Over time, disease-carrying mosquito populations will dwindle. Other countries, including Brazil, have tried this method and found it successful, suggesting this could be a solution for countries severely affected by mosquito-borne illnesses. This method is also a “non-chemical way of dealing with mosquitoes,” so offers an alternative to pesticide-based vector control.

In this regular feature on Breakthroughs, we highlight some of the most interesting reads in global health research from the past week. GAVI, the Vaccine Alliance has partnered with the wearable tech company Kushi Baby to bridge the immunization gap for infants in low-income communities. About 1.5 million children die every year from vaccine-preventable illnesses, and one in three do not receive the immunizations they need simply because health professionals "do not know they exist." This partnership will provide children with a wearable necklace technology that remotely tracks and updates their immunization history. The technology allows health professionals to more accurately provide the supplies needed when traveling to rural communities and reach children in need of immunization. This year 1,500 infants in Northern India received the necklaces. The partnership has a goal of increasing distribution to 5,000 necklaces by the end of the year. A new vaccine under development may lower pneumonia incidence and mortality rates by targeting additional strains of the bacteria, according to a new study published in Science Advances. Current pneumonia vaccines only target the most common strains of the illness, but this vaccine candidate targets dozens of additional strains. The candidate may also help maintain the body’s microbiome—a collection of healthy bacteria often killed during the immunization process—by “attack[ing] [bacteria] only if it breaks away from the colony to cause an illness.” The World Health Organization Strategic Advisory Group of Experts on Immunization (SAGE) has recommended a new typhoid fever vaccine that has demonstrated up to 87 percent effectiveness during a clinical study. This typhoid vaccine is the first of its kind licensed for use in children under two years of age. SAGE recommended the vaccine be given to children 6 months old and that catch-up campaigns be administered to immunize children between the ages of 6 months and 15 years of age. With drug-resistant typhoid growing in typhoid-endemic communities, the vaccine will also be a valuable tool in combatting antimicrobial resistance.